(19)
(11)EP 3 747 873 B1

(12)EUROPEAN PATENT SPECIFICATION

(45)Mention of the grant of the patent:
07.09.2022 Bulletin 2022/36

(21)Application number: 19796361.4

(22)Date of filing:  02.05.2019
(51)International Patent Classification (IPC): 
C07D 251/24(2006.01)
H01L 51/00(2006.01)
C07D 209/86(2006.01)
C07D 239/26(2006.01)
C07D 403/04(2006.01)
C07D 409/04(2006.01)
C07C 13/72(2006.01)
H01L 51/50(2006.01)
C07D 213/06(2006.01)
C07D 239/74(2006.01)
C07D 405/04(2006.01)
C07D 491/048(2006.01)
(52)Cooperative Patent Classification (CPC):
C07C 13/72; C07D 251/24; C07D 213/06; C07D 239/26; C07D 405/04; C07D 409/04; C07D 403/04; C07D 239/74; C07D 209/86; C07D 491/048; H01L 51/0096; H01L 51/0056
(86)International application number:
PCT/KR2019/005993
(87)International publication number:
WO 2019/212325 (07.11.2019 Gazette  2019/45)

(54)

NOVEL COMPOUND AND ORGANIC LIGHT EMITTING DIODE USING SAME

NEUARTIGE VERBINDUNG UND ORGANISCHE LICHTEMITTIERENDE DIODE DAMIT

NOUVEAU COMPOSÉ ET DIODE ÉLECTROLUMINESCENTE ORGANIQUE L'UTILISANT


(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: 03.05.2018 KR 20180051361

(43)Date of publication of application:
09.12.2020 Bulletin 2020/50

(73)Proprietor: LG CHEM, LTD.
Yeongdeungpo-gu, Seoul 07336 (KR)

(72)Inventors:
  • KIM, Sunmin
    Daejeon 34122 (KR)
  • CHA, Yongbum
    Daejeon 34122 (KR)
  • JEON, Sang Young
    Daejeon 34122 (KR)
  • KIM, Yeon Hwan
    Daejeon 34122 (KR)

(74)Representative: Hoffmann Eitle 
Patent- und Rechtsanwälte PartmbB Arabellastraße 30
81925 München
81925 München (DE)


(56)References cited: : 
KR-A- 20090 035 974
KR-A- 20140 008 213
KR-A- 20170 095 602
KR-A- 20130 139 105
KR-A- 20140 124 029
  
      
    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

    [Technical Field]



    [0001] The present invention relates to a novel compound and to an organic light emitting device comprising the same.

    [Background Art]



    [0002] In general, an organic light emitting phenomenon refers to a phenomenon where electric energy is converted into light energy by using an organic material. The organic light emitting device using the organic light emitting phenomenon has characteristics such as a wide viewing angle, an excellent contrast, a fast response time, an excellent luminance, driving voltage and response speed, and thus many studies have proceeded.

    [0003] The organic light emitting device generally has a structure which comprises an anode, a cathode, and an organic material layer interposed between the anode and the cathode. The organic material layer frequently has a multilayered structure that comprises different materials in order to enhance efficiency and stability of the organic light emitting device, and for example, the organic material layer may be formed of a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, an electron injection layer and the like. In the structure of the organic light emitting device, if a voltage is applied between two electrodes, the holes are injected from an anode into the organic material layer and the electrons are injected from the cathode into the organic material layer, and when the injected holes and electrons meet each other, an exciton is formed, and light is emitted when the exciton falls to a ground state again.

    [0004] There is a continuing need for the development of new materials for the organic materials used in these organic light emitting devices.

    [Prior Art Literature]


    [Patent Literature]



    [0005] (Patent Literature 0001) Korean Patent Laid-open Publication No. 10-2000-0051826

    [0006] KR 10-2017-0095602 relates to a compound for an organic electric device, the organic electric device using the same, and an electronic device.

    [DETAILED DESCRIPTION OF THE INVENTION]


    [Technical Problem]



    [0007] It is an object of the present invention to provide a novel compound and an organic light emitting device including the same.

    [Technical Solution]



    [0008] In one aspect of the invention, there is provided a compound represented by the following Chemical Formula 1:

    in Chemical Formula 1,

    L is a single bond; a substituted or unsubstituted C6-60 arylene; or a substituted or unsubstituted C2-60 heteroarylene containing at least one selected from the group consisting of N, O and S, and

    Ar is any one selected from the group consisting of the following:

    wherein,

    X1 to X3 are N, or CH, with the proviso that at least one of X1 to X3 is N,

    Ar1 and Ar2 are each independently a substituted or unsubstituted C6-60 aryl; or a substituted or unsubstituted C2-60 heteroaryl containing at least one selected from the group consisting of N, O and S,

    X4 and X5 are N, or CH, with the proviso that at least one of X4 and X5 is N,

    Ar3 is independently a substituted or unsubstituted C6-60 aryl; or a substituted or unsubstituted C2-60 heteroaryl containing at least one selected from the group consisting of N, O and S,

    Y is N(Ar5), O, or S,

    Ar4 is hydrogen, a substituted or unsubstituted C6-60 aryl, or a substituted or unsubstituted C2-60 heteroaryl containing at least one selected from the group consisting of N, O and S, and

    Ar5 is a substituted or unsubstituted C6-60 aryl



    [0009] In another aspect of the invention, there is provided an organic light emitting device including a first electrode; a second electrode provided opposite to the first electrode; and one or more organic material layers provided between the first electrode and the second electrode, wherein one or more layers of the organic material layers includes the compound represented by the Chemical Formula 1.

    [ADVANTAGEOUS EFFECTS]



    [0010] The compound represented by the Chemical Formula 1 described above can be used as a material of an organic material layer of an organic light emitting device, and may improve the efficiency, achieve low driving voltage and/or improve lifetime characteristics in the organic light emitting device. In particular, the compound represented by the Chemical Formula 1 described above can be used as a material for hole injection, hole transport, hole injection and transport, light emitting, electron transport, or electron injection.

    [BRIEF DESCRIPTION OF DRAWINGS]



    [0011] 

    FIG. 1 shows an example of an organic light emitting device comprising a substrate 1, an anode 2, an organic material layer 3, and a cathode 4.

    FIG. 2 shows an example of an organic light emitting device comprising a substrate 1, an anode 2, a hole injection layer 5, a hole transport layer 6, an electron blocking layer 7, a light emitting layer 8, a hole blocking layer 9, an electron transport layer 10, an electron injection layer 11, and a cathode 4.


    [DETAILED DESCRIPTION OF THE EMBODIMENTS]



    [0012] Hereinafter, the present invention will be described in more detail to help understanding of the present invention.

    [0013] In one embodiment of the invention, there is provided a compound represented by the Chemical Formula 1.

    [0014] As used herein, the notation,

    means a bond linked to another substituent group.

    [0015] As used herein, the term "substituted or unsubstituted" means being unsubstituted or substituted with one or more substituents selected from the group consisting of deuterium; a halogen group; a nitrile group; a nitro group; a hydroxy group; a carbonyl group; an ester group; an imide group; an amino group; a phosphine oxide group; an alkoxy group; an aryloxy group; an alkylthioxy group; an arylthioxy group; an alkylsulfoxy group; an arylsulfoxy group; a silyl group; a boron group; an alkyl group; a cycloalkyl group; an alkenyl group; an aryl group; an aralkyl group; an aralkenyl group; an alkylaryl group; an alkylamine group; an aralkylamine group; a heteroarylamine group; an arylamine group; an arylphosphine group; and a hetero-cyclic group containing at least one of N, O and S atoms, or being unsubstituted or substituted with a substituent to which two or more substituents are linked among the substituents exemplified above. For example, "the substituent to which two or more substituents are linked" may be a biphenyl group. That is, the biphenyl group may also be an aryl group, and may be interpreted as a substituent to which two phenyl groups are linked.

    [0016] In the present specification, the number of carbon atoms of a carbonyl group is not particularly limited, but is preferably 1 to 40. Specifically, the carbonyl group may be a compound having the following structural formulae, but is not limited thereto.





    [0017] In the present specification, for an ester group, the oxygen of the ester group may be substituted with a straight-chain, branched-chain, or cyclic alkyl group having 1 to 25 carbon atoms, or an aryl group having 6 to 25 carbon atoms. Specifically, the ester group may be a compound having the following structural formulae, but is not limited thereto.





    [0018] In the present specification, the number of carbon atoms of an imide group is not particularly limited, but is preferably 1 to 25. Specifically, the imide group may be a compound having the following structural formulae, but is not limited thereto.





    [0019] In the present specification, a silyl group specifically includes a trimethylsilyl group, a triethylsilyl group, a t-butyldimethylsilyl group, a vinyldimethylsilyl group, a propyldimethylsilyl group, a triphenylsilyl group, a diphenylsilyl group, a phenylsilyl group and the like, but is not limited thereto.

    [0020] In the present specification, a boron group specifically includes a trimethylboron group, a triethylboron group, a t-butyldimethylboron group, a triphenylboron group, and a phenylboron group, but is not limited thereto.

    [0021] In the present specification, examples of a halogen group include fluorine, chlorine, bromine, or iodine.

    [0022] In the present specification, the alkyl group may be a straight chain or branched chain, and the number of carbon atoms thereof is not particularly limited, but is preferably 1 to 40. According to one embodiment, the number of carbon atoms of the alkyl group is 1 to 20. According to another embodiment, the number of carbon atoms of the alkyl group is 1 to 10. According to another embodiment, the number of carbon atoms of the alkyl group is 1 to 6. Specific examples of the alkyl group include methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, sec-butyl, 1-methyl-butyl, 1-ethyl-butyl, pentyl, n-pentyl, isopentyl, neopentyl, tert-pentyl, hexyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 4-methyl-2-pentyl, 3,3-dimethylbutyl, 2-ethylbutyl, heptyl, n-heptyl, 1-methylhexyl, cyclopentylmethyl, cyclohexylmethyl, octyl, n-octyl, tert-octyl, 1-methylheptyl, 2-ethylhexyl, 2-propylpentyl, n-nonyl, 2,2-dimethylheptyl, 1-ethylpropyl, 1,1-dimethyl-propyl, isohexyl, 2-methylpentyl, 4-methylhexyl, 5-methylhexyl, and the like, but are not limited thereto.

    [0023] In the present specification, the alkenyl group may be a straight chain or branched chain, and the number of carbon atoms thereof is not particularly limited, but is preferably 2 to 40. According to one embodiment, the number of carbon atoms of the alkenyl group is 2 to 20. According to another embodiment, the number of carbon atoms of the alkenyl group is 2 to 10. According to still another embodiment, the number of carbon atoms of the alkenyl group is 2 to 6. Specific examples thereof include vinyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 3-methyl-1-butenyl, 1,3-butadienyl, allyl, 1-phenylvinyl-1-yl, 2-phenylvinyl-1-yl, 2,2-diphenylvinyl-1-yl, 2-phenyl-2-(naphthyl-1-yl)vinyl-1-yl, 2,2-bis(diphenyl-1-yl)vinyl-1-yl, a stilbenyl group, a styrenyl group, and the like, but are not limited thereto.

    [0024] In the present specification, a cycloalkyl group is not particularly limited, but the number of carbon atoms thereof is preferably 3 to 60. According to one embodiment, the number of carbon atoms of the cycloalkyl group is 3 to 30. According to another embodiment, the number of carbon atoms of the cycloalkyl group is 3 to 20. According to still another embodiment, the number of carbon atoms of the cycloalkyl group is 3 to 6. Specific examples thereof include cyclopropyl, cyclobutyl, cyclopentyl, 3-methylcyclopentyl, 2,3-dimethylcyclopentyl, cyclohexyl, 3-methylcyclohexyl, 4-methylcyclohexyl, 2,3-dimethylcyclohexyl, 3,4,5-trimethylcyclohexyl, 4-tert-butylcyclohexyl, cycloheptyl, cyclooctyl, and the like, but are not limited thereto.

    [0025] In the present specification, an aryl group is not particularly limited, but preferably has 6 to 60 carbon atoms, and may be a monocyclic aryl group or a polycyclic aryl group. According to one embodiment, the number of carbon atoms of the aryl group is 6 to 30. According to one embodiment, the number of carbon atoms of the aryl group is 6 to 20. The aryl group may be a phenyl group, a biphenyl group, a terphenyl group or the like as the monocyclic aryl group, but is not limited thereto. Examples of the polycyclic aryl group include a naphthyl group, an anthracenyl group, a phenanthryl group, a pyrenyl group, a perylenyl group, a chrysenyl group and a fluorenyl group or the like, but is not limited thereto.

    [0026] In the present specification, a fluorenyl group may be substituted, and two substituent groups may be bonded to each other to form a spiro structure. In the case where the fluorenyl group is substituted,

    and the like can be formed. However, the structure is not limited thereto.

    [0027] In the present specification, a heterocyclic group is a heterocyclic group including one or more of O, N, Si and S as a heteroatom, and the number of carbon atoms thereof is not particularly limited, but is preferably 2 to 60. Examples of the heterocyclic group include a thiophene group, a furan group, a pyrrole group, an imidazole group, a thiazole group, an oxazol group, an oxadiazol group, a triazol group, a pyridyl group, a bipyridyl group, a pyrimidyl group, a triazine group, an acridyl group, a pyridazine group, a pyrazinyl group, a quinolinyl group, a quinazoline group, a quinoxalinyl group, a phthalazinyl group, a pyridopyrimidinyl group, a pyridopyrazinyl group, a pyrazinopyrazinyl group, an isoquinoline group, an indole group, a carbazole group, a benzoxazole group, a benzimidazole group, a benzothiazol group, a benzocarbazole group, a benzothiophene group, a dibenzothiophene group, a benzofuranyl group, a phenanthroline group, an isoxazolyl group, a thiadiazolyl group, a phenothiazinyl group, a dibenzofuranyl group, and the like, but are not limited thereto.

    [0028] In the present specification, the aryl group in the aralkyl group, the aralkenyl group, the alkylaryl group, and the arylamine group is the same as the aforementioned examples of the aryl group. In the present specification, the alkyl group in the aralkyl group, the alkylaryl group and the alkylamine group is the same as the aforementioned examples of the alkyl group. In the present specification, the heteroaryl in the heteroarylamine can be applied to the aforementioned description of the heterocyclic group. In the present specification, the alkenyl group in the aralkenyl group is the same as the aforementioned examples of the alkenyl group. In the present specification, the aforementioned description of the aryl group may be applied except that the arylene is a divalent group. In the present specification, the aforementioned description of the heterocyclic group can be applied except that the heteroarylene is a divalent group. In the present specification, the aforementioned description of the aryl group or cycloalkyl group can be applied except that the hydrocarbon ring is not a monovalent group but formed by combining two substituent groups. In the present specification, the aforementioned description of the heterocyclic group can be applied, except that the heterocycle is not a monovalent group but formed by combining two substituent groups.

    [0029] Preferably, the Chemical Formula 1 is represented by the following Chemical Formula 1-1, 1-2 or 1-3:







    [0030] Preferably, L is a single bond, phenylene, or carbazoldiyl. More preferably, L is a single bond, 1,4-phenylene, 1,3-phenylene, 1,2-phenylene, or



    [0031] Ar is any one selected from the group consisting of the following:

    wherein,

    X1 to X3 are N, or CH, with the proviso that at least one of X1 to X3 is N,

    Ar1 and Ar2 are each independently a substituted or unsubstituted C6-60 aryl; or a substituted or unsubstituted C2-60 heteroaryl containing at least one selected from the group consisting of N, O and S,

    X4 and X5 are N, or CH, with the proviso that at at least one of X4 and X5 is N,

    Ar3 is independently a substituted or unsubstituted C6-60 aryl; or a substituted or unsubstituted C2-60 heteroaryl containing at least one selected from the group consisting of N, O and S,

    Y is N(Ar5), O or S,

    Ar4 is hydrogen, a substituted or unsubstituted C6-60 aryl, or a substituted or unsubstituted C2-60 heteroaryl containing at least one selected from the group consisting of N, O and S, and

    Ar5 is a substituted or unsubstituted C6-60 aryl.



    [0032] Preferably, Ar1 and Ar2 are each independently phenyl, biphenylyl, terphenylyl, naphthyl, phenanthrenyl, triphenylenyl, dibenzofuranyl, dibenzothiophenyl, or 9-phenyl-9H-carbazolyl.

    [0033] Preferably, Ar3 is phenyl, biphenylyl, or naphthyl.

    [0034] Preferably, Ar4 is hydrogen, phenyl, biphenylyl, or naphthyl.

    [0035] Preferably, Ar5 is phenyl.

    [0036] Representative examples of the compound represented by the Chemical Formula 1 are as follows:











































































































    [0037] In another embodiment of the invention, there is provided a process for preparing a compound represented by the Chemical Formula 1 as shown in the following reaction scheme 1 or 2.







    [0038] In the reaction schemes 1 and 2, L and Ar are same as those defined above, X' is halogen, preferably bromo, or chloro. The reaction schemes 1 and 2 are Suzuki coupling reactions, which are preferably carried out in the presence of a palladium catalyst and a base, and the reactive group for the Suzuki coupling reaction can be modified as known in the art. The above preparation method can be further specified in Preparation Examples to be described later.

    [0039] In still another embodiment of the invention, there is provided an organic light emitting device including a compound represented by the Chemical Formula 1. As an example, there is provided an organic light emitting device including: a first electrode; a second electrode provided opposite to the first electrode; and one or more organic material layers provided between the first electrode and the second electrode, wherein one or more layers of the organic material layers includes the compound represented by the Chemical Formula 1.

    [0040] The organic material layer of the organic light emitting device of the present invention may have a single layer structure, or it may have a multilayered structure in which two or more organic material layers are stacked. For example, the organic light emitting device of the present disclosure may have a structure comprising a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, an electron injection layer and the like as the organic material layer. However, the structure of the organic light emitting device is not limited thereto, and it may include a smaller number of organic layers.

    [0041] Further, the organic material layer may include a light emitting layer, wherein the light emitting layer includes a compound represented by the Chemical Formula 1. In particular, the compound according to the present invention can be used as a dopant in a light emitting layer.

    [0042] Further, the organic material layer may include an electron transport layer, or an electron injection layer, wherein the electron transport layer, or the electron injection layer includes a compound represented by the Chemical Formula 1.

    [0043] Further, the electron transport layer, the electron injection layer, or a layer simultaneously performing electron transport and electron injection include a compound represented by the Chemical Formula 1.

    [0044] Further, the organic material layer includes a light emitting layer and an electron transport layer, wherein the electron transport layer may include a compound represented by the Chemical Formula 1.

    [0045] Further, the organic light emitting device according to the present invention may be a normal type organic light emitting device in which an anode, one or more organic material layers, and a cathode are sequentially stacked on a substrate. Further, the organic light emitting device according to the present disclosure may be an inverted type organic light emitting device in which a cathode, one or more organic material layers and an anode are sequentially stacked on a substrate. For example, the structure of an organic light emitting device according to an embodiment of the present disclosure is illustrated in FIGS. 1 and 2.

    [0046] FIG. 1 shows an example of an organic light emitting device comprising a substrate 1, an anode 2, an organic material layer 3, and a cathode 4. In such a structure, the compound represented by the Chemical Formula 1 may be included in the organic material layer.

    [0047] FIG. 2 shows an example of an organic light emitting device comprising a substrate 1, an anode 2, a hole injection layer 5, a hole transport layer 6, an electron blocking layer 7, a light emitting layer 8, a hole blocking layer 9, an electron transport layer 10, an electron injection layer 11, and a cathode 4. In such a structure, the compound represented by the Chemical Formula 1 may be included in one or more layers of the hole injection layer, the hole transport layer, the electron blocking layer, the light emitting layer, the hole blocking layer, the electron transport layer, and the electron injection layer.

    [0048] The organic light emitting device according to the present invention may be manufactured by materials and methods known in the art, except that one or more layers of the organic material layers includes the compound represented by the Chemical Formula 1. In addition, when the organic light emitting device includes a plurality of organic material layers, the organic material layers may be formed of the same material or different materials.

    [0049] For example, the organic light emitting device according to the present invention can be manufactured by sequentially stacking a first electrode, an organic material layer and a second electrode on a substrate. In this case, the organic light emitting device may be manufactured by depositing a metal, metal oxides having conductivity, or an alloy thereof on the substrate using a PVD (physical vapor deposition) method such as a sputtering method or an e-beam evaporation method to form an anode, forming organic material layers including the hole injection layer, the hole transport layer, the light emitting layer, and the electron transport layer thereon, and then depositing a material that can be used as the cathode thereon. In addition to such a method, the organic light emitting device may be manufactured by sequentially depositing a cathode material, an organic material layer and an anode material on a substrate.

    [0050] In addition, the compound represented by the Chemical Formula 1 may be formed into an organic layer by a solution coating method as well as a vacuum deposition method at the time of manufacturing an organic light emitting device. Herein, the solution coating method means a spin coating, a dip coating, a doctor blading, an inkjet printing, a screen printing, a spray method, a roll coating, or the like, but is not limited thereto.

    [0051] In addition to such a method, the organic light emitting device may be manufactured by sequentially depositing a cathode material, an organic material layer and an anode material on a substrate (International Publication WO2003/012890). However, the manufacturing method is not limited thereto.

    [0052] As an example, the first electrode is an anode, and the second electrode is a cathode, or alternatively the first electrode is a cathode and the second electrode is an anode.

    [0053] As the anode material, generally, a material having a large work function is preferably used so that holes can be smoothly injected into the organic material layer. Specific examples of the anode material include metals such as vanadium, chrome, copper, zinc, and gold, or an alloy thereof; metal oxides such as zinc oxides, indium oxides, indium tin oxides (ITO), and indium zinc oxides (IZO); a combination of metals and oxides, such as ZnO:AI or SnO2:Sb; conductive polymers such as poly(3-methylthiophene), poly[3,4-(ethylene-1,2-dioxy)thiophene] (PEDOT), polypyrrole, and polyaniline, and the like, but are not limited thereto.

    [0054] As the cathode material, generally, a material having a small work function is preferably used so that electrons can be easily injected into the organic material layer. Specific examples of the cathode material include metals such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin, and lead, or an alloy thereof; a multilayered structure material such as LiF/AI or LiO2/Al, and the like, but are not limited thereto.

    [0055] The hole injection layer is a layer for injecting holes from the electrode, and the hole injection material is preferably a compound which has a capability of transporting the holes, thus has a hole injecting effect in the anode and an excellent hole injecting effect to the light emitting layer or the light emitting material, prevents excitons produced in the light emitting layer from moving to an electron injection layer or the electron injection material, and is excellent in the ability to form a thin film. It is preferable that a HOMO (highest occupied molecular orbital) of the hole injection material is between the work function of the anode material and a HOMO of a peripheral organic material layer. Specific examples of the hole injection material include metal porphyrine, oligothiophene, an arylamine-based organic material, a hexanitrilehexaazatriphenylene-based organic material, a quinacridone-based organic material, a perylene-based organic material, anthraquinone, polyaniline and polythiophene-based conductive polymer, and the like, but are not limited thereto.

    [0056] The hole transport layer is a layer that receives holes from a hole injection layer and transports the holes to the light emitting layer. The hole transport material is suitably a material having large mobility to the holes, which may receive holes from the anode or the hole injection layer and transfer the holes to the light emitting layer. Specific examples thereof include an arylamine-based organic material, a conductive polymer, a block copolymer in which a conjugate portion and a non-conjugate portion are present together, and the like, but are not limited thereto.

    [0057] The light emitting material is preferably a material which may receive holes and electrons transported from a hole transport layer and an electron transport layer, respectively, and combine the holes and the electrons to emit light in a visible ray region, and has good quantum efficiency to fluorescence or phosphorescence. Specific examples of the light emitting material include an 8-hydroxy-quinoline aluminum complex (Alq3); a carbazole-based compound; a dimerized styryl compound; BAIq; a 10-hydroxybenzoquinoline-metal compound; a benzoxazole, benzthiazole and benzimidazole-based compound; a poly(p-phenylenevinylene)(PPV)-based polymer; a spiro compound; polyfluorene, lubrene, and the like, but are not limited thereto.

    [0058] The light emitting layer may include a host material and a dopant material. The host material may be a fused aromatic ring derivative, a heterocycle-containing compound or the like. Specific examples of the fused aromatic ring derivatives include anthracene derivatives, pyrene derivatives, naphthalene derivatives, pentacene derivatives, phenanthrene compounds, fluoranthene compounds, and the like. Examples of the heterocyclic-containing compounds include carbazole derivatives, dibenzofuran derivatives, ladder-type furan compounds, pyrimidine derivatives, and the like, but are not limited thereto.

    [0059] Examples of the dopant material include an aromatic amine derivative, a styrylamine compound, a boron complex, a fluoranthene compound, a metal complex, and the like. Specifically, the aromatic amine derivative is a substituted or unsubstituted fused aromatic ring derivative having an arylamino group, and examples thereof include pyrene, anthracene, chrysene, periflanthene and the like, which have an arylamino group. The styrylamine compound is a compound where at least one arylvinyl group is substituted in substituted or unsubstituted arylamine, in which one or two or more substituent groups selected from the group consisting of an aryl group, a silyl group, an alkyl group, a cycloalkyl group, and an arylamino group are substituted or unsubstituted. Specific examples thereof include styrylamine, styryldiamine, styryltriamine, styryltetramine, and the like, but are not limited thereto. Further, the metal complex includes an iridium complex, a platinum complex, and the like, but is not limited thereto.

    [0060] The electron transport layer is a layer which receives electrons from an electron injection layer and transports the electrons to a light emitting layer, and an electron transport material is suitably a material which may receive electrons well from a cathode and transfer the electrons to a light emitting layer, and has a large mobility for electrons. Specific examples of the electron transport material include: an Al complex of 8-hydroxyquinoline; a complex including Alq3; an organic radical compound; a hydroxyflavone-metal complex, and the like, but are not limited thereto. The electron transport layer may be used with any desired cathode material, as used according to the related art. In particular, appropriate examples of the cathode material are a typical material which has a low work function, followed by an aluminum layer or a silver layer. Specific examples thereof include cesium, barium, calcium, ytterbium, and samarium, in each case followed by an aluminum layer or a silver layer.

    [0061] The electron injection layer is a layer which injects electrons from an electrode, and is preferably a compound which has a capability of transporting electrons, has an effect of injecting electrons from a cathode and an excellent effect of injecting electrons into a light emitting layer or a light emitting material, prevents excitons produced from the light emitting layer from moving to a hole injection layer, and is also excellent in the ability to form a thin film. Specific examples of the electron injection layer include fluorenone, anthraquinodimethane, diphenoquinone, thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid, fluorenylidene methane, anthrone, and the like, and derivatives thereof, a metal complex compound, a nitrogen-containing 5-membered ring derivative, and the like, but are not limited thereto.

    [0062] Examples of the metal complex compound include 8-hydroxyquinolinato lithium, bis(8-hydroxyquinolinato)zinc, bis(8-hydroxyquinolinato)copper, bis(8-hydroxyquinolinato)manganese, tris(8-hydroxyquinolinato)aluminum, tris(2-methyl-8-hydroxyquinolinato)aluminum, tris(8-hydroxyquinolinato)gallium, bis(10-hydroxybenzo[h]quinolinato)beryllium, bis(10-hydroxybenzo[h]quinolinato)zinc, bis(2-methyl-8-quinolinato)chlorogallium, bis(2-methyl-8-quinolinato)(o-cresolato)gallium, bis(2-methyl-8-quinolinato)(1-naphtholato)aluminum, bis(2-methyl-8-quinolinato)(2-naphtholato)gallium, and the like, but are not limited thereto.

    [0063] The organic light emitting device according to the present invention may be a front side emission type, a back side emission type, or a double side emission type according to the used material.

    [0064] In addition, the compound represented by the Chemical Formula 1 may be included in an organic solar cell or an organic transistor in addition to an organic light emitting device.

    [0065] The preparation of the compound represented by the Chemical Formula 1 and the organic light emitting device comprising the same will be described in detail in the following examples. However, these examples are presented for illustrative purposes only, and are not intended to limit the scope of the present invention.

    [Example]


    Example 1: Preparation of Compound 1



    [0066] 



    [0067] Compound A (7.50 g, 20.05 mmol) and Compound a-1 (7.43 g, 21.06 mmol) were completely dissolved in tetrahydrofuran (240 ml) in a 500-ml round bottom flask under a nitrogen atmosphere, to which a 2 M aqueous potassium carbonate solution (120 ml) was added and tetrakis-(triphenylphosphine)palladium (0.70 g, 0.60 mmol) was added, and then the resulting mixture was heated and stirred for 4 hours. The temperature was lowered to normal temperature, the aqueous layer was removed, and the resulting product was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure, and recrystallized with tetrahydrofuran (180 ml) to prepare Compound 1 (8.76 g, yield: 67%).

    [0068] MS: [M+H]+ = 648

    Example 2: Preparation of Compound 2



    [0069] 



    [0070] Compound A (6.50 g, 17.38 mmol) and Compound a-2 (6.44 g, 18.25 mmol) were completely dissolved in tetrahydrofuran (260 ml) in a 500-ml round bottom flask under a nitrogen atmosphere, to which a 2 M aqueous potassium carbonate solution (130 ml) was added and tetrakis-(triphenylphosphine)palladium (0.60 g, 0.52 mmol) was added, and then the resulting mixture was heated and stirred for 3 hours. The temperature was lowered to normal temperature, the aqueous layer was removed, and the resulting product was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure, and recrystallized with ethyl acetate (270 ml) to prepare Compound 2 (7.46 g, yield: 66%).

    [0071] MS: [M+H]+ = 648

    Example 3: Preparation of Compound 3



    [0072] 



    [0073] Compound A (8.50 g, 22.73 mmol) and Compound a-3 (8.42 g, 23.86 mmol) were completely dissolved in tetrahydrofuran (240 ml) in a 500-ml round bottom flask under a nitrogen atmosphere, to which a 2 M aqueous potassium carbonate solution (120 ml) was added and tetrakis-(triphenylphosphine)palladium (0.79 g, 0.68 mmol) was added, and then the resulting mixture was heated and stirred for 2 hours. The temperature was lowered to normal temperature, the aqueous layer was removed, and the resulting product was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure, and recrystallized with ethyl acetate (210 ml) to prepare Compound 3 (7.89 g, yield: 54%).

    [0074] MS: [M+H]+ = 647

    Example 4: Preparation of Compound 4



    [0075] 



    [0076] Compound A (7.50 g, 20.05 mmol) and Compound a-4 (9.03 g, 21.06 mmol) were completely dissolved in tetrahydrofuran (220 ml) in a 500-ml round bottom flask under a nitrogen atmosphere, to which a 2 M aqueous potassium carbonate solution (110 ml) was added and tetrakis-(triphenylphosphine)palladium (0.70 g, 0.60 mmol) was added, and then the resulting mixture was heated and stirred for 5 hours. The temperature was lowered to normal temperature, the aqueous layer was removed, and the resulting product was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure, and recrystallized with ethyl acetate (320 ml) to prepare Compound 4 (9.11 g, yield: 63%).

    [0077] MS: [M+H]+ = 724

    Example 5: Preparation of Compound 5



    [0078] 



    [0079] Compound A-1 (15.58 g, 33.43 mmol) and Compound a-5 (8.50 g, 31.84 mmol) were completely dissolved in tetrahydrofuran (240 ml) in a 500-ml round bottom flask under a nitrogen atmosphere, to which a 2 M aqueous potassium carbonate solution (120 ml) was added and tetrakis-(triphenylphosphine)palladium (1.10 g, 0.96 mmol) was added, and then the resulting mixture was heated and stirred for 4 hours. The temperature was lowered to normal temperature, the aqueous layer was removed, and the resulting product was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure, and recrystallized with ethyl acetate (280 ml) to prepare Compound 5 (11.24 g, yield: 62%).

    [0080] MS: [M+H]+ = 572

    Example 6: Preparation of Compound 6



    [0081] 



    [0082] Compound A-1 (12.13 g, 26.02 mmol) and Compound a-6 (8.50 g, 24.78 mmol) were completely dissolved in tetrahydrofuran (260 ml) in a 500-ml round bottom flask under a nitrogen atmosphere, to which a 2 M aqueous potassium carbonate solution (130 ml) was added and tetrakis-(triphenylphosphine)palladium (0.86 g, 0.74 mmol) was added, and then the resulting mixture was heated and stirred for 5 hours. The temperature was lowered to normal temperature, the aqueous layer was removed, and the resulting product was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure, and recrystallized with ethyl acetate (270 ml) to prepare Compound 6 (10.67 g, yield: 66%).

    [0083] MS: [M+H]+ = 648

    Example 7: Preparation of Compound 7



    [0084] 



    [0085] Compound A-1 (10.28 g, 22.06 mmol) and Compound a-7 (7.50 g, 21.01 mmol) were completely dissolved in tetrahydrofuran (280 ml) in a 500-ml round bottom flask under a nitrogen atmosphere, to which a 2 M aqueous potassium carbonate solution (140 ml) was added and tetrakis-(triphenylphosphine)palladium (0.73 g, 0.63 mmol) was added, and then the resulting mixture was heated and stirred for 5 hours. The temperature was lowered to normal temperature, the aqueous layer was removed, and the resulting product was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure, and recrystallized with ethyl acetate (310 ml) to prepare Compound 7 (8.84 g, yield: 64%).

    [0086] MS: [M+H]+ = 662

    Example 8: Preparation of Compound 8



    [0087] 



    [0088] Compound B (8.50 g, 23.81 mmol) and Compound a-1 (11.65 g, 25.01 mmol) were completely dissolved in tetrahydrofuran (280 ml) in a 500-ml round bottom flask under a nitrogen atmosphere, to which a 2 M aqueous potassium carbonate solution (140 ml) was added and tetrakis-(triphenylphosphine)palladium (0.83 g, 0.71 mmol) was added, and then the resulting mixture was heated and stirred for 4 hours. The temperature was lowered to normal temperature, the aqueous layer was removed, and the resulting product was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure, and recrystallized with ethyl acetate (280 ml) to prepare Compound 8 (10.22 g, yield: 65%).

    [0089] MS: [M+H]+ = 648

    Example 9: Preparation of Compound 9



    [0090] 



    [0091] Compound B-1 (10.70 g, 22.96 mmol) and Compound a-6 (7.50 g, 21.87 mmol) were completely dissolved in tetrahydrofuran (180 ml) in a 500-ml round bottom flask under a nitrogen atmosphere, to which a 2 M aqueous potassium carbonate solution (90 ml) was added and tetrakis-(triphenylphosphine)palladium (0.76 g, 0.66 mmol) was added, and then the resulting mixture was heated and stirred for 4 hours. The temperature was lowered to normal temperature, the aqueous layer was removed, and the resulting product was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure, and recrystallized with ethyl acetate (280 ml) to prepare Compound 9 (8.71 g, yield: 60%).

    [0092] MS: [M+H]+ = 650

    Example 10: Preparation of Compound 10



    [0093] 



    [0094] Compound C (9.50 g, 22.73 mmol) and Compound a-8 (9.62 g, 23.86 mmol) were completely dissolved in tetrahydrofuran (260 ml) in a 500-ml round bottom flask under a nitrogen atmosphere, to which a 2 M aqueous potassium carbonate solution (130 ml) was added and tetrakis-(triphenylphosphine)palladium (0.79 g, 0.68 mmol) was added, and then the resulting mixture was heated and stirred for 4 hours. The temperature was lowered to normal temperature, the aqueous layer was removed, and the resulting product was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure, and recrystallized with ethyl acetate (240 ml) to prepare Compound 10 (9.82 g, yield: 62%).

    [0095] MS: [M+H]+ = 698

    Example 11: Preparation of Compound 11



    [0096] 



    [0097] Compound C-1 (8.51 g, 21.11 mmol) and Compound a-9 (4.63 g, 9.91 mmol) were completely dissolved in tetrahydrofuran (260 ml) in a 500-ml round bottom flask under a nitrogen atmosphere, to which a 2 M aqueous potassium carbonate solution (130 ml) was added and tetrakis-(triphenylphosphine)palladium (0.70 g, 0.60 mmol) was added, and then the resulting mixture was heated and stirred for 5 hours. The temperature was lowered to normal temperature, the aqueous layer was removed, and the resulting product was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure, and recrystallized with ethyl acetate (310 ml) to prepare Compound 11 (7.85 g, yield: 58%).

    [0098] MS: [M+H]+ = 678

    [Experimental Example]


    Experimental Example 1



    [0099] A glass substrate on which ITO (indium tin oxide) was coated as a thin film to a thickness of 1,000 Å was put into distilled water in which a detergent was dissolved, and ultrasonically cleaned. In this case, a product manufactured by Fischer Co., was used as the detergent, and as the distilled water, distilled water filtered twice using a filter manufactured by Millipore Co., was used. After the ITO was cleaned for 30 minutes, ultrasonic cleaning was repeated twice using distilled water for 10 minutes. After the cleaning with distilled water was completed, the substrate was ultrasonically cleaned with solvents of isopropyl alcohol, acetone, and methanol, then dried, and then transferred to a plasma cleaner. In addition, the substrate was cleaned for 5 minutes using oxygen plasma, and then transferred to a vacuum depositor.

    [0100] On the ITO transparent electrode which is the anode electrode thus prepared, the following compound HI1 and the following compound HI2 were thermally vacuum deposited at a ratio of 98: 2 (molar ratio) to have a thickness of 100 Å, thereby forming a hole injection layer. The following compound HT1 was vacuum deposited on the hole injection layer to a thickness of 1150 Å to form a hole transfer layer. The following compound EB1 was vacuum deposited on the hole transport layer to a thickness of 50 Å to form an electron blocking layer. Then, the following compound BH and the following compound BD were vacuum deposited at a weight ratio of 25: 1 on the electron blocking layer to a thickness of 200 Å to form a light emitting layer. The Compound 1 prepared in Example 1 above was vacuum deposited on the light emitting layer to a thickness of 50 Å to form a hole blocking layer. The following compound ET1 and the following compound LiQ were vacuum deposited at a ratio of 1: 1 on the hole blocking layer to a thickness of 310 Å to form an electron injection and transport layer. Lithium fluoride (LiF) and aluminum were sequentially deposited to have a thickness of 12 Å and 1,000 Å, respectively, on the electron injection and transport layer, thereby forming a cathode.







    [0101] In the above-mentioned process, the vapor deposition rate of the organic material was maintained at 0.4 to 0.7 Å/sec, the deposition rates of lithium fluoride and aluminum of the cathode were maintained at 0.3 Å/sec and at 2 Å/sec, respectively, and the degree of vacuum during the deposition was maintained at 2×10-7 to 5×10-6 torr, thereby manufacturing an organic light emitting device.

    Experimental Examples 2 to 11



    [0102] An organic light emitting device was manufactured in the same manner as in Experimental Example 1, except that the compounds shown in Table 1 below were used instead of Compound 1.

    Comparative Experimental Examples 1 to 3



    [0103] An organic light emitting device was manufactured in the same manner as in Experimental Example 1, except that the compounds shown in Table 1 below were used instead of Compound 1. Compounds HB1, HB2 and HB3 shown in Table 1 below are as follows:



    [0104] The voltage, efficiency, color coordinate, and lifetime were measured by applying a current to the organic light emitting devices manufactured in the Experimental Examples and Comparative Experimental Examples, and the results are shown in Table 1 below. At this time, T95 means the time required for the luminance to be reduced to 95% of the initial luminance (1600 nit).
    [Table 1]
     Compound (hole blocking layer)Voltage (V@10mA/cm 2)Efficiency (cd/A @10mA/cm2)Color coordinate (x,y)T95 (hr @10mA/cm2)
    Experimental Example 1 Compound 1 4.47 6.59 (0.145, 0.042) 255
    Experimental Example 2 Compound 2 4.48 6.54 (0.144, 0.045) 265
    Experimental Example 3 Compound 3 4.43 6.58 (0.146, 0.046) 255
    Experimental Example 4 Compound 4 4.45 6.54 (0.147, 0.047) 240
    Experimental Example 5 Compound 5 4.42 6.56 (0.146, 0.044) 250
    Experimental Example 6 Compound 6 4.44 6.52 (0.144, 0.045) 265
    Experimental Example 7 Compound 7 4.45 6.58 (0.145, 0.046) 255
    Experimental Example 8 Compound 8 4.55 6.49 (0.146, 0.047) 245
    Experimental Example 9 Compound 9 4.51 6.48 (0.146, 0.046) 235
    Experimental Example 10 Compound 10 4.66 6.34 (0.144, 0.045) 245
    Experimental Example 11 Compound 11 4.67 6.31 (0.145, 0.046) 230
    Comparative Experimental Example 1 Compound HB1 6.12 2.35 (0.145, 0.045) 15
    Comparative Experimental Example 2 Compound HB2 4.98 5.23 (0.146, 0.046) 180
    Comparative Experimental Example 3 Compound HB3 5.14 5.60 (0.147, 0.044) 195


    [0105] As shown in Table 1, the organic light emitting device using the compound of the present invention as the hole blocking layer exhibited excellent characteristics in terms of efficiency, driving voltage and stability of the organic light emitting device. In particular, compared to the organic light emitting devices of Comparative Experimental Examples 2 and 3 manufactured using Compounds HB2 and HB3 in which triazine substituents are linked to 9,9'-spirobi [fluorene] and 9,9-diphenyl-9H-fluorene cores, the organic light emitting devices of Experimental Examples 1 to 11 using the compound of the present invention exhibited low voltage, high efficiency and long lifetime characteristics. In addition, the organic light emitting device of Comparative Experimental Example 1 manufactured using Compound HB-1 having a structure in which an amine-based substituent was substituted for the core of the present invention, did not exhibit these characteristics.
    [Explanation of Sign]
    1: substrate 2: anode
    3: organic material layer 4: cathode
    5: hole injection layer 6: hole transport layer
    7: electron blocking layer 8: light emitting layer
    9: hole blocking layer 10: electron transport layer
    11: electron injection layer    



    Claims

    1. A compound represented by the following Chemical Formula 1: [Chemical Formula 1]

    in Chemical Formula 1,

    L is a single bond; a substituted or unsubstituted C6-60 arylene; or a substituted or unsubstituted C2-60 heteroarylene containing at least one selected from the group consisting of N, O and S, and

    Ar is any one selected from the group consisting of the following:

    wherein,

    X1 to X3 are N, or CH, with the proviso that at least one of X1 to X3 is N,

    Ar1 and Ar2 are each independently a substituted or unsubstituted C6-60 aryl; or a substituted or unsubstituted C2-60 heteroaryl containing at least one selected from the group consisting of N, O and S,

    X4 and X5 are N, or CH, with the proviso that at least one of X4 and X5 is N,

    Ar3 is independently a substituted or unsubstituted C6-60 aryl; or a substituted or unsubstituted C2-60 heteroaryl containing at least one selected from the group consisting of N, O and S,

    Y is N(Ar5), O, or S,

    Ar4 is hydrogen, a substituted or unsubstituted C6-60 aryl, or a substituted or unsubstituted C2-60 heteroaryl containing at least one selected from the group consisting of N, O and S, and

    Ar5 is a substituted or unsubstituted C6-60 aryl.


     
    2. The compound according to claim 1,
    wherein the Chemical Formula 1 is represented by the following Chemical Formula 1-1, 1-2 or 1-3.







    wherein L and Ar have the same definitions as in claim 1.
     
    3. The compound according to claim 1,
    wherein L is a single bond, phenylene, or carbazoldiyl.
     
    4. The compound according to claim 1,
    wherein Ar1 and Ar2 are each independently phenyl, biphenylyl, terphenylyl, naphthyl, phenanthrenyl, triphenylenyl, dibenzofuranyl, dibenzothiophenyl, or 9-phenyl-9H-carbazolyl.
     
    5. The compound according to claim 1,
    wherein Ar3 is phenyl, biphenylyl, or naphthyl.
     
    6. The compound according to claim 1,
    wherein Ar4 is hydrogen, phenyl, biphenylyl, or naphthyl.
     
    7. The compound according to claim 1,
    wherein Ar5 is phenyl.
     
    8. The compound according to claim 1,
    wherein the compound represented by the Chemical Formula 1 is selected from the group consisting of the following:










































































































     
    9. An organic light emitting device comprising a first electrode; a second electrode provided opposite to the first electrode; and one or more organic material layers provided between the first electrode and the second electrode, wherein one or more layers of the organic material layers comprise the compound according to any one of claims 1 to 8.
     


    Ansprüche

    1. Verbindung, dargestellt durch die folgende Chemische Formel 1:

    in Chemische Formel 1,

    ist L eine Einfachbindung; ein substituiertes oder unsubstituiertes C6-60-Arylen; oder ein substituiertes oder unsubstituiertes C2-60-Heteroarylen, enthaltend mindestens eines ausgewählt aus der Gruppe bestehend aus N, O und S, und

    ist Ar eine beliebige Verbindung ausgewählt aus der Gruppe bestehend aus den folgenden Verbindungen:

    wobei,

    X1 bis X3 N, oder CH sind, mit der Maßgabe, dass mindestens eines von X1 bis X3 N ist,

    Ar1 und Ar2 sind jeweils unabhängig voneinander ein substituiertes oder unsubstituiertes C6-60-Aryl; oder ein substituiertes oder unsubstituiertes C2-60-Heteroaryl, enthaltend mindestens eines ausgewählt aus der Gruppe bestehend aus N, O und S,

    X4 und X5 sind N, oder CH, mit der Maßgabe, dass mindestens eines von X4 und X5 N ist,

    Ar3 ist unabhängig ein substituiertes oder unsubstituiertes C6-60-Aryl; oder ein substituiertes oder unsubstituiertes C2-60-Heteroaryl, enthaltend mindestens eines ausgewählt aus der Gruppe bestehend aus N, O und S,

    Y ist N(Ar5), O, oder S,

    Ar4 ist Wasserstoff, ein substituiertes oder unsubstituiertes C6-60-Aryl; oder ein substituiertes oder unsubstituiertes C2-60-Heteroaryl, enthaltend mindestens eines ausgewählt aus der Gruppe bestehend aus N, O und S, und

    Ar5 ist ein substituiertes oder unsubstituiertes C6-60-Aryl.


     
    2. Verbindung gemäß Anspruch 1,
    wobei die Chemische Formel 1 durch die folgende Chemische Formel 1-1, 1-2 oder 1-3 dargestellt wird:







    wobei L und Ar dieselben Definitionen wie in Anspruch 1 haben.
     
    3. Verbindung gemäß Anspruch 1, wobei L eine Einfachbindung, Phenylen oder Carbazoldiyl ist.
     
    4. Verbindung gemäß Anspruch 1, wobei Ar1 und Ar2 jeweils unabhängig voneinander Phenyl, Biphenylyl, Terphenylyl, Naphthyl, Phenanthrenyl, Triphenylenyl, Dibenzofuranyl, Dibenzothiophenyl oder 9-Phenyl-9H-carbazolyl sind.
     
    5. Verbindung gemäß Anspruch 1, wobei Ar3 Phenyl, Biphenylyl oder Naphthyl ist.
     
    6. Verbindung gemäß Anspruch 1, wobei Ar4 Wasserstoff, Phenyl, Biphenylyl oder Naphthyl ist.
     
    7. Verbindung gemäß Anspruch 1, wobei Ar5 Phenyl ist.
     
    8. Verbindung gemäß Anspruch 1, wobei die durch die Chemische Formel 1 dargestellte Verbindung ausgewählt ist aus der Gruppe bestehend aus den folgenden Verbindungen:










































































































     
    9. Organische lichtemittierende Vorrichtung, umfassend eine erste Elektrode; eine gegenüber der ersten Elektrode vorgesehene zweite Elektrode; und eine oder mehrere Schichten aus organischem Material, welche zwischen der ersten Elektrode und der zweiten Elektrode vorgesehen sind, wobei eine oder mehrere Schichten der Schichten aus organischem Material die Verbindung gemäß einem der Ansprüche 1 bis 8 umfassen.
     


    Revendications

    1. Composé représenté par la Formule Chimique 1 suivante :

    dans la Formule Chimique 1,

    L est une liaison simple; un arylène en C6-60 substitué ou non substitué; ou un hétéroarylène en C2-60 substitué ou non substitué contenant au moins un sélectionné dans le groupe consistant en N, O et S, et

    Ar est l'un quelconque sélectionné dans le groupe consistant en les suivants :

    dans lequel,

    X1 à X3 sont N, ou CH, à condition qu'au moins un parmi X1 à X3 soit N,

    Ar1 et Ar2 sont chacun indépendamment un aryle en C6-60 substitué ou non substitué ; ou un hétéroaryle en C2-60 substitué ou non substitué contenant au moins un sélectionné dans le groupe consistant en N, O et S,

    X4 et X5 sont N, ou CH, à condition qu'au moins un parmi X4 et X5 soit N,

    Ar3 est indépendamment un aryle en C6-60 substitué ou non substitué ; ou un hétéroaryle en C2-60 substitué ou non substitué contenant au moins un sélectionné dans le groupe consistant en N, O et S,

    Y est N(Ar5), O, ou S,

    Ar4 est un hydrogène, un aryle en C6-60 substitué ou non substitué, ou un hétéroaryle en C2-60 substitué ou non substitué contenant au moins un sélectionné dans le groupe consistant en N, O et S, et

    Ar5 est un aryle en C6-60 substitué ou non substitué.


     
    2. Composé selon la revendication 1,
    dans lequel la Formule Chimique 1 est représentée par la Formule Chimique 1-1, 1 - 2 ou 1-3 suivante.





    dans lequel L et Ar ont les mêmes définitions que dans la revendication 1.
     
    3. Composé selon la revendication 1,
    dans lequel L est une liaison simple, un phénylène, ou un carbazoldiyle.
     
    4. Composé selon la revendication 1,
    dans lequel Ar1 et Ar2 sont chacun indépendamment un phényle, un biphénylyle, un terphénylyle, un naphtyle, un phénanthrényle, un triphénylényle, un dibenzofuranyle, un dibenzothiophényle, ou un 9-phényl-9H-carbazolyle.
     
    5. Composé selon la revendication 1,
    dans lequel Ar3 est un phényle, un biphénylyle, ou un naphtyle.
     
    6. Composé selon la revendication 1,
    dans lequel Ar4 est un hydrogène, un phényle, un biphénylyle, ou un naphtyle.
     
    7. Composé selon la revendication 1,
    dans lequel Ar5 est un phényle.
     
    8. Composé selon la revendication 1,
    dans lequel le composé représenté par la Formule Chimique 1 est sélectionné dans le groupe consistant en les suivants :










































































































     
    9. Dispositif électroluminescent organique comprenant une première électrode ; une seconde électrode disposée à l'opposé de la première électrode ; et une ou plusieurs couches de matériau organique disposées entre la première électrode et la seconde électrode, dans lequel une ou plusieurs couches des couches de matériau organique comprennent le composé selon l'une quelconque des revendications 1 à 8.
     




    Drawing








    Cited references

    REFERENCES CITED IN THE DESCRIPTION



    This list of references cited by the applicant is for the reader's convenience only. It does not form part of the European patent document. Even though great care has been taken in compiling the references, errors or omissions cannot be excluded and the EPO disclaims all liability in this regard.

    Patent documents cited in the description