IP Library Granted Patent US 8,168,327
Granted Patent B2
US 8,168,327 · App. 11/619,787 · Granted May 1, 2012

Imide derivative, material for organic electroluminescent device and organic electroluminescent device using the same

Assignee: Idemitsu Kosan Co., Ltd.
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Quick Facts
Patent No.
US 8,168,327
App. No.
11/619,787
Granted
May 1, 2012
Kind
B2
Abstract

An imide derivative represented by the following formula (A): wherein R a and R b are each a hydrogen atom, a halogen atom, a cyano group, an alkyl group, a fluoroalkyl group or an aryl group; at least one of R a and R b is a fluoroalkyl group; and R c and R d are each a substituted or unsubstituted benzyl group, an aryl group, a heterocycle, a fluoroalkyl group or an imide group.

Claims (16)

1. A material represented by the following formula (II):

wherein R 11 to R 20 are each a hydrogen atom, a fluorine atom, a fluoroalkyl group or a cyano group, provided that a material wherein all of R 11 to R 20 are a hydrogen atom is excluded.

2. A material according to claim 1 which has a reduction potential (vs saturated calomel electrode) in a dimethylformamide solution of −0.5 V or more.

3. An organic electroluminescent device comprising:

an anode,

a cathode, and

one or a plurality of organic thin layers, including an emitting layer, the organic thin layers being interposed between the anode and the cathode;

at least one of the organic thin layers comprising the material of claim 1 .

4. The organic electroluminescent device according to claim 3 wherein the organic thin layers are a multilayer body in which a hole transporting layer, an emitting layer and an electron transporting layer are stacked in this order from the anode.

5. The organic electroluminescent device according to claim 4 wherein the hole transporting layer comprises the material.

6. The organic electroluminescent device according to claim 3 wherein the organic thin layers are a multilayer body in which a hole injecting layer, a hole transporting layer, an emitting layer, and an electron transporting layer are stacked in this order from the anode; the hole injection layer comprising the material.

7. The organic electroluminescent device according to claim 5 wherein the hole transporting layer comprising the material further comprises a phenylenediamine compound represented by the following formula (III):

wherein R 21 to R 26 are a hydrogen atom, a halogen atom, a trifluoromethyl group, an alkyl group, an aryl group, or a heterocycle; R 21 to R 26 may form a naphthalene skeleton, a carbazole skeleton, or a fluorene skeleton with a phenyl group bonded; and n represents 1 or 2.

8. The organic electroluminescent device according to claim 6 wherein the hole injecting layer comprising the material further comprises a phenylenediamine compound represented by the following formula (III):

wherein R 21 to R 26 are a hydrogen atom, a halogen atom, a trifluoromethyl group, an alkyl group, an aryl group, or a heterocycle; R 21 to R 26 may form a naphthalene skeleton, a carbazole skeleton, or a fluorene skeleton with a phenyl group bonded; and n represents 1 or 2.

9. A material according to claim 1 , which has the following formulae (II-8) or (II-9):

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 19, 2007
From: MORISHITA, HIRONOBU; KAWAMURA, HISAYUKI; HOSOKAWA, CHISHIO
To: IDEMITSU KOSAN CO. LTD.
Reel/Frame 019029/0756 →
Priority Claims (2)
JP 2006-003714 · Jan 11, 2006 · national
JP 2006-094411 · Mar 30, 2006 · national
Continuity (1)
Related Publication 20070160905A1 · Jul 12, 2007