Light-emitting material for organic electroluminescent device, organic electroluminescent device using same, and material for organic electroluminescent device

Patent metadata

Field	Value
Publication number	US-10069074-B2
Application number	US-201715709114-A
Country	US
Kind code	B2
Filing date	Sep 19, 2017
Priority date	Dec 19, 2003
Publication date	Sep 4, 2018
Grant date	Sep 4, 2018

Abstract

Disclosed is a light-emitting material for organic electroluminescent (EL) devices which is composed of an asymmetric anthracene derivative of a specific structure. Also disclosed are a material for organic EL devices and an organic EL device wherein an organic thin film layer composed of one or more layers including at least a light-emitting layer is interposed between a cathode and an anode. At least one layer composed of the organic thin film layer contains the material for organic EL devices by itself or as a component of a mixture. Consequently, the organic EL device has a high efficiency and a long life. Also disclosed are a light-emitting material for organic EL devices and material for organic devices which enable to realize such an organic EL device.

First claim

What we claim is:

1. A light emitting material for an organic electroluminescent device comprising an asymmetric anthracene derivative represented by formula (1):

wherein,
A 1 represents 1-naphthyl group, 1-phenanthryl group, 2-phenanthryl group, 3-phenanthryl group, 4-phenanthryl group, or 9-phenanthryl group;
A 2 represents 2-naphthyl group, 1-phenanthryl group, 2-phenanthryl group, 3-phenanthryl group, 4-phenanthryl group, or 9-phenanthryl group;
Ar 1 represents a substituted or unsubstituted condensed aromatic hydrocarbon ring group having ring carbon atoms of 6 to 50;
Ar 2 represents a hydrogen atom or a substituted or unsubstituted condensed aromatic hydrocarbon ring group having ring carbon atoms of 6 to 50;
R 1 to R 8 each independently represents a hydrogen atom;
R 9 represents a hydrogen atom or a substituted or unsubstituted aromatic hydrocarbon ring group having ring carbon atoms of 6 to 50;
R 10 represents a hydrogen atom or a substituted or unsubstituted aromatic hydrocarbon ring group having ring carbon atoms of 6 to 50;
Ar 1 , Ar 2 , R 9 and R 10 each may be a plural number, and two neighboring groups thereof may form a saturated or unsaturated ring structure; and
the substituent groups at 9th and 10th positions of the anthracene core in formula (1) are different from each other.

2. The light emitting material for the organic electroluminescent device according to claim 1 , wherein,
Ar 1 and Ar 2 each independently represents any one of phenyl group, 1-naphthyl group, 2-naphthyl group, 1-phenanthryl group, 2-phenanthryl group, 3-phenanthryl group, 4-phenanthryl group, 9-phenanthryl group, 1-naphthacenyl group, 2-naphthacenyl group, 9-naphthacenyl group, 1-pyrenyl group, 2-pyrenyl group, 4-pyrenyl group, 2-biphenylyl group, 3-biphenylyl group, 4-biphenylyl group, p-terphenyl-4-yl group, p-terphenyl-3-yl group, p-terphenyl-2-yl group, m-terphenyl-4-yl group, m-terphenyl-3-yl group, m-terphenyl-2-yl group, o-tolyl group, m-tolyl group, p-tolyl group, p-t-butylphenyl group, p-(2-phenylpropyl) phenyl group, 3-methyl-2-naphthyl group, 4-methyl-1-naphthyl group, 4-methyl-1-anthryl group, 4′-methylbiphenylyl group, and 4″-t-butyl-p-terphenyl-4-yl group.

3. The light emitting material for the organic electroluminescent device according to claim 1 , wherein,
Ar 1 and Ar 2 each independently represents any one of phenyl group, 1-naphthyl group, 2-naphthyl group, 1-phenanthryl group, 2-phenanthryl group, 3-phenanthryl group, 4-phenanthryl group, 9-phenanthryl group, 2-biphenylyl group, 3-biphenylyl group, and 4-biphenylyl group.

4. The light emitting material for the organic electroluminescent device according to claim 1 , wherein A 1 represents 1-naphthyl group.

5. The light emitting material for the organic electroluminescent device according to claim 1 , wherein A 2 represents 2-naphthyl group.

6. The light emitting material for the organic electroluminescent device according to claim 1 , wherein R 9 represents a hydrogen atom, and R 10 represents a hydrogen atom.

7. The light emitting material for the organic electroluminescent device according to claim 1 , wherein,
Ar 1 and Ar 2 each independently represents any one of phenyl group, 1-naphthyl group, 2-naphthyl group, 1-phenanthryl group, 2-phenanthryl group, 3-phenanthryl group, 4-phenanthryl group, 9-phenanthryl group, 1-naphthacenyl group, 2-naphthacenyl group, 9-naphthacenyl group, 1-pyrenyl group, 2-pyrenyl group, 4-pyrenyl group, 2-biphenylyl group, 3-biphenylyl group, 4-biphenylyl group, p-terphenyl-4-yl group, p-terphenyl-3-yl group, p-terphenyl-2-yl group, m-terphenyl-4-yl group, m-terphenyl-3-yl group, m-terphenyl-2-yl group, o-tolyl group, m-tolyl group, p-tolyl group, p-t-butylphenyl group, p-(2-phenylpropyl) phenyl group, 3-methyl-2-naphthyl group, 4-methyl-1-naphthyl group, 4-methyl-1-anthryl group, 4′-methylbiphenylyl group, and 4″-t-butyl-p-terphenyl-4-yl group;
R 9 represents a hydrogen atom; and
R 10 represents a hydrogen atom.

8. The light emitting material for the organic electroluminescent device according to claim 1 , wherein,
Ar 1 and Ar 2 each independently represents any one of phenyl group, 1-naphthyl group, 2-naphthyl group, 1-phenanthryl group, 2-phenanthryl group, 3-phenanthryl group, 4-phenanthryl group, 9-phenanthryl group, 1-naphthacenyl group, 2-naphthacenyl group, 9-naphthacenyl group, 1-pyrenyl group, 2-pyrenyl group, 4-pyrenyl group, 2-biphenylyl group, 3-biphenylyl group, 4-biphenylyl group, p-terphenyl-4-yl group, p-terphenyl-3-yl group, p-terphenyl-2-yl group, m-terphenyl-4-yl group, m-terphenyl-3-yl group, m-terphenyl-2-yl group, o-tolyl group, m-tolyl group, p-tolyl group, p-t-butylphenyl group, p-(2-phenylpropyl) phenyl group, 3-methyl-2-naphthyl group, 4-methyl-1-naphthyl group, 4-methyl-1-anthryl group, 4′-methylbiphenylyl group, and 4″-t-butyl-p-terphenyl-4-yl group;
A 1 represents 1-naphthyl group;
R 9 represents a hydrogen atom; and
R 10 represents a hydrogen atom.

9. The light emitting material for the organic electroluminescent device according to claim 1 , wherein,
Ar 1 and Ar 2 each independently represents any one of phenyl group, 1-naphthyl group, 2-naphthyl group, 1-phenanthryl group, 2-phenanthryl group, 3-phenanthryl group, 4-phenanthryl group, 9-phenanthryl group, 1-naphthacenyl group, 2-naphthacenyl group, 9-naphthacenyl group, 1-pyrenyl group, 2-pyrenyl group, 4-pyrenyl group, 2-biphenylyl group, 3-biphenylyl group, 4-biphenylyl group, p-terphenyl-4-yl group, p-terphenyl-3-yl group, p-terphenyl-2-yl group, m-terphenyl-4-yl group, m-terphenyl-3-yl group, m-terphenyl-2-yl group, o-tolyl group, m-tolyl group, p-tolyl group, p-t-butylphenyl group, p-(2-phenylpropyl) phenyl group, 3-methyl-2-naphthyl group, 4-methyl-1-naphthyl group, 4-methyl-1-anthryl group, 4′-methylbiphenylyl group, and 4″-t-butyl-p-terphenyl-4-yl group;
A 1 represents 1-naphthyl group;
A 2 represents 2-naphthyl group;
R 9 represents a hydrogen atom; and
R 10 represents a hydrogen atom.

10. The light emitting material for the organic electroluminescent device according to claim 1 , wherein,
Ar 1 and Ar 2 each independently represents any one of phenyl group, 1-naphthyl group, 2-naphthyl group, 1-phenanthryl group, 2-phenanthryl group, 3-phenanthryl group, 4-phenanthryl group, 9-phenanthryl group, 2-biphenylyl group, 3-biphenylyl group, and 4-biphenylyl group;
R 9 represents a hydrogen atom; and
R 10 represents a hydrogen atom.

11. The light emitting material for the organic electroluminescent device according to claim 1 , wherein,
Ar 1 and Ar 2 each independently represents any one of phenyl group, 1-naphthyl group, 2-naphthyl group, 1-phenanthryl group, 2-phenanthryl group, 3-phenanthryl group, 4-phenanthryl group, 9-phenanthryl group, 2-biphenylyl group, 3-biphenylyl group, and 4-biphenylyl group;
A 1 represents 1-naphthyl group;
R 9 represents a hydrogen atom; and
R 10 represents a hydrogen atom.

12. The light emitting material for the organic electroluminescent device according to claim 1 , wherein,
Ar 1 and Ar 2 each independently represents any one of phenyl group, 1-naphthyl group, 2-naphthyl group, 1-phenanthryl group, 2-phenanthryl group, 3-phenanthryl group, 4-phenanthryl group, 9-phenanthryl group, 2-biphenylyl group, 3-biphenylyl group, and 4-biphenylyl group;
A 1 represents 1-naphthyl group;
A 2 represents 2-naphthyl group;
R 9 represents a hydrogen atom; and
R 10 represents a hydrogen atom.

13. A light emitting material for an organic electroluminescent de

Assignees

• Idemitsu Kosan Co

Inventors

• Kubota Mineyuki
• Funahashi Masakazu
• Hosokawa Chishio

Classifications

• C07C15/28 Primary

  Anthracenes · CPC title

• H05B33/14

  characterised by the chemical or physical composition or the arrangement of the electroluminescent material {, or by the simultaneous addition of the electroluminescent material in or onto the light source} · CPC title

• C07C2603/50

  Pyrenes; Hydrogenated pyrenes · CPC title

• C09K2211/1007

  Non-condensed systems · CPC title

• C07C15/38

  containing four rings · CPC title