IP Library Granted Patent US 10,734,589
Granted Patent B2
US 10,734,589 · App. 15/674,943 · Granted Aug 4, 2020

Organic compound, light-emitting element, light-emitting device, electronic device, and lighting device

Inventors: Hiroki Suzuki (Kanagawa, JP); Tomoya Yamaguchi (Kanagawa, JP); Hideko Yoshizumi (Kanagawa, JP); Satoshi Seo (Kanagawa, JP); Tatsuyoshi Takahashi (Kanagawa, JP); Hiromitsu Kido (Kanagawa, JP); Satomi Watabe (Kanagawa, JP)
Assignee: Semiconductor Energy Laboratory Co., Ltd.
H01L51/0071C07D491/048H01L51/0074H05B33/20C09K11/06C09K2211/1007C09K2211/1044C09K2211/185H01L51/0085H01L51/5012H01L51/5016H01L51/5072H01L2251/308
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Quick Facts
Patent No.
US 10,734,589
App. No.
15/674,943
Granted
Aug 4, 2020
Kind
B2
Abstract

A novel organic compound is provided. That is, a novel organic compound that is effective in improving the element characteristics and reliability is provided. The organic compound has a benzofuroquinoxaline skeleton or a benzothienoquinoxaline skeleton. The organic compound is represented by General Formula (G1). In the formula, Q represents O or S, and each of R1 to R8 independently represents any of hydrogen, a halogeno group, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group having 6 to 12 carbon atoms, and a substituted or unsubstituted heteroaryl group having 3 to 12 carbon atoms. At least one of R1 to R8 includes a substituted or unsubstituted condensed aromatic or heteroaromatic ring having 3 to 24 carbon atoms.

Claims (61)

1. An organic compound represented by General Formula (G1):

wherein Q represents O,

wherein each of R 1 to R 8 independently represents any of hydrogen, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group having 6 to 12 carbon atoms, and a substituted or unsubstituted heteroaryl group having 3 to 12 carbon atoms, and

wherein at least one of R 1 to R 8 comprises a substituted or unsubstituted condensed aromatic ring having 3 to 24 carbon atoms or a substituted or unsubstituted condensed heteroaromatic ring having 3 to 24 carbon atoms.

2. The organic compound according to claim 1 ,

wherein at least one of R 1 to R 4 and at least one of R 5 to R 8 each comprise a substituted or unsubstituted condensed aromatic ring having 3 to 24 carbon atoms or a substituted or unsubstituted condensed heteroaromatic ring having 3 to 24 carbon atoms.

3. The organic compound according to claim 1 ,

wherein at least one of R 1 to R 8 comprises any of substituted or unsubstituted naphthalene, fluorene, phenanthrene, triphenylene, dibenzothiophene, dibenzofuran, and carbazole rings.

4. The organic compound according to claim 1 ,

wherein at least one of R 1 to R 4 and at least one of R 5 to R 8 each comprise any of substituted or unsubstituted naphthalene, fluorene, phenanthrene, triphenylene, dibenzothiophene, dibenzofuran, and carbazole rings.

5. The organic compound according to claim 1 ,

wherein at least one of R 1 to R 8 comprises A via a substituted or unsubstituted arylene group having 6 to 24 carbon atoms or a substituted or unsubstituted heteroarylene group having 3 to 24 carbon atoms, A being represented by any of General Formulae (A-1) to (A-4):

wherein each of R 11 to R 18 independently represents any of hydrogen, an alkyl group having 1 to 6 carbon atoms, and a substituted or unsubstituted phenyl group.

6. The organic compound according to claim 1 ,

wherein at least one of R 1 to R 4 and at least one of R 5 to R 8 each comprise A via a substituted or unsubstituted arylene group having 6 to 24 carbon atoms or a substituted or unsubstituted heteroarylene group having 3 to 24 carbon atoms, A being represented by any of General Formulae (A-1) to (A-4):

wherein each of R 11 to R 18 independently represents any of hydrogen, an alkyl group having 1 to 6 carbon atoms, and a substituted or unsubstituted phenyl group.

7. The organic compound according to claim 1 ,

wherein at least one of R 1 to R 8 comprises A represented by any of General Formulae (A-1) to (A-4):

wherein each of R 11 to R 18 independently represents any of hydrogen, an alkyl group having 1 to 6 carbon atoms, and a substituted or unsubstituted phenyl group.

8. The organic compound according to claim 1 ,

wherein at least one of R 1 to R 4 and at least one of R 5 to R 8 each comprise A represented by any of General Formulae (A-1) to (A-4):

wherein each of R 11 to R 18 independently represents any of hydrogen, an alkyl group having 1 to 6 carbon atoms, and a substituted or unsubstituted phenyl group.

9. The organic compound according to claim 1 , wherein the organic compound is represented by Structural Formula (100):

10. The organic compound according to claim 1 , wherein the organic compound is represented by Structural Formula (200) or Structural Formula (262):

11. A light-emitting element comprising an organic compound represented by General Formula (G1):

wherein Q represents O,

wherein each of R 1 to R 8 independently represents any of hydrogen, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted aryl group having 6 to 12 carbon atoms, and a substituted or unsubstituted heteroaryl group having 3 to 12 carbon atoms, and

wherein at least one of R 1 to R 8 comprises a substituted or unsubstituted condensed aromatic ring having 3 to 24 carbon atoms or a substituted or unsubstituted condensed heteroaromatic ring having 3 to 24 carbon atoms.

12. The light-emitting element according to claim 11 , comprising an EL layer between a pair of electrodes,

wherein the EL layer comprises the organic compound.

13. The light-emitting element according to claim 11 , comprising an EL layer between a pair of electrodes,

wherein the EL layer comprises a light-emitting layer, and

wherein the light-emitting layer comprises the organic compound.

14. The light-emitting element according to claim 11 , comprising an EL layer between a pair of electrodes,

wherein the EL layer comprises a light-emitting layer, and

wherein the light-emitting layer comprises the organic compound and an organometallic complex represented by the following formula:

15. A light-emitting device comprising:

the light-emitting element according to claim 11 ; and

a transistor or a substrate.

16. An electronic device comprising:

the light-emitting device according to claim 15 ; and

a microphone, a camera, an operation button, an external connection portion, or a speaker.

17. A lighting device comprising:

the light-emitting device according to claim 15 ; and

a housing, a cover, or a support.

18. A light-emitting element comprising:

an organic compound having a benzofuro[2,3-b]quinoxaline skeleton; and

a light-emitting substance,

wherein the organic compound having the benzofuro[2,3-b]quinoxaline skeleton is a host material.

19. The light-emitting element according to claim 18 , wherein the light-emitting substance comprises a substance converting triplet excitation energy into light emission.

20. The light-emitting element according to claim 18 , wherein the light-emitting substance comprises a phosphorescence material.

21. The light-emitting element according to claim 18 , wherein the light-emitting substance comprises a TADF material.

22. A light-emitting device comprising:

the light-emitting element according to claim 18 ; and

a transistor or a substrate.

23. An electronic device comprising:

the light-emitting device according to claim 22 ; and

a microphone, a camera, an operation button, an external connection portion, or a speaker.

24. A lighting device comprising:

the light-emitting device according to claim 22 ; and

a housing, a cover, or a support.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 11, 2017
From: SUZUKI, HIROKI; YAMAGUCHI, TOMOYA; YOSHIZUMI, HIDEKO; SEO, SATOSHI; TAKAHASHI, TATSUYOSHI; KIDO, HIROMITSU; WATABE, SATOMI
To: SEMICONDUCTOR ENERGY LABORATORY CO., LTD.
Reel/Frame 043269/0824 →
Priority Claims (2)
JP 2016-159794 · Aug 17, 2016 · national
JP 2017-102066 · May 23, 2017 · national
Continuity (1)
Related Publication 20180053903A1 · Feb 22, 2018
Cited By (2)
US 12,415,812 US 12,660,054