IP Library Granted Patent US 8,062,769
Granted Patent B2
US 8,062,769 · App. 12/439,787 · Granted Nov 22, 2011

Indolocarbazole compound for use in organic electroluminescent device and organic electroluminescent device

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Quick Facts
Patent No.
US 8,062,769
App. No.
12/439,787
Granted
Nov 22, 2011
Kind
B2
Abstract

Provided is an organic electroluminescent device (organic EL device) that is improved in luminous efficiency, fully secured of driving stability, and simply constructed. The EL device has a light-emitting layer disposed between an anode and a cathode stacked one upon another on a substrate and the light-emitting layer comprises a phosphorescent dopant and an indolocarbazole derivative as a host material. Examples of the indolocarbazole compounds include a compound represented by the following formula (2) or (3), wherein X is N or CH, at least one of Xs is N, and Ar 1 to Ar 3 each is a substituted or unsubstituted aromatic group.

Claims (14)

1. A compound for use in an organic electroluminescent device represented by the following general formulas (2)-(7):

wherein:

X is CH or N and at least one of Xs is a nitrogen atom;

Ar 1 to Ar 3 each is independently a substituted or unsubstituted non-condensed aromatic hydrocarbon group or a substituted or unsubstituted non-condensed aromatic heterocyclic group and Ar 2 or Ar 3 may form a condensed ring with the X-containing ring;

R is hydrogen or a monovalent substituent.

2. A compound for use in an organic electroluminescent device as described in claim 1 wherein R in formulas (2)-(7) is independently hydrogen, an alkyl group, an aralkyl group, an alkenyl group, an alkynyl group, a cyano group, a dialkylamino group, a diarylamino group, a diaralkylamino group, an amino group, a nitro group, an acyl group, an alkoxycarbonyl group, a carboxyl group, an alkoxyl group, an alkylsulfonyl group, a haloalkyl group, a hydroxyl group, an amide group, a substituted or unsubstituted aromatic hydrocarbon group, or a substituted or unsubstituted aromatic heterocyclic group.

3. A compound for use in an organic electroluminescent device as described in claim 1 wherein R in formulas (2)-(7) is independently hydrogen, a substituted or unsubstituted aromatic hydrocarbon group of 5 to 18 carbon atoms, or a substituted or unsubstituted aromatic heterocyclic group of 3 to 17 carbon atoms.

4. A compound for use in an organic electroluminescent device as described in claim 1 wherein Ar 1 to Ar 3 each in formulas (2)-(7) is independently a substituted or unsubstituted phenyl group or a substituted or unsubstituted aromatic heterocyclic group of 2 to 5 carbon atoms.

5. A compound for use in an organic electroluminescent device as described in claim 1 wherein the said compound is represented by formula (2) or by formula (3).

6. An organic electroluminescent device which contains an organic layer comprising the compound for use in an organic electroluminescent device described in any one of claims 1 to 5 .

7. An organic electroluminescent device as described in claim 6 wherein the organic layer comprising the compound for use in an organic electroluminescent device is at least one layer selected from a light-emitting layer, a hole-transporting layer, an electron-transporting layer, and a hole-blocking layer.

8. An organic electroluminescent device as described in claim 6 wherein the organic layer comprising the compound for use in an organic electroluminescent device is a light-emitting layer of the said device disposed between an anode and a cathode stacked one upon another on a substrate and the said light-emitting layer comprises a phosphorescent dopant and the said compound for use in an organic electroluminescent device as a host material.

9. An organic electroluminescent device as described in claim 8 wherein a hole-injecting/transporting layer is disposed between the anode and the light-emitting layer and an electron-injecting/transporting layer is disposed between the cathode and the light-emitting layer.

10. An organic electroluminescent device as described in claim 9 wherein the hole-blocking layer is disposed between the light-emitting layer and the electron-injecting/transporting layer.

Assignments (2)
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 →