IP Library Granted Patent US 10,868,261
Granted Patent B2
US 10,868,261 · App. 14/887,955 · Granted Dec 15, 2020

Organic electroluminescent materials and devices

Inventors: Bin Ma (Ewing, NJ); Chuanjun Xia (Ewing, NJ)
Assignee: UNIVERSAL DISPLAY CORPORATION
H01L51/0085C07F15/0033C09K11/025C09K11/06H01L51/0054H01L51/0074C09K2211/1007C09K2211/1029C09K2211/1033C09K2211/1088C09K2211/185H01L51/5016
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Quick Facts
Patent No.
US 10,868,261
App. No.
14/887,955
Granted
Dec 15, 2020
Kind
B2
Abstract

This invention discloses iridium complexes containing phenylpyridine ligand wherein there is an aryl or heterocyclic ring fused into phenyl ring. This invention also discloses organic light emitting devices comprising an anode, a cathode, and an organic layer disposed between the anode and the cathode, the organic layer comprising an iridium complex, and formulations comprising iridium complexes. The iridium complexes showed desired device performance.

Claims (63)

1. A compound of Formula II

wherein R has the following structure and is fused to ring A:

Z 1 to Z 8 is independently selected from nitrogen or carbon;

and the wave lines indicate the bonds to two of the adjacent Z 1 to Z 4 of ring A;

wherein when two of the adjacent Z 1 to Z 4 are used to fuse to R, those two of the adjacent Z 1 to Z 4 are carbon;

R 1 and R 4 independently represent mono, di, tri, or tetra substitutions, or no substitution;

R 2 and R 3 independently represent mono, or di substitutions, or no substitution;

R 7 and R 8 independently represent mono, di, tri, or tetra substitutions, or no substitution;

wherein X is O or S;

wherein R 1 , R 2 , R 3 , R 4 , R 7 , and R 8 are each independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

wherein any two adjacent substituents R 1 , R 2 , R 3 , R 4 , R 7 , and R 8 are optionally joined to form a ring, which can be further substituted;

wherein R 5 and R 6 are independently branched alkyl which is partially deuterated, or linear alkyl which is partially deuterated; or

R 5 and R 6 are alkyl and together join to form a ring which is substituted with hydrogen, deuterium, alkyl, cycloalkyl, or combinations thereof.

2. The compound of claim 1 , wherein each of Z 1 to Z 4 is carbon.

3. The compound of claim 1 , wherein each of Z 5 to Z 8 is carbon.

4. The compound of claim 1 , wherein each of Z 1 to Z 8 is carbon.

5. The compound of claim 1 , wherein at least one of Z 5 to Z 8 is nitrogen.

6. The compound of claim 1 , wherein X is O.

7. The compound of claim 1 , wherein R 5 and R 6 are alkyl and together join to form a ring which is substituted with hydrogen, deuterium, alkyl, cycloalkyl, or combinations thereof.

8. The compound of claim 1 , wherein the Formula II includes a ligand L A selected from the group consisting of:

9. The compound of claim 1 , wherein the Formula II includes a ligand L B selected from the group consisting of:

10. The compound of claim 8 , wherein the compound has the formula Ir(L A )(L B ) 2 ;

wherein L B is selected from the group consisting of:

11. The compound of claim 1 , wherein R 5 and R 6 are independently branched alkyl which is partially deuterated.

12. The compound of claim 1 , wherein R 5 and R 6 are independently linear alkyl which is partially deuterated.

13. An organic light emitting device (OLED) comprising:

an anode;

a cathode; and

an organic layer disposed between the anode and the cathode, the organic layer comprising a compound of Formula II

wherein R has the following structure and is fused to ring A:

Z 1 to Z 8 is independently selected from nitrogen or carbon;

and the wave lines indicate the bonds to two of the adjacent Z 1 to Z 4 of ring A;

wherein when two of the adjacent Z 1 to Z 4 are used to fuse to R, those two of the adjacent Z 1 to Z 4 are carbon;

R 1 and R 4 independently represent mono, di, tri, or tetra substitutions, or no substitution;

R 2 and R 3 independently represent mono, or di substitutions, or no substitution;

R 7 and R 8 independently represent mono, di, tri, or tetra substitutions, or no substitution;

wherein X is O or S;

wherein R 1 , R 2 , R 3 , R 4 , R 7 , and R 8 are each independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

wherein any two adjacent substituents R 1 , R 2 , R 3 , R 4 , R 7 , and R 8 are optionally joined to form a ring, which can be further substituted;

wherein R 5 and R 6 are independently branched alkyl which is partially deuterated, or linear alkyl which is partially deuterated; or

R 5 and R 6 are alkyl and together join to form a ring which is substituted with hydrogen, deuterium, alkyl, cycloalkyl, or combinations thereof.

14. The OLED of claim 13 , wherein the OLED is incorporated into a device selected from the group consisting of a consumer product, an electronic component module, and a lighting panel.

15. The OLED of claim 13 , wherein the organic layer is an emissive layer and the compound is an emissive dopant or a non-emissive dopant.

16. The OLED of claim 13 , wherein the organic layer further comprises a host; wherein the host comprises a triphenylene containing benzo-fused thiophene or benzo-fused furan;

wherein any substituent in the host is an unfused substituent independently selected from the group consisting of C n H 2n+1 , OC n H 2n+1 , OAr 1 , N(C n H 2n+1 ) 2 , N(Ar 1 )(Ar 2 ), CH═CH—C n H 2n+1 , C≡CC n H 2n+1 , Ar 1 , Ar 1 -Ar 2 , and C n H 2n —Ar 1 , or the host has no substitution;

wherein n is from 1 to 10; and

wherein Ar 1 and Ar 2 are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof.

17. The OLED of claim 13 , wherein the organic layer further comprises a host, wherein the host comprises at least one chemical group selected from the group consisting of triphenylene, carbazole, dibenzothiphene, dibenzofuran, dibenzoselenophene, azatriphenylene, azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene.

18. The OLED of claim 13 , wherein the organic layer further comprises a host and the host is selected from the group consisting of:

and combinations thereof.

19. A formulation comprising a compound of Formula II

wherein R has the following structure and is fused to ring A:

Z 1 to Z 8 is independently selected from nitrogen or carbon;

and the wave lines indicate the bonds to two of the adjacent Z 1 to Z 4 of ring A;

wherein when two of the adjacent Z 1 to Z 4 are used to fuse to R, those two of the adjacent Z 1 to Z 4 are carbon;

R 1 and R 4 independently represent mono, di, tri, or tetra substitutions, or no substitution;

R 2 and R 3 independently represent mono, or di substitutions, or no substitution;

R 7 and R 8 independently represent mono, di, tri, or tetra substitutions, or no substitution;

wherein X is O or S;

wherein R 1 , R 2 , R 3 , R 4 , R 7 , and R 8 are each independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

wherein any two adjacent substituents R 1 , R 2 , R 3 , R 4 , R 7 , and R 8 are optionally joined to form a ring, which can be further substituted;

wherein R 5 and R 6 are independently branched alkyl which is partially deuterated, or linear alkyl which is partially deuterated; or

R 5 and R 6 are alkyl and together join to form a ring which is substituted with hydrogen, deuterium, alkyl, cycloalkyl, or combinations thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 20, 2015
From: MA, BIN; XIA, CHUANJUN
To: UNIVERSAL DISPLAY CORPORATION
Reel/Frame 036835/0735 →
Continuity (2)
Provisional Application 62077469 · Nov 10, 2014
Related Publication 20160141522A1 · May 19, 2016
Cited By (3)
US 12,201,011 US 12,201,012 US 12,325,719