IP Library Granted Patent US 11,380,855
Granted Patent B2
US 11,380,855 · App. 16/658,316 · Granted Jul 5, 2022

Organic electroluminescent materials and devices

Inventors: Scott Beers (Flemington, NJ); Chuanjun Xia (Lawrenceville, NJ); Harvey Wendt (Medford Lakes, NJ); Suman Layek (Lawrenceville, NJ)
Assignee: UNIVERSAL DISPLAY CORPORATION
H01L51/0085C07F15/0033C09K11/025C09K11/06C09K2211/1007C09K2211/1033C09K2211/185H01L51/5016
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Quick Facts
Patent No.
US 11,380,855
App. No.
16/658,316
Granted
Jul 5, 2022
Kind
B2
Abstract

Novel iridium complexes containing phenylpyridine and pyridyl aza-benzo fused ligands are described. These complexes are useful as light emitters when incorporated into OLEDs.

Claims (59)

1. A compound having the formula Ir(L A ) n (L B ) 3-n , having the structure:

wherein A 1 , A 2 , A 3 , A 4 , A 6 , A 7 , and A 8 comprise carbon;

wherein A 5 is nitrogen;

wherein ring B is bonded to ring A through a C—C bond;

wherein the iridium is bonded to ring A through a Ir—C bond;

wherein (i) A 4 is bonded to ring B and A 3 is bonded to Ir, (ii) A 3 is bonded to ring B and A 2 is bonded to Ir, (iii) A 2 is bonded to ring B and A 1 is bonded to Ir, (iv) A 1 is bonded to ring B and A 2 is bonded to Ir, or (v) A 3 is bonded to ring B and A 4 is bonded to Ir;

wherein X is O, S, or Se;

wherein R 1 , R 2 , R 3 , and R 4 independently represent mono-, di-, tri-, tetra-substitution, or no substitution;

wherein any adjacent substitutions in R 1 , R 2 , R 3 , and R 4 are optionally linked together to form a ring;

wherein R 1 , R 2 , R 3 , and R 4 are 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; and

wherein n is an integer from 1 to 2.

2. The compound of claim 1 , wherein n is 1.

3. The compound of claim 1 , wherein the compound has the formula:

4. The compound of claim 3 , wherein the compound has the formula:

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

6. The compound of claim 1 , wherein R 1 , R 2 , R 3 , and R 4 are independently selected from the group consisting of hydrogen, deuterium, alkyl, and combinations thereof.

7. The compound of claim 1 , wherein at least one R 2 is alkyl.

8. The compound of claim 1 , wherein at least one R 3 is alkyl.

9. The compound of claim 1 , wherein L B is selected from the group consisting of:

10. The compound of claim 1 , wherein (ii) A 3 is bonded to ring B and A 2 is bonded to Ir.

11. The compound of claim 1 , wherein (iii) A 2 is bonded to ring B and A 1 is bonded to Ir.

12. The compound of claim 1 , wherein (iv) A 1 is bonded to ring B and A 2 is bonded to Ir.

13. The compound of claim 1 , wherein (v) A 3 is bonded to ring B and A 4 is bonded to Ir.

14. A first device comprising a first organic light emitting device, comprising:

an anode;

a cathode; and

an organic layer, disposed between the anode and the cathode, comprising a compound having the formula Ir(L A ) n (L B ) 3-n , having the structure:

wherein A 1 , A 2 , A 3 , A 4 , A 6 , A 7 , and A 8 comprise carbon;

wherein A 5 is nitrogen;

wherein ring B is bonded to ring A through a C—C bond;

wherein the iridium is bonded to ring A through a Ir—C bond;

wherein (i) A 4 is bonded to ring B and A 3 is bonded to Ir, (ii) A 3 is bonded to ring B and A 2 is bonded to Ir, (iii) A 2 is bonded to ring B and A 1 is bonded to Ir, (iv) A 1 is bonded to ring B and A 2 is bonded to Ir, or (v) A 3 is bonded to ring B and A 4 is bonded to Ir;

wherein X is O, S, or Se;

wherein R 1 , R 2 , R 3 , and R 4 independently represent mono-, di-, tri-, tetra-substitution, or no substitution;

wherein any adjacent substitutions in R 1 , R 2 , R 3 , and R 4 are optionally linked together to form a ring;

wherein R 1 , R 2 , R 3 , and R 4 are 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; and

wherein n is an integer from 1 to 2.

15. The first device of claim 14 , wherein the organic layer is an emissive layer and the compound is an emissive dopant or a non-emissive dopant.

16. The first device of claim 14 , wherein the organic layer further comprises a host, and 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 2 —Ar 1 ;

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 first device of claim 14 , wherein the organic layer further comprises a host, and wherein the host comprises at least one chemical group selected from the group consisting of carbazole, dibenzothiphene, dibenzofuran, dibenzoselenophene, azacarbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophene.

18. The first device of claim 14 , wherein the organic layer further comprises a host, and wherein the host is selected from the group consisting of:

and combinations thereof.

19. A consumer product comprising an organic light-emitting device comprising:

an anode;

a cathode; and

an organic layer, disposed between the anode and the cathode, comprising a compound having the formula Ir(L A ) n (L B ) 3-n , having the structure:

wherein A 1 , A 2 , A 3 , A 4 , A 6 , A 7 , and A 8 comprise carbon;

wherein A 5 is nitrogen;

wherein ring B is bonded to ring A through a C—C bond;

wherein the iridium is bonded to ring A through a Ir—C bond;

wherein (i) A 4 is bonded to ring B and A 3 is bonded to Ir, (ii) A 3 is bonded to ring B and A 2 is bonded to Ir, (iii) A 2 is bonded to ring B and A 1 is bonded to Ir, (iv) A 1 is bonded to ring B and A 2 is bonded to Ir, or (v) A 3 is bonded to ring B and A 4 is bonded to Ir;

wherein X is O, S, or Se;

wherein R 1 , R 2 , R 3 , and R 4 independently represent mono-, di-, tri-, tetra-substitution, or no substitution;

wherein any adjacent substitutions in R 1 , R 2 , R 3 , and R 4 are optionally linked together to form a ring;

wherein R 1 , R 2 , R 3 , and R 4 are 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; and

wherein n is an integer from 1 to 2.

20. The consumer product of claim 19 , wherein the consumer product is selected from the group consisting of flat panel displays, computer monitors, medical monitors, televisions, billboards, lights for interior or exterior illumination and/or signaling, heads-up displays, fully or partially transparent displays, flexible displays, laser printers, telephones, mobile phones, tablets, phablets, personal digital assistants (PDAs), wearable devices, laptop computers, digital cameras, camcorders, viewfinders, micro-displays, 3-D displays, virtual reality or augmented reality displays, vehicles, wall screens, theater or stadium screens, and signs.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 21, 2019
From: BEERS, SCOTT; XIA, CHUANJUN; WENDT, HARVEY; LAYEK, SUMAN
To: UNIVERSAL DISPLAY CORPORATION
Reel/Frame 050776/0847 →
Continuity (3)
Continuation 15455838 · Mar 10, 2017
Continuation 13673338 · Nov 9, 2012
Related Publication 20200066999A1 · Feb 27, 2020
Cited By (1)
US 12,453,280