IP Library Patent Application 14421792
Patent Application
App. No. 14/421,792

COMPOUND FOR ORGANIC ELECTROLUMINESCENT ELEMENTS, AND ORGANIC ELECTROLUMINESCENT ELEMENT

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Patent No.
US None
App. No.
14/421,792
Abstract

Provided are an organic EL device practically satisfactory in terms of its light-emitting characteristics, driving voltage, and durability, and a compound for an organic EL device to be used in the device. The organic EL device has a structure in which an anode, a plurality of organic layers including a light-emitting layer, and a cathode are laminated on a substrate, and the organic EL device contains an indolocarbazole compound in at least one organic layer selected from the light-emitting layer, a hole-transporting layer, an electron-transporting layer, a hole-blocking layer, and an electron-blocking layer. The indolocarbazole compound is a compound having, in a molecule thereof, at least one boron-containing group having such a structure that boron of the boron-containing group is bonded to an atom on a linking group bonded to a nitrogen atom of an indolocarbazole ring or to a carbon atom of the ring.

Claims (18)

1 . A compound for an organic electroluminescent device, which is represented by the following general formula (1):

wherein:

a ring I represents an aromatic hydrocarbon ring represented by the formula (1a) to be fused to adjacent rings at arbitrary positions and a ring II represents a heterocycle represented by the formula (1b) to be fused to adjacent rings at arbitrary positions;

L 1 and L 2 each independently represent an i+1-valent or k+1-valent group selected from a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 17 carbon atoms, and a linked aromatic group formed by linking two to six of aromatic rings of the substituted or unsubstituted aromatic hydrocarbon groups and the substituted or unsubstituted aromatic heterocyclic groups, the linked aromatic group may be linear or branched, and the aromatic rings to be linked may be identical to or different from each other;

Z represents a boron-containing group represented by the formula (1c);

Rs each independently represent deuterium, an alkyl group having 1 to 12 carbon atoms, an aralkyl group having 7 to 19 carbon atoms, an alkenyl group having 2 to 12 carbon atoms, an alkynyl group having 2 to 12 carbon atoms, a cyano group, a dialkylamino group having 2 to 24 carbon atoms, a diarylamino group having 6 to 36 carbon atoms, a diaralkylamino group having 14 to 38 carbon atoms, an amino group, a nitro group, an acyl group having 2 to 12 carbon atoms, an alkoxycarbonyl group having 2 to 12 carbon atoms, as carboxyl group, an alkoxyl group having 1 to 12 carbon atoms, an alkylsulfonyl group having 1 to 12 carbon atoms, a haloalkyl group having 1 to 12 carbon atoms, a hydroxyl group, an amide group, a phenoxy group, an alkylthio group having 1 to 12 carbon atoms, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having, 3 to 17 carbon atoms, or a boron-containing group represented by the formula (1c);

A 1 and A 2 each independently represent hydrogen, deuterium, an alkyl group having 1 to 12 carbon atoms, an alkenyl group having 2 to 12 carbon atoms, an alkynyl group having 2 to 12 carbon atoms, an alkoxyl group having 1 to 12 carbon atoms, a hydroxyl group, chlorine, bromine, fluorine, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, or a substituted or unsubstituted aromatic heterocyclic group having 3 to 17 carbon atoms, and A 1 and A 2 may be bonded to adjacent A 1 and A 2 or substituents of A 1 and A 2 to form a ring; and

p and q each independently represent an integer of from 0 to 4, r represents an integer of from 0 to 2, and i and k each represent an integer of from 0 to 5, provided that p+q+r+i+k≧1 and when both of i and k represent 0, at least one of Rs represents a boron-containing group represented by the formula (1c), and when p, q, r, i, and k each represent 2 or more, Rs and Zs may be identical to or different from each other.

2 . A compound for an organic electroluminescent device according to claim 1 , wherein the compound is represented by any one of the general formulae (2) to (5):

in the general formulae (2) to (5), L 1 , L 2 , Z, R, p, q, r, i, and k each have the same meaning as that of the general formula (1).

3 . A compound for an organic electroluminescent device according to claim 1 , wherein:

Rs each independently represent deuterium, an alkyl group having 1 to 12 carbon atoms, an aralkyl group having 7 to 19 carbon atoms, an alkenyl group having 2 to 12 carbon atoms, an alkynyl group having 2 to 12 carbon atoms, a dialkylamino group having 2 to 24 carbon atoms, a diarylamino group having 6 to 36 carbon atoms, a diaralkylamino group having 14 to 38 carbon atoms, an acyl group having 2 to 12 carbon atoms, an alkoxycarbonyl group having 2 to 12 carbon atoms, an alkoxyl group having 1 to 12 carbon atoms, an alkylsulfonyl group having 1 to 12 carbon atoms, a haloalkyl group having 1 to 12 carbon atoms, a phenoxy group, an alkylthio group having 1 to 12 carbon atoms, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 17 carbon atoms, or a boron-containing group represented by the formula (1c); and

A 1 and A 2 each independently represent an alkyl group having 1 to 12 carbon atoms, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, or a substituted or unsubstituted aromatic heterocyclic group having 3 to 17 carbon atoms.

4 . A compound for an organic electroluminescent device according to claim 1 , wherein i+k is 1 or more and Rs each represent a group except a boron-containing group.

5 . A compound for an organic electroluminescent device according to claim 1 , wherein A 1 and A 2 each independently represent a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, or a substituted or unsubstituted aromatic heterocyclic group having 3 to 17 carbon atoms.

6 . An organic electroluminescent device, comprising an organic layer containing the compound for an organic electroluminescent device according to claim 1 .

7 . An organic electroluminescent device according to claim 6 , wherein the organic layer containing the compound for an organic electroluminescent device comprises at least one layer selected from a light-emitting layer, a hole-transporting layer, a hole-injecting layer, an electron-transporting layer, and an electron-injecting layer.

8 . An organic electroluminescent device according to claim 6 , wherein the organic layer containing the compound for an organic electroluminescent device comprises a light-emitting layer, and the light-emitting layer contains a phosphorescent light-emitting dopant and the compound for an organic electroluminescent device as a host material.

Assignments (3)
CHANGE OF ADDRESS Recorded Nov 13, 2019
From: NIPPON STEEL CHEMICAL & MATERIAL CO., LTD.
To: NIPPON STEEL CHEMICAL & MATERIAL CO., LTD.
Reel/Frame 050998/0200 →
CHANGE OF NAME Recorded Dec 18, 2018
From: NIPPON STEEL & SUMIKIN CHEMICAL CO., LTD.
To: NIPPON STEEL CHEMICAL & MATERIAL CO., LTD.
Reel/Frame 047805/0595 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 13, 2015
From: SANNOMIYA, RUMI; KAI, TAKAHIRO; KOMORI, MASAKI; YAMAMOTO, TOSHIHIRO; TADA, MASASHI
To: NIPPON STEEL & SUMIKIN CHEMICAL CO., LTD.
Reel/Frame 034963/0587 →