(19)
(11)EP 3 502 107 B1

(12)EUROPEAN PATENT SPECIFICATION

(45)Mention of the grant of the patent:
26.01.2022 Bulletin 2022/04

(21)Application number: 18213749.7

(22)Date of filing:  18.12.2018
(51)International Patent Classification (IPC): 
C07D 405/12(2006.01)
H01L 51/50(2006.01)
C07D 307/91(2006.01)
(52)Cooperative Patent Classification (CPC):
H01L 51/0073; H01L 51/5056; C07D 307/91; H01L 51/0072; C07D 409/14; C07D 405/14; H01L 51/0061; C07D 405/12; H01L 51/0052

(54)

1-AMINODIBENZOFURAN-BASED COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

1-AMINODIBENZOFURAN-BASIERTE VERBINDUNG UND ORGANISCHE LICHTEMITTIERENDE VORRICHTUNG DAMIT

COMPOSÉ BASÉ SUR LE 1-AMINODIBENZOFURANE ET DISPOSITIF ÉLECTROLUMINESCENT ORGANIQUE LE COMPRENANT


(84)Designated Contracting States:
AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

(30)Priority: 20.12.2017 KR 20170176483
09.11.2018 KR 20180137609

(43)Date of publication of application:
26.06.2019 Bulletin 2019/26

(73)Proprietor: Samsung Display Co., Ltd.
Yongin-si Gyeonggi-do (KR)

(72)Inventors:
  • Kim, Jongwoo
    Gyeonggi-do (KR)
  • Baek, Jangyeol
    Gyeonggi-do (KR)
  • Jeong, Eunjae
    Gyeonggi-do (KR)
  • Han, Sanghyun
    Gyeonggi-do (KR)
  • Youngkook, Kim
    Gyeonggi-do (KR)
  • Hwang, Seokhwan
    Gyeonggi-do (KR)

(74)Representative: Russell, Tim 
Venner Shipley LLP 200 Aldersgate
London EC1A 4HD
London EC1A 4HD (GB)


(56)References cited: : 
EP-A1- 2 930 168
EP-A1- 3 305 782
WO-A1-2013/039184
WO-A1-2014/088285
WO-A1-2017/012687
WO-A1-2017/016632
WO-A1-2017/142308
WO-A1-2017/148565
WO-A1-2018/091435
WO-A1-2019/054599
WO-A1-2019/124903
CN-A- 107 382 749
US-A1- 2016 028 020
US-A1- 2016 126 469
US-A1- 2016 365 517
US-A1- 2017 213 971
US-A1- 2017 279 050
EP-A1- 3 018 128
EP-A1- 3 321 341
WO-A1-2013/039184
WO-A1-2015/130069
WO-A1-2017/012687
WO-A1-2017/038728
WO-A1-2017/148564
WO-A1-2017/207596
WO-A1-2018/216903
WO-A1-2019/095920
CN-A- 105 349 134
US-A1- 2013 087 776
US-A1- 2016 093 810
US-A1- 2016 181 543
US-A1- 2017 213 970
US-A1- 2017 213 972
  
      
    Note: Within nine months from the publication of the mention of the grant of the European patent, any person may give notice to the European Patent Office of opposition to the European patent granted. Notice of opposition shall be filed in a written reasoned statement. It shall not be deemed to have been filed until the opposition fee has been paid. (Art. 99(1) European Patent Convention).


    Description

    CROSS-REFERENCE TO RELATED APPLICATION


    BACKGROUND


    1. Field



    [0001] One or more embodiments relate to an amine-based compound and an organic light-emitting device comprising the same.

    2. Description of the Related Art



    [0002] Organic light-emitting devices (OLEDs) are self-emission devices that, as compared with related art devices, have wide viewing angles, high contrast ratios, short response times, and excellent brightness, driving voltage, and response speed characteristics, and produce full-color images.

    [0003] OLEDs may comprise a first electrode disposed on a substrate, and may comprise a hole transport region, an emission layer, an electron transport region, and a second electrode sequentially disposed on the first electrode. Holes provided from the first electrode may move toward the emission layer through the hole transport region. Electrons provided from the second electrode may move toward the emission layer through the electron transport region. Carriers, such as holes and electrons, may recombine in the emission layer to produce excitons. These excitons transit from an excited state to a ground state to thereby generate light.

    SUMMARY



    [0004] In a first aspect, the present invention provides an organic light-emitting device according to claim 1.

    BRIEF DESCRIPTION OF THE DRAWINGS



    [0005] 

    FIG. 1 is a schematic cross-sectional view of an embodiment of an organic light-emitting device.

    FIG. 2 is a schematic cross-sectional view of an embodiment of an organic light-emitting device.

    FIG. 3 is a schematic cross-sectional view of an embodiment of an organic light-emitting device.

    FIG. 4 is a schematic cross-sectional view of an embodiment of an organic light-emitting device.


    DETAILED DESCRIPTION



    [0006] Reference will now be made in more detail to embodiments, examples of which are illustrated in the accompanying drawings, wherein like reference numerals refer to like elements throughout. In this regard, the present embodiments may have different forms and should not be construed as being limited to the descriptions set forth herein. Accordingly, the embodiments are merely described below, by referring to the figures, to explain aspects of the present description. As used herein, the term "and/or" includes any and all combinations of one or more of the associated listed items. Expressions such as "at least one of', when preceding a list of elements, modify the entire list of elements and do not modify the individual elements of the list. Further, the use of "may" when describing embodiments of the present invention refers to "one or more embodiments of the present invention."

    [0007] As used herein, the terms "substantially," "about," and similar terms are used as terms of approximation and not as terms of degree, and are intended to account for the inherent deviations in measured or calculated values that would be recognized by those of ordinary skill in the art. Also, any numerical range recited herein is intended to include all sub-ranges of the same numerical precision subsumed within the recited range. For example, a range of "1.0 to 10.0" is intended to include all subranges between (and including) the recited minimum value of 1.0 and the recited maximum value of 10.0, that is, having a minimum value equal to or greater than 1.0 and a maximum value equal to or less than 10.0, such as, for example, 2.4 to 7.6. Any maximum numerical limitation recited herein is intended to include all lower numerical limitations subsumed therein and any minimum numerical limitation recited in this specification is intended to include all higher numerical limitations subsumed therein. Accordingly, Applicant reserves the right to amend this specification, including the claims, to expressly recite any sub-range subsumed within the ranges expressly recited herein.

    [0008] As the inventive concept allows various modifications and includes various embodiments, examplary embodiments will be illustrated in the drawings and described in more detail in the written description. Effects, features, and a method of achieving the inventive concept will become apparent by reference to the examplary embodiments of the inventive concept, together with the accompanying drawings. The inventive concept may, however, be embodied in many different forms and should not be construed as being limited to the examplary embodiments set forth herein.

    [0009] Hereinafter, the inventive concept will be described in more detail by explaining examplary embodiments of the inventive concept with reference to the attached drawings. Like reference numerals in the drawings denote like elements, and thus their description will not be repeated.

    [0010] In the embodiments described in the present specification, an expression used in the singular encompasses the expression of the plural, unless it has a clearly different meaning in the context.

    [0011] In the present specification, it is to be understood that the terms such as "including," "having," and "comprising" are intended to indicate the existence of the features or components disclosed in the specification, and are not intended to preclude the possibility that one or more other features or components may exist or may be added.

    [0012] It will be understood that when a layer, region, or component is referred to as being "on" or "onto" another layer, region, or component, it may be directly or indirectly formed over the other layer, region, or component. That is, for example, intervening layers, regions, or components may be present.

    [0013] Sizes of components in the drawings may be exaggerated for convenience of explanation. In other words, because sizes and thicknesses of components in the drawings are arbitrarily illustrated for convenience of explanation, the following embodiments are not limited thereto.

    [0014] All subject matter not present in the claims is seen as not forming part of the invention and being present as reference information.

    [0015] An exemplary amine-based compound can be represented by one of Formulae 1A and 1B:







    [0016] wherein, in Formulae 1A and 1B, A1 to A5 are independently selected from a C5-C30 carbocyclic group and a C1-C30 heterocyclic group.

    [0017] In some embodiments, in Formulae 1A and 1B, A1 to A5 may each independently be selected from a benzene group, an indene group, a naphthalene group, an anthracene group, a fluorene group, a phenanthrene group, a triphenylene group, a pyrene group, a chrysene group, a naphthacene group, a pyrrole group, an imidazole group, a pyrazole group, a pyridine group, a pyrimidine group, a pyrazine group, a pyridazine group, an indole group, an isoindole group, an indazole group, a quinoline group, an isoquinoline group, a benzoquinoline group, a naphthyridine group, a quinoxaline group, a quinazoline group, a cinnoline group, a carbazole group, a phenanthridine group, an acridine group, a phenanthroline group, a phenazine group, a benzimidazole group, a furan group, a benzofuran group, a thiophene group, a benzothiophene group, a thiazole group, an isothiazole group, a benzothiazole group, an isoxazole group, an oxazole group, a triazole group, an oxadiazole group, a triazine group, a benzoxazole group, a dibenzofuran group, a dibenzothiophene group, a benzocarbazole group, and a dibenzocarbazole group.

    [0018] In some embodiments, in Formulae 1A and 1B, A1 to A5 may each independently be selected from a benzene group, an indene group, a naphthalene group, an anthracene group, a fluorene group, a phenanthrene group, a pyridine group, a pyrimidine group, a pyrazine group, a pyridazine group, and a carbazole group, but embodiments are not limited thereto.

    [0019] In some embodiments, in Formulae 1A and 1B, A1 to A5 may each independently be selected from a benzene group and a naphthalene group, but embodiments are not limited thereto.

    [0020] In some embodiments, in Formulae 1A and 1B, A1 to A5 may each independently be a benzene group, but embodiments are not limited thereto.

    [0021] In Formulae 1A and 1B, X1 may be O, S, N-(L1)a1-(R1)b1, or C(R9)(R10), and X2 may be O, S, or C(R11)(R12).

    [0022] In some embodiments, in Formulae 1A and 1B, X1 may be N-(L1)a1-(R1)b1, and X2 may be O, S, or C(R11)(R12); or X1 may be O, and X2 may be C(R11)(R12), but embodiments are not limited thereto.

    [0023] In Formulae 1A and 1B, L1 to L3 may each independently be selected from a single bond, a substituted or unsubstituted C5-C60 carbocyclic group, and a substituted or unsubstituted C1-C60 heterocyclic group.

    [0024] In some embodiments, in Formulae 1A and 1B, L1 to L3 may each independently be selected from a single bond, a benzene group, a pentalene group, an indene group, a naphthalene group, an azulene group, a heptalene group, an indacene group, an acenaphthalene group, a fluorene group, a spiro-bifluorene group, a benzofluorene group, a phenalene group, a phenanthrene group, an anthracene group, a fluoranthene group, a triphenylene group, a pyrene group, a chrysene group, a naphthacene group, a picene group, a perylene group, a pentaphenylene group, a hexacene group, a pyrrole group, an imidazole group, a pyrazole group, a pyridine group, a pyrazine group, a pyrimidine group, a pyridazine group, an isoindole group, an indole group, an indazole group, a purine group, a quinoline group, an isoquinoline group, a benzoquinoline group, a phthalazine group, a naphthyridine group, a quinoxaline group, a quinazoline group, a cinnoline group, a carbazole group, a phenanthridine group, an acridine group, a phenanthroline group, a phenazine group, a benzimidazole group, a furan group, a benzofuran group, a thiophene group, a benzothiophene group, a thiazole group, an isothiazole group, a benzothiazole group, an iso-oxazole group, an oxazole group, a triazole group, a tetrazole group, an oxadiazole group, a triazine group, a benzoxazole group, a dibenzofuran group, a dibenzothiophene group, a benzocarbazole group, and a dibenzocarbazole group; and

    [0025] a benzene group, a pentalene group, an indene group, a naphthalene group, an azulene group, a heptalene group, an indacene group, an acenaphthalene group, a fluorene group, a spiro-bifluorene group, a benzofluorene group, a phenalene group, a phenanthrene group, an anthracene group, a fluoranthene group, a triphenylene group, a pyrene group, a chrysene group, a naphthacene group, a picene group, a perylene group, a pentaphenylene group, a hexacene group, a pyrrole group, an imidazole group, a pyrazole group, a pyridine group, a pyrazine group, a pyrimidine group, a pyridazine group, an isoindole group, an indole group, an indazole group, a purine group, a quinoline group, an isoquinoline group, a benzoquinoline group, a phthalazine group, a naphthyridine group, a quinoxaline group, a quinazoline group, a cinnoline group, a carbazole group, a phenanthridine group, an acridine group, a phenanthroline group, a phenazine group, a benzimidazole group, a furan group, a benzofuran group, a thiophene group, a benzothiophene group, a thiazole group, an isothiazole group, a benzothiazole group, an iso-oxazole group, an oxazole group, a triazole group, a tetrazole group, an oxadiazole group, a triazine group, a benzoxazole group, a dibenzofuran group, a dibenzothiophene group, a benzocarbazole group, and a dibenzocarbazole group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a C6-C20 aryl group, a C1-C20 heteroaryl group, and - Si(Q31XQ32)(Q33),

    [0026] wherein, Q31 to Q33 may each independently be selected from hydrogen, deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a C1-C60 alkyl group, a C2-C60 alkenyl group, a C2-C60 alkynyl group, a C1-C60 alkoxy group, a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C6-C60 aryl group substituted with a C1-C60 alkyl group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, a biphenyl group, and a terphenyl group.

    [0027] In some embodiments, in Formulae 1A and 1B, L1 to L3 may each independently be selected from a single bond and groups represented by Formulae 3-1 to 3-46:



















    wherein, in Formulae 3-1 to 3-46,

    Y1 may be O, S, C(Z3)(Z4), N(Z5), or Si(Z6)(Z7),

    Z1 to Z7 may each independently be selected from hydrogen, deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclopentenyl group, a cyclohexenyl group, a phenyl group, a biphenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a phenalenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a naphthyridinyl group, a quinoxalinyl group, a quinazolinyl group, a carbazolyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a triazinyl group, a dibenzofuranyl group, a dibenzothiophenyl group, and -Si(Q31)(Q32)(Q33),

    d2 may be an integer from 0 to 2; when d2 is 2, at least two Z1 groups may be identical to or different from each other,

    d3 may be an integer from 0 to 3; when d3 is 2 or greater, at least two Z1 groups (in (Z1)d3) may be identical to or different from each other, and at least two Z2 groups (in (Z2)d3) may be identical to or different from each other,

    d4 may be an integer from 0 to 4; when d4 is 2 or greater, at least two Z1 groups (in (Z1)d4) may be identical to or different from each other, and at least two Z2 groups (in (Z2)d4) may be identical to or different from each other,

    d5 may be an integer from 0 to 5; when d5 is 2 or greater, at least two Z1 groups (in (Z1)d5) may be identical to or different from each other, and at least two Z2 groups (in (Z2)d5) may be identical to or different from each other,

    d6 may be an integer from 0 to 6; when d6 is 2 or greater, at least two Z1 groups (in (Z1)d6) may be identical to or different from each other, and at least two Z2 groups (in (Z2)d6) may be identical to or different from each other,

    d8 may be an integer from 0 to 8; when d8 is 2 or greater, at least two Z1 groups may be identical to or different from each other, and

    and ' each indicate a binding site to an adjacent atom.



    [0028] In some examples, L1 to L3 may each independently be selected from a single bond and groups represented by Formulae 3-1 to 3-7, 3-31 to 3-34, 3-42, and 3-43.

    [0029] In some examples, L1 to L3 may each independently be selected from a single bond and groups represented by Formulae 3-1, 3-2, and 3-34.

    [0030] In some examples, in Formulae 3-1 to 3-46, Z1 to Z7 may each independently be selected from hydrogen, deuterium, -F, a cyano group, a methyl group, an ethyl group, an n-propyl group, a tert-butyl group, a phenyl group, and a naphthyl group, but embodiments are not limited thereto.

    [0031] In some examples, in Formulae 1A and 1B, L1 to L3 may each independently be selected from a single bond and a benzene group; and
    a benzene group substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a C6-C20 aryl group, a C1-C20 heteroaryl group, and -Si(Q31)(Q32)(Q33), but embodiments are not limited thereto.

    [0032] In Formulae 1A and 1B, a1 to a3 are each independently an integer from 1 to 5. a1 indicates the number of L1 groups; when a1 is 2 or greater, at least two L1 groups may be identical to or different from each other. Descriptions for a2 and a3 may be understood by referring to (may be the same as) the descriptions for a1 provided herein.

    [0033] In some examples, in Formulae 1A and 1B, a1 to a3 may each independently be an integer from 1 to 3.

    [0034] For example, a1 to a3 may each be 1, but examplesare not limited thereto.

    [0035] For the avoidance of doubt, when a1 is 2 or more, the moiety -(L1)a1- does not comprise a plurality of adjacent single bonds.

    [0036] In Formulae 1A and 1B, R1 to R8 each independently are selected from hydrogen, deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a substituted or unsubstituted C1-C60 alkyl group, a substituted or unsubstituted C2-C60 alkenyl group, a substituted or unsubstituted C2-C60 alkynyl group, a substituted or unsubstituted C1-C60 alkoxy group, a substituted or unsubstituted C3-C10 cycloalkyl group, a substituted or unsubstituted C1-C10 heterocycloalkyl group, a substituted or unsubstituted C3-C10 cycloalkenyl group, a substituted or unsubstituted C1-C10 heterocycloalkenyl group, a substituted or unsubstituted C6-C60 aryl group, a substituted or unsubstituted C6-C60 aryloxy group, a substituted or unsubstituted C6-C60 arylthio group, a substituted or unsubstituted C1-C60 heteroaryl group, a substituted or unsubstituted C1-C60 heteroaryloxy group, a substituted or unsubstituted monovalent non-aromatic condensed C8 to C60 polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed 8-to 60-membered heteropolycyclic group, -Si(Q1)(Q2)(Q3), -B(Q1)(Q2), and -C(=O)(Q1),

    R9 and R10 and/or R11 and R12 are as described herein in connection with R1 to R8 or are bound to each other to form a substituted or unsubstituted C5-C30 carbocyclic group or a substituted or unsubstituted C1-C30 heterocyclic group,

    wherein, Q1 to Q3 are each independently selected from hydrogen, deuterium, - F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a C1-C60 alkyl group, a C2-C60 alkenyl group, a C2-C60 alkynyl group, a C1-C60 alkoxy group, a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C6-C60 aryl group substituted with a C1-C60 alkyl group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, a biphenyl group, and a terphenyl group.



    [0037] In some examples, in Formulae 1A and 1B, R1 and R2 may each independently be selected from a C6-C60 aryl group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, and a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group; and
    a C6-C60 aryl group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, and a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a C1-C60 alkyl group, a C1-C60 alkoxy group, a C6-C60 aryl group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, -N(Q31)(Q32), and -Si(Q31)(Q32)(Q33).

    [0038] In some examples, in Formulae 1A and 1B, R1 and R2 may each independently be selected from a phenyl group, a pentalenyl group, an indenyl group, a naphthyl group, an azulenyl group, a heptalenyl group, an indacenyl group, an acenaphthyl group, a fluorenyl group, a spiro-fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a phenalenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a naphthacenyl group, a picenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pyrrolyl group, an imidazolyl group, a pyrazolyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, an isoindolyl group, an indolyl group, an indazolyl group, a purinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a phthalazinyl group, a naphthyridinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a carbazolyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a benzoxazolyl group, a benzimidazolyl group, a furanyl group, a benzofuranyl group, a thiophenyl group, a benzothiophenyl group, a thiazolyl group, an isothiazolyl group, a benzothiazolyl group, an isoxazolyl group, an oxazolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a triazinyl group, a benzoxazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, and a dibenzocarbazolyl group; and
    a phenyl group, a pentalenyl group, an indenyl group, a naphthyl group, an azulenyl group, a heptalenyl group, an indacenyl group, an acenaphthyl group, a fluorenyl group, a spiro-fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a phenalenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a naphthacenyl group, a picenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pyrrolyl group, an imidazolyl group, a pyrazolyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, an isoindolyl group, an indolyl group, an indazolyl group, a purinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a phthalazinyl group, a naphthyridinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a carbazolyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a benzoxazolyl group, a benzimidazolyl group, a furanyl group, a benzofuranyl group, a thiophenyl group, a benzothiophenyl group, a thiazolyl group, an isothiazolyl group, a benzothiazolyl group, an isoxazolyl group, an oxazolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a triazinyl group, a benzoxazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, and a dibenzocarbazolyl group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a C6-C20 aryl group, a C1-C20 heteroaryl group, and - Si(Q31)Q32)(Q33), but embodiments are not limited thereto.

    [0039] In some examples, in Formulae 1A and 1B, R1 and R2 may each independently be selected from groups represented by Formulae 5-1 to 5-79, but embodiments are not limited thereto:







































    ,

    wherein, in Formulae 5-1 to 5-79,

    Y31 may be O, S, C(Z33)(Z34), N(Z35), or Si(Z36)(Z37),

    Z31, Z32 and Z35 to Z37 may each independently be selected from hydrogen, deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclopentenyl group, a cyclohexenyl group, a phenyl group, a biphenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a spiro-fluorene-benzofluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenalenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a naphthyridinyl group, a quinoxalinyl group, a quinazolinyl group, a carbazolyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a triazinyl group, a dibenzofuranyl group, a dibenzothiophenyl group, and -Si(Q31)(Q32)(Q33),

    Z33 and Z34 may be as defined for Z31, Z32 and Z35 to Z37, or may be bound to form a substituted or unsubstituted C5-C30 carbocyclic group or a substituted or unsubstituted C1-C30 heterocyclic group,

    e2 may be an integer from 0 to 2; when e2 is 2, at least two Z31 groups may be identical to or different from each other, and at least two Z32 groups may be identical to or different from each other,

    e3 may be an integer from 0 to 3; when e3 is 2 or greater, at least two Z31 groups (in (Z31)e3) may be identical to or different from each other, and at least two Z32 groups (in (Z32)e3) may be identical to or different from each other,

    e4 may be an integer from 0 to 4; when e4 is 2 or greater, at least two Z31 groups (in (Z31)e4) may be identical to or different from each other, and at least two Z32 groups (in (Z32)e4) may be identical to or different from each other,

    e5 may be an integer from 0 to 5; when e5 is 2 or greater, at least two Z31 groups (in (Z31)e5) may be identical to or different from each other, and at least two Z32 groups (in (Z32)e5) may be identical to or different from each other,

    e6 may be an integer from 0 to 6; when e6 is 2 or greater, at least two Z31 groups (in (Z31)e6) may be identical to or different from each other, and at least two Z32 groups (in (Z32)e6) may be identical to or different from each other,

    e7 may be an integer from 0 to 7; when e7 is 2 or greater, at least two Z31 groups may be identical to or different from each other,

    e9 may be an integer from 0 to 9; when e9 is 2 or greater, at least two Z31 groups may be identical to or different from each other, and

    indicates a binding site to an adjacent atom.



    [0040] In some examples, in Formulae 1A and 1B, R1 and R2 may each independently be selected from groups represented by Formulae 5-1 to 5-20, but examplesare not limited thereto.

    [0041] In some examples, in Formulae 1A and 1B, R1 and R2 may each independently be selected from groups represented by Formulae 5-1 to 5-3, 5-13 to 5-16, and 5-20, but examplesare not limited thereto.

    [0042] In some examples, in Formulae 5-1 to 5-79, Z31 to Z37 may each independently be selected from hydrogen, deuterium, -F, a cyano group, a methyl group, an ethyl group, an n-propyl group, a tert-butyl group, a phenyl group, and a naphthyl group, but examplesare not limited thereto.

    [0043] In some examples, in Formulae 1A and 1B, R1 and R2 may each independently be selected from groups represented by Formulae 6-1 to 6-42, but examplesare not limited thereto:

















    ,

    wherein, in Formulae 6-1 to 6-42,

    "Ph" represents a phenyl group, and

    indicates a binding site to an adjacent atom.



    [0044] In Formulae 1A and 1B, R3 to R12 may each independently be selected from hydrogen, deuterium, -F, -Cl, -Br, -I, a C1-C60alkyl group, a C1-C60alkoxy group, a C6-C60 aryl group, a C6-C60 aryloxy group, a C6-C60 arylthio group, a C1-C60heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, -Si(Q1)(Q2)(Q3), and - N(Q1)(Q2);

    a C1-C60 alkyl group and a C1-C60alkoxy group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a cyano group, and a nitro group; and

    a C6-C60 aryl group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, and a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a cyano group, a nitro group, a methyl group, a methoxy group, a phenyl group, a naphthyl group, and a biphenyl group, but examplesare not limited thereto.



    [0045] In some examples, R3 to R12 may each independently be selected from hydrogen, deuterium, -F, -Cl, -Br, -I, a methyl group, an ethyl group, a propyl group, an iso-propyl group, an n-butyl group, an isobutyl group, a sec-butyl group, a ter-butyl group, a pentyl group, an iso-amyl group, a hexyl group, a phenyl group, and a biphenyl group, but examplesare not limited thereto.

    [0046] In some embodiments, R2 is not a group represented by



    [0047] In Formulae 1A and 1B, b1 to b3 and b5 to b8 are each independently an integer from 1 to 10, and b4 is an integer from 1 to 3.
    b1 indicates the number of R1 groups; when b1 is 2 or greater, at least two R1 groups may be identical to or different from each other. Descriptions for b2 to b8 may each be understood by referring to (may be the same as) the descriptions for b1 provided herein.

    [0048] The substituted C5-C60 carbocyclic group, the substituted C1-C60 heterocyclic group, the substituted C1-C60 alkyl group, the substituted C2-C60 alkenyl group, the substituted C2-C60 alkynyl group, the substituted C1-C60 alkoxy group, the substituted C3-C10 cycloalkyl group, the substituted C1-C10 heterocycloalkyl group, the substituted C3-C10 cycloalkenyl group, the substituted C1-C10 heterocycloalkenyl group, the substituted C6-C60 aryl group, the substituted C6-C60 aryloxy group, the substituted C6-C60 arylthio group, the substituted C1-C60 heteroaryl group, the substituted C1-C60 heteroaryloxy group, the substituted monovalent non-aromatic condensed C8 to C60 polycyclic group, and the substituted monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group are each independently substituted by one or more substituents (e.g. 1, 2,3, 4 or 5 substiuents)selected from:

    deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a C1-C60 alkyl group, a C2-C60 alkenyl group, a C2-C60 alkynyl group, and a C1-C60alkoxy group;

    a C1-C60 alkyl group, a C2-C60 alkenyl group, a C2-C60 alkynyl group, and a C1-C60 alkoxy group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, - I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C6-C60 aryloxy group, a C6-C60 arylthio group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, -Si(Q11)(Q12)(Q13), -N(Q11)(Q12), - B(Q11)(Q12), -C(=O)(Q11), -S(=O)2(Q11), and -P(=O)(Q11)(Q12);

    a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C6-C60 aryloxy group, a C6-C60 arylthio group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, a biphenyl group, and a terphenyl group;

    a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C6-C60 aryloxy group, a C6-C60 arylthio group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, a biphenyl group, and a terphenyl group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a C1-C60 alkyl group, a C2-C60 alkenyl group, a C2-C60 alkynyl group, a C1-C60 alkoxy group, a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C6-C60 aryloxy group, a C6-C60 arylthio group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, a biphenyl group, a terphenyl group, -Si(Q21)(Q22)(Q23), - N(Q21)(Q22), -B(Q21(Q22), -C(=O)(Q21), -S(=O)2(Q21), and -P(=O)(Q21)(Q22); and

    -Si(Q31)(Q32)(Q33), -N(Q31)(Q32), -B(Q31)(Q32), -C(=O)(Q31), -S(=O)2(Q31), and - P(=O)(Q31)(Q32),

    wherein Q1 to Q3, Q11 to Q13, Q21 to Q23, and Q31 to Q33 are each independently selected from hydrogen, deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a C1-C60 alkyl group, a C2-C60 alkenyl group, a C2-C60 alkynyl group, a C1-C60 alkoxy group, a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C6-C60 aryl group substituted with a C1-C60 alkyl group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, a biphenyl group, and a terphenyl group.



    [0049] According to an embodiment, the amine-based compound is represented by Formula 1D,:

    wherein, in Formulae and 1D,

    descriptions for substituent groups may be understood by referring to the claims

    b4, b6, and b8 may each independently be an integer from 1 to 3, and

    b3, b5, and b7 may each independently be an integer from 1 to 4.



    [0050] In some examples, the compound represented by one of Formulae 1A and 1B maybe represented by one of Formulae 1A-1 to 1A-4 and 1B-1 to 1B-16, but embodiments are not limited thereto:





















































    wherein, in Formulae 1A-1 to 1A-4 and 1B-1 to 1B-16,

    descriptions for X1, X2, L1 L2, a2, a3, R2 to R8, and b2 may be understood by referring to (may be the same as) the descriptions for those of Formulae 1A and 1B,

    b4, b6, and b8 may each independently be an integer from 1 to 3, and

    b3, b5, and b7 may each independently be an integer from 1 to 4.



    [0051] In some examples, in Formulae 1A-1 to 1A-4 and 1B-1 to 1B-16, X1 may be N-(L1)a1-(R1)b1, and X2 may be O, S, or C(R11)(R12),

    X1 may be O, and X2 may be C(R11)(R12), or

    X1 may be C(R9)(R10), and X2 may be C(R11)(R12), but examplesare not limited thereto.



    [0052] In some examples, in Formulae 1A-1 to 1A-4 and 1B-1 to 1B-16, L1 to L3 may each independently be selected from a single bond and a benzene group; and
    a benzene group substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a C6-C20 aryl group, a C1-C20 heteroaryl group, and -Si(Q31)(Q32)(Q33), but examplesare not limited thereto.

    [0053] In some examples, in Formulae 1A-1 to 1A-4 and 1B-1 to 1B-16, R1 and R2 may each independently be selected from Formulae 6-1 to 6-42, but examplesare not limited thereto.

    [0054] In some examples, in Formulae 1A and 1B, R9 and R10 and/or R11 and R12 may be bound to each other to form a group represented by one of Formulae 7-1 to 7-3:



    [0055] In Formulae 7-1 to 7-3,

    Z51 and Z52 may each independently be selected from hydrogen, deuterium, -F, - Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclopentenyl group, a cyclohexenyl group, a phenyl group, a biphenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a spiro-fluorene-benzofluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenalenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a naphthyridinyl group, a quinoxalinyl group, a quinazolinyl group, a carbazolyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a triazinyl group, a dibenzofuranyl group, a dibenzothiophenyl group, and -Si(Q31)(Q32)(Q33),

    n1 may be an integer from 1 to 8,

    n2 may be an integer from 1 to 10,

    n3 and n4 may each independently be an integer from 1 to 4, and

    indicates a carbon atom bound to R9 and R10 or bound to R11 and R12.



    [0056] In some embodiments, the compound represented by one of Formula 1Dmay be selected from Compounds 42-45, 47-50, 56-59, 61-64, 70-73, 75-78, 84-87, and 89-92. Compounds 1-41, 46, 51-55, 60, 65-69, 74, 79-83, 88, 93to 265, 267 to 284, 207A, 208A and 226A are included only for reference and do not form part of the claimed invention:

















































































































































    [0057] The amine-based compound represented by one of Formulae 1A and 1B has a structure in which nitrogen (N) is bound to a substituent represented by Formula 1A', and thus the compound may have a molecular structure having a large steric hindrance. Accordingly, the amine-based compound may maintain optimum intermolecular density. Further, the amine-based compound may have excellent hole transportability due to the increased interaction of an unshared electron pair of oxygen (O), which is relatively sterically exposed:



    [0058] Furthermore, the amine-based compound comprises an amine group in a molecule. Thus, the amine-based compound may have a suitable energy level, as compared with a compound comprising at least two amine groups. Accordingly, the amine-based compound may have improved hole mobility due to reduced hole transport barrier and hole injection barrier.

    [0059] Therefore, an electronic device, e.g., an organic light-emitting device, employing the amine-based compound may have a low driving voltage, high efficiency, and long lifespan.

    [0060] Methods of synthesizing the amine-based compound represented by one of Formulae 1A and 1B and 1D should be readily apparent to those of ordinary skill in the art by referring to Examples described herein.

    [0061] Accordingly, there is provided an organic light-emitting device comprising a first electrode; a second electrode facing the first electrode; and an organic layer between the first electrode and the second electrode, wherein the organic layer comprises an emission layer and at least one amine-based compound represented by Formula 1D.

    [0062] As used herein, the expression "(for example, the organic layer) comprising at least one amine-based compound" refers to that "(the organic layer) comprising an amine-based compound represented by one of Formulae 1A and 1B, or at least two different amine-based compounds represented by one of Formulae 1A and 1B".

    [0063] For example, the organic layer may contain only Compound 1 as the amine-based compound. In this embodiment, Compound 1 may be contained in the emission layer of the organic light-emitting device. In some embodiments, the organic layer may contain Compounds 1 and 2 as the amine-based compounds. In this embodiment, Compounds 1 and 2 may be present in the same layer (for example, Compounds 1 and 2 may be both present in an emission layer), or in different layers (for example, Compound 1 may be present in an emission layer, and Compound 2 may be present in an electron transport layer).

    [0064] In some embodiments, the first electrode may be an anode, the second electrode may be a cathode, and the organic layer may further comprise a hole transport region between the first electrode and the emission layer and an electron transport region between the emission layer and the second electrode, wherein the hole transport region may comprise a hole injection layer, a hole transport layer, an emission auxiliary layer, an electron blocking layer, or a combination thereof, and the electron transport region may comprise a hole blocking layer, an electron transport layer, an electron injection layer, or a combination thereof.

    [0065] In some embodiments, the hole transport region may comprise the amine-based compound.

    [0066] In some embodiments, the hole transport region may comprise a hole injection layer and a hole transport layer, wherein at least one of the hole injection layer and the hole transport layer may comprise the amine-based compound.

    [0067] In some embodiments, the hole transport region may comprise a hole transport layer, wherein the hole transport layer may comprise the amine-based compound.

    [0068] In some embodiments, examples of the p-dopant may include at least one selected from a quinone derivative, a metal oxide, and a cyano group-containing compound.

    [0069] In some embodiments, the hole transport region may comprise a hole injection layer comprising the p-dopant.

    [0070] The term "organic layer" as used herein refers to a single and/or a plurality of layers between the first electrode and the second electrode in an organic light-emitting device. A material comprised in the "organic layer" is not limited to an organic material.

    Description of FIG. 1



    [0071] FIG. 1 illustrates a schematic cross-sectional view of an organic light-emitting device 10 according to an embodiment. The organic light-emitting device 10 may comprise a first electrode 110, an organic layer 150, and a second electrode 190.

    [0072] Hereinafter, the structure of the organic light-emitting device 10 according to an embodiment and a method of manufacturing an organic light-emitting device 10 according to an embodiment will be described in connection with FIG. 1.

    First electrode 110



    [0073] In FIG. 1, a substrate may be additionally disposed under the first electrode 110 or above the second electrode 190. The substrate may be a glass substrate or a plastic substrate, each having excellent mechanical strength, thermal stability, transparency, surface smoothness, ease of handling, and water resistance.

    [0074] The first electrode 110 may be formed by vacuum-depositing or sputtering, onto the substrate, a material for forming the first electrode 110. When the first electrode 110 is an anode, the material for the first electrode 110 may be selected from materials with a high work function to facilitate hole injection.

    [0075] The first electrode 110 may be a reflective electrode, a semi-transmissive electrode, or a transmissive electrode. When the first electrode 110 is a transmissive electrode, as a material for forming the first electrode 110, indium tin oxide (ITO), indium zinc oxide (IZO), tin oxide (SnO2), zinc oxide (ZnO), and any combination thereof may be utilized, but embodiments are not limited thereto. When the first electrode 110 is a semi-transmissive electrode or a reflective electrode, as a material for forming the first electrode 110, magnesium (Mg), aluminum (Al), aluminum-lithium (Al-Li), calcium (Ca), magnesium-indium (Mg-In), magnesium-silver (Mg-Ag), and any combination thereof may be utilized, but embodiments are not limited thereto.

    [0076] The first electrode 110 may have a single-layered structure, or a multi-layered structure comprising two or more layers. In some embodiments, the first electrode 110 may have a triple-layered structure of ITO/Ag/ITO, but embodiments are not limited thereto.

    Organic layer 150



    [0077] The organic layer 150 may be on the first electrode 110. The organic layer 150 may comprise an emission layer.

    [0078] The organic layer 150 may further comprise a hole transport region between the first electrode 110 and the emission layer and an electron transport region between the emission layer and the second electrode 190.

    Hole transport region in organic layer 150



    [0079] The hole transport region may have i) a single-layered structure including a single layer including a single material, ii) a single-layered structure including a single layer comprising a plurality of different materials, or iii) a multi-layered structure having a plurality of layers, each comprising a single or a plurality of different materials.

    [0080] The hole transport region may comprise at least one selected from a hole injection layer, a hole transport layer, an emission auxiliary layer, and an electron blocking layer.

    [0081] For example, the hole transport region may have a single-layered structure including a single layer comprising a plurality of different materials or a multi-layered structure, e.g., a structure of hole injection layer/hole transport layer, a structure of hole injection layer/hole transport layer/emission auxiliary layer, a structure of hole injection layer/emission auxiliary layer, a structure of hole transport layer/emission auxiliary layer, or a structure of hole injection layer/hole transport layer/electron blocking layer, wherein layers of each structure are sequentially stacked on the first electrode 110 in each stated order, but embodiments are not limited thereto.

    [0082] The hole transport region may comprise the amine-based compound represented by one of Formulae 1A and 1B.

    [0083] The hole transport region may comprise, in addition to the amine-based compound represented by one of Formulae 1A and 1B, at least one selected from m-MTDATA, TDATA, 2-TNATA, NPB (NPD), β-NPB, TPD, spiro-TPD, spiro-NPB, methylated-NPB, TAPC, HMTPD, 4,4',4"-tris(N-carbazolyl)triphenylamine (TCTA), polyaniline/dodecylbenzenesulfonic acid (PANI/DBSA), poly(3,4-ethylenedioxythiophene)/poly(4-styrenesulfonate) (PEDOT/PSS), polyaniline/camphor sulfonic acid (PANI/CSA), (polyaniline)/poly(4-styrenesulfonate) (PANI/PSS), a compound represented by Formula 201, and a compound represented by Formula 202:











    In Formulae 201 and 202,

    L201 to L204 may each independently be selected from a substituted or unsubstituted C3-C10 cycloalkylene group, a substituted or unsubstituted C1-C10 heterocycloalkylene group, a substituted or unsubstituted C3-C10 cycloalkenylene group, a substituted or unsubstituted C1-C10 heterocycloalkenylene group, a substituted or unsubstituted C6-C60 arylene group, a substituted or unsubstituted C1-C60 heteroarylene group, a substituted or unsubstituted divalent non-aromatic condensed C8 to C60 polycyclic group, and a substituted or unsubstituted divalent non-aromatic condensed 8-to 60-membered heteropolycyclic group,

    L205 may be selected from -O-', -S-', -N(Q201)-', a substituted or unsubstituted C1-C20 alkylene group, a substituted or unsubstituted C2-C20 alkenylene group, a substituted or unsubstituted C3-C10 cycloalkylene group, a substituted or unsubstituted C1-C10 heterocycloalkylene group, a substituted or unsubstituted C3-C10 cycloalkenylene group, a substituted or unsubstituted C1-C10 heterocycloalkenylene group, a substituted or unsubstituted C6-C60 arylene group, a substituted or unsubstituted C1-C60 heteroarylene group, a substituted or unsubstituted divalent non-aromatic condensed C8 to C60 polycyclic group, and a substituted or unsubstituted divalent non-aromatic condensed 8- to 60-membered heteropolycyclic group,

    xa1 to xa4 may each independently be an integer from 0 to 3,

    xa5 may be an integer from 1 to 10, and

    R201 to R204 and Q201 may each independently be selected from a substituted or unsubstituted C3-C10 cycloalkyl group, a substituted or unsubstituted C1-C10 heterocycloalkyl group, a substituted or unsubstituted C3-C10 cycloalkenyl group, a substituted or unsubstituted C1-C10 heterocycloalkenyl group, a substituted or unsubstituted C6-C60 aryl group, a substituted or unsubstituted C6-C60 aryloxy group, a substituted or unsubstituted C6-C60 arylthio group, a substituted or unsubstituted C1-C60 heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed C8 to C60 polycyclic group, and a substituted or unsubstituted monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group.



    [0084] In some embodiments, in Formula 202, R201 and R202 may optionally be linked to each other via a single bond, a dimethyl-methylene group, or a diphenyl-methylene group, and R203 and R204 may optionally be linked to each other via a single bond, a dimethyl-methylene group, or a diphenyl-methylene group.

    [0085] In one embodiment, in Formulae 201 and 202, L201 to L205 may each independently be selected from

    a phenylene group, a pentalenylene group, an indenylene group, a naphthylene group, an azulenylene group, a heptalenylene group, an indacenylene group, an acenaphthylene group, a fluorenylene group, a spiro-bifluorenylene group, a benzofluorenylene group, a dibenzofluorenylene group, a phenalenylene group, a phenanthrenylene group, an anthracenylene group, a fluoranthenylene group, a triphenylenylene group, a pyrenylene group, a chrysenylene group, a naphthacenylene group, a picenylene group, a perylenylene group, a pentaphenylene group, a hexacenylene group, a pentacenylene group, a rubicenylene group, a coronenylene group, an ovalenylene group, a thiophenylene group, a furanylene group, a carbazolylene group, an indolylene group, an isoindolylene group, a benzofuranylene group, a benzothiophenylene group, a dibenzofuranylene group, a dibenzothiophenylene group, a benzocarbazolylene group, a dibenzocarbazolylene group, a dibenzosilolylene group, and a pyridinylene group; and

    a phenylene group, a pentalenylene group, an indenylene group, a naphthylene group, an azulenylene group, a heptalenylene group, an indacenylene group, an acenaphthylene group, a fluorenylene group, a spiro-bifluorenylene group, a benzofluorenylene group, a dibenzofluorenylene group, a phenalenylene group, a phenanthrenylene group, an anthracenylene group, a fluoranthenylene group, a triphenylenylene group, a pyrenylene group, a chrysenylene group, a naphthacenylene group, a picenylene group, a perylenylene group, a pentaphenylene group, a hexacenylene group, a pentacenylene group, a rubicenylene group, a coronenylene group, an ovalenylene group, a thiophenylene group, a furanylene group, a carbazolylene group, an indolylene group, an isoindolylene group, a benzofuranylene group, a benzothiophenylene group, a dibenzofuranylene group, a dibenzothiophenylene group, a benzocarbazolylene group, a dibenzocarbazolylene group, a dibenzosilolylene group, and a pyridinylene group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclopentenyl group, a cyclohexenyl group, a phenyl group, a biphenyl group, a terphenyl group, a phenyl group substituted with a C1-C10 alkyl group, a phenyl group substituted with -F, a pentalenyl group, an indenyl group, a naphthyl group, an azulenyl group, a heptalenyl group, an indacenyl group, an acenaphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenalenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a naphthacenyl group, a picenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a rubicenyl group, a coronenyl group, an ovalenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, a pyridinyl group, -Si(Q31)(Q32)(Q33), and -N(Q31)(Q32),

    wherein Q31 to Q33 may each independently be selected from a C1-C10 alkyl group, a C1-C10 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, and a naphthyl group.



    [0086] In one or more embodiments, xa1 to xa4 may each independently be 0, 1, or 2.

    [0087] In one or more embodiments, xa5 may be 1, 2, 3, or 4.

    [0088] In one or more embodiments, R201 to R204 and Q201 may each independently be selected from a phenyl group, a biphenyl group, a terphenyl group, a pentalenyl group, an indenyl group, a naphthyl group, an azulenyl group, a heptalenyl group, an indacenyl group, an acenaphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenalenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a naphthacenyl group, a picenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a rubicenyl group, a coronenyl group, an ovalenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, and a pyridinyl group; and

    a phenyl group, a biphenyl group, a terphenyl group, a pentalenyl group, an indenyl group, a naphthyl group, an azulenyl group, a heptalenyl group, an indacenyl group, an acenaphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenalenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a naphthacenyl group, a picenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a rubicenyl group, a coronenyl group, an ovalenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, and a pyridinyl group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclopentenyl group, a cyclohexenyl group, a phenyl group, a biphenyl group, a terphenyl group, a phenyl group substituted with a C1-C10 alkyl group, a phenyl group substituted with -F, a pentalenyl group, an indenyl group, a naphthyl group, an azulenyl group, a heptalenyl group, an indacenyl group, an acenaphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenalenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a naphthacenyl group, a picenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a rubicenyl group, a coronenyl group, an ovalenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, a pyridinyl group, -Si(Q31)(Q32)(Q33), and -N(Q31)(Q32),

    wherein descriptions for Q31 to Q33 may be understood by referring to (may be the same as) the descriptions for those provided herein.



    [0089] In one or more embodiments, in Formula 201, at least one of R201 to R203 may each independently be selected from

    a fluorenyl group, a spiro-bifluorenyl group, a carbazolyl group, a dibenzofuranyl group, and a dibenzothiophenyl group; and

    a fluorenyl group, a spiro-bifluorenyl group, a carbazolyl group, a dibenzofuranyl group, and a dibenzothiophenyl group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclopentenyl group, a cyclohexenyl group, a phenyl group, a biphenyl group, a terphenyl group, a phenyl group substituted with a C1-C10 alkyl group, a phenyl group substituted with -F, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a carbazolyl group, a dibenzofuranyl group, and a dibenzothiophenyl group, but embodiments are not limited thereto.



    [0090] In one or more embodiments, in Formula 202, i) R201 may be linked to R202 via a single bond, and/or ii) R203 may be linked to R204 via a single bond.

    [0091] In one or more embodiments, in Formula 202, at least one of R201 to R204 may be selected from

    a carbazolyl group; and

    a carbazolyl group substituted with at least one selected from deuterium, -F, - Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclopentenyl group, a cyclohexenyl group, a phenyl group, a biphenyl group, a terphenyl group, a phenyl group substituted with a C1-C10 alkyl group, a phenyl group substituted with -F, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a carbazolyl group, a dibenzofuranyl group, and a dibenzothiophenyl group, but embodiments are not limited thereto.



    [0092] The compound represented by Formula 201 may be represented by Formula 201A:



    [0093] In some embodiments, the compound represented by Formula 201 may be represented by Formula 201A(1), but embodiments are not limited thereto:



    [0094] In some embodiments, the compound represented by Formula 201 may be represented by Formula 201A-1, but embodiments are not limited thereto:



    [0095] The compound represented by Formula 202 may be represented by Formula 202A:





    [0096] In some embodiments, the compound represented by Formula 202 may be represented by Formula 202A-1:



    [0097] In Formulae 201A, 201A(1), 201A-1, 202A, and 202A-1,

    descriptions for L201 to L203, xa1 to xa3, xa5, and R202 to R204 may each be understood by referring to (may be the same as) the descriptions for those provided herein,

    descriptions for R211 and R212 may each be be understood by referring to (may be the same as) the descriptions for those for R203 provided herein, and

    R213 to R217 may each independently be selected from hydrogen, deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclopentenyl group, a cyclohexenyl group, a phenyl group, a biphenyl group, a terphenyl group, a phenyl group substituted with a C1-C10 alkyl group, a phenyl group substituted with -F, a pentalenyl group, an indenyl group, a naphthyl group, an azulenyl group, a heptalenyl group, an indacenyl group, an acenaphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenalenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a naphthacenyl group, a picenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a rubicenyl group, a coronenyl group, an ovalenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, and a pyridinyl group.



    [0098] The hole transport region may comprise at least one compound selected from Compounds HT1 to HT39, but embodiments are not limited thereto:



























    [0099] The thickness of the hole transport region may be in a range of 100 (Angstroms) Å to 10,000 Å, and in some embodiments, 100 Å to 1,000 Å. When the hole transport region comprises at least one of a hole injection layer and a hole transport layer, a thickness of the hole injection layer may be in a range of 100 Å to 9,000 Å, for example, 100 Å to 1,000 Å, and a thickness of the hole transport layer may be in a range of 50 Å to 2,000 Å, for example, 100 Å to 1,500 Å. When the thicknesses of the hole transport region, the hole injection layer, and the hole transport layer are within the above-described ranges, excellent hole transport characteristics may be obtained without a substantial increase in driving voltage.

    [0100] The emission auxiliary layer may increase light emission efficiency by compensating for an optical resonance distance according to the wavelength of light emitted by an emission layer. The electron blocking layer may reduce or eliminate the flow of electrons from an electron transport region. The emission auxiliary layer and the electron blocking layer may comprise the aforementioned materials.

    p-dopant



    [0101] The hole transport region may comprise a charge generating material as well as the aforementioned materials, to improve conductive properties of the hole transport region. The charge generating material may be substantially homogeneously or non-homogeneously dispersed in the hole transport region.

    [0102] The charge generating material may comprise, for example, a p-dopant.

    [0103] In some embodiments, the LUMO energy level of the p-dopant may be about - 3.5 eV or less.

    [0104] Examples of the p-dopant may include at least one selected from a quinone derivative, a metal oxide, and a cyano group-containing compound, but embodiments are not limited thereto.

    [0105] In some embodiments, examples of the p-dopant may include:

    a quinone derivative, such as tetracyanoquinodimethane (TCNQ) or 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane (F4-TCNQ);

    a metal oxide, such as tungsten oxide or molybdenum oxide;

    1,4,5,8,9,12-hexaazatriphenylene-hexacarbonitrile (HAT-CN); and

    a compound represented by Formula 221, but embodiments are not limited thereto:







    [0106] In Formula 221,
    R221 to R223 may each independently be selected from a substituted or unsubstituted C3-C10 cycloalkyl group, a substituted or unsubstituted C1-C10 heterocycloalkyl group, a substituted or unsubstituted C3-C10 cycloalkenyl group, a substituted or unsubstituted C1-C10 heterocycloalkenyl group, a substituted or unsubstituted C6-C60 aryl group, a substituted or unsubstituted C1-C60 heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed C8 to C60 polycyclic group, and a substituted or unsubstituted monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, provided that at least one of R221 to R223 may include at least one substituent selected from a cyano group, -F, -Cl, -Br, -I, a C1-C20 alkyl group substituted with -F, a C1-C20 alkyl group substituted with -Cl, a C1-C20 alkyl group substituted with -Br, and a C1-C20 alkyl group substituted with -I.

    Emission layer in organic layer 150



    [0107] When the organic light-emitting device 10 is a full color organic light-emitting device, the emission layer may be patterned into a red emission layer, a green emission layer, or a blue emission layer, according to a sub-pixel. In some embodiments, the emission layer may have a stacked structure. The stacked structure may comprise two or more layers selected from a red emission layer, a green emission layer, and a blue emission layer. The two or more layers may be in direct contact with each other. Alternatively, the two or more layers may be separated from each other. In one or more embodiments, the emission layer may comprise two or more materials. The two or more materials may comprise a red light-emitting material, a green light-emitting material, or a blue light-emitting material. The two or more materials may be mixed with each other in a single layer. The two or more materials mixed with each other in the single layer may emit white light.

    [0108] The emission layer may comprise a host and a dopant. The dopant may comprise at least one of a fluorescent dopant and a phosphorescent dopant.

    [0109] The amount of the dopant in the emission layer may be, in general, in a range of about 0.01 parts to about 15 parts by weight based on 100 parts by weight of the host, but embodiments are not limited thereto.

    [0110] The thickness of the emission layer may be in a range of about 100 Å to about 1,000 Å, and in some embodiments, about 200 Å to about 600 Å. When the thickness of the emission layer is within the above-described ranges, improved luminescence characteristics may be obtained without a substantial increase in driving voltage.

    Host in emission layer



    [0111] The host may include a compound represented by Formula 301:

            Formula 301     [Ar301]xb11-[(L301)xb1-R301]xb21

    wherein, in Formula 301,

    Ar301 may be a substituted or unsubstituted C5-C60 carbocyclic group or a substituted or unsubstituted C1-C60 heterocyclic group,

    xb11 may be 1, 2, or 3,

    L301 may be selected from a substituted or unsubstituted C3-C10 cycloalkylene group, a substituted or unsubstituted C1-C10 heterocycloalkylene group, a substituted or unsubstituted C3-C10 cycloalkenylene group, a substituted or unsubstituted C1-C10 heterocycloalkenylene group, a substituted or unsubstituted C6-C60 arylene group, a substituted or unsubstituted C1-C60 heteroarylene group, a substituted or unsubstituted divalent non-aromatic condensed C8 to C60 polycyclic group, and a substituted or unsubstituted divalent non-aromatic condensed 8- to 60-membered heteropolycyclic group,

    xb1 may be an integer from 0 to 5,

    R301 may be selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a substituted or unsubstituted C1-C60 alkyl group, a substituted or unsubstituted C2-C60 alkenyl group, a substituted or unsubstituted C2-C60 alkynyl group, a substituted or unsubstituted C1-C60 alkoxy group, a substituted or unsubstituted C3-C10 cycloalkyl group, a substituted or unsubstituted C1-C10 heterocycloalkyl group, a substituted or unsubstituted C3-C10 cycloalkenyl group, a substituted or unsubstituted C1-C10 heterocycloalkenyl group, a substituted or unsubstituted C6-C60 aryl group, a substituted or unsubstituted C6-C60 aryloxy group, a substituted or unsubstituted C6-C60 arylthio group, a substituted or unsubstituted C1-C60 heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed C8 to C60 polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, -Si(Q301)(Q302)(Q303), -N(Q301)(Q302), -B(Q301)(Q302), -C(=O)(Q301), - S(=O)2(Q301), and -P(=O)(Q301)(Q302),

    xb2i may be an integer from 1 to 5,

    wherein Q301 to Q303 may each independently be selected from a C1-C10 alkyl group, a C1-C10 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, and a naphthyl group, but embodiments are not limited thereto.



    [0112] In some embodiments, Ar301 in Formula 301 may be selected from

    a naphthalene group, a fluorene group, a spiro-bifluorene group, a benzofluorene group, a dibenzofluorene group, a phenalene group, a phenanthrene group, an anthracene group, a fluoranthene group, a triphenylene group, a pyrene group, a chrysene group, a naphthacene group, a picene group, a perylene group, a pentaphene group, an indenoanthracene group, a dibenzofuran group, and a dibenzothiophene group; and

    a naphthalene group, a fluorene group, a spiro-bifluorene group, a benzofluorene group, a dibenzofluorene group, a phenalene group, a phenanthrene group, an anthracene group, a fluoranthene group, a triphenylene group, a pyrene group, a chrysene group, a naphthacene group, a picene group, a perylene group, a pentaphene group, an indenoanthracene group, a dibenzofuran group, and a dibenzothiophene group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, -Si(Q31)(Q32)(Q33), -N(Q31)(Q32), -B(Q31)(Q32), - C(=O)(Q31), -S(=O)2(Q31), and -P(=O)(Q31)(Q32),

    wherein Q31 to Q33 may each independently be selected from a C1-C10 alkyl group, a C1-C10 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, and a naphthyl group, but embodiments are not limited thereto.



    [0113] When xb11 in Formula 301 is 2 or greater, at least two Ar301 groups may be linked via a single bond.

    [0114] In one or more embodiments, the compound represented by Formula 301 may be represented by Formula 301-1 or 301-2:





    [0115] In Formulae 301-1 to 301-2,

    A301 to A304 may each independently be selected from a benzene group, a naphthalene group, a phenanthrene group, a fluoranthene group, a triphenylene group, a pyrene group, a chrysene group, a pyridine group, a pyrimidine group, an indene group, a fluorene group, a spiro-bifluorene group, a benzofluorene group, a dibenzofluorene group, an indole group, a carbazole group, a benzocarbazole group, a dibenzocarbazole group, a furan group, a benzofuran group, a dibenzofuran group, a naphthofuran group, a benzonaphthofuran group, a dinaphthofuran group, a thiophene group, a benzothiophene group, a dibenzothiophene group, a naphthothiophene group, a benzonapthothiophene group, and a dinaphthothiophene group,

    X301 may be O, S, or N-[(L304)xb4-R304],

    R311 to R314 may each independently be selected from hydrogen, deuterium, -F, - Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, -Si(Q31)(Q32)(Q33), -N(Q31)(Q32), - B(Q31)(Q32), -C(=O)(Q31), -S(=O)2(Q31), and -P(=O)(Q31)(Q32),

    xb22 and xb23 may each independently be 0, 1, or 2,

    descriptions for L301, xbi, R301, and Q31 to Q33 may each independently be understood by referring to (may be the same as) the descriptions for those provided herein,

    descriptions for L302 to L304 may be understood by referring to (may be the same as) those for L301 provided herein,

    descriptions for xb2 to xb4 may each independently be understood by referring to (may be the same as) those for xb1 provided herein, and

    descriptions for R302 to R304 may each independently be understood by referring to (may be the same as) those for R301 provided herein.



    [0116] In some embodiments, in Formulae 301, 301-1, and 301-2, L301 to L304 may each independently be selected from

    a phenylene group, a naphthylene group, a fluorenylene group, a spiro-bifluorenylene group, a benzofluorenylene group, a dibenzofluorenylene group, a phenanthrenylene group, an anthracenylene group, a fluoranthenylene group, a triphenylenylene group, a pyrenylene group, a chrysenylene group, a perylenylene group, a pentaphenylene group, a hexacenylene group, a pentacenylene group, a thiophenylene group, a furanylene group, a carbazolylene group, an indolylene group, an isoindolylene group, a benzofuranylene group, a benzothiophenylene group, a dibenzofuranylene group, a dibenzothiophenylene group, a benzocarbazolylene group, a dibenzocarbazolylene group, a dibenzosilolylene group, a pyridinylene group, an imidazolylene group, a pyrazolylene group, a thiazolylene group, an isothiazolylene group, an oxazolylene group, an isoxazolylene group, a thiadiazolylene group, an oxadiazolylene group, a pyrazinylene group, a pyrimidinylene group, a pyridazinylene group, a triazinylene group, a quinolinylene group, an isoquinolinylene group, a benzoquinolinylene group, a phthalazinylene group, a naphthyridinylene group, a quinoxalinylene group, a quinazolinylene group, a cinnolinylene group, a phenanthridinylene group, an acridinylene group, a phenanthrolinylene group, a phenazinylene group, a benzimidazolylene group, an isobenzothiazolylene group, a benzoxazolylene group, an isobenzoxazolylene group, a triazolylene group, a tetrazolylene group, an imidazopyridinylene group, an imidazopyrimidinylene group, and an azacarbazolylene group; and

    a phenylene group, a naphthylene group, a fluorenylene group, a spiro-bifluorenylene group, a benzofluorenylene group, a dibenzofluorenylene group, a phenanthrenylene group, an anthracenylene group, a fluoranthenylene group, a triphenylenylene group, a pyrenylene group, a chrysenylene group, a perylenylene group, a pentaphenylene group, a hexacenylene group, a pentacenylene group, a thiophenylene group, a furanylene group, a carbazolylene group, an indolylene group, an isoindolylene group, a benzofuranylene group, a benzothiophenylene group, a dibenzofuranylene group, a dibenzothiophenylene group, a benzocarbazolylene group, a dibenzocarbazolylene group, a dibenzosilolylene group, a pyridinylene group, an imidazolylene group, a pyrazolylene group, a thiazolylene group, an isothiazolylene group, an oxazolylene group, an isoxazolylene group, a thiadiazolylene group, an oxadiazolylene group, a pyrazinylene group, a pyrimidinylene group, a pyridazinylene group, a triazinylene group, a quinolinylene group, an isoquinolinylene group, a benzoquinolinylene group, a phthalazinylene group, a naphthyridinylene group, a quinoxalinylene group, a quinazolinylene group, a cinnolinylene group, a phenanthridinylene group, an acridinylene group, a phenanthrolinylene group, a phenazinylene group, a benzimidazolylene group, an isobenzothiazolylene group, a benzoxazolylene group, an isobenzoxazolylene group, a triazolylene group, a tetrazolylene group, an imidazopyridinylene group, an imidazopyrimidinylene group, and an azacarbazolylene group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, a pyridinyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a thiadiazolyl group, an oxadiazolyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a phthalazinyl group, a naphthyridinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a benzimidazolyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an imidazopyridinyl group, an imidazopyrimidinyl group, an azacarbazolyl group, -Si(Q31)(Q32)(Q33), - N(Q31)(Q32), -B(Q31)(Q32), -C(=O)(Q31), -S(=O)2(Q31), and -P(=O)(Q31)(Q32),

    wherein descriptions for Q31 to Q33 may each independently be understood by referring to (may be the same as) the descriptions for those provided herein.



    [0117] In some embodiments, in Formulae 301, 301-1, and 301-2, R301 to R304 may each independently be selected from

    a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, a pyridinyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a thiadiazolyl group, an oxadiazolyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a phthalazinyl group, a naphthyridinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a benzimidazolyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an imidazopyridinyl group, an imidazopyrimidinyl group, and an azacarbazolyl group; and

    a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, a pyridinyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a thiadiazolyl group, an oxadiazolyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a phthalazinyl group, a naphthyridinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a benzimidazolyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an imidazopyridinyl group, an imidazopyrimidinyl group, and an azacarbazolyl group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, a pyridinyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a thiadiazolyl group, an oxadiazolyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a phthalazinyl group, a naphthyridinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a benzimidazolyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an imidazopyridinyl group, an imidazopyrimidinyl group, an azacarbazolyl group, -Si(Q31)(Q32)(Q33), -N(Q31)(Q32), -B(Q31)(Q32), -C(=O)(Q31), - S(=O)2(Q31), and -P(=O)(Q31)(Q32),

    wherein descriptions for Q31 to Q33 may each independently be understood by referring to (may be the same as) the descriptions for those provided herein.



    [0118] In some embodiments, the host may include an alkaline earth metal complex. For example, the host may include a beryllium (Be) complex, e.g., Compound H55, a magnesium (Mg) complex, or a zinc (Zn) complex.

    [0119] The host may include at least one selected from 9,10-di(2-naphthyl)anthracene (ADN), 2-methyl-9,10-bis(naphthalen-2-yl)anthracene (MADN), 9,10-di-(2-naphthyl)-2-t-butyl-anthracene (TBADN), 4,4'-bis(N-carbazolyl)-1,1'-biphenyl (CBP), 1,3-di-9-carbazolylbenzene (mCP), 1,3,5-tri(carbazol-9-yl)benzene (TCP), and Compounds Hi to H55, but embodiments are not limited thereto:






























    Phosphorescent dopant comprised in emission layer of organic layer 150



    [0120] Examples of the phosphorescent dopant may include an organic metal complex represented by Formula 401:

            Formula 401     M(L401)xc1(L402)xc2







    [0121] In Formulae 401 and 402,

    M may be selected from iridium (Ir), platinum (Pt), palladium (Pd), osmium (Os), titanium (Ti), zirconium (Zr), hafnium (Hf), europium (Eu), terbium (Tb), rhodium (Rh), and thulium (Tm),

    L401 may be selected from ligands represented by Formula 402, xc1 may be an integer selected from 1, 2, and 3; when xc1 is two or greater, at least two L401 groups may be identical to or different from each other,

    L402 may be an organic ligand, xc2 may be an integer from 0 to 4; when xc2 is 2 or greater, at least two L402 groups may be identical to or different from each other,

    X401 to X404 may each independently be nitrogen or carbon,

    X401 and X403 may be linked via a single bond or a double bond, X402 and X404 may be linked via a single bond or a double bond,

    A401 and A402 may each independently be a C5-C60 carbocyclic group or a C1-C60 heterocyclic group,

    X405 may be a single bond, -O-', -S-∗', -C(=O)-', -N(Q411)-', -C(Q411)(Q412)-', -C(Q411)=C(Q412)-', -C(Q411)=', or =C=', wherein Q411 and Q412 may each independently be hydrogen, deuterium, a C1-C20 alkyl group, a C1-C20 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, or a naphthyl group,

    X406 may be a single bond, O, or S,

    R401 and R402 may each independently be selected from hydrogen, deuterium, - F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a substituted or unsubstituted C1-C20 alkyl group, a substituted or unsubstituted C1-C20 alkoxy group, a substituted or unsubstituted C3-C10 cycloalkyl group, a substituted or unsubstituted C1-C10 heterocycloalkyl group, a substituted or unsubstituted C3-C10 cycloalkenyl group, a substituted or unsubstituted C1-C10 heterocycloalkenyl group, a substituted or unsubstituted C6-C60 aryl group, a substituted or unsubstituted C6-C60 aryloxy group, a substituted or unsubstituted C6-C60 arylthio group, a substituted or unsubstituted C1-C60 heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed C8 to C60 polycyclic group and a substituted or unsubstituted monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, -Si(Q401)(Q402)(Q403), -N(Q401)(Q402), -B(Q401)(Q402), -C(=O)(Q401), - S(=O)2(Q401), and -P(=O)(Q401)(Q402), wherein Q401 to Q403 may each independently be selected from a C1-C10 alkyl group, a C1-C10 alkoxy group, a C6-C20 aryl group, and a C1-C20 heteroaryl group,

    xc11 and xc12 may each independently be an integer from 0 to 10, and

    and ' in Formula 402 each indicate a binding site to M in Formula 401.

    In one embodiment, A401 and A402 in Formula 402 may each independently be selected from a benzene group, a naphthalene group, a fluorene group, a spiro-bifluorene group, an indene group, a pyrrole group, a thiophene group, a furan group, an imidazole group, a pyrazole group, a thiazole group, an isothiazole group, an oxazole group, an isoxazole group, a pyridine group, a pyrazine group, a pyrimidine group, a pyridazine group, a quinoline group, an isoquinoline group, a benzoquinoline group, a quinoxaline group, a quinazoline group, a carbazole group, a benzimidazole group, a benzofuran group, a benzothiophene group, an isobenzothiophene group, a benzoxazole group, an isobenzoxazole group, a triazole group, a tetrazole group, an oxadiazole group, a triazine group, a dibenzofuran group, and a dibenzothiophene group.



    [0122] In one or more embodiments, in Formula 402, i) X401 may be nitrogen, and X402 may be carbon, or ii) X401 and X402 may each be nitrogen.

    [0123] In one or more embodiments, in Formula 402, R401 and R402 may each independently be selected from

    hydrogen, deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, and a C1-C20 alkoxy group;

    a C1-C20 alkyl group and a C1-C20 alkoxy group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a phenyl group, a naphthyl group, a cyclopentyl group, a cyclohexyl group, an adamantyl group, a norbornanyl group, and a norbornenyl group;

    a cyclopentyl group, a cyclohexyl group, an adamantyl group, a norbornanyl group, a norbornenyl group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a carbazolyl group, a dibenzofuranyl group, and a dibenzothiophenyl group;

    a cyclopentyl group, a cyclohexyl group, an adamantyl group, a norbornanyl group, a norbornenyl group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a carbazolyl group, a dibenzofuranyl group, and a dibenzothiophenyl group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a cyclopentyl group, a cyclohexyl group, an adamantanyl group, a norbornanyl group, a norbornenyl group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a carbazolyl group, a dibenzofuranyl group, and a dibenzothiophenyl group; and

    -Si(Q401)(Q402)(Q403), -N(Q401)(Q402), -B(Q401)(Q402), -C(=O)(Q401), -S(=O)2(Q401) and -P(=O)(Q401)(Q402),

    wherein Q401 to Q403 may each independently be selected from a C1-C10 alkyl group, a C1-C10 alkoxy group, a phenyl group, a biphenyl group, and a naphthyl group, but embodiments are not limited thereto.



    [0124] In one or more embodiments, when xc1 in Formula 401 is 2 or greater, two A401(s) in at least two L401(s) may optionally be linked to each other via X407, which is a linking group; or two A402(s) in at least two L401(s) may optionally be linked to each other via X408, which is a linking group (see Compounds PD1 to PD4 and PD7). X407 and X408 may each independently be selected from a single bond, -O-', -S-', -C(=O)-', -N(Q413)-', -C(Q413)(Q414)-', and -C(Q413)=C(Q414)-', wherein Q413 and Q414 may each independently be hydrogen, deuterium, a C1-C20 alkyl group, a C1-C20 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, or a naphthyl group, but embodiments are not limited thereto.

    [0125] L402 in Formula 401 may be any suitable monovalent, divalent, or trivalent organic ligand. In some embodiments, L402 may be selected from halogen, diketone (e.g., acetylacetonate), a carboxylic acid (e.g., picolinate), -C(=O), isonitrile, -CN, and phosphorus (e.g., phosphine or phosphite), but embodiments are not limited thereto.

    [0126] In some embodiments, examples of the phosphorescent dopant may include, for example, at least one selected from Compounds PD1 to PD25, but embodiments are not limited thereto:










    Fluorescent dopant in emission layer



    [0127] Examples of the fluorescent dopant may include an arylamine compound or a styrylamine compound.

    [0128] The host may include a compound represented by Formula 501:





    [0129] In Formula 501,

    Ar501 may be a substituted or unsubstituted C5-C60 carbocyclic group or a substituted or unsubstituted C1-C60 heterocyclic group,

    L501 to L503 may be each independently selected from a substituted or unsubstituted C3-C10 cycloalkylene group, a substituted or unsubstituted C1-C10 heterocycloalkylene group, a substituted or unsubstituted C3-C10 cycloalkenylene group, a substituted or unsubstituted C1-C10 heterocycloalkenylene group, a substituted or unsubstituted C6-C60 arylene group, a substituted or unsubstituted C1-C60 heteroarylene group, a substituted or unsubstituted divalent non-aromatic condensed C8 to C60 polycyclic group, and a substituted or unsubstituted divalent non-aromatic condensed 8-to 60-membered heteropolycyclic group,

    xd1 to xd3 may each independently be an integer from 0 to 3,

    R501 and R502 may each independently be selected from a substituted or unsubstituted C3-C10 cycloalkyl group, a substituted or unsubstituted C1-C10 heterocycloalkyl group, a substituted or unsubstituted C3-C10 cycloalkenyl group, a substituted or unsubstituted C1-C10 heterocycloalkenyl group, a substituted or unsubstituted C6-C60 aryl group, a substituted or unsubstituted C6-C60 aryloxy group, a substituted or unsubstituted C6-C60 arylthio group, a substituted or unsubstituted C1-C60 heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed C8 to C60 polycyclic group, and a substituted or unsubstituted monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, and

    xd4 may be an integer from 1 to 6.



    [0130] In some embodiments, Ar501 in Formula 501 may be selected from

    a naphthalene group, a heptalene group, a fluorene group, a spiro-bifluorene group, a benzofluorene group, a dibenzofluorene group, a phenalene group, a phenanthrene group, an anthracene group, a fluoranthene group, a triphenylene group, a pyrene group, a chrysene group, a naphthacene group, a picene group, a perylene group, a pentaphene group, an indenoanthracene group, and an indenophenanthrene group; and

    a naphthalene group, a heptalene group, a fluorene group, a spiro-bifluorene group, a benzofluorene group, a dibenzofluorene group, a phenalene group, a phenanthrene group, an anthracene group, a fluoranthene group, a triphenylene group, a pyrene group, a chrysene group, a naphthacene group, a picene group, a perylene group, a pentaphene group, an indenoanthracene group, and an indenophenanthrene group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, and a naphthyl group.



    [0131] In one or more embodiments, in Formula 501, L501 to L503 may each independently be selected from

    a phenylene group, a naphthylene group, a fluorenylene group, a spiro-bifluorenylene group, a benzofluorenylene group, a dibenzofluorenylene group, a phenanthrenylene group, an anthracenylene group, a fluoranthenylene group, a triphenylenylene group, a pyrenylene group, a chrysenylene group, a perylenylene group, a pentaphenylene group, a hexacenylene group, a pentacenylene group, a thiophenylene group, a furanylene group, a carbazolylene group, an indolylene group, an isoindolylene group, a benzofuranylene group, a benzothiophenylene group, a dibenzofuranylene group, a dibenzothiophenylene group, a benzocarbazolylene group, a dibenzocarbazolylene group, a dibenzosilolylene group, and a pyridinylene group; and

    a phenylene group, a naphthylene group, a fluorenylene group, a spiro-bifluorenylene group, a benzofluorenylene group, a dibenzofluorenylene group, a phenanthrenylene group, an anthracenylene group, a fluoranthenylene group, a triphenylenylene group, a pyrenylene group, a chrysenylene group, a perylenylene group, a pentaphenylene group, a hexacenylene group, a pentacenylene group, a thiophenylene group, a furanylene group, a carbazolylene group, an indolylene group, an isoindolylene group, a benzofuranylene group, a benzothiophenylene group, a dibenzofuranylene group, a dibenzothiophenylene group, a benzocarbazolylene group, a dibenzocarbazolylene group, a dibenzosilolylene group, and a pyridinylene group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, and a pyridinyl group.



    [0132] In one or more embodiments, in Formula 501, R501 and R502 may each independently be selected from

    a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, and a pyridinyl group; and

    a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, and a pyridinyl group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, a pyridinyl group, and -Si(Q31)(Q32)(Q33),

    wherein Q31 to Q33 may each independently be selected from a C1-C10 alkyl group, a C1-C10 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, and a naphthyl group.



    [0133] In one or more embodiments, xd4 in Formula 501 may be 2, but embodiments are not limited thereto.

    [0134] In some embodiments, the fluorescent dopant may be selected from Compounds FD1 to FD22:



















    [0135] In some embodiments, the fluorescent dopant may be selected from the following compounds, but embodiments are not limited thereto:






    Electron transport region in organic layer 150



    [0136] The electron transport region may have i) a single-layered structure including a single layer comprising a single material, ii) a single-layered structure including a single layer comprising a plurality of different materials, or iii) a multi-layered structure having a plurality of layers comprising a plurality of different materials.

    [0137] The electron transport region may comprise at least one selected from a buffer layer, a hole blocking layer, an electron control layer, an electron transport layer, and an electron injection layer, but embodiments are not limited thereto.

    [0138] In some embodiments, the electron transport region may have a structure of an electron transport layer/electron injection layer, a structure of a hole blocking layer/electron transport layer/electron injection layer, a structure of an electron control layer/electron transport layer/electron injection layer, or a structure of a buffer layer/electron transport layer/electron injection layer, wherein layers of each structure are sequentially stacked on the emission layer in each stated order, but embodiments are not limited thereto.

    [0139] The electron transport region, e.g., a buffer layer, a hole blocking layer, an electron control layer, or an electron transport layer in the electron transport region, may comprise a metal-free compound. The metal-free compound may include at least one π electron-depleted nitrogen-containing ring.

    [0140] The term "π electron-depleted nitrogen-containing ring" as used herein refers to a C1-C60 heterocyclic group having at least one -N=' moiety as a ring-forming moiety.

    [0141] For example, the "π electron-depleted nitrogen-containing ring" may be i) a 5-membered to 7-membered heteromonocyclic group having at least one -N=' moiety, ii) a heteropolycyclic group in which two or more 5-membered to 7-membered heteromonocyclic groups, each having at least one -N=' moiety, are condensed, or iii) a heteropolycyclic group in which at least one 5-membered to 7-membered heteromonocyclic group, having at least one -N=' moiety, is condensed with at least one C5-C60 carbocyclic group.

    [0142] Examples of the π electron-depleted nitrogen-containing ring may include an imidazole, a pyrazole, a thiazole, an isothiazole, an oxazole, an isoxazole, a pyridine, a pyrazine, a pyrimidine, a pyridazine, an indazole, a purine, a quinoline, an isoquinoline, a benzoquinoline, a phthalazine, a naphthyridine, a quinoxaline, a quinazoline, a cinnoline, a phenanthridine, an acridine, a phenanthroline, a phenazine, a benzimidazole, an iso-benzothiazole, a benzoxazole, an isobenzoxazole, a triazole, a tetrazole, an oxadiazole, a triazine, a thiadiazole, an imidazopyridine, an imidazopyrimidine, and an azacarbazole, but embodiments are not limited thereto.

    [0143] In some embodiments, the electron transport region may comprise a compound represented by Formula 601:

            Formula 601     [Ar601]xe11-[(L601)xe1-R601]xe21

    wherein, in Formula 601,

    Ar601 may be a substituted or unsubstituted C5-C60 carbocyclic group or a substituted or unsubstituted C1-C60 heterocyclic group,

    xe11 may be 1, 2, or 3,

    L601 may be selected from a substituted or unsubstituted C3-C10 cycloalkylene group, a substituted or unsubstituted C1-C10 heterocycloalkylene group, a substituted or unsubstituted C3-C10 cycloalkenylene group, a substituted or unsubstituted C1-C10 heterocycloalkenylene group, a substituted or unsubstituted C6-C60 arylene group, a substituted or unsubstituted C1-C60 heteroarylene group, a substituted or unsubstituted divalent non-aromatic condensed C8 to C60 polycyclic group, and a substituted or unsubstituted divalent non-aromatic condensed 8- to 60-membered heteropolycyclic group,

    xe1 may be an integer from 0 to 5,

    R601 may be selected from a substituted or unsubstituted C3-C10 cycloalkyl group, a substituted or unsubstituted C1-C10 heterocycloalkyl group, a substituted or unsubstituted C3-C10 cycloalkenyl group, a substituted or unsubstituted C1-C10 heterocycloalkenyl group, a substituted or unsubstituted C6-C60 aryl group, a substituted or unsubstituted C6-C60 aryloxy group, a substituted or unsubstituted C6-C60 arylthio group, a substituted or unsubstituted C1-C60 heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed C8 to C60 polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, -Si(Q601)(Q602)(Q603), -C(=O)(Q601), -S(=O)2(Q601), and - P(=O)(Q601)(Q602),

    wherein Q601 to Q603 may each independently be a C1-C10 alkyl group, a C1-C10 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, or a naphthyl group, and

    xe2i may be an integer from 1 to 5.



    [0144] In one embodiment, at least one of Ar601 groups in the number of xe11 and R601 groups in the number of xe2i may comprise the π electron-depleted nitrogen-containing ring.

    [0145] In some embodiments, Ar601 in Formula 601 may be selected from

    a benzene group, a naphthalene group, a fluorene group, a spiro-bifluorene group, a benzofluorene group, a dibenzofluorene group, a phenalene group, a phenanthrene group, an anthracene group, a fluoranthene group, a triphenylene group, a pyrene group, a chrysene group, a naphthacene group, a picene group, a perylene group, a pentaphene group, an indenoanthracene group, a dibenzofuran group, a dibenzothiophene group, a carbazole group, an imidazole group, a pyrazole group, a thiazole group, an isothiazole group, an oxazole group, an isoxazole group, a pyridine group, a pyrazine group, a pyrimidine group, a pyridazine group, an indazole group, a purine group, a quinoline group, an isoquinoline group, a benzoquinoline group, a phthalazine group, a naphthyridine group, a quinoxaline group, a quinazoline group, a cinnoline group, a phenanthridine group, an acridine group, a phenanthroline group, a phenazine group, a benzimidazole group, an iso-benzothiazole group, a benzoxazole group, an isobenzoxazole group, a triazole group, a tetrazole group, an oxadiazole group, a triazine group, a thiadiazole group, an imidazopyridine group, an imidazopyrimidine group, and an azacarbazole group; and

    a benzene group, a naphthalene group, a fluorene group, a spiro-bifluorene group, a benzofluorene group, a dibenzofluorene group, a phenalene group, a phenanthrene group, an anthracene group, a fluoranthene group, a triphenylene group, a pyrene group, a chrysene group, a naphthacene group, a picene group, a perylene group, a pentaphene group, an indenoanthracene group, a dibenzofuran group, a dibenzothiophene group, a carbazole group, an imidazole group, a pyrazole group, a thiazole group, an isothiazole group, an oxazole group, an isoxazole group, a pyridine group, a pyrazine group, a pyrimidine group, a pyridazine group, an indazole group, a purine group, a quinoline group, an isoquinoline group, a benzoquinoline group, a phthalazine group, a naphthyridine group, a quinoxaline group, a quinazoline group, a cinnoline group, a phenanthridine group, an acridine group, a phenanthroline group, a phenazine group, a benzimidazole group, an iso-benzothiazole group, a benzoxazole group, an isobenzoxazole group, a triazole group, a tetrazole group, an oxadiazole group, a triazine group, a thiadiazole group, an imidazopyridine group, an imidazopyrimidine group, and an azacarbazole group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, -Si(Q31)(Q32)(Q33), - S(=O)2(Q31), and -P(=O)(Q31)(Q32),

    wherein Q31 to Q33 may each independently be selected from a C1-C10 alkyl group, a C1-C10 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, and a naphthyl group.



    [0146] When xe11 in Formula 601 is 2 or greater, at least two Ar601 groups may be linked via a single bond.

    [0147] In one or more embodiments, Ar601 in Formula 601 may be an anthracene group.

    [0148] In some embodiments, the compound represented by Formula 601 may be represented by Formula 601-1:



    [0149] In Formula 601-1,

    X614 may be N or C(R614), X615 may be N or C(R615), X616 may be N or C(R616), and at least one selected from X614 to X616 may be N,

    descriptions for L611 to L613 may each independently be understood by referring to (may be the same as) the descriptions for those for L601 provided herein,

    descriptions for xe611 to xe613 may each independently be understood by referring to (may be the same as) the descriptions for those for xe1 provided herein,

    descriptions for R611 to R613 may each independently be understood by referring to (may be the same as) the descriptions for those for R601 provided herein, and

    R614 to R616 may each independently be selected from hydrogen, deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, and a naphthyl group.



    [0150] In one embodiment, in Formulae 601 and 601-1, L601 and L611 to L613 may each independently be selected from

    a phenylene group, a naphthylene group, a fluorenylene group, a spiro-bifluorenylene group, a benzofluorenylene group, a dibenzofluorenylene group, a phenanthrenylene group, an anthracenylene group, a fluoranthenylene group, a triphenylenylene group, a pyrenylene group, a chrysenylene group, a perylenylene group, a pentaphenylene group, a hexacenylene group, a pentacenylene group, a thiophenylene group, a furanylene group, a carbazolylene group, an indolylene group, an isoindolylene group, a benzofuranylene group, a benzothiophenylene group, a dibenzofuranylene group, a dibenzothiophenylene group, a benzocarbazolylene group, a dibenzocarbazolylene group, a dibenzosilolylene group, a pyridinylene group, an imidazolylene group, a pyrazolylene group, a thiazolylene group, an isothiazolylene group, an oxazolylene group, an isoxazolylene group, a thiadiazolylene group, an oxadiazolylene group, a pyrazinylene group, a pyrimidinylene group, a pyridazinylene group, a triazinylene group, a quinolinylene group, an isoquinolinylene group, a benzoquinolinylene group, a phthalazinylene group, a naphthyridinylene group, a quinoxalinylene group, a quinazolinylene group, a cinnolinylene group, a phenanthridinylene group, an acridinylene group, a phenanthrolinylene group, a phenazinylene group, a benzimidazolylene group, an isobenzothiazolylene group, a benzoxazolylene group, an isobenzoxazolylene group, a triazolylene group, a tetrazolylene group, an imidazopyridinylene group, an imidazopyrimidinylene group, and an azacarbazolylene group; and

    a phenylene group, a naphthylene group, a fluorenylene group, a spiro-bifluorenylene group, a benzofluorenylene group, a dibenzofluorenylene group, a phenanthrenylene group, an anthracenylene group, a fluoranthenylene group, a triphenylenylene group, a pyrenylene group, a chrysenylene group, a perylenylene group, a pentaphenylene group, a hexacenylene group, a pentacenylene group, a thiophenylene group, a furanylene group, a carbazolylene group, an indolylene group, an isoindolylene group, a benzofuranylene group, a benzothiophenylene group, a dibenzofuranylene group, a dibenzothiophenylene group, a benzocarbazolylene group, a dibenzocarbazolylene group, a dibenzosilolylene group, a pyridinylene group, an imidazolylene group, a pyrazolylene group, a thiazolylene group, an isothiazolylene group, an oxazolylene group, an isoxazolylene group, a thiadiazolylene group, an oxadiazolylene group, a pyrazinylene group, a pyrimidinylene group, a pyridazinylene group, a triazinylene group, a quinolinylene group, an isoquinolinylene group, a benzoquinolinylene group, a phthalazinylene group, a naphthyridinylene group, a quinoxalinylene group, a quinazolinylene group, a cinnolinylene group, a phenanthridinylene group, an acridinylene group, a phenanthrolinylene group, a phenazinylene group, a benzimidazolylene group, an isobenzothiazolylene group, a benzoxazolylene group, an isobenzoxazolylene group, a triazolylene group, a tetrazolylene group, an imidazopyridinylene group, an imidazopyrimidinylene group, and an azacarbazolylene group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, a pyridinyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a thiadiazolyl group, an oxadiazolyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a phthalazinyl group, a naphthyridinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a benzimidazolyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an imidazopyridinyl group, an imidazopyrimidinyl group, and an azacarbazolyl group, but embodiments are not limited thereto.



    [0151] In one or more embodiments, in Formulae 601 and 601-1, xe1 and xe611 to xe613, may each independently be 0, 1, or 2.

    [0152] In one or more embodiments, in Formulae 601 and 601-1, R601 and R611 to R613 may each independently be selected from

    a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, a pyridinyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a thiadiazolyl group, an oxadiazolyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a phthalazinyl group, a naphthyridinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a benzimidazolyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an imidazopyridinyl group, an imidazopyrimidinyl group, and an azacarbazolyl group;

    a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, a pyridinyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a thiadiazolyl group, an oxadiazolyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a phthalazinyl group, a naphthyridinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a benzimidazolyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an imidazopyridinyl group, an imidazopyrimidinyl group, and an azacarbazolyl group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a perylenyl group, a pentaphenyl group, a hexacenyl group, a pentacenyl group, a thiophenyl group, a furanyl group, a carbazolyl group, an indolyl group, an isoindolyl group, a benzofuranyl group, a benzothiophenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzosilolyl group, a pyridinyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a thiadiazolyl group, an oxadiazolyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a phthalazinyl group, a naphthyridinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a benzimidazolyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an imidazopyridinyl group, an imidazopyrimidinyl group, and an azacarbazolyl group; and

    -S(=O)2(Q601) and -P(=O)(Q601)(Q602),

    wherein descriptions for Q601 and Q602 may each independently be understood by referring to (may be the same as) the descriptions for those provided herein.



    [0153] The electron transport region may comprise at least one compound selected from Compounds ET1 to ET36, but embodiments are not limited thereto:

























    [0154] In some embodiments, the electron transport region may comprise at least one compound selected from 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP), 4,7-diphenyl-1,10-phenanthroline (Bphen), Alq3, BAlq, 3-(biphenyl-4-yl)-5-(4-tert-butylphenyl)-4-phenyl-4H-1,2,4-triazole (TAZ), and NTAZ:





    [0155] The thicknesses of the buffer layer, the hole blocking layer, or the electron control layer may each independently be in a range of about 20 Å to about 1,000 Å, and in some embodiments, about 30 Å to about 300 Å. When the thicknesses of the buffer layer, the hole blocking layer or the electron control layer are within the above-described ranges, excellent hole blocking characteristics or excellent electron controlling characteristics may be obtained without a substantial increase in driving voltage.

    [0156] The thickness of the electron transport layer may be in a range of about 100 Å to about 1,000 Å, and in some embodiments, about 150 Å to about 500 Å. When the thickness of the electron transport layer is within the above-described ranges, excellent electron transport characteristics may be obtained without a substantial increase in driving voltage.

    [0157] The electron transport region (e.g., the electron transport layer in the electron transport region) may further comprise, in addition to the materials described above, a material comprising metal (e.g., a metal ion).

    [0158] The material comprising metal may comprise at least one selected from an alkali metal complex and an alkaline earth metal complex. The alkali metal complex may comprise a metal ion selected from a lithium (Li) ion, a sodium (Na) ion, a potassium (K) ion, a rubidium (Rb) ion, and a cesium (Cs) ion. The alkaline earth metal complex may comprise a metal ion selected from a beryllium (Be) ion, a magnesium (Mg) ion, a calcium (Ca) ion, an strontium (Sr) ion, and a barium (Ba) ion. Each ligand coordinated with the metal ion of the alkali metal complex and the alkaline earth metal complex may independently be selected from a hydroxyquinoline, a hydroxyisoquinoline, a hydroxybenzoquinoline, a hydroxyacridine, a hydroxyphenanthridine, a hydroxyphenyloxazole, a hydroxyphenylthiazole, a hydroxyphenyl oxadiazole, a hydroxyphenyl thiadiazole, a hydroxyphenyl pyridine, a hydroxyphenyl benzimidazole, a hydroxyphenyl benzothiazole, a bipyridine, a phenanthroline, and a cyclopentadiene, but embodiments are not limited thereto.

    [0159] Examples of the material comprising metal may include a Li complex. Examples of the Li complex may include, e.g., Compound ET-Di (lithium quinolate, LiQ) or Compound ET-D2:



    [0160] The electron transport region may comprise an electron injection layer that facilitates injection of electrons from the second electrode 190. The electron injection layer may be in direct contact with the second electrode 190.

    [0161] The electron injection layer may have i) a single-layered structure including a single layer including a single material, ii) a single-layered structure including a single layer comprising a plurality of different materials, or iii) a multi-layered structure having a plurality of layers, each comprising a plurality of different materials.

    [0162] The electron injection layer may comprise an alkali metal, an alkaline earth metal, a rare earth metal, an alkali metal compound, an alkaline earth metal compound, a rare earth metal compound, an alkali metal complex, an alkaline earth metal complex, a rare earth metal complex, or a combination thereof.

    [0163] The alkali metal may be selected from Li, Na, K, Rb, and Cs. In one embodiment, the alkali metal may be Li, Na, or Cs. In one or more embodiments, the alkali metal may be Li or Cs, but embodiments are not limited thereto.

    [0164] The alkaline earth metal may be selected from Mg, Ca, Sr, and Ba.

    [0165] The rare earth metal may be selected from Sc, Y, Ce, Tb, Yb, and Gd.

    [0166] The alkali metal compound, the alkaline earth metal compound, and the rare earth metal compound may each independently be selected from oxides and halides (e.g., fluorides, chlorides, bromides, or iodines) of the alkali metal, the alkaline earth metal, and the rare earth metal, respectively.

    [0167] The alkali metal compound may be selected from alkali metal oxides (such as Li2O, Cs2O, or K2O), and alkali metal halides (such as LiF, NaF, CsF, KF, LiI, NaI, CsI, KI, or RbI). In one embodiment, the alkali metal compound may be selected from LiF, Li2O, NaF, LiI, NaI, CsI, and KI, but embodiments are not limited thereto.

    [0168] The alkaline earth metal compound may be selected from alkaline earth metal compounds such as BaO, SrO, CaO, BaxSr1-xO (where 0<x<1), and BaxCa1-xO (where 0<x<1). In one embodiment, the alkaline earth metal compound may be selected from BaO, SrO, and CaO, but embodiments are not limited thereto.

    [0169] The rare earth metal compound may be selected from YbF3, ScF3, ScO3, Y2O3, Ce2O3, GdF3, and TbF3. In one embodiment, the rare earth metal compound may be selected from YbF3, ScF3, TbF3, YbI3, ScI3, and TbI3, but embodiments are not limited thereto.

    [0170] The alkali metal complex, the alkaline earth metal complex, and the rare earth metal complex may each comprise ions of the above-described alkali metal, alkaline earth metal, and rare earth metal. Each ligand coordinated with the metal ion of the alkali metal complex, the alkaline earth metal complex, and the rare earth metal complex may independently be selected from a hydroxyquinoline, a hydroxyisoquinoline, a hydroxybenzoquinoline, a hydroxyacridine, a hydroxyphenanthridine, a hydroxyphenyl oxazole, a hydroxyphenyl thiazole, a hydroxyphenyl oxadiazole, a hydroxyphenyl thiadiazole, a hydroxyphenyl pyridine, a hydroxyphenyl benzimidazole, a hydroxyphenyl benzothiazole, a bipyridine, a phenanthroline, and a cyclopentadiene, but embodiments are not limited thereto.

    [0171] The electron injection layer may comprise (e.g., consist of) an alkali metal, an alkaline earth metal, a rare earth metal, an alkali metal compound, an alkaline earth metal compound, a rare earth metal compound, an alkali metal complex, an alkaline earth metal complex, a rare earth metal complex, or a combination thereof, as described above. In some embodiments, the electron injection layer may further comprise an organic material. When the electron injection layer further comprises an organic material, the alkali metal, the alkaline earth metal, the rare earth metal, the alkali metal compound, the alkaline earth metal compound, the rare earth metal compound, the alkali metal complex, the alkaline earth metal complex, the rare earth metal complex, or a combination thereof may be homogeneously or non-homogeneously dispersed in a matrix comprising the organic material.

    [0172] The thickness of the electron injection layer may be in a range of about 1 Å to about 100 Å, and in some embodiments, about 3 Å to about 90 Å. When the thickness of the electron injection layer is within the above-described ranges, excellent electron injection characteristics maybe obtained without a substantial increase in driving voltage.

    Second electrode 190



    [0173] The second electrode 190 may be on the organic layer 150. In an embodiment, the second electrode 190 may be a cathode that is an electron injection electrode. In this embodiment, a material for forming the second electrode 190 may be a material having a low work function, for example, a metal, an alloy, an electrically conductive compound, or a combination thereof.

    [0174] The second electrode 190 may comprise at least one selected from lithium (Li), silver (Ag), magnesium (Mg), aluminum (Al), aluminum-lithium (Al-Li), calcium (Ca), magnesium-indium (Mg-In), magnesium-silver (Mg-Ag), ITO, and IZO, but embodiments are not limited thereto. The second electrode 190 may be a transmissive electrode, a semi-transmissive electrode, or a reflective electrode.

    [0175] The second electrode 190 may have a single-layered structure, or a multi-layered structure comprising two or more layers.

    Description of FIGS. 2 to 4



    [0176] Referring to FIG. 2, an organic light-emitting device 20 has the structure of a first capping layer 210, the first electrode 110, the organic layer 150, and the second electrode 190, wherein the layers are sequentially stacked in this stated order. Referring to FIG. 3, an organic light-emitting device 30 has the structure of the first electrode 110, the organic layer 150, the second electrode 190, and a second capping layer 220, wherein the layers are sequentially stacked in this stated order. Referring to FIG. 4, an organic light-emitting device 40 has the structure of the first capping layer 210, the first electrode 110, the organic layer 150, the second electrode 190, and the second capping layer 220, wherein the layers are stacked in this stated order.

    [0177] The first electrode 110, the organic layer 150, and the second electrode 190 illustrated in FIGS. 2 to 4 may be substantially the same as those illustrated in FIG. 1.

    [0178] In the organic light-emitting devices 20 and 40, light emitted from the emission layer in the organic layer 150 may pass through the first electrode 110 (which may be a semi-transmissive electrode or a transmissive electrode) and through the first capping layer 210 to the outside. In the organic light-emitting devices 30 and 40, light emitted from the emission layer in the organic layer 150 may pass through the second electrode 190 (which may be a semi-transmissive electrode or a transmissive electrode) and through the second capping layer 220 to the outside.

    [0179] The first capping layer 210 and the second capping layer 220 may improve the external luminescence efficiency based on the principle of constructive interference.

    [0180] The first capping layer 210 and the second capping layer 220 may each independently be an organic capping layer comprising an organic material, an inorganic capping layer comprising an inorganic material, or a composite capping layer comprising an organic material and an inorganic material.

    [0181] At least one of the first capping layer 210 and the second capping layer 220 may each independently comprise at least one material selected from carbocyclic compounds, heterocyclic compounds, amine-based compounds, porphine derivatives, phthalocyanine derivatives, naphthalocyanine derivatives, alkali metal complexes, and alkaline earth metal complexes. The carbocyclic compound, the heterocyclic compound, and the amine-based compound may optionally be substituted with a substituent containing at least one element selected from O, N, S, Se, Si, F, Cl, Br, and I. In one embodiment, at least one of the first capping layer 210 and the second capping layer 220 may each independently comprise an amine-based compound.

    [0182] In one or more embodiments, at least one of the first capping layer 210 and the second capping layer 220 may each independently comprise a compound represented by Formula 201 or a compound represented by Formula 202.

    [0183] In one or more embodiments, at least one of the first capping layer 210 and the second capping layer 220 may each independently comprise a compound selected from Compounds HT28 to HT33 and Compound CP1 to CP5, but embodiments are not limited thereto:





    [0184] Hereinbefore, the organic light-emitting device has been described with reference to FIGS. 1 to 4, but embodiments are not limited thereto.

    [0185] The layers constituting the hole transport region, the emission layer, and the layers constituting the electron transport region may be formed in a specific region (e.g., in a respective region) utilizing one or more suitable methods, such as vacuum deposition, spin coating, casting, Langmuir-Blodgett (LB) deposition, ink-jet printing, laser printing, and/or laser-induced thermal imaging.

    [0186] When the layers constituting the hole transport region, the emission layer, and/or the layers constituting the electron transport region are each formed by vacuum deposition, the vacuum deposition may be performed at a deposition temperature in a range of about 100°C to about 500°C at a vacuum degree in a range of about 10-8 torr to about 10-3 torr, and at a deposition rate in a range of about 0.01 Angstroms per second (Å/sec) to about 100 Å/sec, depending on the material to be included in each layer and the structure of each layer to be formed.

    [0187] When the layers constituting the hole transport region, the emission layer, and/or the layers constituting the electron transport region are each formed by spin coating, the spin coating may be performed at a coating rate of about 2,000 revolutions per minute (rpm) to about 5,000 rpm and at a heat treatment temperature of about 80°C to about 200°C, depending on the material to be included in each layer and the structure of each layer to be formed.

    General definitions of substituents



    [0188] The term "C1-C60 alkyl group" as used herein refers to a linear or branched aliphatic hydrocarbon monovalent group having 1 to 60 carbon atoms, e.g. 1 to 30 carbon atoms, 1 to 20 carbon atoms, 1 to 10 carbon atoms, 1 to 6 carbon atoms or 1 to 4 carbon atoms. Examples thereof may include a methyl group, an ethyl group, a propyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, a pentyl group, an iso-amyl group, and a hexyl group. The term "C1-C60 alkylene group" as used herein refers to a divalent group having the same structure as the C1-C60 alkyl group.

    [0189] The term "C2-C60 alkenyl group" as used herein refers to a hydrocarbon group having at least one carbon-carbon double bond in the middle or at the terminus of the C2-C60 alkyl group. Examples thereof may include an ethenyl group, a propenyl group, and a butenyl group. The term "C2-C60 alkenylene group" as used herein refers to a divalent group having the same structure as the C2-C60 alkenyl group.

    [0190] The term "C2-C60 alkynyl group" as used herein refers to a hydrocarbon group having at least one carbon-carbon triple bond in the middle or at the terminus of the C2-C60 alkyl group. Examples thereof may include an ethynyl group and a propynyl group. The term "C2-C60 alkynylene group" as used herein refers to a divalent group having the same structure as the C2-C60 alkynyl group.

    [0191] The term "C1-C60 alkoxy group" as used herein refers to a monovalent group represented by -OA101 (wherein A101 is a C1-C60 alkyl group). Examples thereof may include a methoxy group, an ethoxy group, and an isopropyloxy group.

    [0192] The term "C3-C10 cycloalkyl group" as used herein refers to a monovalent monocyclic saturated hydrocarbon group having 3 to 10 carbon atoms. Examples thereof may include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, and a cycloheptyl group. The term "C3-C10 cycloalkylene group" as used herein refers to a divalent group having the same structure as the C3-C10 cycloalkyl group.

    [0193] The term "C1-C10 heterocycloalkyl group" as used herein refers to a monovalent monocyclic group having at least one heteroatom (e.g. 1, 2, 3, 4 or 5 heteroatoms) selected from N, O, Si, P, and S as a ring-forming atom and 1 to 10 carbon atoms, e.g. 1, 2, 3, 4 or 5 ring carbon atoms. Examples thereof may include a 1,2,3,4-oxatriazolidinyl group, a tetrahydrofuranyl group, and a tetrahydrothiophenyl group. The term "C1-C10 heterocycloalkylene group" as used herein refers to a divalent group having the same structure as the C1-C10 heterocycloalkyl group.

    [0194] The term "C3-C10 cycloalkenyl group" as used herein refers to a monovalent monocyclic group having 3 to 10 carbon atoms and at least one carbon-carbon double bond in its ring, wherein the molecular structure as a whole is non-aromatic. Examples thereof may include a cyclopentenyl group, a cyclohexenyl group, and a cycloheptenyl group. The term "C3-C10 cycloalkenylene group" as used herein refers to a divalent group having the same structure as the C3-C10 cycloalkenyl group.

    [0195] The term "C1-C10 heterocycloalkenyl group" as used herein refers to a monovalent monocyclic group having at least one heteroatom (e.g. 1, 2, 3, 4 or 5 heteroatoms) selected from N, O, Si, P, and S as a ring-forming atom, 1 to 10 carbon atoms, e.g. 1, 2, 3, 4 or 5 ring carbon atoms, and at least one double bond in its ring. Examples of the C1-C10 heterocycloalkenyl group may include a 4,5-dihydro-1,2,3,4-oxatriazolyl group, a 2,3-dihydrofuranyl group, and a 2,3-dihydrothiophenyl group. The term "C1-C10 heterocycloalkenylene group" as used herein refers to a divalent group having the same structure as the C1-C10 heterocycloalkenyl group.

    [0196] The term "C6-C60 aryl group" as used herein refers to a monovalent group having a carbocyclic aromatic system having 6 to 60 carbon atoms, e.g. 6 to 20 ring carbon atoms, 6 to 14 ring cabon atoms or 6 to 10 ring carbon atoms. The term "C6-C60 arylene group" as used herein refers to a divalent group having a carbocyclic aromatic system having 6 to 60 carbon atoms, e.g. 6 to 20 ring carbon atoms, 6 to 14 ring cabon atoms or 6 to 10 ring carbon atoms. Examples of the C6-C60 aryl group may include a phenyl group, a naphthyl group, an anthracenyl group, a phenanthrenyl group, a pyrenyl group, and a chrysenyl group. When the C6-C60 aryl group and the C6-C60 arylene group each independently comprise two or more rings, the respective rings may be fused.

    [0197] The term "C1-C60 heteroaryl group" as used herein refers to a monovalent group having a heterocyclic aromatic system having at least one heteroatom (e.g. 1, 2, 3, 4 or 5 hereoatoms) selected from N, O, Si, P, and S as a ring-forming atom and 1 to 60 carbon atoms, e.g. 1 to 19 ring carbon atoms, 1 to 13 ring cabon atoms or 1 to 9 ring carbon atoms. The term "C1-C60 heteroarylene group" as used herein refers to a divalent group having a heterocyclic aromatic system having at least one heteroatom (e.g. 1, 2, 3, 4 or 5 hereoatoms) selected from N, O, Si, P, and S as a ring-forming atom and 1 to 60 carbon atoms, e.g. 1 to 19 ring carbon atoms, 1 to 13 ring cabon atoms or 1 to 9 ring carbon atoms. Examples of the C1-C60 heteroaryl group may include a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, and an isoquinolinyl group. When the C1-C60 heteroaryl group and the C1-C60 heteroarylene group each independently comprise two or more rings, the respective rings may be fused.

    [0198] The term "C6-C60 aryloxy group" as used herein refers to a group represented by -OA102 (where A102 is a C6-C60 aryl group). The term "C6-C60 arylthio group" as used herein refers to a group represented by -SA103 (where A103 is a C6-C60 aryl group).

    [0199] The term "monovalent non-aromatic condensed C8 to C60 polycyclic group" as used herein refers to a monovalent group that has two or more rings condensed and 8 to 60 carbon atoms as ring forming atoms (e.g., 8 to 20, 8 to 14 or 8 to 10 ring carbon atoms), wherein the entire molecular structure is non-aromatic (e.g., the molecular structure does not have overall aromaticity). An example of the monovalent non-aromatic condensed C8 to C60 polycyclic group may be a fluorenyl group. The term "divalent non-aromatic condensed C8 to C60 polycyclic group" as used herein refers to a divalent group having the same structure as the monovalent non-aromatic condensed C8 to C60 polycyclic group.

    [0200] The term "monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group" as used herein refers to a monovalent group that has having 8- to 60- ring-forming atoms and two or more condensed rings and at least one heteroatom (e.g. 1, 2, 3, 4 or 5 hereoatoms) selected from N, O, Si, P, and S, in addition to carbon atoms (e.g., 1 to 59, 2 to 59, 2 to 19, 2 to 13 or 2 to 9 ring carbon atoms), as a ring-forming atom, wherein the entire molecular structure is non-aromatic (e.g., the molecular structure does not have overall aromaticity). An example of the monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group is a carbazolyl group. The term "divalent non-aromatic condensed 8- to 60-membered heteropolycyclic group" as used herein refers to a divalent group having the same structure as the monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group.

    [0201] The term "C5-C6. carbocyclic group" as used herein refers to a monocyclic group or a polycyclic group having 5 to 60 carbon atoms e.g. 5 to 20 ring carbon atoms, 5 to 14 ring cabon atoms or 5 to 10 ring carbon atoms, in which the only ring-forming atoms are carbon atoms. The C5-C60 carbocyclic group may be an aromatic carbocyclic group or a non-aromatic carbocyclic group. The term "C5-C60 carbocyclic group" as used herein refers to a ring (e.g., a benzene group), a monovalent group (e.g., a phenyl group), or a divalent group (e.g., a phenylene group). In one or more embodiments, depending on the number of substituents connected to the C5-C60 carbocyclic group, the C5-C60 carbocyclic group may be a trivalent group or a quadrivalent group.

    [0202] The term "C1-C60 heterocyclic group" as used herein refers to a group having substantially the same structure as the C5-C60 carbocyclic group, except that at least one heteroatom (e.g. 1, 2, 3, 4 or 5 hereoatoms) selected from N, O, Si, P, and S is used as a ring-forming atom, in addition to 1 to 60 carbon atoms (e.g.,1 to 20 ring carbon atoms, 1 to 14 ring cabon atoms or 1 to 10 ring carbon atoms).

    [0203] Certain groups are specified herein as being substituted or unsubstituted. Unless otherwise specified, when a group is substituted it is typically substituted with 1, 2, 3 or 4 substituents. For example, when a group is substituted it may be substituted with 1, 2 or 3 substituents; 1 or 2 substituents; or 1 substituent. Groups which are not specified as being substituted or unsubstituted are typically unsubstituted. Unless otherwise specified, when a group is substituted it is typically substituted with at least one substituent (e.g. 1, 2, 3 or 4 substituents) selected from:

    [0204] deuterium (-D), -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C60 alkyl group, a C2-C60 alkenyl group, a C2-C60 alkynyl group, and a C1-C60 alkoxy group;

    [0205] a C1-C60 alkyl group, a C2-C60 alkenyl group, a C2-C60 alkynyl group, and a C1-C60 alkoxy group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, - I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C6-C60 aryloxy group, a C6-C60 arylthio group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, -Si(Q11)(Q12)(Q13), -N(Q11)(Q12), -B(Q11)(Q12), - C(=O)(Q11), -S(=O)2(Q11), and -P(=O)(Q11)(Q12);

    [0206] a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C6-C60 aryloxy group, a C6-C60 arylthio group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, and a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group;

    [0207] a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C6-C60 aryloxy group, a C6-C60 arylthio group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, and a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C60 alkyl group, a C2-C60 alkenyl group, a C2-C60 alkynyl group, a C1-C60 alkoxy group, a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C6-C60 aryloxy group, a C6-C60 arylthio group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8-to 60-membered heteropolycyclic group, -Si(Q21)(Q22)(Q23), -N(Q21)(Q22), -B(Q21)(Q22), - C(=O)(Q21), -S(=O)2(Q21), and -P(=O)(Q21)(Q22); and

    [0208] -Si(Q31)(Q32)(Q33), -N(Q31)(Q32), -B(Q31)(Q32), -C(=O)(Q31), -S(=O)2(Q31) and - P(=O)(Q31)(Q32),

    [0209] wherein Q11 to Q13, Q21 to Q23, and Q31 to Q33 may each independently be selected from hydrogen, deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C60 alkyl group, a C2-C60 alkenyl group, a C2-C60 alkynyl group, a C1-C60 alkoxy group, a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, a biphenyl group, and a terphenyl group.

    [0210] The term "Ph" as used herein represents a phenyl group. The term "Me" as used herein represents a methyl group. The term "Et" as used herein represents an ethyl group. The term "ter-Bu" or "But" as used herein represents a tert-butyl group. The term "OMe" as used herein represents a methoxy group.

    [0211] The term "biphenyl group" as used herein refers to a phenyl group substituted with a phenyl group. The "biphenyl group" belongs to "a substituted phenyl group" having a "C6-C60 aryl group" as a substituent.

    [0212] The term "terphenyl group" as used herein refers to a phenyl group substituted with a biphenyl group. The "terphenyl group" belongs to "a substituted phenyl group" having a "C6-C60 aryl group substituted with a C6-C60 aryl group" as a substituent.

    [0213] The symbols and ' as used herein, unless defined otherwise, each indicate a binding site to an adjacent atom in the corresponding formula.

    [0214] Hereinafter, compounds and an organic light-emitting device according to one or more embodiments will be described in more detail with reference to Synthesis Examples and Examples. The wording "B was utilized instead of A" used in describing Synthesis Examples means that an amount of B utilized was identical to an amount of A utilized in terms of molar equivalents.

    Synthesis Examples


    Synthesis Example 1: Synthesis of Compound 1



    [0215] 


    (1) Synthesis of Intermediate 1-1



    [0216] 5 grams (g) of 1-bromodibenzo[b,d]furan (Intermediate (a)), 6.4 g of 9,9-dimethyl-9H-fluoren-2-amine (Intermediate (b)), 6.4 g of potassium tert-butoxide (KtOBu), 0.3 g of P(tBu)3, and 0.4 g of Pd2(dba)3 were diluted in toluene, followed by stirring at a temperature of 100°C under reflux. After a 20-hour lapse, the temperature was lowered to room temperature. Subsequently, the reaction was terminated utilizing water. An organic layer was extracted therefrom three times utilizing ethyl acetate. Then, the organic layer was dried utilizing anhydrous magnesium sulfate, followed by filtration under reduced pressure. The obtained residue was separated and purified through column chromatography to thereby obtain 6.5 g of Intermediate 1-1 (yield: 86%). The compound thus obtained was identified by liquid chromatography-mass spectrometry (LC-MS). C27H21NO : calc'd : M+ 375.16 foun'd : 375.26

    (2) Synthesis of Compound 1



    [0217] Compound 1 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 3.8 g of Intermediate 1-1 was utilized instead of Intermediate (b), and 3.7 g of 3-iodo-9-phenyl-9H-carbazole (Intermediate (c)) was utilized instead of 1-bromodibenzo[b,d]furan (Intermediate (a)).

    [0218] C45H32N2O : calc'd : M+ 616.25 foun'd : 616.35

    Synthesis Example 2: Synthesis of Compound 2



    [0219] 


    (1) Synthesis of Intermediate 2-1



    [0220] 8.2 g of Intermediate 2-1 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 8 g of Intermediate (d) was utilized instead of Intermediate (b) (yield: 82%). C37H25NO: calc'd : M+ 499.19 foun'd : 499.29

    (2) Synthesis of Compound 2



    [0221] Compound 2 was obtained in substantially the same manner as in Synthesis of Compound 1, except that 5 g of Intermediate 2-1 was utilized instead of Intermediate 1-1. C55H36N2O : calc'd : M+ 740.28 foun'd : 740.38

    Synthesis Example 3: Synthesis of Compound 3



    [0222] 


    (1) Synthesis of Intermediate 3-1



    [0223] 5.2 g of Intermediate 3-1 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 8 g of Intermediate (e) was utilized instead of Intermediate (b) (yield: 52%). C37H25NO: calc'd : M+ 497.18 foun'd : 497.28

    (2) Synthesis of Compound 3



    [0224] 7.4 g of Compound 3 was obtained in substantially the same manner as in Synthesis of Compound 1, except that 5 g of Intermediate 3-1 was utilized instead of Intermediate 1-1 (yield: 75%). C55H36N2O : calc'd : M+ 740.28 foun'd : 740.38

    Synthesis Example 4: Synthesis of Compound 4



    [0225] 


    (1) Synthesis of Intermediate 4-1



    [0226] 5.1 g of Intermediate 4-1 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 4.9 g of 1-bromodibenzo[b,d]furan was utilized instead of 5 g of Intermediate (a), and 7.1 g of spiro[cyclopentane-1,9'-fluoren]-2'-amine was utilized instead of Intermediate (b) (yield: 64 %).

    [0227] C29H23NO : calc'd : M+ 401.18 foun'd : 401.20

    (2) Synthesis of Compound 4



    [0228] 4.6 g of Compound 4 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 4 g of Intermediate 4-1 was utilized instead of Intermediate (b), and 3.7 g of 3-iodo-9-phenyl-9H-carbazole was utilized instead of 5 g of Intermediate (a) (yield: 72 %).

    [0229] C47H34N2O : calc'd : M+ 647.27 foun'd : 647.28

    [0230] 1H NMR (500 MHz, CDCl3) δ= 8.22(m, 1H), 7.79(dd, 2H), 7.72(dd, 1H), 7.67(d, 1H), 7.54-7.14(m, 17H), 6.95(d, 1H), 6.90(dd, 1H), 6.66(dd, 1H),. 6.54(dd, 1H), 2.19-2.08(m, 2H), 1.95-1.72(m, 6H)

    Synthesis Example 5: Synthesis of Compound 5



    [0231] 



    [0232] 4.7 g of Compound 5 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 3.8 g of Intermediate 1-1 was utilized instead of Intermediate (b), and 3.4 g of 3-bromo-9-(4-fluorophenyl)-9H-carbazole was utilized instead of Intermediate (a) (yield: 75%). C45H31FN2O : calc'd : M+ 634.24 foun'd : 634.34

    Synthesis Example 6: Synthesis of Compound 6



    [0233] 



    [0234] 5.2 g of Compound 6 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 5 g of Intermediate 2-1 was utilized instead of Intermediate (b), and 3.4 g of 3-bromo-9-(4-fluorophenyl)-9H-carbazole was utilized instead of Intermediate (a) (yield: 68%). C55H35FN2O : calc'd : M+ 758.27 foun'd : 758.37

    Synthesis Example 7: Synthesis of Compound 8



    [0235] 



    [0236] 5 g of Compound 8 was obtained in substantially the same manner as in Synthesis of Compound 4, except that 4 g of Intermediate 4-1 and 3.9 g of 9-(4-fluorophenyl)-3-iodo-9H-carbazole were utilized (yield: 76 %).

    [0237] C47H33FN2O : calc'd : M+ 660.26 foun'd : 660.27

    [0238] 1H NMR (500 MHz, CDCl3) δ= 8.22(m, 1H), 7.79(dd, 2H), 7.72(dd, 1H), 7.67(d, 1H), 7.48-7.23(m, 13H), 7.18-7.14(m, 1H), 7.09-7.04(m, 2H), 6.95(d, 1H), 6.90(dd, 1H), 6.66(dd, 1H),. 6.54(dd, 1H), 2.19-2.08(m, 2H), 1.95-1.72(m, 6H)

    Synthesis Example 8: Synthesis of Compound 16



    [0239] 



    [0240] 4.7 g of Compound 16 was obtained in substantially the same manner as in Synthesis of Compound 4, except that 4 g of Intermediate 4-1 and 4 g of 9-([1,1'-biphenyl]-4-yl)-3-bromo-9H-carbazole were utilized (yield: 66 %).

    [0241] C53H38N2O : calc'd : M+ 718.30 foun'd : 718.33

    [0242] 1H NMR (500 MHz, CDCl3) δ= 8.22(m, 1H), 7.79(dd, 2H), 7.72(dd, 1H), 7.67(d, 1H), 7.63-7.59(m, 2H), 7.57-7.23(m, 18H), 7.18(dt, 1H), 6.95(d, 1H), 6.90(dd, 1H), 6.66(dd, 1H), 6.59(dd, 1H), 2.19-2.08(m, 2H), 1.95-1.72(m, 6H)

    Synthesis Example 9: Synthesis of Compound 21



    [0243] 



    [0244] 4.3 g of Compound 21 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 3.8 g of Intermediate 1-1 was utilized instead of Intermediate (b), and 2.5 g of 2-bromodibenzo[b,d]furan was utilized instead of Intermediate (a) (yield: 80%). C45H31FN2O: calc'd : M+ 541.20 foun'd : 541.30

    Synthesis Example 10: Synthesis of Compound 37



    [0245] 



    [0246] 3.8 g of Compound 37 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 2.6 g of Intermediate 37-1 was utilized instead of Intermediate (b), and 3.7 g of Intermediate (c) was utilized instead of Intermediate (a) (yield: 76%).

    [0247] C36H24N2OM+ calc'd : 500.19 foun'd : 500.29

    Synthesis Example 11: Synthesis of Compound 93



    [0248] 



    [0249] 5.1 g of Compound 93 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 3.8 g of Intermediate 1-1 was utilized instead of Intermediate (b), and 4 g of Intermediate 93-1 was utilized instead of Intermediate (a) (yield: 74%).

    [0250] C51H36N2O M+ calc'd : 692.28 foun'd : 692.38

    Synthesis Example 12: Synthesis of Compound 94



    [0251] 



    [0252] 6.3 g of Compound 94 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 5 g of Intermediate 2-1 was utilized instead of Intermediate (b), and 4 g of Intermediate 93-1 was utilized instead of Intermediate (a) (yield: 77%).

    [0253] C61H40N2O M+ calc'd : 816.31 foun'd : 816.41

    Synthesis Example 13: Synthesis of Compound 95



    [0254] 



    [0255] 6.1 g of Compound 95 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 5 g of Intermediate 3-1 was utilized instead of Intermediate (b), and 4 g of Intermediate 93-1 was utilized instead of Intermediate (a) (yield: 75%).

    [0256] C61H38N2O M+ calc'd : 814.30 foun'd : 814.40

    Synthesis Example 14: Synthesis of Compound 101



    [0257] 



    [0258] 7.1 g of Compound 101 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 3.8 g of Intermediate 1-1 was utilized instead of Intermediate (b), and 4.2 g of Intermediate 101-1 was utilized instead of Intermediate (a) (yield: 75%).

    [0259] C51H35FN2O M+ calc'd : 710.27 foun'd : 710.37

    Synthesis Example 15: Synthesis of Compound 187



    [0260] 



    [0261] 3.1 g of Compound 187 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 2.5 g of Intermediate 2-1 was utilized instead of Intermediate (b), and 2 g of 2-bromo-9,9'-spirobi[fluorene] was utilized instead of Intermediate (a) (yield: 77%).

    [0262] C62H39NO : calc'd : M+ 813.30 foun'd : 813.34

    [0263] 1H NMR (500 MHz, CDCl3) δ= 7.92-7.84(m, 4H), 7.79(m, 1H), 7.72(dd, 1H), 7.61(d, 1H), 7.58(d, 1H), 7.48-7.41(m, 5H), 7.36-7.28(m, 3H), 7.21-7.06(m, 14H), 6.92(dd, 1H), 6.81-6.72(m, 5H), 6.66(dd, 1H), 6.57(d, 1H), 6.43(d, 1H)

    Synthesis Example 16: Synthesis of Compound 188



    [0264] 



    [0265] 3.3 g of Compound 188 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 2.5 g of Intermediate 3-1 was utilized instead of Intermediate (b), and 2 g of 2-bromo-9,9'-spirobi[fluorene] was utilized instead of Intermediate (a) (yield: 81 %).

    [0266] C62H37NO : calc'd : M+ 811.29 foun'd : 811.31

    [0267] 1H NMR (500 MHz, CDCl3) δ= 7.92(dd, 4H), 7.89(dd, 2H), 7.79(td, 1H), 7.72(dd, 1H), 7.61(d, 2H), 7.48-7.41(m, 7H), 7.36-7.26(m, 3H), 7.21-7.15(m, 6H), 6.92(dd, 2H), 6.77-6.73(m, 6H), 6.68(dd, 1H), 6.43(d, 2H)

    Synthesis Example 17: Synthesis of Compound 204



    [0268] 



    [0269] 3.8 g of Compound 204 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 5 g of Intermediate 2-1 was utilized instead of Intermediate (b), and 2.3 g of 2-bromo-1,1'-biphenyl was utilized instead of Intermediate (a) (yield: 58%).

    [0270] C49H33NO : M+ calc'd : 651.26 foun'd : 651.36

    Synthesis Example 18: Synthesis of Compound 210



    [0271] 


    (1) Synthesis of Intermediate 210-1



    [0272] 3 g of Intermediate 210-1 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 2.5 g of [1,1'-biphenyl]-2-amine was utilized instead of Intermediate (b), and 2.5 g of 1-bromodibenzo[b,d]furan was utilized instead of 5 g of Intermediate (a) (yield: 91%).

    [0273] C24H17NO: calc'd : M+ 335.13 foun'd : 335.14

    (2) Synthesis of Compound 210



    [0274] 5.1 g of Compound 210 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 3 g of Intermediate 210-1 was utilized instead of Intermediate (b), and 3.7 g of 2-bromo-9,9'-spirobi[fluorene] was utilized instead of Intermediate (a) (yield: 86 %).

    [0275] C49H31NO: calc'd : M+649.24 foun'd : 649.25

    [0276] 1H NMR (500 MHz, CDCl3) δ= 7.92(dd, 2H), 7.89(dd, 1H), 7.80(d, 1H), 7.72(d, 1H), 7.59-7.51(m, 5H), 7.49-7.41(m, 5H), 7.32-7.27(m, 3H), 7.21-7.14(m, 5H), 7.01(t, 1H), 6.77-6.73(m, 4H), 6.66(dd, 1H), 6.61(dd, 1H),5.47(d, 1H)

    Synthesis Example 19: Synthesis of Compound 213



    [0277] 




    (1) Synthesis of Intermediate 213-2



    [0278] 4.7 g of 2,7-dibromo-9,9'-spirobi[fluorene] and 3.4 g of phenyl boronic acid were dilluted with 60 mL of tetrahydrofuran and 20 mL of water. 4.1 g of K2CO3 and 580 mg of Pd(PPh3)4 were added dropwise thereto, followed by stirring at a temperature of 65 °C under reflux. Once the reaction was complete, the temperature was lowered to room temperature, and filtration was performed three times utilizing ethyl acetate under reduced pressure. Then, the residue obtained by distillation under reduced pressure was separated and purified through column chromatography to obtain 4.4 g of Intermediate 213-2 (yield: 93 %).

    [0279] C31H19Br : calc'd : M+ 470.07 foun'd : 470.08

    (2) Synthesis of Intermediate 213-1



    [0280] 3 g of Intermediate 213-1 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 2.5 g of [1,1'-biphenyl]-4-amine was utilized instead of Intermediate (b), and 2.5 g of 1-bromodibenzo[b,d]furan was utilized instead of 5 g of Intermediate (a) (yield: 91%).

    [0281] C24H17NO: calc'd : M+ 335.13 foun'd : 335.14

    (3) Synthesis of Compound 213



    [0282] 5.1g of Compound 213 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 4.4 g of Intermediate 213-2 was utilized instead of Intermediate (a), and 3 g of Intermediate 213-1 was utilized instead of Intermediate (b) (yield: 79 %).

    [0283] C55H35NO: calc'd : M+ 725.27 foun'd : 725.30

    [0284] 1H NMR (500 MHz, CDCl3) δ= 7.93(dd, 2H), 7.79-7.78(111, 2H), 7.72-7.59(111, 6H), 7.54-7.28(m, 15H), 7.20(t, 2H), 6.89(m, 2H), 6.75(dd, 2H), 6.68(dd, 1H), 6.56-6.54(m, 2H), 5.68(d, 1H)

    Synthesis Example 20: Synthesis of Compound 219



    [0285] 



    [0286] 3.1 g of Compound 219 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 2.4 g of Intermediate 213-2 was utilized instead of Intermediate (a), and 1.9 g of Intermediate 1-1 was utilized instead of Intermediate (b) (yield: 81 %).

    [0287] C58H39NO : calc'd : M+ 765.30 foun'd : 765.34

    [0288] 1H NMR (500 MHz, CDCl3) δ= 7.93(dd, 2H), 7.79-7.67(m, 6H), 7.62(d, 1H), 7.53-7.28(m, 11H), 7.18(dt, 2H), 7.11(dd, 2H), 6.89-6.82(m, 3H), 6.75(dd, 2H), 6.68(dd, 1H), 6.50(d, 1H). 6.10(d, 1H), 1.61(s, 6H)

    Synthesis Example 21: Synthesis of Compound 240



    [0289] 



    [0290] 2.5 g of Compound 240 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 2 g of 6-bromo-2,9-diphenyl-9H-carbazole was utilized instead of Intermediate (a), and 1.7 g of Intermediate 213-1 was utilized instead of Intermediate (b) (yield: 78 %).

    [0291] C48H32N2O: calc'd : M+ 625.25 foun'd : 625.29

    [0292] 1H NMR (500 MHz, CDCl3) δ= 7.86(dd, 1H), 7.79-7.76(m, 2H), 7.73-7.70(m, 3H), 7.65-7.61(m, 2H), 7.55-7.28(m, 18H), 7.24-7.21(m, 2H), 6.70-6.65(m, 3H), 6.59(dd, 1H)

    Synthesis Example 22: Synthesis of Compound 251



    [0293] 


    (1) Synthesis of Intermediate 251-1



    [0294] 3.1 g of Intermediate 251-1 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 2.1 g of 9,9-dimethyl-9H-fluoren-1-amine was utilized instead of Intermediate (b), and 2.5 g of 1-bromodibenzo[b,d]furan was utilized instead of 5 g of Intermediate (a) (yield: 83 %).

    [0295] C27H21NO: calc'd : M+ 375.16 foun'd : 375.19

    (2) Synthesis of Compound 251



    [0296] 4 g of Compound 251 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 3.1 g of Intermediate 251-1 was utilized instead of Intermediate (b), and 3.1 g of 3-iodo-9-phenyl-9H-carbazole was utilized instead of Intermediate (a) (yield: 78 %).

    [0297] C45H32N2O: calc'd : M+ 616.25 foun'd : 616.29

    [0298] 1H NMR (500 MHz, CDCl3) δ= 8.22(d, 1H), 7.82(d,1 H), 7.77(td, 1H), 7.70(dd, 1H), 7.54-7.44(m, 7H), 7.39-7.22(m, 10H), 7.11(dd, 1H), 6.96(dd, 1H), 6.57-6.47(m, 3H), 1.68(s, 6H)

    Synthesis Example 23: Synthesis of Compound 253



    [0299] 


    (1) Synthesis of Intermediate 253-1



    [0300] 3.5 g of Intermediate 253-1 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 2.1 g of 9,9-dimethyl-9H-fluoren-4-amine was utilized instead of Intermediate (b), and 2.5 g of 1-bromodibenzo[b,d]furan was utilized instead of 5 g of Intermediate (a) (yield: 92 %).

    [0301] C27H21NO: calc'd : M+ 375.16 foun'd : 375.19

    (2) Synthesis of Compound 253



    [0302] 4.6 g of Compound 253 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 3.5 g of Intermediate 253-1 was utilized instead of Intermediate (b), and 3.6 g of 3-iodo-9-phenyl-9H-carbazole was utilized instead of Intermediate (a) (yield: 81 %).

    [0303] C45H32N2O: calc'd : M+ 616.25 foun'd : 616.29

    [0304] 1H NMR (500 MHz, CDCl3) δ= 8.22(d, 1H), 7.82(d,1 H), 7.72(d, 1H), 7.63(dd,1 H), 7.51-7.21(m, 16H), 7.14-7.07(m, 2H), 6.86(dd, 1H), 6.61-6.59(m, 1H), 6.53(dd, 1H), 6.24(td, 1H), 1.61(s, 6H)

    Synthesis Example 24: Synthesis of Compound 256



    [0305] 



    [0306] 5.0 g of Compound 256 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 3.5 g of Intermediate 253-1 was utilized instead of Intermediate (b), and 3.2 g of 3-bromo-9-(4-fluorophenyl)-9H-carbazole was utilized instead of Intermediate (a) (yield: 84 %).

    [0307] C45H31FN2O: calc'd : M+ 634.24 foun'd : 634.25

    [0308] 1H NMR (500 MHz, CDCl3) δ= 8.23(d, 1H), 7.82(d, 1H), 7.72(td,1 H), 7.62(dd, 1H), 7.58-7.35(m, 3H), 7.34-7.21(m, 10H), 7.14-7.03(m, 4H), 6.86(dd, 1H), 6.61(m, 1H), 6.53(dd,1 H), 6.24(dd, 1H, 1.61(s, 6H)

    Synthesis Example 25: Synthesis of Compound 268



    [0309] 


    (1) Synthesis of Intermediate 268-1



    [0310] 3.2 g of Intermediate 268-1 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 2.1 g of 9,9-dimethyl-9H-fluoren-2-amine was utilized instead of Intermediate (b), and 2.5 g of 1-bromodibenzo[b,d]furan was utilized instead of 5 g of Intermediate (a) (yield: 85 %).

    [0311] C27H21NO: calc'd : M+ 375.16 foun'd : 375.18

    (2) Synthesis of Compound 268



    [0312] 5.7 g of Compound 268 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 3.2 g of Intermediate 268-1 was utilized instead of Intermediate (b), and 4.0 g of Intermediate 213-2 was utilized instead of Intermediate (a) (yield: 88 %).

    [0313] C58H39NO: calc'd : M+ 765.30 foun'd : 765.32

    [0314] 1H NMR (500 MHz, CDCl3) δ= 7.93(dd, 2H), 7.79-7.66(m, 6H). 7.62(d, 1H), 7.53-7.29(m, 11H), 7.20(dt,2 H), 7.11-7.04(m, 4H), 6.89(d,1H), 6.87(t, 1H), 6.75(t, 1H), 6.74(d, 1H), 6.66(dd, 1H), 6.42(dd,1 H), 5.68(d,1 H), 1.52(s, 6H)

    Synthesis Example 26: Synthesis of Compound 269



    [0315] 



    [0316] 4.8 g of Compound 269 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 3.2 g of Intermediate 253-1 was utilized instead of Intermediate (b), and 4.0 g of Intermediate 213-2 was utilized instead of Intermediate (a) (yield: 74 %).

    [0317] C58H39NO: calc'd : M+ 765.30 foun'd : 765.32

    [0318] 1H NMR (500 MHz, CDCl3) δ= 7.93(d,2H), 7.82(d, 1H), 7.80(d, 1H), 7.72-7.58(m, 5H), 7.53-7.36(m, 7H), 7.33-7.05(m, 9H), 6.87-6.84(m, 2H), 6.79(dd,1 H), 6.75(dd,2 H), 6.61(m, 1H), 6.23(d, 1H), 5.49(d, 1H), 1.61(s, 6H)

    Synthesis Example 27: Synthesis of Compound 278



    [0319] 



    [0320] 4.3 g of Compound 278 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 3.2 g of Intermediate 253-1 was utilized instead of Intermediate (b), and 3.8 g of 2-bromo-9,9'-spirobi[fluorene] was utilized instead of Intermediate (a) (yield: 86 %).

    [0321] C52H35NO: calc'd : M+ 689.27 foun'd : 689.28

    [0322] 1H NMR (500 MHz, CDCl3) δ= 7.92(d, 2H), 7.89(d, 1H), 7.82(d,1 H), 7.72(d, 1H), 7.62(dd, 1H), 7.59(d,1 H), 7.48-7.41(m, 4H), 7.32-7.06(m, 10H), 6.87(d, 1H), 6.81(dd,1 H), 6.77-6.73(m, 3H), 6.61(m,1 H), 6.23(d, 1H), 5.72(dd, 1H), 1.61(s, 6H)

    Synthesis Example 28: Synthesis of Compound 281



    [0323] 


    (1) Synthesis of Intermediate 281-1



    [0324] 3.8 g of Intermediate 281-1 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 3.3 g of 9,9-diphenyl-9H-fluoren-4-amine was utilized instead of Intermediate (b), and 2.5 g of 1-bromodibenzo[b,d]furan was utilized instead of 5 g of Intermediate (a) (yield: 77 %).

    [0325] C37H25NO: calc'd : M+ 499.19 foun'd : 499.23

    (2) Synthesis of Compound 281



    [0326] 4.9 g of Compound 281 was obtained in substantially the same manner as in Synthesis of Intermediate 1-1, except that 3.8 g of Intermediate 281-1 was utilized instead of Intermediate (b), and 3.2 g of 2-bromo-9,9'-spirobi[fluorene] was utilized instead of Intermediate (a) (yield: 79 %).

    [0327] C62H39NO: calc'd : M+ 813.30 foun'd : 813.33

    [0328] 1H NMR (500 MHz, CDCl3) δ= 7.92(d, 2H), 7.89(d,1 H), 7.82(d,1 H), 7.72(d,1 H), 7.59(dd, 2H), 7.49-7.40(m, 4H), 7.33-7.26(m, 4H), 7.21-7.05(m, 14H), 6.81-6.71(m, 6H), 6.62(m, 1H), 6.56(dd, 1H), 5.72(d, 1H), 5.68(t, 1H)

    [0329] Compounds synthesized in Synthesis Examples 1 to 28 were identified by 1H nuclear magnetic resonance (NMR). The results thereof are shown in Tables 1 and 2. Methods of synthesizing compounds other than compounds shown in Tables 1 and 2 may be easily understood to those skilled in the art by referring to the synthesis pathways and raw materials described above.
    Table 1
    Compound1H NMR (400 Mhz)
    1 8.25(d, 1H), 7.85(d, 2H), 7.80-7.75(m,2H), 7.73-7.70(m, 1H), 7.56(d, 1H), 7.53-7.21(m, 14H), 7.15-7.09(m, 2H), 7.00(dd, 3H), 6.85(dd, 1H), 6.65(dd, 1H), 6.55(dd, 1H), 1.61(s, 6H)
    2 8.22-8.20(m, 1H), 7.86(td, 1H), 7.79-7.77(m, 1H), 7.72(m,1H), 7.58(d, 1H), 7.51-7.23(m, 15H), 7.21-7.05(m, 11H), 6.81(td, 1H), 6.73(dd, 1H), 6.65(dd, 1H), 6.53-6.48(m, 2H)
    3 8.22-8.20(m, 1H), 7.90(dd, 2H), 7.87(dd, 1H), 7.79(m, 1H), 7.72(m, 1H), 7.61(d,1H), 7.54-7.12(m, 20H), 6.92(dd, 1H), 6.77-6.73(m, 3H), 6.66(dd, 1H), 6.51(dd, 1H), 5.97(q, 1H)
    5 8.22-8.20(m, 1H), 7.85(m, 1H), 7.79-7.76(m, 2H), 7.71(m, 1H), 7.57(m, 1H), 7.46(dd, 1H), 7.40-7.21(m, 10H), 7.14-7.03(m, 4H), 7.01(dd,1H), 6.85(dd, 1H), 6.66(dd, 1H), 6.54(dd, 1H), 1.61(s, 6H)
    6 8.22-8.20(m, 1H), 7.86(td, 1H), 7.79-7.77(m, 1H), 7.72-7.70(m, 1H), 7.58(d, 1H). 7.48-7.23(m, 12H), 7.20-7.03(m, 13H), 6.81(dd, 1H), 6.73(dd, 1H), 6.66(dd, 1H), 6.53(q, 1H), 6.51(dd, 1H)
    21 7.84-7.82(m, 1H), 7.79-7.75(m, 2H), 7.73-7.70(m, 2H),7.68-7.65(m, 1H), 7.57-7.40(m, 5H), 7.34-7.25(m, 4H), 7.14-7.09(m, 2H), 7.03(dd, 1H), 6.85(m, 1H), 6.66(dd, 1H), 6.54(dd, 1H), 1.61(s, 6H)
    37 8.22-8.20(m, 1H), 7.79(m, 1H), 7.72(m, 1H), 7.54-7.21(m, 14H), 7.08-7.02(m, 2H), 6.67-6.53(m, 3H), 6.34-6.31(m, 2H)
    93 8.24-8.22(m, 1H), 8.15(m, 1H), 7.79-7.70(m, 4H), 7.67(d, 1H), 7.58-7.42(m, 8H), 7.39-7.25(m, 7H), 7.21-7.19(m, 1H), 7.14-7.09(m, 2H), 6.84(dd, 1H), 6.68(dd, 1H), 6.63-6.59(m, 2H), 6.49(m, 1H), 1.61(s, 6H)
    94 8.24-8.22(m, 1H), 8.15(m, 1H), 7.86(td, 1H), 7.79-7.70(m, 3H), 7.67(d, 1H), 7.60-7.53(m, 3H),7.50-7.25(m, 12H), 7.21-7.03(m, 12H), 6.81(td, 1H), 6.75(dd, 1H), 6.68(dd, 1H), 6.63-6.57(m, 3H), 6.44(d, 1H)
    95 8.24-8.22(m, 1H), 8.15(m, 1H), 8.02-7.87(m, 3H), 7.79-7.70(m, 3H), 7.67(d, 1H), 7.60-7.53(m, 3H),7.50-7.25(m, 14H), 7.23-7.15(m, 4H), 6.92(dd, 1H), 6.77-6.71(m, 3H), 6.68(dd, 1H), 6.63-6.57(m, 3H), 5.95(d, 1H)
    101 8.24-8.22(m, 1H), 8.15(m, 1H), 7.79-7.70(m, 4H), 7.67(d, 1H), 7.58-7.52(m, 3H), 7.48-7.44(m, 1H),7.39-7.25(m, 8H), 7.21-7.19(m, 1H), 7.14-7.03(m, 4H), 6.84(dd, 1H), 6.68(dd, 1H), 6.63-6.59(m, 2H), 6.49(m, 1H), 1.61(s, 6H)
    204 7.92-7.87(m, 3H), 7.79(m, 1H), 7.72(m,1H), 7.63-7.58(m, 3H), 7.52-7.24(m,12H), 7.21-7.15(m, 3H), 6.92(dd, 1H), 6.77-6.71(m, 3H), 6.68-6.66(dd, 1H), 6.58-6.54(m, 2H), 5.95(dd, 1H)
    Table 2
    Compound1H NMR (sooMhz)
    4 8.22(m, 1H), 7.79(dd, 2H), 7.72(dd, 1H), 7.67(d, 1H), 7.54-7.14(m, 17H), 6.95(d, 1H), 6.90(dd, 1H), 6.66(dd, 1H),. 6.54(dd, 1H), 2.19-2.08(m, 2H), 1.95-1.72(m, 6H)
    8 8.22(m, 1H), 7.79(dd, 2H), 7.72(dd, 1H), 7.67(d, 1H), 7.48-7.23(m, 13H), 7.18-7.14(m, 1H), 7.09-7.04(m, 2H), 6.95(d, 1H), 6.90(dd, 1H), 6.66(dd, 1H),. 6.54(dd, 1H), 2.19-2.08(m, 2H), 1.95-1.72(m, 6H)
    16 8.22(m, 1H), 7.79(dd, 2H), 7.72(dd, 1H), 7.67(d, 1H), 7.63-7.59(m, 2H), 7.57-7.23(m, 18H), 7.18(dt, 1H), 6.95(d, 1H), 6.90(dd, 1H), 6.66(dd, 1H), 6.59(dd, 1H), 2.19-2.08(m, 2H), 1.95-1.72(m, 6H)
    187 7.92-7.84(m, 4H), 7.79(m, 1H), 7.72(dd, 1H), 7.61(d, 1H), 7.58(d, 1H), 7.48-7.41(m, 5H), 7.36-7.28(m, 3H), 7.21-7.06(m, 14H), 6.92(dd, 1H), 6.81-6.72(m, 5H), 6.66(dd, 1H), 6.57(d, 1H), 6.43(d, 1H)
    188 7.92(dd, 4H), 7.89(dd, 2H), 7.79(td, 1H), 7.72(dd, 1H), 7.61(d, 2H), 7.48-7.41(m, 7H), 7.36-7.26(m, 3H), 7.21-7.15(m, 6H), 6.92(dd, 2H), 6.77-6.73(m, 6H), 6.68(dd, 1H), 6.43(d, 2H)
    210 7.92(dd, 2H), 7.89(dd, 1H), 7.80(d, 1H), 7.72(d, 1H), 7.59-7.51(m, 5H), 7.49-7.41(m, 5H), 7.32-7.27(m, 3H), 7.21-7.14(m, 5H), 7.01(t, 1H), 6.77-6.73(m, 4H), 6.66(dd, 1H), 6.61(dd, 1H),5.47(d, 1H)
    213 7.93(dd, 2H), 7.79-7.78(m, 2H), 7.72-7.59(m, 6H), 7.54-7.28(m, 15H), 7.20(t, 2H), 6.89(m, 2H), 6.75(dd, 2H), 6.68(dd, 1H), 6.56-6.54(m, 2H), 5.68(d, 1H)
    219 7.93(dd, 2H), 7.79-7.67(m, 6H), 7.62(d, 1H), 7.53-7.28(m, 11H), 7.18(dt, 2H), 7.11(dd, 2H), 6.89-6.82(m, 3H), 6.75(dd, 2H), 6.68(dd, 1H), 6.50(d, 1H). 6.10(d, 1H), 1.61(s, 6H)
    240 7.86(dd, 1H), 7.79-7.76(m, 2H), 7.73-7.70(m, 3H), 7.65-7.61(m, 2H), 7.55-7.28(m, 18H), 7.24-7.21(m, 2H), 6.70-6.65(m, 3H), 6.59(dd, 1H)
    251 8.22(d, 1H), 7.82(d,1 H), 7.77(td, 1H), 7.70(dd, 1H), 7.54-7.44(m, 7H), 7.39-7.22(m, 10H), 7.11(dd, 1H), 6.96(dd, 1H), 6.57-6-47(m, 3H), 1.68(s, 6H)
    253 8.22(d, 1H), 7.82(d,1 H), 7.72(d, 1H), 7.63(dd,1 H), 7.51-7.21(m, 16H), 7.14-7.07(m, 2H), 6.86(dd, 1H), 6.61-6.59(m, 1H), 6.53(dd, 1H), 6.24(td, 1H), 1.61(s, 6H)
    256 8.23(d, 1H), 7.82(d, 1H), 7.72(td,1 H), 7.62(dd, 1H), 7.58-7.35(m, 3H), 7.34-7.21(m, 10H), 7.14-7.03(m, 4H), 6.86(dd, 1H), 6.61(m, 1H), 6.53(dd,1 H), 6.24(dd, 1H, 1.61(s, 6H)
    268 7.93(dd, 2H), 7.79-7.66(m, 6H). 7.62(d, 1H), 7.53-7.29(m, 11H), 7.20(dt,2 H), 7.11-7.04(m, 4H), 6.89(d,1 H), 6.87(t, 1H), 6.75(t, 1H), 6.74(d, 1H), 6.66(dd, 1H), 6.42(dd,1 H), 5.68(d,1 H), 1.52(s, 6H)
    269 7.93(d, 2H), 7.82(d, 1H), 7.80(d, 1H), 7.72-7.58(m, 5H), 7.53-7.36(m, 7H), 7.33-7.05(m, 9H), 6.87-6.84(m, 2H), 6.79(dd,1 H), 6.75(dd,2 H), 6.61(m, 1H), 6.23(d, 1H), 5.49(d, 1H), 1.61(s, 6H)
    278 7.92(d, 2H), 7.89(d, 1H), 7.82(d,1 H), 7.72(d, 1H), 7.62(dd, 1H), 7.59(d,1 H), 7.48-7.41(m, 4H), 7.32-7.06(m, 10H), 6.87(d, 1H), 6.81(dd,1 H), 6.77-6.73(m, 3H), 6.61(m,1 H), 6.23(d, 1H), 5.72(dd, 1H), 1.61(s, 6H)
    281 7.92(d, 2H), 7.89(d,1 H), 7.82(d,1 H), 7.72(d,1 H), 7.59(dd, 2H), 7.49-7.40(m, 4H), 7.33-7.26(m, 4H), 7.21-7.05(m, 14H), 6.81-6.71(m, 6H), 6.62(m, 1H), 6.56(dd, 1H), 5.72(d, 1H), 5.68(t, 1H)

    Examples


    Comparative Example 1



    [0330] A Corning 15 Ohms per square centimeter (Ω/cm2) (1,200 Å) ITO glass substrate was cut to a size of 50 millimeters (mm)×50 mm×0.7 mm, sonicated in isopropyl alcohol and pure water for 5 minutes in each solvent, and cleaned by exposure to ultraviolet rays and ozone for 30 minutes to utilize the glass substrate as an anode. Then, the glass substrate was mounted to a vacuum-deposition apparatus.

    [0331] 2-TNATA was vacuum-deposited on the glass substrate to form a hole injection layer having a thickness of 600 Å. Thereafter, 4,4'-bis[N-(1-naphthyl)-N-phenylamino]biphenyl (hereinafter referred to as "NPB"), which is a hole transport material, as a hole transporting compound was vacuum-deposited on the hole injection layer to form a hole transport layer having a thickness of 300 Å.

    [0332] 9,10-di(naphthalen-2-yl)anthracene (hereinafter referred to as "DNA"), which is a known blue fluorescent host, and 4,4'-bis[2-(4-(N,N-diphenylamino)phenyl)vinyl]biphenyl (hereinafter referred to as "DPAVBi"), which is a known blue fluorescent dopant, were co-deposited on the hole transport layer in a weight ratio of about 98:2 to form an emission layer having a thickness of 300 Å.





    [0333] Subsequently, Alq3 was deposited on the emission layer to form an electron transport layer having a thickness of 300 Å. Subsequently, LiF, which is halogenated alkali metal, was deposited on the electron transport layer to form an electron injection layer having a thickness of 10 Å. Finally, Al was vacuum-deposited on the electron injection layer to form a cathode having a thickness of 3,000 Å to form a LiF/Al electrode, thereby completing the manufacture of an organic light-emitting device.

    Examples 1 to 28



    [0334] An organic light-emitting device was manufactured substantially in the same manner as in Comparative Example 1, except that Compounds shown in Table 3 were utilized instead of NPB in the formation of a hole transport layer.

    Comparative Example 2



    [0335] An organic light-emitting device was manufactured substantially in the same manner as in Comparative Example 1, except that Compound A was utilized instead of NPB in the formation of a hole transport layer.


    Comparative Example 3



    [0336] An organic light-emitting device was manufactured substantially in the same manner as in Comparative Example 1, except that Compound B was utilized instead of NPB in the formation of a hole transport layer.


    Comparative Example 4



    [0337] An organic light-emitting device was manufactured substantially in the same manner as in Comparative Example 1, except that Compound C was utilized instead of NPB in the formation of a hole transport layer.


    Comparative Example 5



    [0338] An organic light-emitting device was manufactured in substantially the same manner as in Comparative Example 1, except that Compound D was utilized instead of NPB in the formation of a hole transport layer.


    Comparative Example 6



    [0339] An organic light-emitting device was manufactured in substantially the same manner as in Comparative Example 1, except that Compound E was utilized instead of NPB in the formation of a hole transport layer.

    Compound E



    [0340] 


    Comparative Example 7



    [0341] An organic light-emitting device was manufactured in substantially the same manner as in Comparative Example 1, except that Compound F was utilized instead of NPB in the formation of a hole transport layer.


    Comparative Example 8



    [0342] An organic light-emitting device was manufactured in substantially the same manner as in Comparative Example 1, except that Compound G was utilized instead of NPB in the formation of a hole transport layer.


    Comparative Example 9



    [0343] An organic light-emitting device was manufactured in substantially the same manner as in Comparative Example 1, except that Compound H was utilized instead of NPB in the formation of a hole transport layer.



    [0344] The performances (driving voltage, luminance, efficiency, and color-coordinate) of the organic light-emitting devices manufactured in Examples 1 to 28 and Comparative Examples 1 to 9 while driving at a current density of 50 mA/cm2 were evaluated. The half lifespan was also measured at a current density of 100 mA/cm2, which indicates time (hour) for the luminance of each organic light-emitting device to decline to 50% of its initial luminance. The evaluation results are shown in Table 3.

    [0345] The luminance was measured utilizing a luminance meter PR650 powered by a current voltmeter (Keithley SMU 236).

    [0346] The efficiency was measured utilizing a luminance meter PR650 powered by a current voltmeter (Keithley SMU 236).
    Table 3
     Hole transport materialDriving voltage (V)Current density (mA/cm2)Luminance (cd/ m2)Efficiency (cd/A)Emission colorHalf lifespan (hr @100 mA/cm2)
    Example 1 Compound 1 4.32 50 3670 7.34 Blue 362
    Example 2 Compound 2 4.21 50 3715 7.43 Blue 353
    Example 3 Compound 3 4.22 50 3665 7.33 Blue 372
    Example 4 Compound 4 4.85 50 3876 7.75 Blue 374
    Example 5 Compound 5 4.26 50 3730 7.46 Blue 374
    Example 6 Compound 6 4.26 50 3730 7.46 Blue 374
    Example 7 Compound 8 4.67 50 3985 7.97 Blue 356
    Example 8 Compound 16 4.72 50 3451 6.90 Blue 382
    Example 9 Compound 21 4.25 50 3630 7.26 Blue 384
    Example 10 Compound 37 4.41 50 3725 7.45 Blue 343
    Example 11 Compound9 3 4.26 50 3630 7.26 Blue 366
    Example 12 Compound 94 4.32 50 3670 7.34 Blue 378
    Example 13 Compound 95 4.45 50 3440 6.88 Blue 325
    Example 14 Compound 101 4.60 50 3490 6.98 Blue 330
    Example 15 Compound 187 4.55 50 3655 7.31 Blue 375
    Example 16 Compound 188 4.69 50 3492 6.98 Blue 356
    Example 17 Compound 204 4.82 50 3540 7.08 Blue 381
    Example 18 Compound 210 4.96 50 3987 7.97 Blue 351
    Example 19 Compound 213 4.74 50 3859 7.72 Blue 348
    Example 20 Compound 219 4.73 50 3565 7.13 Blue 316
    Example 21 Compound 240 4.89 50 3529 7.06 Blue 355
    Example 22 Compound 251 4.82 50 3983 7.97 Blue 327
    Example 23 Compound 253 4.76 50 3852 7.70 Blue 331
    Example 24 Compound 256 4.96 50 3874 7.75 Blue 326
    Example 25 Compound 268 4.81 50 3721 7.44 Blue 312
    Example 26 Compound 269 4.53 50 3652 7.30 Blue 332
    Example 27 Compound 278 4.56 50 3552 7.10 Blue 351
    Example 28 Compound 281 4.66 50 3512 7.02 Blue 366
    Comparati ve Example 1 NPB 7.01 50 2645 5.29 Blue 258
    Comparati ve Example 2 Compound A 6.50 50 2805 5.61 Blue 220
    Comparati ve Example 3 Compound B 5.81 50 3105 6.21 Blue 180
    Comparati ve Example 4 Compound C 6.02 50 3205 6.41 Blue 210
    Comparati ve Example 5 Compound D 8.21 50 1851 3.70 Blue 127
    Comparati ve Example 6 Compound E 6.01 50 2353 5.98 Blue 231
    Comparati ve Example 7 Compound F 7.32 50 2553 5.90 Blue 221
    Comparati ve Example 8 Compound G 5.88 50 2678 5.34 Blue 231
    Comparati ve Example 9 Compound H 5.68 50 2635 5.27 Blue 235


    [0347] As apparent from Table 3, when the compound according to one or more embodiments is utilized as a hole transport material in organic light-emitting devices, the organic light-emitting devices of the Examples comprising the compound according to one or more embodiments were found to have improved driving voltage, excellent I-V-L characteristics with improved efficiency, and particularly, significant improvement of lifespan due to its lifespan improving effects, as compared with the organic light-emitting device of the Comparative Example 1 comprising NPB. In addition, even in comparison with Comparative Examples 2 to 9, in which Compounds A, B, C, D, E, F, G, and H were respectively utilized, the organic light-emitting device of the Examples were found to have improved driving voltage, improved luminance, improved luminescence efficiency, and improved half lifespan.

    [0348] As apparent from the foregoing description, an organic light-emitting device comprising the amine-based compound may have a low driving voltage, high efficiency, long lifespan, and high maximum quantum efficiency.

    [0349] It should be understood that embodiments described herein should be considered in a descriptive sense only and not for purposes of limitation.

    [0350] While one or more embodiments have been described with reference to the figures, it will be understood by those of ordinary skill in the art that various changes in form and details may be made therein without departing from the scope as defined by the following claims, with due account being taken of equivalents thereof.


    Claims

    1. An organic light-emitting device comprising:

    a first electrode;

    a second electrode facing the first electrode; and

    an organic layer between the first electrode and the second electrode, and comprising an emission layer,

    wherein the organic layer comprises at least one amine-based compound represented by Formula 1D:

    wherein, in Formula 1D,

    X1 is N-(L1)a1-(R1)b1,

    X2 is O, or S,

    L1 and L2 are each independently selected from a single bond, a benzene group, a pentalene group, an indene group, a naphthalene group, an azulene group, a heptalene group, an indacene group, an acenaphthalene group, a phenalene group, a phenanthrene group, an anthracene group, a fluoranthene group, a triphenylene group, a pyrene group, a chrysene group, a naphthacene group, a picene group, a perylene group, a pentaphenylene group, a hexacene group, a pyrrole group, an imidazole group, a pyrazole group, a pyridine group, a pyrazine group, a pyrimidine group, a pyridazine group, an isoindole group, an indole group, an indazole group, a purine group, a quinoline group, an isoquinoline group, a benzoquinoline group, a phthalazine group, a naphthyridine group, a quinoxaline group, a quinazoline group, a cinnoline group, a carbazole group, a phenanthridine group, an acridine group, a phenanthroline group, a phenazine group, a benzimidazole group, a furan group, a benzofuran group, a thiophene group, a benzothiophene group, a thiazole group, an isothiazole group, a benzothiazole group, an iso-oxazole group, an oxazole group, a triazole group, a tetrazole group, an oxadiazole group, a triazine group, a benzoxazole group, a dibenzofuran group, a dibenzothiophene group, a benzocarbazole group, and a dibenzocarbazole group; and

    a benzene group, a pentalene group, an indene group, a naphthalene group, an azulene group, a heptalene group, an indacene group, an acenaphthalene group, a phenalene group, a phenanthrene group, an anthracene group, a fluoranthene group, a triphenylene group, a pyrene group, a chrysene group, a naphthacene group, a picene group, a perylene group, a pentaphenylene group, a hexacene group, a pyrrole group, an imidazole group, a pyrazole group, a pyridine group, a pyrazine group, a pyrimidine group, a pyridazine group, an isoindole group, an indole group, an indazole group, a purine group, a quinoline group, an isoquinoline group, a benzoquinoline group, a phthalazine group, a naphthyridine group, a quinoxaline group, a quinazoline group, a cinnoline group, a carbazole group, a phenanthridine group, an acridine group, a phenanthroline group, a phenazine group, a benzimidazole group, a furan group, a benzofuran group, a thiophene group, a benzothiophene group, a thiazole group, an isothiazole group, a benzothiazole group, an iso-oxazole group, an oxazole group, a triazole group, a tetrazole group, an oxadiazole group, a triazine group, a benzoxazole group, a dibenzofuran group, a dibenzothiophene group, a benzocarbazole group, and a dibenzocarbazole group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a C6-C20 aryl group, a C1-C20 heteroaryl group, and -Si(Q31)(Q32)(Q33),

    L3 is a single bond,

    a1 and a2 are each independently an integer from 1 to 5, a3 is 1;

    R1 is independently selected from groups represented by Formulae 5-1 to 5-9, 5-13 to 5-19, and 5-21 to 5-79:







































    wherein, in Formulae 5-1 to 5-9, 5-13 to 5-19, and 5-21 to 5-79,

    Y31 is O, S, N(Z35), or Si(Z36)(Z37),

    Z31, Z32 and Z35 to Z37 are each independently selected from hydrogen, deuterium, - F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclopentenyl group, a cyclohexenyl group, a phenyl group, a biphenyl group, a naphthyl group, a phenalenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a naphthyridinyl group, a quinoxalinyl group, a quinazolinyl group, a carbazolyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a triazinyl group, a dibenzofuranyl group, a dibenzothiophenyl group, and -Si(Q31)(Q32)(Q33),

    e2 is an integer from 0 to 2; when e2 is 2, two Z31 groups are identical to or different from each other, and two Z32 groups are identical to or different from each other,

    e3 is an integer from 0 to 3; when e3 is 2 or greater, at least two Z31 groups are identical to or different from each other and at least two Z32 groups are identical to or different from each other,

    e4 is an integer from 0 to 4; when e4 is 2 or greater, at least two Z31 groups are identical to or different from each other and at least two Z32 groups are identical to or different from each other,

    e5 is an integer from 0 to 5; when e5 is 2 or greater, at least two Z31 groups are identical to or different from each other and at least two Z32 groups are identical to or different from each other,

    e6 is an integer from 0 to 6; when e6 is 2 or greater, at least two Z31 groups are identical to or different from each other and at least two Z32 groups are identical to or different from each other,

    e7 is an integer from 0 to 7; when e7 is 2 or greater, at least two Z31 groups are identical to or different from each other,

    e9 is an integer from 0 to 9; when e9 is 2 or greater, at least two Z31 groups are identical to or different from each other, and

    indicates a binding site to an adjacent atom,

    R3 to R8 are each independently selected from hydrogen, deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a substituted or unsubstituted C1-C60 alkyl group, a substituted or unsubstituted C2-C60 alkenyl group, a substituted or unsubstituted C2-C60 alkynyl group, a substituted or unsubstituted C1-C60 alkoxy group, a substituted or unsubstituted C3-C10 cycloalkyl group, a substituted or unsubstituted C1-C10 heterocycloalkyl group, a substituted or unsubstituted C3-C10 cycloalkenyl group, a substituted or unsubstituted C1-C10 heterocycloalkenyl group, a substituted or unsubstituted C6-C60 aryl group, a substituted or unsubstituted C6-C60 aryloxy group, a substituted or unsubstituted C6-C60 arylthio group, a substituted or unsubstituted C1-C60 heteroaryl group, a substituted or unsubstituted C1-C60 heteroaryloxy group, a substituted or unsubstituted monovalent non-aromatic condensed C8 to C60 polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, -Si(Q1)(Q2)(Q3), -B(Q1)(Q2), and -C(=O)(Q1),

    b1 is an integer from 1 to 10,

    b3, b5, and b7 are each independently an interger from 1 to 4,

    b4, b6, and b8 are each independently an integer from 1 to 3, and

    the substituted C1-C60 alkyl group, the substituted C2-C60 alkenyl group, the substituted C2-C60 alkynyl group, the substituted C1-C60 alkoxy group, the substituted C3-C10 cycloalkyl group, the substituted C1-C10 heterocycloalkyl group, the substituted C3-C10 cycloalkenyl group, the substituted C1-C10 heterocycloalkenyl group, the substituted C6-C60 aryl group, the substituted C6-C60 aryloxy group, the substituted C6-C60 arylthio group, the substituted C1-C60 heteroaryl group, the substituted C1-C60 heteroaryloxy group, the substituted monovalent non-aromatic condensed C8 to C60 polycyclic group, and the substituted monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group are each independently substituted with one or more substituents independently selected from:

    deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a C1-C60 alkyl group, a C2-C60 alkenyl group, a C2-C60 alkynyl group, and a C1-C60 alkoxy group;

    a C1-C60 alkyl group, a C2-C60 alkenyl group, a C2-C60 alkynyl group, and a C1-C60 alkoxy group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C6-C60 aryloxy group, a C6-C60 arylthio group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, -Si(Q11)(Q12)(Q13), -N(Q11)(Q12), - B(Q11)(Q12), -C(=O)(Q11), -S(=O)2(Q11), and -P(=O)(Q11)(Q12);

    a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C6-C60 aryloxy group, a C6-C60 arylthio group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, a biphenyl group, and a terphenyl group;

    a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C6-C60 aryloxy group, a C6-C60 arylthio group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, a biphenyl group, and a terphenyl group, each substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a C1-C60 alkyl group, a C2-C60 alkenyl group, a C2-C60 alkynyl group, a C1-C60 alkoxy group, a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C6-C60 aryloxy group, a C6-C60 arylthio group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, a biphenyl group, a terphenyl group, -Si(Q21)(Q22)(Q23), - N(Q21)(Q22), -B(Q21)(Q22), -C(=O)(Q21), -S(=O)2(Q21), and -P(=O)(Q21)(Q22); and

    -Si(Q31)(Q32)(Q33), -N(Q31)(Q32), -B(Q31)(Q32), -C(=O)(Q31), -S(=O)2(Q31), and - P(=O)(Q31)(Q32),

    wherein Q1 to Q3, Q11 to Q13, Q21 to Q23, and Q31 to Q33 are each independently selected from hydrogen, deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a C1-C60 alkyl group, a C2-C60 alkenyl group, a C2-C60 alkynyl group, a C1-C60 alkoxy group, a C3-C10 cycloalkyl group, a C1-C10 heterocycloalkyl group, a C3-C10 cycloalkenyl group, a C1-C10 heterocycloalkenyl group, a C6-C60 aryl group, a C6-C60 aryl group substituted with a C1-C60 alkyl group, a C1-C60 heteroaryl group, a monovalent non-aromatic condensed C8 to C60 polycyclic group, a monovalent non-aromatic condensed 8- to 60-membered heteropolycyclic group, a biphenyl group, and a terphenyl group.


     
    2. The organic light-emitting device of claim 1, wherein

    the first electrode is an anode,

    the second electrode is a cathode,

    the organic layer further comprises a hole transport region between the first electrode and the emission layer and an electron transport region between the emission layer and the second electrode,

    the hole transport region comprises a hole injection layer, a hole transport layer, an emission auxiliary layer, an electron blocking layer, or a combination thereof, and

    the electron transport region comprises a hole blocking layer, an electron transport layer, an electron injection layer, or a combination thereof;

    preferably wherein the hole transport region comprises the at least one amine-based compound;

    more preferably wherein the hole transport region comprises the hole transport layer, and the hole transport layer comprises the at least one amine-based compound.


     
    3. An amine-based compound represented by Formula 1D:

    wherein, Formula 1D is as defined in claim 1.
     
    4. The amine-based compound of any one of claims 3, wherein

    (A) L1 and L2 are each independently selected from:

    a single bond and a benzene group; and

    a benzene group substituted with at least one selected from deuterium, -F, -Cl, -Br, -I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazino group, a hydrazono group, a C1-C20 alkyl group, a C1-C20 alkoxy group, a C6-C20 aryl group, a C1-C20 heteroaryl group, and -Si(Q31)(Q32)(Q33);

    L3 is a single bond,
    and/or

    (B) R3 to R12 are each independently selected from hydrogen, deuterium, -F, - Cl, -Br, -I, a methyl group, an ethyl group, a propyl group, an iso-propyl group, an n-butyl group, an isobutyl group, a sec-butyl group, a ter-butyl group, a pentyl group, an iso-amyl group, a hexyl group, a phenyl group, and a biphenyl group.


     
    5. The amine-based compound of any one of claims 3 to 4, wherein R1 is selected from groups represented by Formulae 6-1 to 6-10 and 6-12 to 6-26:









    wherein, in Formulae 6-1 to 6-10 and 6-12 to 6-26,
    indicates a binding site to an adjacent atom.
     
    6. The amine-based compound of any one of claims 3 to 5, wherein the amine-based compound represented by Formula 1D is represented by one of Formulae 1B-1 to 1B-16:









































    wherein, in Formulae 1B-1 to 1B-16,
    X1, X2, L2, L3, a2, a3, R3 to R8, b3 to b8 are each independently the same as defined in claims 1 and 4 to 5.
     
    7. An amine-based compound according to claim 3, wherein the amine-based compound is selected from Compounds 42-45, 47-50, 56-59, 61-64, 70-73, 75-78, 84-87, 89-92, 232-239, 243-250:






































     
    8. The organic light-emitting device according to any one of claims 1 or 2, wherein the amine based compound is as defined in any one of claims 3 to 7.
     


    Ansprüche

    1. Organische lichtemittierende Vorrichtung, umfassend:

    eine erste Elektrode;

    eine zweite Elektrode, die der ersten Elektrode gegenüberliegt; und

    eine organische Schicht zwischen der ersten Elektrode und der zweiten Elektrode, und eine Emissionsschicht umfassend,

    wobei die organische Schicht mindestens eine Verbindung auf Aminbasis, dargestellt durch Formel 1D, umfasst:

    wobei, in Formel 1D,

    X1 N-(L1)a1-(R1)b1 ist,

    X2 O oder S ist,

    L1 und L2 jeweils unabhängig voneinander ausgewählt sind aus einer Einfachbindung, einer Benzolgruppe, einer Pentalengruppe, einer Indengruppe, einer Naphthalingruppe, einer Azulengruppe, einer Heptalengruppe, einer Indacengruppe, einer Acenaphthalingruppe, einer Phenalengruppe, einer Phenanthrengruppe, einer Anthracengruppe, einer Fluoranthengruppe, einer Triphenylengruppe, einer Pyrengruppe, einer Chrysengruppe, einer Naphthacengruppe, einer Picengruppe, einer Perylengruppe, einer Pentaphenylengruppe, einer Hexacengruppe, einer Pyrrolgruppe, einer Imidazolgruppe, einer Pyrazolgruppe, einer Pyridingruppe, einer Pyrazingruppe, einer Pyrimidingruppe, einer Pyridazingruppe, einer Isoindolgruppe, einer Indolgruppe, einer Indazolgruppe, einer Puringruppe, einer Chinolingruppe, einer Isochinolingruppe, einer Benzochinolingruppe, einer Phthalazingruppe, einer Naphthyridingruppe, einer Chinoxalingruppe, einer Chinazolingruppe, einer Cinnolingruppe, einer Carbazolgruppe, einer Phenanthridingruppe, einer Acridingruppe, einer Phenanthrolingruppe, einer Phenazingruppe, einer Benzimidazolgruppe, einer Furangruppe, einer Benzofurangruppe, einer Thiophengruppe, einer Benzothiophengruppe, einer Thiazolgruppe, einer Isothiazolgruppe, einer Benzothiazolgruppe, einer Isooxazolgruppe, einer Oxazolgruppe, einer Triazolgruppe, einer Tetrazolgruppe, einer Oxadiazolgruppe, einer Triazingruppe, einer Benzoxazolgruppe, einer Dibenzofurangruppe, einer Dibenzothiophengruppe, einer Benzocarbazolgruppe und einer Dibenzocarbazolgruppe; und

    einer Benzolgruppe, einer Pentalengruppe, einer Indengruppe, einer Naphthalingruppe, einer Azulengruppe, einer Heptalengruppe, einer Indacengruppe, einer Acenaphthalingruppe, einer Phenalengruppe, einer Phenanthrengruppe, einer Anthracengruppe, einer Fluoranthengruppe, einer Triphenylengruppe, einer Pyrengruppe, einer Chrysengruppe, einer Naphthacengruppe, einer Picengruppe, einer Perylengruppe, einer Pentaphenylengruppe, einer Hexacengruppe, einer Pyrrolgruppe, einer Imidazolgruppe, einer Pyrazolgruppe, einer Pyridingruppe, einer Pyrazingruppe, einer Pyrimidingruppe, einer Pyridazingruppe, einer Isoindolgruppe, einer Indolgruppe, einer Indazolgruppe, einer Puringruppe, einer Chinolingruppe, einer Isochinolingruppe, einer Benzochinolingruppe, einer Phthalazingruppe, einer Naphthyridingruppe, einer Chinoxalingruppe, einer Chinazolingruppe, einer Cinnolingruppe, einer Carbazolgruppe, einer Phenanthridingruppe, einer Acridingruppe, einer Phenanthrolingruppe, einer Phenazingruppe, einer Benzimidazolgruppe, einer Furangruppe, einer Benzofurangruppe, einer Thiophengruppe, einer Benzothiophengruppe, einer Thiazolgruppe, einer Isothiazolgruppe, einer Benzothiazolgruppe, einer Isooxazolgruppe, einer Oxazolgruppe, einer Triazolgruppe, einer Tetrazolgruppe, einer Oxadiazolgruppe, einer Triazingruppe, einer Benzoxazolgruppe, einer Dibenzofurangruppe, einer Dibenzothiophengruppe, einer Benzocarbazolgruppe und einer Dibenzocarbazolgruppe, jeweils substituiert mit mindestens einem, ausgewählt aus Deuterium, -F, -Cl, -Br, -I, einer Hydroxylgruppe, einer Cyanogruppe, einer Nitrogruppe, einer Aminogruppe, einer Amidinogruppe, einer Hydrazinogruppe, einer Hydrazonogruppe, einem C1-C20-Alkylrest, einem C1-C20-Alkoxyrest, einem C6-C20-Arylrest, einem C1-C20-Heteoarylrest und -Si(Q31)(Q32)(Q33),

    L3 eine Einfachbindung ist,

    a1 und a2 jeweils unabhängig voneinander eine ganze Zahl von 1 bis 5 sind, a3 1 ist;

    R1 unabhängig ausgewählt ist aus Resten, dargestellt durch die Formeln 5-1 bis 5-9, 5-13 bis 5-19 und 5-21 bis 5-79:







































    wobei, in den die Formeln 5-1 bis 5-9, 5-13 bis 5-19 und 5-21 bis 5-79,

    Y31 O, S, N(Z35) oder Si(Z36)(Z37) ist,

    Z31, Z32 und Z35 bis Z37 jeweils unabhängig voneinander ausgewählt sind aus Wasserstoff, Deuterium, -F, -Cl, -Br, -I, einer Hydroxylgruppe, einer Cyanogruppe, einer Nitrogruppe, einer Amidinogruppe, einer Hydrazinogruppe, einer Hydrazonogruppe, einem C1-C20-Alkylrest,einem C1-C20-Alkoxyrest, einer Cyclopentylgruppe, einer Cyclohexylgruppe, einer Cycloheptylgruppe, einer Cyclopentenylgruppe, einer Cyclohexenylgruppe, einer Phenylgruppe, einer Biphenylgruppe, einer Naphthylgruppe, einer Phenalenylgruppe, einer Phenanthrenylgruppe, einer Anthracenylgruppe, einer Fluoranthenylgruppe, einer Triphenylenylgruppe, Pyridinylgruppe, einer Pyrazinylgruppe, einer Pyrimidinylgruppe, einer Chinolinylgruppe, einer Isochinolinylgruppe, einer Benzochinolinylgruppe, einer Naphthyridinylgruppe, einer Chinoxalinylgruppe, einer Chinazolinylgruppe, einer Carbazolylgruppe, einer Phenanthridinylgruppe, einer Acridinylgruppe, einer Phenanthrolinylgruppe, einer Phenazinylgruppe, einer Triazinylgruppe, einer Dibenzofuranylgruppe, einer Dibenzothiophenylgruppe und -Si(Q31)(Q32)(Q33),

    e2 eine ganze Zahl von 0 bis 2 ist; wenn e2 2 ist, zwei Reste Z31 miteinander identisch sind oder sich voneinander unterscheiden und zwei Reste Z32 miteinander identisch sind oder sich voneinander unterscheiden,

    e3 eine ganze Zahl von 0 bis 3 ist; wenn e3 2 oder größer ist, mindestens zwei Reste Z31 miteinander identisch sind oder sich voneinander unterscheiden und mindestens zwei Reste Z32 miteinander identisch sind oder sich voneinander unterscheiden,

    e4 eine ganze Zahl von 0 bis 4 ist; wenn e4 2 oder größer ist, mindestens zwei Reste Z31 miteinander identisch sind oder sich voneinander unterscheiden und mindestens zwei Reste Z32 miteinander identisch sind oder sich voneinander unterscheiden,

    e5 eine ganze Zahl von 0 bis 5 ist; wenn e5 2 oder größer ist, mindestens zwei Reste Z31 miteinander identisch sind oder sich voneinander unterscheiden und mindestens zwei Reste Z32 miteinander identisch oder sich voneinander unterscheiden,

    e6 eine ganze Zahl von 0 bis 6 ist; wenn e6 2 oder größer ist, mindestens zwei Reste Z31 miteinander identisch sind oder sich voneinander unterscheiden und mindestens zwei Reste Z32 miteinander identisch sind oder sich voneinander unterscheiden,

    e7 eine ganze Zahl von 0 bis 7 ist; wenn e7 2 oder größer ist, mindestens zwei Reste Z31 miteinander identisch sind oder sich voneinander unterscheiden,

    e9 eine ganze Zahl von 0 bis 9 ist; wenn e9 2 oder größer ist, mindestens zwei Reste Z31 miteinander identisch sind oder sich voneinander unterscheiden, und

    eine Bindungsstelle zu einem benachbarten Atom kennzeichnet,

    R3 bis R8 jeweils unabhängig voneinander ausgewählt sind aus Wasserstoff, Deuterium, -F, -Cl, -Br, -I, einer Hydroxylgruppe, einer Cyanogruppe, einer Nitrogruppe, einer Aminogruppe, einer Amidinogruppe, einer Hydrazinogruppe, einer Hydrazonogruppe, einem substituierten oder unsubstituierten C1-C60-Alkylrest, einem substituierten oder unsubstituierten C2-C60-Alkenylrest, einem substituierten oder unsubstituierten C2-C60-Alkinylrest, einem substituierten oder unsubstituierten C1-C60-Alkoxyrest, einem substituierten oder unsubstituierten C3-C10-Cycloalkylrest, einem substituierten oder unsubstituierten C1-C10-Heterocycloalkylrest, einem substituierten oder unsubstituierten C3-C10-Cycloalkenylrest, einem substituierten oder unsubstituierten C1-C10-Heterocycloalkenylrest, einem substituierten oder unsubstituierten C6-C60-Arylrest, einem substituierten oder unsubstituierten C6-C60-Aryloxyrest, einem substituierten oder unsubstituierten C6-C60-Arylthiorest, einem substituierten oder unsubstituierten C1-C60-Heteroarylrest, einem substituierten oder unsubstituierten C1-C60-Heteroaryloxyrest, einem substituierten oder unsubstituierten einwertigen, nichtaromatischen, kondensierten polycyclischen C8 bis C60-Rest , einem substituierten oder unsubstituierten einwertigen, nichtaromatischen, kondensierten heteropolycyclischen 8- bis 60-gliedrigen Rest, -Si(Q1)(Q2)(Q3), -B(Q1)(Q2) und -C(=O)(Q1),

    b1 eine ganze Zahl von 1 bis 10 ist,

    b3, b5 und b7 jeweils unabhängig voneinander eine ganze Zahl von 1 bis 4 sind,

    b4, b6 und b8 jeweils unabhängig voneinander eine ganze Zahl von 1 bis 3 sind, und

    der substituierte C1-C60-Alkylrest, der substituierte C2-C60-Alkenylrest, der substituierte C2-C60-Alkinylrest, der substituierte C1-C60-Alkoxyrest, der substituierte C3-C10-Cycloalkylrest, der substituierte C1-C10-Heterocycloalkylrest, der substituierte C3-C10-Cycloalkenylrest, der substituierte C1-C10-Heterocycloalkenylrest, der substituierte C6-C60-Arylrest, der substituierte C6-C60-Aryloxyrest, der substituierte C6-C60-Arylthiorest, der substituierte C1-C60-Heteroarylrest, der substituierte C1-C60-Heteroaryloxyrest, der substituierte einwertige, nichtaromatische, kondensierte polycyclische C8 bis C60-Rest und der substituierte einwertige, nichtaromatische, kondensierte heteropolycyclische 8- bis 60-gliedrige Rest jeweils unabhängig voneinander substituiert sind mit einem oder mehreren Substituenten, unabhängig voneinander ausgewählt aus:

    Deuterium, -F, -Cl, -Br, -I, einer Hydroxylgruppe, einer Cyanogruppe, einer Nitrogruppe, einer Aminogruppe, einer Amidinogruppe, einer Hydrazinogruppe, einer Hydrazonogruppe, einem C1-C60-Alkylrest, einem C2-C60-Alkenylrest, einem C2-C60-Alkinylrest und einem C1-C60-Alkoxyrest;

    einem C1-C60-Alkylrest, einem C2-C60-Alkenylrest, einem C2-C60-Alkinylrest und einem C1-C60-Alkoxyrest, jeweils substituiert mit mindestens einem, ausgewählt aus Deuterium, -F, -Cl, -Br, -I, einer Hydroxylgruppe, einer Cyanogruppe, einer Nitrogruppe, einer Aminogruppe, einer Amidinogruppe, einer Hydrazinogruppe, einer Hydrazonogruppe, einem C3-C10-Cycloalkylrest, einem C1-C10-Heterocycloalkylrest, einem C3-C10-Cycloalkenylrest, einem C1-C10-Heterocycloalkenylrest, einem C6-C60-Arylrest, einem C6-C60-Aryloxyrest, einem C6-C60-Arylthiorest, einem C1-C60-Heteoarylrest, einem einwertigen, nichtaromatischen, kondensierten polycyclischen C8 bis C60-Rest, einem einwertigen, nichtaromatischen, kondensierten heteropolycyclischen 8- bis 60-gliedrigen Rest, -Si(Q11)(Q12)(Q13), -N(Q11)(Q12), -B(Q11)(Q12), -C(=O)(Q11), -S(=O)2(Q11) und -P(=O)(Q11)(Q12);

    einem C3-C10-Cycloalkylrest, einem C1-C10-Heterocycloalkylrest, einem C3-C10-Cycloalkenylrest, einem C1-C10-Heterocycloalkenylrest, einem C6-C60-Arylrest, einem C6-C60-Aryloxyrest, einem C6-C60-Arylthiorest, einem C1-C60-Heteoarylrest, einem einwertigen, nichtaromatischen, kondensierten polycyclischen C8 bis C60-Rest, einem einwertigen, nichtaromatischen, kondensierten heteropolycyclischen 8- bis 60-gliedrigen Rest, einer Biphenylgruppe und einer Terphenylgruppe;

    einem C3-C10-Cycloalkylrest, einem C1-C10-Heterocycloalkylrest, einem C3-C10-Cycloalkenylrest, einem C1-C10-Heterocycloalkenylrest, einem C6-C60-Arylrest, einem C6-C60-Aryloxyrest, einem C6-C60-Arylthiorest, einem C1-C60-Heteoarylrest, einem einwertigen, nichtaromatischen, kondensierten polycyclischen C8 bis C60-Rest, einem einwertigen, nichtaromatischen, kondensierten heteropolycyclischen 8- bis 60-gliedrigen Rest, einer Biphenylgruppe und einer Terphenylgruppe, jeweils substituiert mit mindestens einem, ausgewählt aus Deuterium, -F, -Cl, -Br, -I, einer Hydroxylgruppe, einer Cyanogruppe, einer Nitrogruppe, einer Aminogruppe, einer Amidinogruppe, einer Hydrazinogruppe, einer Hydrazonogruppe, einem C1-C60-Alkylrest, einem C2-C60-Alkenylrest, einem C2-C60-Alkinylrest, einem C1-C60-Alkoxyrest, einem C3-C10-Cycloalkylrest, einem C1-C10-Heterocycloalkylrest, einem C3-C10-Cycloalkenylrest, einem C1-C10-Heterocycloalkenylrest, einem C6-C60-Arylrest, einem C6-C60-Aryloxyrest, einem C6-C60-Arylthiorest, einem C1-C60-Heteoarylrest, einem einwertigen, nichtaromatischen, kondensierten polycyclischen C8 bis C60-Rest, einem einwertigen, nichtaromatischen, kondensierten heteropolycyclischen 8- bis 60-gliedrigen Rest, einer Biphenylgruppe, einer Terphenylgruppe, -Si(Q21)(Q22)(Q23), -N(Q21)(Q22), -B(Q21)(Q22), -C(=O)(Q21), -S(=O)2(Q21) und -P(=O)(Q21)(Q22); und

    -Si(Q31)(Q32)(Q33), -N(Q31)(Q32), -B(Q31)(Q32), -C(=O)(Q31), -S(=O)2(Q31) und -P(=O)(Q31)(Q32),

    wobei Q1 bis Q3, Q11 bis Q13, Q21 bis Q23 und Q31 bis Q33 jeweils unabhängig voneinander ausgewählt sind aus Wasserstoff, Deuterium, -F, -Cl, -Br, -I, einer Hydroxylgruppe, einer Cyanogruppe, einer Nitrogruppe, einer Aminogruppe, einer Amidinogruppe, einer Hydrazinogruppe, einer Hydrazonogruppe, einem C1-C60-Alkylrest, einem C2-C60-Alkenylrest, einem C2-C60-Alkinylrest, einem C1-C60-Alkoxyrest, einem C3-C10-Cycloalkylrest, einem C1-C10-Heterocycloalkylrest, einem C3-C10-Cycloalkenylrest, einem C1-C10-Heterocycloalkenylrest, einem C6-C60-Arylrest, einem mit einem C1-C60-Alkylrest substituierten C6-C60-Arylrest, einem C1-C60-Heteoarylrest, einem einwertigen, nichtaromatischen, kondensierten polycyclischen C8 bis C60-Rest, einem einwertigen, nichtaromatischen, kondensierten heteropolycyclischen 8- bis 60-gliedrigen Rest, einer Biphenylgruppe und einer Terphenylgruppe.


     
    2. Organische lichtemittierende Vorrichtung nach Anspruch 1, wobei

    die erste Elektrode eine Anode ist,

    die zweite Elektrode eine Kathode ist,

    die organische Schicht weiterhin einen Lochtransportbereich zwischen der ersten Elektrode und der Emissionsschicht und einen Elektronentransportbereich zwischen der Emissionsschicht und der zweiten Elektrode umfasst,

    der Lochtransportbereich eine Lochinjektionsschicht, eine Lochtransportschicht, eine Emissionshilfsschicht, eine Elektronenblockierschicht, oder eine Kombination davon umfasst, und

    der Elektronentransportbereich eine Lochblockierschicht, eine Elektronentransportschicht, eine Elektroneninjektionsschicht, oder eine Kombination davon umfasst;

    vorzugsweise wobei der Lochtransportbereich die mindestens eine Verbindung auf Aminbasis umfasst;

    stärker bevorzugt wobei der Lochtransportbereich die Lochtransportschicht umfasst, und die Lochtransportschicht die mindestens eine Verbindung auf Aminbasis umfasst.


     
    3. Verbindung auf Aminbasis, dargestellt durch Formel 1D:

    wobei Formel 1D wie in Anspruch 1 definiert ist.
     
    4. Verbindung auf Aminbasis nach einem der Ansprüche 3, wobei

    (A) L1 und L2 jeweils unabhängig voneinander ausgewählt sind aus:

    einer Einfachbindung und einer Benzolgruppe; und

    einer Benzolgruppe, substituiert mit mindestens einem, ausgewählt aus Deuterium, -F, -Cl, -Br, -I, einer Hydroxylgruppe, einer Cyanogruppe, einer Nitrogruppe, einer Aminogruppe, einer Amidinogruppe, einer Hydrazinogruppe, einer Hydrazonogruppe, einem C1-C20-Alkylrest, einem C1-C20-Alkoxyrest, einem C6-C20-Arylrest, einem C1-C20-Heteoarylrest und -Si(Q31)(Q32)(Q33);

    L3 eine Einfachbindung ist,
    und/oder

    (B) R3 bis R12 jeweils unabhängig voneinander ausgewählt sind aus Wasserstoff, Deuterium, -F, -Cl, -Br, -I, einer Methylgruppe, einer Ethylgruppe, einer Propylgruppe, einer Isopropylgruppe, einer n-Butylgruppe, einer Isobutylgruppe, einer sec-Butylgruppe, einer tert-Butylgruppe, einer Pentylgruppe, einer Isoamylgruppe, einer Hexylgruppe, einer Phenylgruppe und einer Biphenylgruppe.


     
    5. Verbindung auf Aminbasis nach einem der Ansprüche 3 bis 4, wobei R1 ausgewählt ist aus Resten, dargestellt durch die Formeln 6-1 bis 6-10 und 6-12 bis 6-26:









    wobei, in den Formeln 6-1 bis 6-10 und 6-12 bis 6-26,
    eine Bindungsstelle zu einem benachbarten Atom kennzeichnet.
     
    6. Verbindung auf Aminbasis nach einem der Ansprüche 3 bis 5, wobei die durch Formel 1D dargestellte Verbindung auf Aminbasis durch eine der Formeln 1B-1 bis 1B-16 wiedergegeben wird:































    wobei, in den Formeln 1B-1 bis 1B-16,
    X1, X2, L2, L3, a2, a3, R3 bis R8, b3 bis b8 unabhängig voneinander das Gleiche sind, wie in den Ansprüchen 1 und 4 bis 5 definiert.
     
    7. Verbindung auf Aminbasis nach Anspruch 3, wobei die Verbindung auf Aminbasis ausgewählt ist aus den Verbindungen 42-45, 47-50, 56-59, 61-64, 70-73, 75-78, 84-87, 89-92, 232-239, 243-250:






































     
    8. Organische lichtemittierende Vorrichtung nach einem der Ansprüche 1 oder 2, wobei die Verbindung auf Aminbasis wie in einem der Ansprüche 3 bis 7 definiert ist.
     


    Revendications

    1. Dispositif électroluminescent organique comprenant :

    une première électrode ;

    une deuxième électrode faisant face à la première électrode ; et

    une couche organique entre la première électrode et la deuxième électrode, et comprenant une couche d'émission,

    dans lequel la couche organique comprend au moins un composé à base d'amine représenté par la formule 1D :

    où, dans la formule 1D,

    X1 est N-(L1)a1-(R1)b1,

    X2 est O ou S,

    chacun de L1 et L2 est indépendamment choisi parmi une liaison simple, un groupe benzène, un groupe pentalène, un groupe indène, un groupe naphtalène, un groupe azulène, un groupe heptalène, un groupe indacène, un groupe acénaphtalène, un groupe phénalène, un groupe phénanthrène, un groupe anthracène, un groupe fluoranthène, un groupe triphénylène, un groupe pyrène, un groupe chrysène, un groupe naphtacène, un groupe picène, un groupe pérylène, un groupe pentaphénylène, un groupe hexacène, un groupe pyrrole, un groupe imidazole, un groupe pyrazole, un groupe pyridine, un groupe pyrazine, un groupe pyrimidine, un groupe pyridazine, un groupe isoindole, un groupe indole, un groupe indazole, un groupe purine, un groupe quinoline, un groupe isoquinoline, un groupe benzoquinoline, un groupe phtalazine, un groupe naphtyridine, un groupe quinoxaline, un groupe quinazoline, un groupe cinnoline, un groupe carbazole, un groupe phénanthridine, un groupe acridine, un groupe phénanthroline, un groupe phénazine, un groupe benzimidazole, un groupe furane, un groupe benzofurane, un groupe thiophène, un groupe benzothiophène, un groupe thiazole, un groupe isothiazole, un groupe benzothiazole, un groupe isoxazole, un groupe oxazole, un groupe triazole, un groupe tétrazole, un groupe oxadiazole, un groupe triazine, un groupe benzoxazole, un groupe dibenzofurane, un groupe dibenzothiophène, un groupe benzocarbazole et un groupe dibenzocarbazole, et

    un groupe benzène, un groupe pentalène, un groupe indène, un groupe naphtalène, un groupe azulène, un groupe heptalène, un groupe indacène, un groupe acénaphtalène, un groupe phénalène, un groupe phénanthrène, un groupe anthracène, un groupe fluoranthène, un groupe triphénylène, un groupe pyrène, un groupe chrysène, un groupe naphtacène, un groupe picène, un groupe pérylène, un groupe pentaphénylène, un groupe hexacène, un groupe pyrrole, un groupe imidazole, un groupe pyrazole, un groupe pyridine, un groupe pyrazine, un groupe pyrimidine, un groupe pyridazine, un groupe isoindole, un groupe indole, un groupe indazole, un groupe purine, un groupe quinoline, un groupe isoquinoline, un groupe benzoquinoline, un groupe phtalazine, un groupe naphtyridine, un groupe quinoxaline, un groupe quinazoline, un groupe cinnoline, un groupe carbazole, un groupe phénanthridine, un groupe acridine, un groupe phénanthroline, un groupe phénazine, un groupe benzimidazole, un groupe furane, un groupe benzofurane, un groupe thiophène, un groupe benzothiophène, un groupe thiazole, un groupe isothiazole, un groupe benzothiazole, un groupe isoxazole, un groupe oxazole, un groupe triazole, un groupe tétrazole, un groupe oxadiazole, un groupe triazine, un groupe benzoxazole, un groupe dibenzofurane, un groupe dibenzothiophène, un groupe benzocarbazole et un groupe dibenzocarbazole, chacun substitué par au moins l'un choisi parmi le deutérium, -F, -Cl, -Br, -I, un groupe hydroxyle, un groupe cyano, un groupe nitro, un groupe amino, un groupe amidino, un groupe hydrazino, un groupe hydrazono, un groupe alkyle en C1 à C20, un groupe alkoxy en C1 à C20, un groupe aryle en C6 à C20, un groupe hétéroaryle en C1 à C20, et -Si(Q31)(Q32)(Q33),

    L3 est une liaison simple,

    chacun de a1 et a2 est indépendamment un entier de 1 à 5, a3 vaut 1 ;

    R1 est indépendamment choisi parmi les groupes représentés par les formules 5-1 à 5-9, 5-13 à 5-19, et 5-21 à 5-79 :







































    où, dans les formules 5-1 à 5-9, 5-13 à 5-19, et 5-21 à 5-79,

    Y31 est O, S, N(Z35) ou Si(Z36)(Z37),

    chacun de Z31, Z32 et Z35 à Z37 est indépendamment choisi parmi l'hydrogène, le deutérium, -F, -Cl, -Br, -I, un groupe hydroxyle, un groupe cyano, un groupe nitro, un groupe amidino, un groupe hydrazino, un groupe hydrazono, un groupe alkyle en C1 à C20, un groupe alkoxy en C1 à C20, un groupe cyclopentyle, un groupe cyclohexyle, un groupe cycloheptyle, un groupe cyclopentényle, un groupe cyclohexényle, un groupe phényle, un groupe biphényle, un groupe naphtyle, un groupe phénalényle, un groupe phénanthrényle, un groupe anthracényle, un groupe fluoranthényle, un groupe triphénylényle, un groupe pyridinyle, un groupe pyrazinyle, un groupe pyrimidinyle, un groupe quinolinyle, un groupe isoquinolinyle, un groupe benzoquinolinyle, un groupe naphtyridinyle, un groupe quinoxalinyle, un groupe quinazolinyle, un groupe carbazolyle, un groupe phénanthridinyle, un groupe acridinyle, un groupe phénanthrolinyle, un groupe phénazinyle, un groupe triazinyle, un groupe dibenzofuranyle, un groupe dibenzothiophényle, et -Si(Q31)(Q32)(Q33),

    e2 est un entier de 0 à 2 ; quand e2 vaut 2, deux groupes Z31 sont identiques ou différents, et deux groupes Z32 sont identiques ou différents,

    e3 est un entier de 0 à 3 ; quand e3 vaut 2 ou plus, au moins deux groupes Z31 sont identiques ou différents et au moins deux Z32 sont identiques ou différents,

    e4 est un entier de 0 à 4 ; quand e4 vaut 2 ou plus, au moins deux groupes Z31 sont identiques ou différents et au moins deux Z32 sont identiques ou différents,

    e5 est un entier de 0 à 5 ; quand e5 vaut 2 ou plus, au moins deux groupes Z31 sont identiques ou différents et au moins deux Z32 sont identiques ou différents,

    e6 est un entier de 0 à 6 ; quand e6 vaut 2 ou plus, au moins deux groupes Z31 sont identiques ou différents et au moins deux Z32 sont identiques ou différents,

    e7 est un entier de 0 à 7 ; quand e7 vaut 2 ou plus, au moins deux groupes Z31 sont identiques ou différents,

    e9 est un entier de 0 à 9 ; quand e9 vaut 2 ou plus, au moins deux groupes Z31 sont identiques ou différents, et

    * indique un site de liaison à un atome adjacent,

    chacun de R3 à R8 est indépendamment choisi parmi l'hydrogène, le deutérium, -F, -Cl, -Br, -I, un groupe hydroxyle, un groupe cyano, un groupe nitro, un groupe amino, un groupe amidino, un groupe hydrazino, un groupe hydrazono, un groupe alkyle en C1 à C60 substitué ou non substitué, un groupe alcényle en C2 à C60 substitué ou non substitué, un groupe alcynyle en C2 à C60 substitué ou non substitué, un groupe alkoxy en C1 à C60 substitué ou non substitué, un groupe cycloalkyle en C3 à C10 substitué ou non substitué, un groupe hétérocycloalkyle en C1 à C10 substitué ou non substitué, un groupe cycloalcényle en C3 à C10 substitué ou non substitué, un groupe hétérocycloalcényle en C1 à C10 substitué ou non substitué, un groupe aryle en C6 à C60 substitué ou non substitué, un groupe aryloxy en C6 à C60 substitué ou non substitué, un groupe arylthio en C6 à C60 substitué ou non substitué, un groupe hétéroaryle en C1 à C60 substitué ou non substitué, un groupe hétéroaryloxy en C1 à C60 substitué ou non substitué, un groupe polycyclique en C8 à C60 condensé non aromatique monovalent substitué ou non substitué, un groupe hétéropolycyclique à 8 à 60 chaînons condensé non aromatique monovalent substitué ou non substitué, -Si(Q1)(Q2)(Q3), -B(Q1)(Q2), et -C(=O)(Q1),

    b1 est un entier de 1 à 10,

    chacun de b3, b5 et b7 est indépendamment un entier de 1 à 4,

    chacun de b4, b6 et b8 est indépendamment un entier de 1 à 3, et

    chacun du groupe alkyle en C1 à C60 substitué, du groupe alcényle en C2 à C60 substitué, du groupe alcynyle en C2 à C60 substitué, du groupe alkoxy en C1 à C60 substitué, du groupe cycloalkyle en C3 à C10 substitué, du groupe hétérocycloalkyle en C1 à C10 substitué, du groupe cyclo-alcényle en C3 à C10 substitué, du groupe hétérocycloalcényle en C1 à C10 substitué, du groupe aryle en C6 à C60 substitué, du groupe aryloxy en C6 à C60 substitué, du groupe arylthio en C6 à C60 substitué, du groupe hétéroaryle en C1 à C60 substitué, du groupe hétéroaryloxy en C1 à C60 substitué, du groupe polycyclique en C8 à C60 condensé non aromatique monovalent substitué, et du groupe hétéropolycyclique à 8 à 60 chaînons condensé non aromatique monovalent substitué est indépendamment substitué par un ou plusieurs substituants indépendamment choisis parmi :

    le deutérium, -F, -Cl, -Br, -I, un groupe hydroxyle, un groupe cyano, un groupe nitro, un groupe amino, un groupe amidino, un groupe hydrazino, un groupe hydrazono, un groupe alkyle en C1 à C60, un groupe alcényle en C2 à C60, un groupe alcynyle en C2 à C60, et un groupe alkoxy en C1 à C60 ;

    un groupe alkyle en C1 à C60, un groupe alcényle en C2 à C60, un groupe alcynyle en C2 à C60, et un groupe alkoxy en C1 à C60, chacun substitué par au moins l'un choisi parmi le deutérium, -F, -Cl, -Br, -I, un groupe hydroxyle, un groupe cyano, un groupe nitro, un groupe amino, un groupe amidino, un groupe hydrazino, un groupe hydrazono, un groupe cycloalkyle en C3 à C10, un groupe hétérocycloalkyle en C1 à C10, un groupe cycloalcényle en C3 à C10, un groupe hétérocycloalcényle en C1 à C10, un groupe aryle en C6 à C60, un groupe aryloxy en C6 à C60, un groupe arylthio en C6 à C60, un groupe hétéroaryle en C1 à C60, un groupe polycyclique en C8 à C60 condensé non aromatique monovalent, un groupe hétéropolycyclique à 8 à 60 chaînons condensé non aromatique monovalent, -Si(Q11)(Q12)(Q13), -N(Q11)(Q12), -B(Q11)(Q12), -C(=O)(Q11), -S(=O)2(Q11), et -P(=O)(Q11)(Q12) ;

    un groupe cycloalkyle en C3 à C10, un groupe hétérocycloalkyle en C1 à C10, un groupe cycloalcényle en C3 à C10, un groupe hétérocycloalcényle en C1 à C10, un groupe aryle en C6 à C60, un groupe aryloxy en C6 à C60, un groupe arylthio en C6 à C60, un groupe hétéroaryle en C1 à C60, un groupe polycyclique en C8 à C60 condensé non aromatique monovalent, un groupe hétéropolycyclique à 8 à 60 chaînons condensé non aromatique monovalent, un groupe biphényle, et un groupe terphényle ;

    un groupe cycloalkyle en C3 à C10, un groupe hétérocycloalkyle en C1 à C10, un groupe cycloalcényle en C3 à C10, un groupe hétérocycloalcényle en C1 à C10, un groupe aryle en C6 à C60, un groupe aryloxy en C6 à C60, un groupe arylthio en C6 à C60, un groupe hétéroaryle en C1 à C60, un groupe polycyclique en C8 à C60 condensé non aromatique monovalent, un groupe hétéropolycyclique à 8 à 60 chaînons condensé non aromatique monovalent, un groupe biphényle, et un groupe terphényle, chacun substitué par au moins l'un choisi parmi le deutérium, -F, -Cl, -Br, -I, un groupe hydroxyle, un groupe cyano, un groupe nitro, un groupe amino, un groupe amidino, un groupe hydrazino, un groupe hydrazono, un groupe alkyle en C1 à C60, un groupe alcényle en C2 à C60, un groupe alcynyle en C2 à C60, un groupe alkoxy en C1 à C60, un groupe cycloalkyle en C3 à C10, un groupe hétérocycloalkyle en C1 à C10, un groupe cycloalcényle en C3 à C10, un groupe hétérocycloalcényle en C1 à C10, un groupe aryle en C6 à C60, un groupe aryloxy en C6 à C60, un groupe arylthio en C6 à C60, un groupe hétéroaryle en C1 à C60, un groupe polycyclique en C8 à C60 condensé non aromatique monovalent, un groupe hétéropolycyclique à 8 à 60 chaînons condensé non aromatique monovalent, un groupe biphényle, un groupe terphényle, -Si(Q21)(Q22)(Q23), -N(Q21)(Q22), -B(Q21)(Q22), -C(=O)(Q21), -S(=O)2(Q21), et -P(=O)(Q21)(Q22) ; et

    -Si(Q31)(Q32)(Q33), -N(Q31)(Q32), -B(Q31)(Q32), -C(=O)(Q31), -S(=O)2(Q31), et -P(=O)(Q31)(Q32),

    où chacun de Q1 à Q3, Q11 à Q13, Q21 à Q23 et Q31 à Q33 est indépendamment choisi parmi l'hydrogène, le deutérium, -F, -Cl, -Br, -I, un groupe hydroxyle, un groupe cyano, un groupe nitro, un groupe amino, un groupe amidino, un groupe hydrazino, un groupe hydrazono, un groupe alkyle en C1 à C60, un groupe alcényle en C2 à C60, un groupe alcynyle en C2 à C60, un groupe alkoxy en C1 à C60, un groupe cycloalkyle en C3 à C10, un groupe hétérocycloalkyle en C1 à C10, un groupe cycloalcényle en C3 à C10, un groupe hétérocycloalcényle en C1 à C10, un groupe aryle en C6 à C60, un groupe aryle en C6 à C60 substitué par un groupe alkyle en C1 à C60, un groupe hétéroaryle en C1 à C60, un groupe polycyclique en C8 à C60 condensé non aromatique monovalent, un groupe hétéropolycyclique à 8 à 60 chaînons condensé non aromatique monovalent, un groupe biphényle, et un groupe terphényle.


     
    2. Dispositif électroluminescent organique selon la revendication 1, dans lequel

    la première électrode est une anode,

    la deuxième électrode est une cathode,

    la couche organique comprend en outre une région de transport de trous entre la première électrode et la couche d'émission et une région de transport d'électrons entre la couche d'émission et la deuxième électrode,

    la région de transport de trous comprend une couche d'injection de trous, une couche de transport de trous, une couche auxiliaire d'émission, une couche de blocage d'électrons, ou une de leurs combinaisons, et

    la région de transport d'électrons comprend une couche de blocage de trous, une couche de transport d'électrons, une couche d'injection d'électrons, ou une de leurs combinaisons ;

    de préférence dans lequel la région de transport de trous comprend l'au moins un composé à base d'amine ;

    mieux encore dans lequel la région de transport de trous comprend la couche de transport de trous, et la couche de transport de trous comprend l'au moins un composé à base d'aminé.


     
    3. Composé à base d'aminé représenté par la formule 1D :

    où la formule 1D est telle que définie dans la revendication 1.
     
    4. Composé à base d'amine selon la revendication 3, dans lequel

    (A) chacun de L1 et L2 est indépendamment choisi parmi :

    une liaison simple et un groupe benzène ; et

    un groupe benzène substitué par au moins l'un choisi parmi le deutérium, -F, -Cl, -Br, -I, un groupe hydroxyle, un groupe cyano, un groupe nitro, un groupe amino, un groupe amidino, un groupe hydrazino, un groupe hydrazono, un groupe alkyle en C1 à C20, un groupe alkoxy en C1 à C20, un groupe aryle en C6 à C20, un groupe hétéroaryle en C1 à C20, et -Si(Q31)(Q32)(Q33) ;

    L3 est une liaison simple, et/ou

    (B) chacun de R3 à R12 est indépendamment choisi parmi l'hydrogène, le deutérium, -F, -Cl, -Br, -I, un groupe méthyle, un groupe éthyle, un groupe propyle, un groupe isopropyle, un groupe n-butyle, un groupe isobutyle, un groupe sec-butyle, un groupe tert-butyle, un groupe pentyle, un groupe isoamyle, un groupe hexyle, un groupe phényle, et un groupe biphényle.


     
    5. Composé à base d'amine selon l'une quelconque des revendications 3 et 4, dans lequel R1 est choisi parmi les groupes représentés par les formules 6-1 à 6-10 et 6-12 à 6-26 :









    où, dans les formules 6-1 à 6-10 et 6-12 à 6-26,
    * indique un site de liaison à un atome adjacent.
     
    6. Composé à base d'amine selon l'une quelconque des revendications 3 à 5, où le composé à base d'amine représenté par la formule 1D est représenté par l'une des formules 1B-1 à 1B-16 :































    où, dans les formules 1B-1 à 1B-16,
    chacun de X1, X2, L2, L3, a2, a3, R3 à R8, b3 à b8 sont indépendamment tels que définis dans les revendications 1, 4 et 5.
     
    7. Composé à base d'amine selon la revendication 3, où le composé à base d'amine est choisi parmi les composés 42 à 45, 47 à 50, 56 à 59, 61 à 64, 70 à 73, 75 à 78, 84 à 87, 89 à 92, 232 à 239, 243 à 250 :






































     
    8. Dispositif électroluminescent organique selon l'une quelconque des revendications 1 et 2, dans lequel le composé à base d'amine est tel que défini dans l'une quelconque des revendications 3 à 7.
     




    Drawing