IP Library › Granted Patent US 9,065,061
Granted Patent B2
US 9,065,061 · App. 12/914,216 · Granted Jun 23, 2015

Organometallic complex, light-emitting element, display device, electronic device, and lighting device

Inventors: Hideko Inoue (Kanagawa, JP); Tomoka Nakagawa (Kanagawa, JP); Nobuharu Ohsawa (Kanagawa, JP); Satoshi Seo (Kanagawa, JP); Yui Yamada (Kanagawa, JP)
Assignee: Semiconductor Energy Laboratory Co., Ltd.
H01L51/0085C07F15/0033C07F15/0086C09B57/10C09K11/06C09K2211/1059C09K2211/185H01L51/0059H01L51/0072H01L51/0074H01L51/5016H01L51/5036H05B33/14
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Quick Facts
Patent No.
US 9,065,061
App. No.
12/914,216
Granted
Jun 23, 2015
Kind
B2
Abstract

Provided are organometallic complexes that can exhibit phosphorescence. One of the novel organometallic complexes is represented by General Formula (G1). In General Formula (G1), R 1 represents any of an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 5 to 8 carbon atoms which may have a substituent, and an aralkyl group having 7 to 10 carbon atoms which may have a substituent. In addition, R 2 represents any of an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 5 to 8 carbon atoms which may have a substituent, and an aryl group having 6 to 12 carbon atoms which may have a substituent. Further, Ar represents an arylene group having 6 to 13 carbon atoms which may have a substituent. Further, M represents a Group 9 element or a Group 10 element.

Claims (79)

1. An organometallic complex comprising a structure represented by General Formula (G1):

wherein:

R 1 represents any of a substituted or unsubstituted cycloalkyl group having 5 to 8 carbon atoms, and a substituted or unsubstituted aralkyl group having 7 to 10 carbon atoms;

R 2 represents any of an alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted cycloalkyl group having 5 to 8 carbon atoms, and a substituted or unsubstituted aryl group having 6 to 12 carbon atoms;

Ar represents a substituted or unsubstituted arylene group having 6 to 13 carbon atoms; and

M represents a Group 9 element or a Group 10 element.

2. The organometallic complex according to claim 1 ,

wherein the organometallic complex comprises a structure represented by General Formula (G3):

and

wherein:

R 3 to R 6 individually represent any of hydrogen, an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 5 to 8 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, an aryloxy group having 6 to 12 carbon atoms, an alkylthio group having 1 to 4 carbon atoms, an arylthio group having 6 to 12 carbon atoms, an alkylamino group having 1 to 4 carbon atoms, a monoarylamino or diarylamino group having 6 to 24 carbon atoms, a cyano group, a halogen group, a haloalkyl group having 1 to 4 carbon atoms, and an aryl group having 6 to 12 carbon atoms.

3. The organometallic complex according to claim 1 ,

wherein the organometallic complex comprises a structure represented by General Formula (G5):

and

wherein:

R 7 to R 10 individually represent hydrogen or an electron-withdrawing group.

4. The organometallic complex according to claim 3 , wherein the electron-withdrawing group is a cyano group, a fluoro group, a trifluoromethyl group, a phenyl group substituted by a fluoro group, or a phenyl group substituted by a trifluoromethyl group.

5. The organometallic complex according to claim 1 ,

wherein the organometallic complex comprises a structure represented by General Formula (G7):

and

wherein:

R 11 represents a cycloalkyl group having 5 to 8 carbon atoms;

R 12 to R 16 individually represent any of hydrogen, an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 5 to 8 carbon atoms, and a phenyl group; and

R 17 to R 20 individually represent hydrogen or an electron-withdrawing group.

6. The organometallic complex according to claim 5 , wherein the electron-withdrawing group is a cyano group, a fluoro group, a trifluoromethyl group, a phenyl group substituted by a fluoro group, or a phenyl group substituted by a trifluoromethyl group.

7. The organometallic complex according to claim 5 , wherein each of R 12 to R 16 is hydrogen.

8. A light-emitting element comprising the organometallic complex according to claim 1 between a pair of electrodes.

9. A display device comprising a pixel portion, wherein the pixel portion comprises the light-emitting element according to claim 8 .

10. An electronic device comprising a display portion, wherein the display portion comprises the light-emitting element according to claim 8 .

11. A lighting device comprising the light-emitting element according to claim 8 .

12. A light-emitting element comprising;

a first light-emitting unit and a second light-emitting unit between a pair of electrodes,

wherein the first light-emitting unit contains the organometallic complex according to claim 1 , and

wherein the second light-emitting unit contains a light-emitting material that emits light with a longer wavelength than the organometallic complex.

13. A light-emitting element comprising;

a first light-emitting unit, a second light-emitting unit, and a third light-emitting unit between a pair of electrodes,

wherein the first light-emitting unit contains the organometallic complex according to claim 1 ,

wherein the second light-emitting unit contains a first light-emitting material that emits light with a longer wavelength than the organometallic complex, and

wherein the third light-emitting unit contains a second light-emitting material that emits light with a longer wavelength than the organometallic complex and a shorter wavelength than the first light-emitting material.

14. An organometallic complex represented by General Formula (G2):

wherein:

R 1 represents any of a substituted or unsubstituted cycloalkyl group having 5 to 8 carbon atoms, and a substituted or unsubstituted aralkyl group having 7 to 10 carbon atoms;

R 2 represents any of an alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted cycloalkyl group having 5 to 8 carbon atoms, and a substituted or unsubstituted aryl group having 6 to 12 carbon atoms;

Ar represents a substituted or unsubstituted arylene group having 6 to 13 carbon atoms;

M represents a Group 9 element or a Group 10 element; and

n=3 when M is a Group 9 element, and n=2 when M is a Group 10 element.

15. The organometallic complex according to claim 14 ,

wherein the organometallic complex is represented by General Formula (G4):

and

wherein:

R 3 to R 6 individually represent any of hydrogen, an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 5 to 8 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, an aryloxy group having 6 to 12 carbon atoms, an alkylthio group having 1 to 4 carbon atoms, an arylthio group having 6 to 12 carbon atoms, an alkylamino group having 1 to 4 carbon atoms, a monoarylamino or diarylamino group having 6 to 24 carbon atoms, a cyano group, a halogen group, a haloalkyl group having 1 to 4 carbon atoms, and an aryl group having 6 to 12 carbon atoms.

16. The organometallic complex according to claim 14 ,

wherein the organometallic complex is represented by General Formula (G6):

and

wherein:

R 7 to R 10 individually represent hydrogen or an electron-withdrawing group.

17. The organometallic complex according to claim 14 ,

wherein the organometallic complex is represented by General Formula (G8):

and

wherein:

R 11 represents a cycloalkyl group having 5 to 8 carbon atoms;

R 12 to R 16 individually represent any of hydrogen, an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 5 to 8 carbon atoms, and a phenyl group; and

R 17 to R 20 individually represent hydrogen or an electron-withdrawing group.

18. The organometallic complex according to claim 17 , wherein the electron-withdrawing group is a cyano group, a fluoro group, a trifluoromethyl group, a phenyl group substituted by a fluoro group, or a phenyl group substituted by a trifluoromethyl group.

19. The organometallic complex according to claim 17 , wherein each of R 12 to R 16 is hydrogen.

20. The organometallic complex according to claim 16 , wherein the electron-withdrawing group is a cyano group, a fluoro group, a trifluoromethyl group, a phenyl group substituted by a fluoro group, or a phenyl group substituted by a trifluoromethyl group.

21. A light-emitting element comprising the organometallic complex according to claim 14 between a pair of electrodes.

22. A display device comprising a pixel portion, wherein the pixel portion comprises the light-emitting element according to claim 21 .

23. An electronic device comprising a display portion, wherein the display portion comprises the light-emitting element according to claim 21 .

24. A lighting device comprising the light-emitting element according to claim 21 .

25. A light-emitting element comprising;

a first light-emitting unit and a second light-emitting unit between a pair of electrodes,

wherein the first light-emitting unit contains the organometallic complex according to claim 14 , and

wherein the second light-emitting unit contains a light-emitting material that emits light with a longer wavelength than the organometallic complex.

26. A light-emitting element comprising;

a first light-emitting unit, a second light-emitting unit, and a third light-emitting unit between a pair of electrodes,

wherein the first light-emitting unit contains the organometallic complex according to claim 14 ,

wherein the second light-emitting unit contains a first light-emitting material that emits light with a longer wavelength than the organometallic complex, and

wherein the third light-emitting unit contains a second light-emitting material that emits light with a longer wavelength than the organometallic complex and a shorter wavelength than the first light-emitting material.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2011
From: INOUE, HIDEKO; NAKAGAWA, TOMOKA; OHSAWA, NOBUHARU; SEO, SATOSHI; YAMADA, YUI
To: SEMICONDUCTOR ENERGY LABORATORY CO., LTD.
Reel/Frame 025607/0835 →
Priority Claims (2)
JP 2009-252168 · Nov 2, 2009 · national
JP 2010-169870 · Jul 28, 2010 · national
Continuity (1)
Related Publication 20110101854A1 · May 5, 2011