IP Library Granted Patent US 8,759,819
Granted Patent B2
US 8,759,819 · App. 12/744,178 · Granted Jun 24, 2014

Organic electroluminescence device

Inventors: Kazuki Nishimura (Sodegaura, JP); Toshihiro Iwakuma (Sodegaura, JP); Kenichi Fukuoka (Sodegaura, JP); Chishio Hosokawa (Sodegaura, JP); Jun Endo (Sodegaura, JP); Nobuhiro Yabunouchi (Sodegaura, JP); Hiroshi Yamamoto (Sodegaura, JP)
Assignee: Idemitsu Kosan Co., Ltd.
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Quick Facts
Patent No.
US 8,759,819
App. No.
12/744,178
Granted
Jun 24, 2014
Kind
B2
Abstract

An organic electroluminescence device includes an anode, a cathode, and an organic thin-film layer interposed between the anode and the cathode. The organic thin-film layer includes a phosphorescent-emitting layer containing a host and a phosphorescent dopant, and an electron transporting layer that is provided closer to the cathode than the phosphorescent-emitting layer. The host contains a substituted or unsubstituted polycyclic fused aromatic skeleton.

Claims (26)

1. An organic electroluminescence device, comprising:

an anode;

a cathode; and

an organic thin-film layer interposed between the anode and the cathode, where

the organic thin-film layer comprises: a phosphorescent-emitting layer containing a host and a phosphorescent dopant; and an electron transporting layer that is provided closer to the cathode than the phosphorescent layer;

the host contains a host compound comprising a substituted or unsubstituted polycyclic fused aromatic skeleton,

the host compound is at least one compound selected from the group consisting of phenanthrene derivative, chrysene derivative, fluoranthene derivative and triphenylene derivative, wherein the electron transporting layer contains at least one of the compounds represented by formulae (4) or (5) below,

where: X is a fused ring containing a nitrogen atom or sulfur atom; Y is selected from one of or a combination of a single bond, alkyl chain, alkylene chain, cycloalkyl chain, aryl chain, heterocyclic chain, silyl chain, ether chain or thioether chain; and q is an integer of 2 or more, wherein

a molecular weight of the compound represented by the formula (4) is 480 or more, and

where: A represents a substituent having a phenanthroline skeleton or benzoquinoline skeleton; B is a p-valent organic group having a structure represented by a formula (5A) below; and p is an integer of 2 or more,

where: R 4 and R 5 each independently represent an alkyl group or aryl group which includes an aryl group fused to a phenyl group; l and in each independently represent an integer from 0 to 5; and Z is at least one compound selected from compounds represented by a formula (5B) below

2. The organic electroluminescence device according to claim 1 , wherein a minimum triplet energy gap of the host compound is in a range of 2.1 eV to 2.7 eV.

3. The organic electroluminescence device according to claim 1 , wherein a wavelength of the phosphorescent dopant at a maximum luminance intensity is in a range of 470 nm to 700 nm.

4. The organic electroluminescence device according to claim 1 , wherein a reduction-causing dopant is present at an interfacial region between the cathode and the organic thin-film layer.

5. An organic electroluminescence device, comprising:

an anode;

a cathode; and

an organic thin-film layer interposed between the anode and the cathode, wherein

the organic thin-film later comprises: a phosphorescent-emitting layer containing a host and a phosphorescent dopant; and an electron transporting layer that is provided closer to the cathode than the phosphorescent-emitting layer;

the host contains a host compound comprising a substituted or unsubstituted polycyclic fused aromatic skeleton,

the host compound is at least one compound selected from the group consisting of phenanthrene derivative, chrysene derivative, fluoranthene derivative and triphenylene derivative, and

the electron transporting layer contains a compound represented by a formula (4)

where: X is independently selected from the group consisting of a pyridine ring, a quinoxaline ring, a triazole ring, a triazine ring, an oxadiazole ring, a thiophene ring, a diphenyl boron, a quinoline ring, a benzoquinoline ring and a phenanthroline ring, which are substituted or unsubstituted;

Y is selected from the group consisting of a single bond, an alkyl chain, an alkylene chain, a cycloalkyl chain, an aryl chain, a heterocyclic chain, a silyl chain, an ether chain and a thioether chain or combinations thereof; and

q is an integer of 2 or more, wherein

a molecular weight of the compound represented by the formula (4) is 480 or more.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 29, 2010
From: NISHIMURA, KAZUKI; IWAKUMA, TOSHIHIRO; FUKUOKA, KENICHI; HOSOKAWA, CHISHIO; ENDO, JUN; YABUNOUCHI, NOBUHIRO; YAMAMOTO, HIROSHI
To: IDEMITSU KOSAN CO., LTD.
Reel/Frame 024764/0222 →
Priority Claims (1)
JP 2007-303713 · Nov 22, 2007 · national
Continuity (1)
Related Publication 20100283043A1 · Nov 11, 2010