Aromatic amine derivative and organic electroluminescent device using the same

Patent metadata

Field	Value
Publication number	US-10297765-B2
Application number	US-201615174191-A
Country	US
Kind code	B2
Filing date	Jun 6, 2016
Priority date	Dec 28, 2007
Publication date	May 21, 2019
Grant date	May 21, 2019

Abstract

Provided are: an aromatic amine derivative in which a terminal substituent such as a dibenzofuran ring or a dibenzothiophene ring is bonded to a nitrogen atom directly or through an arylene group or the like; an organic electroluminescence device including an organic thin film layer formed of one or more layers including a light emitting layer and interposed between a cathode and an anode in which a layer of the organic thin film layer contains the aromatic amine derivative by itself or as a component of a mixture, and the device has a long lifetime and high luminous efficiency; and an aromatic amine derivative for realizing the device.

First claim

The invention claimed is:

1. An organic electroluminescence device, comprising an organic thin film layer formed of one or more layers including a light emitting layer and interposed between a cathode and an anode, wherein a layer of the organic thin film layer comprises the aromatic amine derivative represented by the following general formula (1) by itself or as a component of a mixture,
wherein the light emitting layer comprises the aromatic amine derivative as a doping material and comprises an anthracene derivative represented by the following general formula (i) as a host material:

where
Ar 0 represents a substituted or unsubstituted, divalent fused aromatic hydrocarbon group having 10 to 50 ring-forming carbon atoms, provided that Ar 0 does not represent a substituted or unsubstituted fluorenylene group, and
Ar 1 to Ar 4 each independently represent a substituted or unsubstituted aryl group having 6 to 50 ring-forming carbon atoms, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring-forming carbon atoms, a substituted or unsubstituted aralkyl group having 7 to 50 ring-forming carbon atoms, or a substituted or unsubstituted heterocyclic group having 5 to 50 ring-forming atoms,
provided that one or more of Ar 1 to Ar 4 each represent a group represented by the following general formula (3):

where
n represents an integer of 1 to 3,
1 represents an integer of 0 to 7,
X represents oxygen (O), sulfur (S), or selenium (Se),
Ar represents a substituted or unsubstituted arylene group having 6 to 60 ring-forming carbon atoms,
R represents a substituted or unsubstituted aryl group having 6 to 60 ring-forming carbon atoms, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, an amino group, a substituted or unsubstituted alkoxy group having 1 to 50 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 50 ring-forming carbon atoms, a substituted or unsubstituted arylthio group having 6 to 50 ring-forming atoms, a substituted or unsubstituted alkoxycarbonyl group having 1 to 50 carbon atoms, a halogen atom, a cyano group, a nitro group, a hydroxyl group, a silyl group, or a carboxyl group,
when n or 1 represents 2 or more, multiple Ar's or multiple R's may be identical to or different from each other, and
when multiple R's are present, the multiple R's may be bonded to each other to form a saturated or unsaturated, five- or six-membered cyclic structure that may be substituted, provided that:
in the general formula (3), a case where (R) 1 and (Ar) n , are bonded to a five-membered ring portion including X is excluded,

where
A 1 and A 2 each independently represent a group derived from a substituted or unsubstituted aromatic ring having 6 to 20 ring-forming carbon atoms,
R 1 to R 8 each independently represent a group selected from a hydrogen atom, a substituted or unsubstituted aryl group having 6 to 50 ring-forming carbon atoms, a substituted or unsubstituted heteroaryl group having 4 to 50 ring-forming atoms, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 ring-forming carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 50 carbon atoms, a substituted or unsubstituted aralkyl group having 7 to 50 ring-forming carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 50 ring-forming carbon atoms, a substituted or unsubstituted arylthio group having 6 to 50 ring-forming carbon atoms, a substituted or unsubstituted alkoxycarbonyl group having 1 to 50 carbon atoms, a substituted or unsubstituted silyl group, a carboxyl group, a halogen atom, a cyano group, a nitro group, and a hydroxyl group.

2. The organic electroluminescence device according to claim 1 , wherein A 1 and A 2 in the general formula (i) represent groups different from each other.

3. The organic electroluminescence device according to claim 1 , wherein Ar 0 in the general formula (1) represents a substituted or unsubstituted naphthylene group, a substituted or unsubstituted anthracenylene group, a substituted or unsubstituted phenanthrylene group, a substituted or unsubstituted chrysenylene group, a substituted or unsubstituted pyrenylene group, or a substituted or unsubstituted benzoanthracenylene group.

4. The organic electroluminescence device according to claim 3 , wherein —NAr 1 Ar 2 and —NAr 3 Ar 4 are bonded to 2- and 6-positions of the naphthylene group, respectively, —NAr 1 Ar 2 and —NAr 3 Ar 4 are bonded to 9- and 10-positions of the anthracenylene group, respectively, —NAr 1 Ar 2 and —NAr 3 Ar 4 are bonded to 2- and 6-positions of the anthracenylene group, respectively, —NAr 1 Ar 2 and —NAr 3 Ar 4 are bonded to 2-and 7-positions of the phenanthrylene group, respectively, —NAr 1 Ar 2 and —NAr 3 Ar 4 are bonded to 6- and 12-positions of the chrysenylene group, respectively, —NAr 1 Ar 2 and —NAr 3 Ar 4 are bonded to 1- and 6-positions of the pyrenylene group, respectively, —NAr 1 Ar 2 and —NAr 3 Ar 4 are bonded to 2- and 7-positions of the pyrenylene group, respectively, or —NAr 1 Ar, and —NAr 3 Ar 4 are bonded to 7- and 12-positions of the benzoanthracenylene group, respectively.

5. The organic electroluminescence device according to claim 1 , wherein Ar 1 and Ar 3 in the general formula (1) each represent a group represented by the general formula (3).

6. The organic electroluminescence device according to claim 1 , wherein all of Ar 1 to Ar 4 in the general formula (1) represent a group represented by the general formula (3).

7. The organic electroluminescence device according to claim 1 , wherein 1 in the general formula (3) represents 0.

8. The organic electroluminescence device according to claim 1 , wherein X in the general formula (3) represents an oxygen atom.

9. The organic electroluminescence device according to claim 1 , wherein Ar in the general formula (3) represents a substituted or unsubstituted phenylene group, a substituted or unsubstituted 2-methylphenylene group, a substituted or unsubstituted 3-methylphenylene group, a substituted or unsubstituted 4-methylphenylene group, a substituted or unsubstituted 4-ethylphenylene group, a substituted or unsubstituted biphenylene group, a substituted or unsubstituted 4-methylbiphenylene group, a substituted or unsubstituted 4-ethylbiphenylenegroup, a substituted or unsubstituted 4-cyclohexylbiphenylene group, a substituted or unsubstituted terphenylene group, a substituted or unsubstituted 3,5-dichlorophenylene group, a substituted or unsubstituted naphthylene group, a substituted or unsubstituted 5-methylnaphthylene group, an substituted or unsubstituted anthrylene group, a substituted or unsubstituted pyrenylene group, a substituted or unsubstituted chrysenylene group, a substituted or unsubstituted fluoranthenylene group, or a substituted or unsubstituted perylenylene group.

10. The organic electroluminescence device according to claim 1 , wherein Ar in the general foiiiiula (3) represents a substituted or unsubstituted arylene group having 6 to 20 ring-forming carbon atoms.

11. The organic electroluminescence device according to claim 1 , wherein Ar in the general fo

Assignees

• Idemitsu Kosan Co

Inventors

• Mizuki Yumiko
• Funahashi Masakazu
• Ito Mitsunori
• Kawamura Masahiro

Classifications

• C07D307/91 Primary

  Dibenzofurans; Hydrogenated dibenzofurans · CPC title

• C09B57/00

  Other synthetic dyes of known constitution · CPC title

• C09K2211/1011

  Condensed systems · CPC title

• H01L51/5012

  Electricity · mapped topic

• H01L51/0058

  Electricity · mapped topic