IP Library Granted Patent US 7,691,494
Granted Patent B2
US 7,691,494 · App. 11/506,002 · Granted Apr 6, 2010

Electronic devices comprising organic iridium compositions

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Quick Facts
Patent No.
US 7,691,494
App. No.
11/506,002
Granted
Apr 6, 2010
Kind
B2
Abstract

The present invention provides electronic devices comprising novel organic iridium compositions which provide for enhanced device performance. The novel iridium compositions employed comprise at least one novel organic iridium compound which comprises at least one cyclometallated ligand and at least one ketopyrrole ligand. The organic iridium compositions employed are referred to as Type (1) organic iridium compositions and are constituted such that no ligand of the novel organic iridium compound has a number average molecular weight of 2,000 grams per mole or greater (as measured by gel permeation chromatography). Type (1) organic iridium compositions are referred to herein as comprising “organic iridium complexes”. In one aspect, the present invention provides optoelectronic devices, such as OLED devices and photovoltaic devices. In another aspect, the invention provides OLED devices exhibiting enhanced color properties and light output efficiencies.

Claims (110)

1. An organic light emitting device comprising:

a cathode;

an anode;

an electroluminescent material; and

a composition comprising an organic iridium complex of structure I

wherein each of the ligands

is independently at each occurrence a cyclometallated ligand which may be the same or different;

R 1 is a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 2 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical; and

“a” is an integer from 0 to 3.

2. The organic light emitting device according to claim 1 , wherein the cyclometallated ligand is derived from a phenyl isoquinoline compound having structure II

wherein R 3 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 4 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

“m” is an integer from 0 to 6; and

“n” is an integer ranging from 0 to 5.

3. The organic light emitting device according to claim 1 , wherein the cyclometallated ligand is derived from a 2-phenyl pyridine compound having structure III

wherein R 5 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 6 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

“p” is an integer from 0 to 4; and

“q” is an integer from 0 to 5.

4. The organic light emitting device according to claim 1 , wherein the cyclometallated ligand is derived from a styryl isoquinoline compound having structure IV

wherein R 7 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 8 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

“d” is an integer from 0 to 6; and

“e” is an integer from 0 to 5.

5. The organic light emitting device according to claim 1 , wherein the cyclometallated ligand

is derived from a 1-phenylisoquinoline, a 2-phenylpyridine, a 1-styryl isoquinoline, or a combination thereof.

6. The organic light emitting device according to claim 1 , wherein the cyclometallated ligand is derived from 1-phenylisoquinoline.

7. The organic light emitting device according to claim 1 , wherein the cyclometallated ligand is derived from 2-phenylpyridine.

8. The organic light emitting device according to claim 1 , wherein the cyclometallated ligand is derived from 1-styrylisoquinoline.

9. The organic light emitting device according to claim 1 , wherein said complex comprises a ketopyrrole ligand derived from a ketopyrrole having structure V

wherein R 1 is a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 2 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical; and

“a” is an integer from 0 to 3.

10. The organic light emitting device according to claim 1 , wherein said complex comprises a ketopyrrole ligand derived from a benzoyl pyrrole compound having structure VI

wherein R 2 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 9 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

“a” is an integer from 0 to 3; and

“s” is an integer from 0 to 5.

11. The organic light emitting device according to claim 1 , wherein said organic iridium complex has structure VII

wherein R 2 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 3 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 4 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 9 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

“a” is an integer from 0 to 3;

“m” is an integer from 0 to 6;

“n” is an integer from 0 to 4; and

“s” is an integer from 0 to 5.

12. The organic light emitting device according to claim 1 , wherein said organic iridium complex has structure IX

wherein R 2 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 5 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 6 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 9 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

“a” is an integer from 0 to 3;

“p” is an integer from 0 to 4;

“q” is an integer from 0 to 4; and

“s” is an integer from 0 to 5.

13. The organic light emitting device according to claim 1 , wherein said organic iridium complex has structure XI

wherein R 2 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 7 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 8 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 9 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

“a” is an integer from 0 to 3;

“d” is an integer from 0 to 6;

“e” is an integer from 0 to 5; and

“s” is an integer from 0 to 5.

14. The organic light emitting device according to claim 1 , wherein said electroluminescent material is a light emitting polymer.

15. The organic light emitting device according to claim 1 wherein said electroluminescent material is a blue light emitting polymer.

16. The organic light emitting device according to claim 1 , further comprising at least one of a hole transport layer and an electron transport layer.

17. An organic light emitting device comprising:

a cathode;

an anode; and

an electrophosphorescent composition comprising at least one organic iridium complex of structure I

wherein each of the ligands

is independently at each occurrence a cyclometallated ligand which may be the same or different;

R 1 is a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 2 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical; and

“a” is an integer from 0 to 3.

18. The organic light emitting device according to claim 17 , wherein said organic iridium complex has structure VII

wherein R 2 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 3 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 4 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 9 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

“a” is an integer from 0 to 3;

“m” is an integer from 0 to 6;

“n” is an integer from 0 to 4; and

“s” is an integer from 0 to 5.

19. The organic light emitting device according to claim 17 , wherein said organic iridium complex has structure IX

wherein R 2 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 5 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 6 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 9 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

“a” is an integer from 0 to 3;

“p” is an integer from 0 to 4;

“q” is an integer from 0 to 4; and

“s” is an integer from 0 to 5.

20. The organic light emitting device according to claim 17 , wherein said organic iridium complex has structure XI

wherein R 2 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 7 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 8 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

R 9 is independently at each occurrence a deuterium atom, a halogen, a nitro group, an amino group, a C 3 -C 40 aromatic radical, a C 1 -C 50 aliphatic radical, or a C 3 -C 40 cycloaliphatic radical;

“a” is an integer from 0 to 3;

“d” is an integer from 0 to 6;

“e” is an integer from 0 to 5; and

“s” is an integer from 0 to 5.

21. An organic light emitting device comprising:

a cathode;

an anode;

an electroluminescent material; and

an organic iridium complex having structure LVII

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 21, 2016
From: GENERAL ELECTRIC COMPANY
To: BOE TECHNOLOGY GROUP CO., LTD.
Reel/Frame 038490/0022 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2016
From: GENERAL ELECTRIC COMPANY
To: BOE TECHNOLOGY GROUP CO., LTD.
Reel/Frame 038439/0315 →