| (19) |
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(11) |
EP 1 341 403 A8 |
| (12) |
CORRECTED EUROPEAN PATENT APPLICATION |
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published in accordance with Art. 158(3) EPC |
| (48) |
Corrigendum issued on: |
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17.12.2003 Bulletin 2003/51 |
| (43) |
Date of publication: |
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03.09.2003 Bulletin 2003/36 |
| (22) |
Date of filing: 22.11.2001 |
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| (51) |
International Patent Classification (IPC)7: H05B 33/22, H05B 33/14, C09K 11/06, C07D 311/96, C07D 471/04, C07D 405/14, C07D 409/14, C07D 413/14, C07D 417/14, C07D 407/14, C07D 335/12, C07D 235/02, C07D 221/10 |
| (86) |
International application number: |
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PCT/JP0110/214 |
| (87) |
International publication number: |
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WO 0204/3449 (30.05.2002 Gazette 2002/22) |
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| (84) |
Designated Contracting States: |
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AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR |
| (30) |
Priority: |
24.11.2000 JP 2000357129 08.06.2001 JP 2001173610
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| (71) |
Applicant: Toray Industries, Inc. |
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Tokyo 103-8666 (JP) |
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| (72) |
Inventors: |
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- TOMINAGA, Tsuyoshi
Otsu-shi, Shiga 520-2152 (JP)
- KITAZAWA, Daisuke
Otsu-shi, Shiga 520-0842 (JP)
- MAKIYAMA, Aki Kosei-Center Toray Industries, Inc
Otsu-shi, Shiga 520-0844 (JP)
- KOHAMA, Akira
Otsu-shi, Shiga 520-0834 (JP)
|
| (74) |
Representative: Coleiro, Raymond et al |
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MEWBURN ELLIS York House 23 Kingsway London WC2B 6HP London WC2B 6HP (GB) |
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| (54) |
LUMINESCENT ELEMENT MATERIAL AND LUMINESCENT ELEMENT COMPRISING THE SAME |
(57) The light emitting device of the present invention relates to a light emitting device
which is characterized in that it is a device with an emissive substance present between
an anode and cathode, and which emits light by means of electrical energy, and said
device has a least one type of compound denoted by (a) to (d) below.
- (a) A compound having a plurality of 1,7-phenanthroline skeletal structures
- (b) A benzoquinoline derivative
- (c) A spiro compound represented by general formula (1) A1 and A2 are each selected
from single bonds, substituted or unsubstituted alkyl chains, ether chains, thioether
chains, ketone chains and substituted or unsubstituted amino chains. However, A1 ≠
A2. Z represents carbon or silicon. R1 to R16 are each selected from hydrogen, alkyl
group, cycloalkyl group, aralkyl group, alkenyl group, cycloalkenyl group, alkynyl
group, hydroxyl group, mercapto group, alkoxy group, alkylthio group, aryl ether group,
aryl thioether group, aryl group, heterocyclic group, halogen, haloalkane, haloalkene,
haloalkyne, cyano group, aldehyde group, carbonyl group, carboxyl group, ester group,
carbamoyl group, amino group, nitro group, silyl group, siloxanyl group and a cyclic
structure formed with an adjacent substituent.
- (d) A tetraphenylmethane derivative represented by general formula (2) R17 to R36
are each selected from hydrogen, alkyl group, cycloalkyl group, aralkyl group, alkenyl
group, cycloalkenyl group, alkynyl group, hydroxyl group, mercapto group, alkoxy group,
alkylthio group, aryl ether group, aryl thioether group, aryl group, heterocyclic
group, halogen, haloalkane, haloalkene, haloalkyne, cyano group, aldehyde group, carbonyl
group, carboxyl group, ester group, carbamoyl group, amino group, nitro group, silyl
group, siloxanyl group and a cyclic structure formed with an adjacent substituent.
However, at least one of R17 to R36 is selected from substituents represented by general
formula (3).―X―Ar X is a single bond or is selected from the following, and Ar denotes
a condensed aromatic ring or heteroaromatic ring. In the case where X is phosphorus
oxide, then Ar represents an aromatic hydrocarbon or heteroaromatic ring.
- n is an natural number.