IP Library Granted Patent US 9,156,843
Granted Patent B2
US 9,156,843 · App. 13/577,238 · Granted Oct 13, 2015

Organic electroluminescent device comprising an organic layer containing an indolocarbazole compound

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Quick Facts
Patent No.
US 9,156,843
App. No.
13/577,238
Granted
Oct 13, 2015
Kind
B2
Abstract

Disclosed is an organic electroluminescent device (organic EL device) that is improved in luminous efficiency, sufficiently secures driving stability, and has a simple configuration. This organic EL device is constituted of an anode, organic layers comprising a phosphorescent light-emitting layer, and a cathode piled one upon another on a substrate and at least one organic layer selected from a light-emitting layer, an electron-transporting layer, and a hole-blocking layer contains an indolocarbazole compound represented by general formula (1). In the case where the indolocarbazole compound is incorporated in the light-emitting layer containing a phosphorescent dopant and a host material, it is incorporated as the host material. Some of such indolocarbazole compounds are represented by the following formula (2): wherein each of A 1 and A 2 is an aromatic hydrocarbon group; each of B 1 and B 2 is an aromatic heterocyclic group; each of R 1 to R 3 is a hydrogen atom, an alkyl group, a cycloalkyl group, an aromatic hydrocarbon group, or an aromatic heterocyclic group; m is an integer of 1 to 3; and n is an integer of 0 to 3.

Claims (36)

1. An organic electroluminescent device comprising an anode, organic layers containing a phosphorescent light-emitting layer, and a cathode piled one upon another on a substrate wherein an organic layer is a light-emitting layer and contains an indolocarbazole compound represented by general formula (1);

in general formula (1), ring A is an aromatic ring or a heterocyclic ring represented by formula (1a) and fused to the adjacent rings at arbitrary positions and ring B is a heterocyclic ring represented by formula (1b) and fused to the adjacent rings at arbitrary positions; in general formula (1) and formulas (1a) and (1b), each of A 1 and A 2 is independently an (m+1)-valent or (n+1)-valent aromatic hydrocarbon group of 6 to 50 carbon atoms and has no substituent or has one to six substituents selected from an alkyl group of 1 to 4 carbon atoms, an alkoxyl group of 1 to 2 carbon atoms, and an acetyl group, provided that when a number of the substituents is 2 or more, they may be identical with or different from one another;

each of B 1 and B 2 is independently:

(i) an aromatic heterocyclic group of 3 to 17 carbon atoms, or

(ii) an aromatic heterocyclic group of 6 to 50 carbon atoms in total in which two to five aromatic heterocyclic rings, each of which have a total of 3 to 17 carbon atoms, are linked together such that any two linked aromatic heterocyclic rings are connected via a single bond, and

each of B 1 and B 2 has no substituent or has one to six substituents selected from an alkoxyl group of 1 to 2 carbon atoms, an acetyl group, and an aromatic hydrocarbon group of 6 to 12 carbon atoms, provided that when a number of the substituents is 2 or more, they may be identical with or different from one another; X is a methine group; each of R 1 and R 2 is independently a hydrogen atom, an aliphatic hydrocarbon group of 1 to 10 carbon atoms, an aromatic hydrocarbon group of 6 to 12 carbon atoms, or an aromatic heterocyclic group of 3 to 11 carbon atoms; R 3 is a hydrogen atom, an aliphatic hydrocarbon group of 1 to 10 carbon atoms, an aromatic hydrocarbon group of 6 to 12 carbon atoms, or an aromatic heterocyclic group of 3 to 11 carbon atoms; m is an integer of 1 to 3; n is an integer of 0 to 3; when m or n is 2 or more, a plurality of B 1 s or B 2 s may be identical with or different from one another.

2. An organic, electroluminescent device as described in claim 1 wherein the indolocarbazole compound represented by general formula (1) is an indolocarbazole compound represented by any one of general formulas (2) to (5);

In general formulas (2) to (5), A 1 , A 2 , B 1 , B 2 , R 1 to R 3 , m, and n respectively have the same meaning as those in general formula (1).

3. An organic electroluminescent device as described in claim 2 wherein the indolocarbazole compound represented by any one of general formulas (2) to (5) is an indolocarbazole compound represented by any one of general formulas (6) to (9);

In general formulas (6) to (9), B 1 , B 2 , R 1 to R 3 , m, and n respectively have the same meaning as those in general formula (1).

4. An organic electroluminescent device as described in claim 1 wherein the organic layer containing an indolocarbazole compound is a light-emitting layer containing a phosphorescent dopant.

5. An organic electroluminescent device as described in claim 2 wherein the organic layer containing an indolocarbazole compound is a light-emitting layer containing a phosphorescent dopant having a peak emission wavelength of 440 to 510 nm and an indolocarbazole compound represented by general formula (4) or (5).

6. An organic electroluminescent device as described in claim 2 wherein the organic layer containing an indolocarbazole compound is a light-emitting layer containing a phosphorescent dopant.

7. An organic electroluminescent device as described in claim 3 wherein the organic layer containing an indolocarbazole compound is a light-emitting layer containing a phosphorescent dopant.

8. An organic electroluminescent device as described in claim 1 wherein each of B 1 and B 2 is independently an aromatic heterocyclic group derived from pyrrole, pyridine, pyrimidine, triazine, indole, quinoline, isoquinoline, quinoxaline, naphthyridine, carbazole, acridine, furan, benzofuran, dibenzofuran, thiopene, benzothiophene, dibenzothiophene, bipyridine, bipyrimidine, bitriazine, pyridylpyrimidine, pyridylcarbazole, pyridylpyrimidine, pyridylcarbazole, or pyrimidylcarbazole,

and may have one to six substituents selected from an alkoxyl group of 1 to 2 carbon atoms, an acetyl group, and an aromatic hydrocarbon group of 6 to 12 carbon atoms, provided that when a number of the substituents is 2 or more, they may be identical with or different from one another.

9. An organic electroluminescent device as described in claim 1 wherein each of A 1 and A 2 is independently an aromatic hydrocarbon group derived from benzene, naphthalene, fluorene, anthracene, phenanthrene, fluoranthene, pyrene, chrysene, biphenyl, terphenyl, phenylnaphthalene, diphenylnaphthalene, phenylanthracene, diphenylanthracene, or diphenylfluorene,

and may have one to six substituents selected from an alkyl group of 1 to 4 carbon atoms, an alkoxyl group of 1 to 2 carbon atoms, and an acetyl group, provided that when a number of the substituents is 2 or more, they may be identical with or different from one another.

10. An organic electroluminescent device comprising an anode, organic layers containing a phosphorescent light-emitting layer, and a cathode piled one upon another on a substrate wherein an organic layer is a light-emitting layer and contains an indolocarbazole compound represented by general formula (1);

in general formula (1), ring A is an aromatic ring or a heterocyclic ring represented by formula (1a) and fused to the adjacent rings at arbitrary positions and ring B is a heterocyclic ring represented by formula (1b) and fused to the adjacent rings at arbitrary positions; in general formula (1) and formulas (1a) and (1b), each of A 1 and A 2 is independently an (m+1)-valent or (n+1)-valent aromatic hydrocarbon group of 6 to 50 carbon atoms and has no substituent or has one to six substituents selected from an alkyl group of 1 to 4 carbon atoms, an alkoxyl group of 1 to 2 carbon atoms, and an acetyl group, provided that when a number of the substituents is 2 or more, they may be identical with or different from one another;

each of B 1 and B 2 is independently:

(i) an aromatic heterocyclic group of 3 to 17 carbon atoms, or

(ii) an aromatic heterocyclic group of 6 to 50 carbon atoms in total in which two to five aromatic heterocyclic rings, each of which have a total of 3 to 17 carbon atoms, are linked together such that any two linked aromatic heterocyclic rings are connected via a single bond, and

each of B 1 and B 2 has no substituent or has one to six substituents, each of said substituents being an aromatic hydrocarbon group of 6 to 12 carbon atoms, provided that when a number of the substituents is 2 or more, they may be identical with or different from one another; X is a methine group; each of R 1 and R 2 is independently a hydrogen atom, an aliphatic hydrocarbon group of 1 to 10 carbon atoms, an aromatic hydrocarbon group of 6 to 12 carbon atoms, or an aromatic heterocyclic group of 3 to 11 carbon atoms; R 3 is a hydrogen atom, an aliphatic hydrocarbon group of 1 to 10 carbon atoms, an aromatic hydrocarbon group of 6 to 12 carbon atoms, or an aromatic heterocyclic group of 3 to 11 carbon atoms; m is an integer of 1 to 3; n is an integer of 0 to 3; when m or n is 2 or more, a plurality of B 1 s or B 2 s may be identical with or different from one another.

11. An organic electroluminescent device as described in claim 10 wherein the indolocarbazole compound represented by general formula (1) is an indolocarbazole compound represented by any one of general formulas (2) to (5);

in general formulas (2) to (5), A 1 , A 2 , B 1 , B 2 , R 1 to R 3 , m, and n respectively have the same meaning as those in general formula (1).

12. An organic electroluminescent device as described in claim 11 wherein the indolocarbazole compound represented by any one of general formulas (2) to (5) is an indolocarbazole compound represented by any one of general formulas (6) to (9);

In general formulas (6) to (9), B 1 , B 2 , R 1 to R 3 , m, and n respectively have the same meaning as those in general formula (1).

13. An organic electroluminescent device as described in claim 10 wherein the organic layer containing an indolocarbazole compound is a light-emitting layer containing a phosphorescent dopant.

14. An organic electroluminescent device as described in claim 11 wherein the organic layer containing an indolocarbazole compound is a light-emitting layer containing a phosphorescent dopant having a peak emission wavelength of 440 to 510 nm and an indolocarbazole compound represented by general formula (4) or (5).

15. An organic electroluminescent device as described in claim 11 wherein the organic layer containing an indolocarbazole compound is a light-emitting layer containing a phosphorescent dopant.

16. An organic electroluminescent device as described in claim 12 wherein the organic layer containing an indolocarbazole compound is a light-emitting layer containing a phosphorescent dopant.

17. An organic electroluminescent device as described in claim 10 wherein each of B 1 and B 2 is independently an aromatic heterocyclic group derived from pyrrole, pyridine, pyrimidine, triazine, indole, quinoline, isoquinoline, quinoxaline, naphthyridine, carbazole, acridine, furan, benzofuran, dibenzofuran, thiopene, benzothiophene, dibenzothiophene, bipyridine, bipyrimidine, bitriazine, pyridylpyrimidine, pyridylcarbazole, pyridylpyrimidine, pyridylcarbazole, or pyrimidylcarbazole,

and may have one to six substituents, each of said substituents being an aromatic hydrocarbon group of 6 to 12 carbon atoms, provided that when a number of the substituents is 2 or more, they may be identical with or different from one another.

18. An organic electroluminescent device as described in claim 10 wherein each of A 1 and A 2 is independently an aromatic hydrocarbon group derived from benzene, naphthalene, fluorene, anthracene, phenanthrene, fluoranthene, pyrene, chrysene, biphenyl, terphenyl, phenylnaphthalene, diphenylnaphthalene, phenylanthracene, diphenylanthracene, or diphenylfluorene,

and may have one to six substituents selected from an alkyl group of 1 to 4 carbon atoms, an alkoxyl group of 1 to 2 carbon atoms, and an acetyl group, provided that when a number of the substituents is 2 or more, they may be identical with or different from one another.

Assignments (3)
MERGER Recorded Oct 21, 2020
From: NIPPON STEEL & SUMIKIN MATERIALS CO., LTD.; NIPPON STEEL & SUMIKIN CHEMICAL CO., LTD.
To: NIPPON STEEL CHEMICAL & MATERIAL CO., LTD.
Reel/Frame 054145/0400 →
CHANGE OF NAME Recorded Mar 20, 2013
From: NIPPON STEEL CHEMICAL CO., LTD.
To: NIPPON STEEL & SUMIKIN CHEMICAL CO., LTD.
Reel/Frame 030049/0771 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 4, 2012
From: KAI, TAKAHIRO; KOMORI, MASAKI; YAMAMOTO, TOSHIHIRO; MATSUMOTO, MEGUMI
To: NIPPON STEEL CHEMICAL CO., LTD.
Reel/Frame 028724/0751 →