IP Library Granted Patent US 8,709,613
Granted Patent B2
US 8,709,613 · App. 11/596,299 · Granted Apr 29, 2014

Aromatic amine derivative, organic electroluminescent element employing the same, and process for producing aromatic amine derivative

Inventor: Masakazu Funahashi (Sodegaura, JP)
Assignee: Idemitsu Kosan Co., Ltd.
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,709,613
App. No.
11/596,299
Granted
Apr 29, 2014
Kind
B2
Abstract

An aromatic amine derivative with a special structure obtained by bonding a diphenylamino group having a substituent to a substituted pyrene structure; and a process for producing the aromatic amine derivative. An organic electroluminescence device which comprises at least one organic thin film layer comprising a light emitting layer sandwiched between a pair of electrodes consisting of an anode and a cathode, wherein at least one of the organic thin film layer comprises the aromatic amine derivative singly or as its mixture component. An organic electroluminescence device having a prolonged lifetime and emits blue light with an enhanced efficiency of light emission and an aromatic amine derivative realizing the device are provided.

Claims (42)

1. An aromatic amine derivative represented by general formula (A):

wherein

R 1 and R 2 are each independently selected from the group consisting of a substituted or unsubstituted aryl group having 5 to 25 carbon atoms, and a substituted or unsubstituted cycloalkyl group having 3 to 25 carbon atoms;

A 1 , A 2 , A 3 and A 4 each independently represents a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 5 to 25 carbon atoms, or a substituted or unsubstituted cycloalkyl group having 3 to 25 carbon atoms,

however, a case where any substituent of each group represented by R 1 , R 2 , A 1 , A 2 , A 3 and A 4 comprises a vinyl group is excluded;

p, q, r and s each independently represents an integer of 1 to 5; when p represents an integer of 2 or greater, each of plural A 1 may be the same with, or different from each other, and may bond each other to form a saturated or unsaturated ring; when q represents an integer of 2 or greater, each of plural A 2 may be the same with, or different from each other, and may bond each other to form a saturated or unsaturated ring; when r represents an integer of 2 or greater, each of plural A 3 may be the same with, or different from each other, and may bond each other to form a saturated or unsaturated ring; and when s represents an integer of 2 or greater, each of plural A 4 may be the same with, or different from each other, and may bond each other to form a saturated or unsaturated ring.

2. The aromatic amine derivative according to claim 1 , wherein at least one of p, q, r and s represents an integer of 2 or greater.

3. An aromatic amine derivative represented by general formula (A′):

wherein

R 1 ′ and R 2 ′ each independently represents a hydrogen atom or an alkyl group having 1 to 20 carbon atoms; excluding a case where both R 1 ′ and R 2 ′ are hydrogen atoms;

A 1 , A 2 , A 3 and A 4 each independently represents a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 5 to 25 carbon atoms, or a substituted or unsubstituted cycloalkyl group having 3 to 25 carbon atoms;

however, at least one of A 1 , A 2 , A 3 and A 4 bonds to meta-position of a bonding position where a nitrogen atom bonds;

further, a case where any substituent of each group represented by R 1 ′, R 2 ′, A 1 , A 2 , A 3 and A 4 comprises a vinyl group is excluded;

p, q, r and s each independently represents an integer of 1 to 5; when p represents an integer of 2 or greater, each of plural A l may be the same with, or different from each other, and may bond each other to form a saturated or unsaturated ring; when q represents an integer of 2 or greater, each of plural A 2 may be the same with, or different from each other, and may bond each other to form a saturated or unsaturated ring; when r represents an integer of 2 or greater, each of plural A 3 may be the same with, or different from each other, and may bond each other to form a saturated or unsaturated ring; and when s represents an integer of 2 or greater, each of plural A 4 may be the same with, or different from each other, and may bond each other to form a saturated or unsaturated ring.

4. An aromatic amine derivative represented by general formula (A″):

wherein

R 1 ′ and R 2 ′ each independently represents a hydrogen atom or an alkyl group selected from the group consisting of a methyl group, an ethyl group, a propyl group, and an isopropyl group; excluding a case where both R 1 ′ and R 2 ′ are hydrogen atoms;

A 1 , A 2 , A 3 and A 4 each independently represents a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 5 to 25 carbon atoms, or a substituted or unsubstituted cycloalkyl group having 3 to 25 carbon atoms;

however, when A 1 , A 2 , A 3 and A 4 all represent alkyl groups, a total sum made by adding numbers of carbon atoms in A 1 , A 2 , A 3 and A 4 does not exceed 10;

further, a case where any substituent of each group represented by R 1 ′, R 2 ′, A 1 , A 2 , A 3 and A 4 comprises a vinyl group is excluded;

p, q, r and s each independently represents an integer of 1 to 5; when p represents an integer of 2 or greater, each of plural A l may be the same with, or different from each other, and may bond each other to form a saturated or unsaturated ring; when q represents an integer of 2 or greater, each of plural A 2 may be the same with, or different from each other, and may bond each other to form a saturated or unsaturated ring; when r represents an integer of 2 or greater, each of plural A 3 may be the same with, or different from each other, and may bond each other to form a saturated or unsaturated ring; and when s represents an integer of 2 or greater, each of plural A 4 may be the same with, or different from each other, and may bond each other to form a saturated or unsaturated ring.

5. The aromatic amine derivative according to claim 1 , which is a doping material for an organic electroluminescence device.

6. An organic electroluminescence device which comprises:

at least one organic thin film layer comprising a light emitting layer sandwiched between a pair of electrodes consisting of an anode and a cathode,

wherein at least one of the at least one organic thin film layer comprises the aromatic amine derivative according to claim 1 singly or as a component of a mixture.

7. The organic electroluminescence device according to claim 6 , wherein the at least one organic thin film layer comprises an organic layer having the aromatic amine derivative between the anode and the light emitting layer.

8. The organic electroluminescence device according to claim 6 , wherein the light emitting layer contains the aromatic amine derivative in an amount of 0.1 to 20% by weight.

9. The aromatic amine derivative according to claim 1 , wherein R 1 and R 2 are each independently selected from the group consisting of phenyl group, o-biphenyl group, 4-methylphenyl group, α,α-dimethylbenzyl group, 4-cyanophenyl group, 2-phenylethyl group, 1-naphthyl group, and 2-naphthyl group;

A 1 , A 2 , A 3 and A 4 are each independently selected from the group consisting of hydrogen atom, methyl group, t-butyl group, isopropyl group, n-propyl group, 2-butyl group, 2-naphthyl group, α,α-dimethylbenzyl group, phenyl group, trifluoromethyl group, and cyclohexyl group; and

p, q, r and s each independently represents an integer of 1 to 3, when any of p, q, r and s is 2 or 3, two A 1 , A 2 , A 3 or A 4 groups may bond each other to form butane-1,4-diyl group or propane-1,3-diyl group.

10. The aromatic amine derivative according to claim 3 , which is a doping material for an organic electroluminescence device.

11. An organic electroluminescence device which comprises:

at least one organic thin film layer comprising a light emitting layer sandwiched between a pair of electrodes consisting of an anode and a cathode,

wherein at least one of the at least one organic thin film layer comprises the aromatic amine derivative according to claim 3 singly or as a component of a mixture.

12. The organic electroluminescence device according to claim 11 , wherein the at least one organic thin film layer comprises an organic layer having the aromatic amine derivative between the anode and the light emitting layer.

13. The organic electroluminescence device according to claim 11 , wherein the light emitting layer comprises the aromatic amine derivative in an amount of 0.1 to 20% by weight.

14. The aromatic amine derivative according to claim 4 , which is a doping material for an organic electroluminescence device.

15. An organic electroluminescence device which comprises:

at least one organic thin film layer comprising a light emitting layer sandwiched between a pair of electrodes consisting of an anode and a cathode,

wherein at least one of the at least one organic thin film layer comprises the aromatic amine derivative according to claim 4 singly or as a component of a mixture.

16. The organic electroluminescence device according to claim 15 , wherein the at least one organic thin film layer comprises an organic layer having the aromatic amine derivative between the anode and the light emitting layer.

17. The organic electroluminescence device according to claim 15 , wherein the light emitting layer comprises the aromatic amine derivative in an amount of 0.1 to 20% by weight.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 18, 2007
From: FUNAHASHI, MASAKAZU
To: IDEMITSU KOSAN CO., LTD.
Reel/Frame 019979/0091 →
Priority Claims (1)
JP 2004-141900 · May 12, 2004 · national
Continuity (1)
Related Publication 20070252511A1 · Nov 1, 2007