IP Library Granted Patent US 7,129,518
Granted Patent B2
US 7,129,518 · App. 10/696,060 · Granted Oct 31, 2006

Electroluminescent iridium compounds with fluorinated phenylpryidines, phenylpyrimidines, and phenylquinolines and devices made with such compounds

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Quick Facts
Patent No.
US 7,129,518
App. No.
10/696,060
Granted
Oct 31, 2006
Kind
B2
Abstract

The present invention is generally directed to electroluminescent Ir(III) compounds, the substituted 2-phenylpyridines, phenylpyrimidines, and phenylquinolines that are used to make the Ir(III) compounds, and devices that are made with the Ir(III) compounds.

Claims (21)

1. An organic electronic device comprising an emitting layer having an emission maximum in the range of 450 to 500 nm, wherein at least 20% by weight of the emitting layer comprises at least one compound having a Sixth Formula below:

IrL a L b L′L″  (Sixth Formula)

where

L′ is selected from a phosphine and an isonitrile;

L″ is selected from F, Cl, Br, and I;

L a and L b have structure (I) below,

wherein:

R 1 through R 8 are independently selected from alkyl, alkoxy, halogen, nitro, cyano, fluoro, fluorinated alkyl and fluorinated alkoxy groups, and at least one of R 1 through R 8 is selected from F, C n F 2n+1 , OC n F 2n+1 , and OCF 2 X, where n is an integer from 1 through 6 and X is H, Cl, or Br, and

A is C;

Wherein L″ is Cl, and L′ is selected from tris[3,5-bis(trifluoromethyl)phenyl]phosphine; 2,6-dimethylphenyl isocyanide; 3-trifluoromethylphenyl isocyanide; and 4-toluenesulfonylmethyl isocyanide.

2. An organic electronic device comprising a light-emitting layer and an electron transport layer, wherein the material in the electron transport layer is selected from

3. An organic electronic device comprising an emitting layer having an emission maximum in the range of 450 to 500 nm, wherein at least 20% by weight of the emitting layer comprises at least one compound having a Sixth Formula below:

IrL a L b L′L″  (Sixth Formula)

where

L′ is an isonitrile;

L″ is selected from F, Cl, Br, and I;

L a and L b have structure (I) below,

wherein:

R 1 through R 8 are independently selected from alkyl, alkoxy, halogen, nitro, cyano, fluoro, fluorinated alkyl and fluorinated alkoxy groups, and at least one of R 1 through R 8 is selected from F, C n F 2n+1 , OC n F 2n+1 , and OCF 2 X, where n is an integer from 1 through 6 and X is H, Cl, or Br, and

A is C;

wherein the isonitrile comprises an isonitrile substituent on an aromatic group.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 22, 2019
From: E. I. DU PONT DE NEMOURS AND COMPANY
To: LG CHEM, LTD.
Reel/Frame 050150/0482 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 24, 2019
From: GRUSHIN, VLADIMIR; LECLOUX, DANIEL DAVID; PETROV, VIACHESLAV A.; WANG, YING
To: E. I. DU PONT DE NEMOURS AND COMPANY
Reel/Frame 048419/0092 →