IP Library Granted Patent US 6,929,872
Granted Patent B2
US 6,929,872 · App. 10/398,234 · Granted Aug 16, 2005

Organic electroluminescent devices

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Quick Facts
Patent No.
US 6,929,872
App. No.
10/398,234
Granted
Aug 16, 2005
Kind
B2
Abstract

This invention relates to highly reliable organic electroluminescent (EL) materials and devices exhibiting high luminance, high light emitting efficiency, minimal deterioration in light emission, usability at high temperature and good storage stability. The organic electroluminescent device of this invention has intermediate layers such as light emitting layer, hole transport layer, hole injection layer and the like arranged between the anode and the cathode and at least one of the intermediate layers comprises a triarylamine derivative represented by general formula (1) (wherein Ar 1 -Ar 3 are substituted or unsubstituted aryl groups and at least one of Ar 1 -Ar 3 is 9-phenanthryl group represented by general formula (2)); (wherein R 1 -R 9 are H, halogen, alkyl group, aralkyl group, alkenyl group, cyano group, acyl group, alkoxycarbonyl group, alkoxy group or the like).

Claims (7)

1. A triarylamine derivative represented by general formula (1)

wherein Ar 1, Ar 2 and Ar 3 are independently phenyl group, phenyl group containing a lower alkyl substituent, phenyl group containing a lower alkoxy substituent, cyanophenyl group, phenoxyphenyl group, halophenyl group, naphthyl group, naphthyl group containing a lower alkyl substituent, naphthyl group containing a lower alkoxy substituent, cyanonaphthyl group, halonaphthyl group, fluorenyl group, carbazolyl group, carbazolyl group containing a lower alkyl substituent, biphenylyl group, biphenylyl group containing a lower alkyl substituent, biphenylyl group containing a lower alkoxy substituent, thiophenyl group, indolyl group, pyridyl group or 9-phenanthryl group represented by general formula (2) and at least two of Ar 1, Ar 2 and Ar 3 are 9-phenanthryl groups represented by general formula (2);

wherein R 1 -R 9 are independently hydrogen, halogen, alkyl group, cyano group, acyl group, alkoxycarbonyl group, alkoxy group, alkylsulfonyl group, or haloalkyl group.

2. An organic electroluminescent device prepared by using the triarylamine derivative described in claim 1 .

3. An organic electroluminescent device as described in claim 2 , wherein the device has a light emitting layer and said light emitting layer comprises the triarylamine derivative.

4. An organic electroluminescent device as described in claim 2 , wherein the device has a hole transport layer and said hole transport layer comprises the triarylamine derivative.

5. An organic electroluminescent device comprising an anode, a cathode, and an organic electroluminescent material layer between the anode and cathode, wherein at least one organic electroluminescent material layer comprises the triarylamine derivative as described in claim 1 .

Assignments (2)
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 11, 2003
From: MORI, TATSUO; MIZUTANI, TERUYOSHI; TAKEDA, TORU; YAMASHITA, KOICHI
To: NIPPON STEEL CHEMICAL CO., LTD.; MORI, TATSUO; MIZUTANI, TERUYOSHI
Reel/Frame 014451/0786 →