Organic electroluminescence device and anthracene derivative

Patent metadata

Field	Value
Publication number	US-9583716-B2
Application number	US-201414301865-A
Country	US
Kind code	B2
Filing date	Jun 11, 2014
Priority date	Aug 23, 2002
Publication date	Feb 28, 2017
Grant date	Feb 28, 2017

Abstract

An organic electroluminescence device which comprises a cathode, an anode and an organic thin film layer comprising at least one layer comprising a light emitting layer and disposed between the cathode and the anode, wherein at least one layer in the organic thin film layer comprises an anthracene derivative having a specific structure singly or as a component of a mixture, and an anthracene derivative having a specific asymmetric structure and providing an organic electroluminescence device exhibiting a great efficiency of light emission and having a long life, are provided.

First claim

The invention claimed is:

1. An organic electroluminescence device which comprises:
a cathode, an anode and an organic thin film layer disposed between the cathode and the anode,
wherein:
the organic thin film layer comprises at least one layer which comprises a light emitting layer; and
the light emitting layer comprises a host and the host is at least one anthracene derivative represented by formula (2):

wherein:
Ar represents a substituted or unsubstituted condensed aromatic group having 10 to 50 nuclear carbon atoms;
Ar′ represents an aromatic group selected from the group consisting of a phenyl group, a 1-naphthyl group, a 2-naphthyl group, a 1-anthryl group, a 2-anthryl group, a 9-anthryl group, a 1-phenanthryl group, a 2-phenanthryl group, a 3-phenanthryl group, a 4-phenanthryl group, a 9-phenanthryl group, a 1-naphthacenyl group, a 2-naphthacenyl group, a 9-naphthacenyl group, a 1-pyrenyl group, a 2-pyrenyl group, a 4-pyrenyl group, a 2-biphenylyl group, a 3-biphenylyl group, a 4-biphenylyl group, a p-terphenyl-4-yl group, a p-terphenyl-3-yl group, a p-terphenyl-2-yl group, a m-terphenyl-4-yl group, m-terphenyl-3-yl group, m-terphenyl-2-yl group, and a fluoranthenyl group, each being optionally substitute;
X represents a substituted or unsubstituted aromatic group having 6 to 50 nuclear carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 5 to 50 nuclear atoms, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted alkoxyl group having 1 to 50 carbon atoms, a substituted or unsubstituted aralkyl group having 6 to 50 carbon atoms, a substituted or unsubstituted aryloxyl group having 5 to 50 nuclear atoms, a substituted or unsubstituted arylthio group having 5 to 50 nuclear atoms, a substituted or unsubstituted alkoxycarbonyl group having 1 to 50 carbon atoms, a carboxyl group, a halogen atom, a cyano group, a nitro group or a hydroxyl group;
a and b each represent an integer of 0 to 4; and
n represents an integer of 1 to 3 and, when n represents 2 or 3, two or three groups represented by:

may be a same or different.

2. The organic electroluminescence device according to claim 1 , wherein Ar represents a condensed aromatic group selected from the group consisting of a 1-naphthyl group, a 2-naphthyl group, a 1-anthryl group, a 2-anthryl group, a 9-anthryl group, a 1-phenanthryl group, a 2-phenanthryl group, a 3-phenanthryl group, a 4-phenanthryl group, a 9-phenanthryl group, a 1-naphthacenyl group, a 2-naphthacenyl group, a 9-naphthacenyl group, a 1-pyrenyl group, a 2-pyrenyl group, a 4-pyrenyl group, and a fluoranthenyl group, each being optionally substituted.

3. The organic electroluminescence device according to claim 1 , wherein Ar represents a group selected from the following groups:

wherein Ar 1 represents a substituted or unsubstituted aromatic group having 6 to 50 nuclear carbon atoms.

4. The organic electroluminescence device according to claim 1 , wherein a and b are both zero.

5. The organic electroluminescence device according to claim 1 , wherein X represents an aromatic group having 6 to 50 nuclear carbon atoms or a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms.

6. The organic electroluminescence device according to claim 1 , wherein n is 1.

7. The organic electroluminescence device according to claim 1 , wherein a and b are both zero and n is 1.

8. The organic electroluminescence device according to claim 1 , wherein X represents an unsubstituted group selected from the group consisting of a phenyl group, a 1-naphthyl group, a 2-naphthyl group, a 1-phenanthryl group, a 2-phenanthryl group, a 3-phenanthryl group, a 4-phenanthryl group, a 9-phenanthryl group, a 2-biphenylyl group, a 3-biphenylyl group, a 4-biphenylyl group, a p-terphenyl-4-yl group, a p-terphenyl-3-yl group, a p-terphenyl-2-yl group, a m-terphenyl-4-yl group, a m-terphenyl-3-yl group, a m-terphenyl-2-yl group, a 1-pyrrolyl group, a 2-pyrrolyl group, a 3-pyrrolyl group, a pyrazinyl group, a 2-pyridinyl group, a 3-pyridinyl group, a 4-pyridinyl group, a 1-indolyl group, a 2-indolylgroup, a 3-indolyl group, a 4-indolyl group, a 5-indolyl group, a 6-indolyl group, a 7-indolyl group, a 1-isoindolyl group, a 2-isoindolyl group, a 3-isoindolyl group, a 4-isoindolyl group, a 5-isoindolyl group, a 6-isoindolyl group, a 7-isoindolyl group, a 2-furyl group, 3-furyl group, a 2-benzofuranyl group, a 3-benzofuranyl group, a 4-benzofuranyl group, a 5-benzofuranyl group, a 6-benzofuranyl group, a 7-benzofuranyl group, a 1-isobenzofuranyl group, a 3-isobenzofuranyl group, a 4-isobenzofuranyl group, a 5-isobenzofuranyl group, a 6-isobenzofuranyl group, a 7-isobenzofuranyl group, a 1-carbazolyl group, a 2-carbazolyl group, a 3-carbazolyl group, a 4-carbazolyl group, a 9-carbazolyl group, a 1-phenanthridinyl group, a 2-phenanthridinyl group, a 3-phenanthridinyl group, a 4-phenanthridinyl group, a 6-phenanthridinyl group, a 7-phenanthridinyl group, a 8-phenanthridinyl group, a 9-phenanthridinyl group, a 10-phenanthridinyl group, a 1-acridinyl group, a 2-acridinyl group, a 3-acridinyl group, a 4-acridinyl group, a 9-acridinyl group, a methyl group, an ethyl group, a propyl group, an isopropyl group, a n-butyl group, a s-butyl group, an isobutyl group, and a t-butyl group.

9. The organic electroluminescence device according to claim 1 , wherein the optional substituent of Ar, Ar′ and X is selected from the group consisting of a halogen atom, a hydroxyl group, a nitro group, a cyano group, an unsubstituted alkyl group, an unsubstituted aryl group, an unsubstituted cycloalkyl group, an unsubstituted alkoxyl group, an unsubstituted aromatic heterocyclic group, an unsubstituted aralkyl group, an unsubstituted aryloxyl group, an unsubstituted arylthio group, an unsubstituted alkoxycarbonyl group, and a carboxyl group.

10. The organic electroluminescence device according to claim 1 , wherein
Ar represents an unsubstituted group selected from the group consisting of a 1-naphthyl group, a 2-naphthyl group, a 1-phenanthryl group, a 2-phenanthryl group, a 3-phenanthryl group, and a 4-phenanthryl group;
Ar′ represents an unsubstituted group selected from the group consisting of a phenyl group, a 2-biphenylyl group, a 3-biphenylyl group, a 4-biphenylyl group, a 1-naphtyl group, a 2-naphtyl group, a 1-phenanthryl group, a 2-phenanthryl group, a 3-phenanthryl group, and a 4-phenanthryl group;
X represents an unsubstituted group selected from the group consisting of a phenyl group, a 1-naphthyl group, a 2-naphthyl group, a 1-phenanthryl group, a 2-phenanthryl group, a 3-phenanthryl group, a 4-phenanthryl group, a 9-phenanthryl group, a methyl group, and a t-butyl group;
a is 0 or 1;
b is 0 or 1; and
n is 1.

11. The organic electroluminescence device according to claim 1 , wherein
Ar represents an unsubstituted 1-naphthyl group or an unsubstituted 2-naphthylgroup;
Ar′ represents an unsubstituted 1-naphthyl group or an unsubstituted 2-naphthyl group;
a is 0;
b is 0; and
n is 1.

12. An anthracene derivative represented by formula (2):

wherein:
Ar represents a substituted or unsubstituted 9-phenanthryl group;
Ar′ represents an aro

Assignees

• Idemitsu Kosan Co

Inventors

• Ikeda Hidetsugu
• Ido Motohisa
• Funahashi Masakazu

Classifications

• C09K2211/1011

  Condensed systems · CPC title

• C09K2211/1007

  Non-condensed systems · CPC title

• C07C43/257

  having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings · CPC title

• C07C2603/26

  Phenanthrenes; Hydrogenated phenanthrenes · CPC title

• C07C2603/50

  Pyrenes; Hydrogenated pyrenes · CPC title