IP Library Granted Patent US 9,200,022
Granted Patent B2
US 9,200,022 · App. 13/446,216 · Granted Dec 1, 2015

Organic light-emitting element, organometallic complex, light-emitting device, electronic appliance, and lighting device

Inventors: Hideko Inoue (Kanagawa, JP); Hiromi Nowatari (Kanagawa, JP); Satoshi Seo (Kanagawa, JP)
Assignee: Semiconductor Energy Laboratory Co., Ltd.
C07F15/0033C07F15/0086
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Quick Facts
Patent No.
US 9,200,022
App. No.
13/446,216
Granted
Dec 1, 2015
Kind
B2
Abstract

Disclosed is a phosphorescent organometallic complex having: a 6-membered aromatic heterocycle having a nitrogen atom; iridium or platinum to which the nitrogen atom coordinates; and an aryl group which is bonded to an α-carbon of the nitrogen atom and is ortho-metalated with the iridium or platinum, where at least one of the aromatic heterocycle and the aryl group has an alicyclic hydrocarbon having an intramolecular carbon-carbon bridged bond as a substituent. The ability of the bulky structure of the alicyclic hydrocarbon to inhibit aggregation of the organometallic complex, concerted with the strong electron-donating property of the alicyclic hydrocarbon to the aromatic heterocycle or the aryl group, contributes to the increase in absorption coefficient and phosphorescent efficiency of the organometallic complex. The improved absorption coefficient and the phosphorescent efficiency allow the formation of a light-emitting element with excellent external quantum efficiency over 25%.

Claims (36)

1. A compound represented by a formula (G3):

wherein R 1 to R 7 are separately selected from hydrogen, halogen, a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 4 carbon atoms, a substituted or unsubstituted alkylthio group having 1 to 4 carbon atoms, a substituted or unsubstituted haloalkyl group having 1 to 4 carbon atoms, and a substituted or unsubstituted aryl group having 6 to 10 carbon atoms, and

wherein at least one of R 1 , R 5 , R 6 , and R 7 is an alicyclic hydrocarbon having an intramolecular carbon-carbon bridged bond.

2. The compound according to claim 1 , wherein R 1 is the alicyclic hydrocarbon.

3. The compound according to claim 1 , wherein the alicyclic hydrocarbon is selected from a tricyclo[5.2.1.0(2,6)]decanyl group, a norbornyl group, and an adamantyl group.

4. A compound represented by a formula (G2):

wherein R 1 to R 7 are separately selected from hydrogen, halogen, a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 4 carbon atoms, a substituted or unsubstituted alkylthio group having 1 to 4 carbon atoms, a substituted or unsubstituted haloalkyl group having 1 to 4 carbon atoms, and a substituted or unsubstituted aryl group having 6 to 10 carbon atoms,

wherein at least one of R 1 , R 5 , R 6 , and R 7 is an alicyclic hydrocarbon having an intramolecular carbon-carbon bridged bond, and

wherein L is a monoanionic ligand represented by any of formulae (L1) to (L7):

and

wherein: R 71 to R 109 separately represent any of hydrogen, a substituted or unsubstituted alkyl group having 1 to 4 carbon atoms, a substituted or unsubstituted haloalkyl group having 1 to 4 carbon atoms, and a substituted or unsubstituted alkoxy group having 1 to 4 carbon atoms,;

A l to A 3 separately represent any of nitrogen, sp 2 carbon bonded to hydrogen, and sp 2 carbon bonded to a substituent R; and R represents any of an alkyl group having 1 to 4 carbon atoms, a haloalkyl group having 1 to 4 carbon atoms, and a phenyl group.

5. The compound according to claim 4 ,

wherein the monoanionic ligand is represented by any of the formula (L1) and (L7).

6. The compound according to claim 4 ,

wherein the compound is represented by any one of formula (100), (111), and (128):

7. The compound according to claim 1 ,

wherein the compound is represented by a formula (108):

8. The compound according to claim 1 ,

wherein:

the halogen is fluorine,

the substituted or unsubstituted alkyl group is selected from a methyl group, an ethyl group, a propyl group, an isopropyl group, a n-butyl group, a sec-butyl group, an isobutyl group, and a tert-butyl group;

the substituted or unsubstituted alkoxy group is selected from a methoxy group, an ethoxy group, a propoxy group, an isopropoxy group, a n-butoxy group, a sec-butoxy group, an isobutoxy group, and a tert-butoxy group;

the substituted or unsubstituted alkylthio group is selected from a methylsulfanyl group, an ethylsulfanyl group, a propylsulfanyl group, an isopropylsulfanyl group, a n-butylsulfanyl group, an isobutylsulfanyl group, a sec-butylsulfanyl group, and tert-butylsulfanyl group; and

the substituted or unsubstituted haloalkyl group is selected from a fluoromethyl group, a difluoromethyl group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, a 3,3,3-trifluoropropyl group, and a 1,1,1,3,3,3-hexafluoroisopropyl group.

9. The compound according to claim 4 ,

wherein:

the halogen is fluorine,

the substituted or unsubstituted alkyl group is selected from a methyl group, an ethyl group, a propyl group, an isopropyl group, a n-butyl group, a sec-butyl group, an isobutyl group, and a tert-butyl group;

the substituted or unsubstituted alkoxy group is selected from a methoxy group, an ethoxy group, a propoxy group, an isopropoxy group, a n-butoxy group, a sec-butoxy group, an isobutoxy group, and a tert-butoxy group;

the substituted or unsubstituted alkylthio group is selected from a methylsulfanyl group, an ethylsulfanyl group, a propylsulfanyl group, an isopropylsulfanyl group, a n-butylsulfanyl group, an isobutylsulfanyl group, a sec-butylsulfanyl group, and tert-butylsulfanyl group; and

the substituted or unsubstituted haloalkyl group is selected from a fluoromethyl group, a difluoromethyl group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, a 3,3,3-trifluoropropyl group, and a 1,1,1,3,3,3-hexafluoroisopropyl group.

10. The compound according to claim 4 ,

wherein: R 71 to R 109 separately represent any of hydrogen, an alkyl group having 1 to 4 carbon atoms, and an alkoxy group having 1 to 4 carbon atoms; A l to A 3 separately represent any of nitrogen, sp 2 carbon bonded to hydrogen, and sp 2 carbon bonded to a substituent R; and R represents any of an alkyl group having 1 to 4 carbon atoms and a phenyl group.

11. The compound according to claim 4 ,

wherein the monoanionic ligand is represented by the formula (L1).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 13, 2012
From: INOUE, HIDEKO; NOWATARI, HIROMI; SEO, SATOSHI
To: SEMICONDUCTOR ENERGY LABORATORY CO., LTD.
Reel/Frame 028042/0174 →
Priority Claims (1)
JP 2011-091514 · Apr 15, 2011 · national
Continuity (1)
Related Publication 20120264936A1 · Oct 18, 2012