IP Library Granted Patent US 10,593,890
Granted Patent B2
US 10,593,890 · App. 15/063,957 · Granted Mar 17, 2020

Organic electroluminescent materials and devices

Inventors: Lichang Zeng (Ewing, NJ); Zeinab Elshenawy (Ewing, NJ); Walter Yeager (Ewing, NJ); Alexey Borisovich Dyatkin (Ewing, NJ); Chuanjun Xia (Ewing, NJ)
Assignee: UNIVERSAL DISPLAY CORPORATION
H01L51/0072C07D405/14C07D487/04C09K11/025C09K11/06H01L51/0052H01L51/0067H01L51/0073H01L51/0074C09K2211/1007C09K2211/1029C09K2211/185H01L51/0085H01L51/5016H01L51/5072H01L2251/5384
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Quick Facts
Patent No.
US 10,593,890
App. No.
15/063,957
Granted
Mar 17, 2020
Kind
B2
Abstract

Organic materials containing dibenzofuran or aza-dibenzofuran moiety are disclosed in this application. These materials are expected to improve OLED device performance.

Claims (61)

1. A compound having Formula I:

wherein G is selected from the group consisting of:

G 1 is a six-member aryl or heteroaryl ring;

L 1 is a direct bond or an organic linker;

n 1 and n 2 are independently an integer of 0 or 1; when n 1 or n 2 is 0, L 2 or L 3 is not present; and

when n 1 or n 2 is 1, L 2 or L 3 is independetly selected from the group consisting of a direct bond, oxygen, CR 1 R 2 , NR 3 , and SiR 4 R 5 ;

Z 1 , Z 2 , and Z 4 to Z 32 are each independently selected from the group consisting of N and CR 6 , and only one of Z 1 , Z 2 , and Z 4 is N;

Ar 1 and Ar 2 are each independently selected from the group consisting of aryl and heteroaryl;

each R 1 , R 2 , R 3 , R 4 , and R 5 are independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, and optionally, any two adjacent R 1 , R 2 , R 3 , R 4 , and R 5 can join to form a ring;

each R 6 is independently selected from the group consisting of a direct bond, hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, and optionally, any two adjacent R 6 can join to form a ring; and

wherein G 1 , Ar 1 , and Ar 2 is independently, optionally substituted by one or more substituents selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

provided that R 6 does not comprise a carbazole.

2. The compound of claim 1 , wherein G is selected from the group consisting of:

wherein Z 33 to Z 38 are each independently selected from the group consisting of N and CR 6 .

3. The compound of claim 1 , wherein one of Z 1 , or Z 2 , is N, and Z 4 to Z 32 are each independently a CR 6 .

4. The compound of claim 1 , wherein Z 1 , Z 2 , and Z 5 to Z 32 are each independently a CR 6 , and Z 4 is N.

5. The compound of claim 1 , wherein the compound is selected from the group consisting of:

6. The compound of claim 1 , wherein ring G 1 is benzene or pyridine.

7. The compound of claim 1 , wherein G is selected from the group consisting of:

wherein Z 33 and Z 34 are each independently selected from the group consisting of N and CR 6 .

8. The compound of claim 1 , wherein G is selected from the group consisting of:

wherein Z 33 to Z 38 are each independently selected from the group consisting of N and CR 6 .

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

an anode;

a cathode; and

an organic layer, disposed between the anode and the cathode, comprising a compound having Formula I:

wherein G is selected from the group consisting of:

G 1 is a six-member aryl or heteroaryl ring;

L 1 is a direct bond or an organic linker;

n 1 and n 2 are independently an integer of 0 or 1; when n 1 or n 2 is 0, L 2 or L 3 is not present; and

when n 1 or n 2 is 1, L 2 or L 3 is independently selected from the group consisting of a direct bond, oxygen, CR 1 R 2 , NR 3 , and SiR 4 R 5 ;

Z 1 , Z 2 , and Z 4 to Z 32 are each independently selected from the group consisting of N and CR 6 , and only one of Z 1 , Z 2 , and Z 4 is N;

Ar 1 and Ar 2 are each independently selected from the group consisting of aryl and heteroaryl;

each R 1 , R 2 , R 3 , R 4 , and R 5 are independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, and optionally, any two adjacent R 1 , R 2 , R 3 , R 4 , and R 5 can join to form a ring;

each R 6 is independently selected from the group consisting of a direct bond, hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, and optionally, any two adjacent R 6 can join to form a ring; and

wherein G 1 , Ar 1 , and Ar 2 is independently, optionally substituted by one or more substituents selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

provided that R 6 does not comprise a carbazole.

10. The OLED of claim 9 , wherein Z 1 and Z 2 are CR 6 , and Z 4 is N.

11. The OLED of claim 9 , wherein the organic layer is an emissive layer and the compound of Formula I is a host, which includes a phosphorescent emissive dopant;

wherein the emissive dopant is a transition metal complex having at least one ligand or part of the ligand if the ligand is more than bidentate selected from the group consisting of:

wherein each X 1 to X 13 are independently selected from the group consisting of carbon and nitrogen;

wherein X is selected from the group consisting of BR′, NR′, PR′, O, S, Se, C═O, S═O, SO 2 , CR′R″, SiR′R″, and GeR′R″;

wherein R′ and R″ are optionally fused or joined to form a ring;

wherein each R a , R b , R c , and R d may represent from mono substitution to the possible maximum number of substitution, or no substitution;

wherein R′, R″, R a , R b , R c , and R d 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; and

wherein any two adjacent substitutents of R a , R b , R c , and R d are optionally fused or joined to form a ring or form a multidentate ligand.

12. The OLED of claim 9 , wherein the organic layer is a blocking layer and the compound of Formula I is a blocking material in the organic layer.

13. The OLED of claim 9 , wherein the organic layer is a transporting layer and the compound of Formula I is a transporting material in the organic layer.

14. The OLED of claim 9 , wherein the OLED is incorporated into a device is selected from the group consisting of a consumer product, an electronic component module, and a lighting panel.

15. A formulation comprising a compound having Formula I:

wherein G is selected from the group consisting of:

G 1 is a six-member aryl or heteroaryl ring;

L 1 is a direct bond or an organic linker;

n 1 and n 2 are independently an integer of 0 or 1; when n 1 or n 2 is 0, L 2 or L 3 is not present; and

when n 1 or n 2 is 1, L 2 or L 3 is independently selected from the group consisting of a direct bond, oxygen, CR 1 R 2 , NR 3 , and SiR 4 R 5 ;

Z 1 , Z 2 , and Z 4 to Z 32 are each independently selected from the group consisting of N and CR 6 , and only one of Z 1 , Z 2 , and Z 4 is N;

Ar 1 and Ar 2 are each independently selected from the group consisting of aryl and heteroaryl;

each R 1 , R 2 , R 3 , R 4 , and R 5 are independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, and optionally, any two adjacent R 1 , R 2 , R 3 , R 4 , and R 5 can join to form a ring;

each R 6 is independently selected from the group consisting of a direct bond, hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, and optionally, any two adjacent R 6 can join to form a ring; and

wherein G 1 , Ar 1 , and Ar 2 is independently, optionally substituted by one or more substituents selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

provided that R 6 does not comprise a carbazole.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 8, 2016
From: ZENG, LICHANG; ELSHENAWY, ZEINAB; YEAGER, WALTER; DYATKIN, ALEXEY BORISOVICH; XIA, CHUANJUN
To: UNIVERSAL DISPLAY CORPORATION
Reel/Frame 037922/0469 →
Continuity (5)
Provisional Application 62143370 · Apr 6, 2015
Provisional Application 62245578 · Oct 23, 2015
Provisional Application 62254299 · Nov 12, 2015
Provisional Application 62274520 · Jan 4, 2016
Related Publication 20160293853A1 · Oct 6, 2016
Cited By (3)
US 12,284,913 US 12,295,262 US 12,715,874