IP Library Granted Patent US 9,540,315
Granted Patent B2
US 9,540,315 · App. 14/605,286 · Granted Jan 10, 2017

Triarylamine derivative, light-emitting substance, light-emitting element, light-emitting device, and electronic device

Inventors: Harue Osaka (Kanagawa, JP); Takahiro Ushikubo (Kanagawa, JP); Nobuharu Ohsawa (Kanagawa, JP); Satoshi Seo (Kanagawa, JP); Tsunenori Suzuki (Kanagawa, JP)
Assignee: Semiconductor Energy Laboratory Co., Ltd.
C07C211/54C09K11/06H01L51/006H01L51/0058H01L51/0059H05B33/14C07C2101/14C09K2211/1007C09K2211/1011C09K2211/1014H01L27/3209H01L51/5012H01L51/5016H01L51/5048H01L51/5056H01L51/5072H01L51/5278Y10S428/917
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Quick Facts
Patent No.
US 9,540,315
App. No.
14/605,286
Granted
Jan 10, 2017
Kind
B2
Abstract

A triarylamine derivative represented by a general formula (G1) given below is provided. Note that in the formula, Ar represents either a substituted or unsubstituted phenyl group or a substituted or unsubstituted biphenyl group; α represents a substituted or unsubstituted naphthyl group; β represents either hydrogen or a substituted or unsubstituted naphthyl group; n and m each independently represent 1 or 2; and R 1 to R 8 each independently represent any of hydrogen, an alkyl group having 1 to 6 carbon atoms, or a phenyl group.

Claims (34)

1. A triarylamine derivative represented by general formula (A2),

wherein Ar represents an aryl group,

wherein β represents a substituent represented by structural formula (β-2) or formula (β-3),

wherein X represents a halogen,

wherein n and m each independently represent 1 or 2, and

wherein R 1 to R 8 each independently represent any of hydrogen, an alkyl group having 1 to 6 carbons atoms, and a phenyl group.

2. The triarylamine derivative according to claim 1 , wherein the halogen is any one of chlorine, bromine, and iodine.

3. The triarylamine derivative according to claim 1 , wherein n and m in the general formula (A2) represent 1.

4. The triarylamine derivative according to claim 1 ,

wherein n in the general formula (A2) represents 2, and

wherein m in the general formula (A2) represents 1.

5. The triarylamine derivative according to claim 1 , wherein Ar is a phenyl group or a biphenyl group.

6. A triarylamine derivative represented by a general formula (A2),

wherein Ar represents a biphenyl group,

wherein β represents a naphthyl group,

wherein X represents halogen,

wherein n and m each independently represent 1 or 2, and

wherein R 1 to R 8 each independently represent any of hydrogen, an alkyl group having 1 to 6 carbon atoms, and a phenyl group.

7. The triarylamine derivative according to claim 6 , wherein β represents a substituent represented by structural formula (β-2) or (β-3),

8. The triarylamine derivative according to claim 6 , wherein the halogen is any one of chlorine, bromine, and iodine.

9. The triarylamine derivative according to claim 6 , wherein n and m in the general formula (A2) represent 1.

10. The triarylamine derivative according to claim 6 ,

wherein n in the general formula (A2) represents 2, and

wherein m in the general formula (A2) represents 1.

11. A triarylamine derivative represented by a general formula (A2),

wherein Ar represents a biphenyl group,

wherein β represents a naphthyl group,

wherein X represents halogen,

wherein n represents 2,

wherein m represents 1, and

wherein R 1 to R 8 each independently represent any of hydrogen, an alkyl group having 1 to 6 carbon atoms, and a phenyl group.

12. The triarylamine derivative according to claim 11 , wherein β represents a substituent represented by structural formula (β-2) or (β-3),

13. The triarylamine derivative according to claim 11 , wherein the halogen is any one of chlorine, bromine, and iodine.

14. The triarylamine derivative according to claim 11 , wherein R 1 to R 8 each independently represents hydrogen.

Priority Claims (3)
JP 2008-129991 · May 16, 2008 · national
JP 2008-300827 · Nov 26, 2008 · national
JP 2009-022314 · Feb 3, 2009 · national
Continuity (3)
Division 13474104 · May 17, 2012
Continuation 12464506 · May 12, 2009
Related Publication 20150141697A1 · May 21, 2015