IP Library Granted Patent US 11,672,175
Granted Patent B2
US 11,672,175 · App. 16/867,696 · Granted Jun 6, 2023

Organic electroluminescent materials and devices

Inventors: Zhiqiang Ji (Ewing, NJ); Lichang Zeng (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 11,672,175
App. No.
16/867,696
Granted
Jun 6, 2023
Kind
B2
Abstract

Indolocarbazole materials with substitution attached at specific positions and methods to synthesize the same are disclosed. The materials are used as hosts for improving performance of organic electroluminescence devices.

Claims (42)

1. A compound of Formula I:

wherein R 1 represents mono, di, tri, or tetra substitution;

wherein R 2 represents mono, di, tri, or tetra substitution, or no substitution;

wherein R 3 represents mono, or di substitution, or no substitution;

wherein R 1 is selected from the group consisting of biphenyl, terphenyl, tetraphenyl, triphenylene, naphthalene, phenanthrene, 9,9-dialkylfluorene, indole, benzofuran, benzothiophene, benzoselenophene, dibenzofuran, dibenzothiophene, dibenzoselenophene, pyrimidine, pyrazine, triazine, aza-carbazole, aza-dibenzofuran, aza-dibenzothiophene, aza-dibenzoselenophene, aza-triphenylene, aza-fluorene, quinoline, isoquinoline, quinoxaline, quinazoline, silyl, halogen, and combinations thereof;

wherein R 1 may be further substituted with a substituent 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 each R 2 , R 3 , R 4 , and R 5 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;

wherein R 4 and R 5 are not thiophene, thiazole, thiadiazole, furan, oxazole, or oxadiazole.

2. The compound of claim 1 , wherein R 1 is selected from the group consisting of triphenylene, 9,9-dialkylfluorene, dibenzofuran, dibenzothiophene, dibenzoselenophene, aza-carbazole, aza-dibenzofuran, aza-dibenzothiophene, aza-dibenzoselenophene, aza-triphenylene, aza-fluorene, and combinations thereof.

3. The compound of claim 1 , wherein each R 2 , R 3 , R 4 , and R 5 are independently selected from the group consisting of aryl, substituted aryl, heteroaryl, and substituted heteroaryl.

4. The compound of claim 1 , wherein R 1 represents mono substitution and the compound has the structure of Formula II:

5. The compound of claim 1 , wherein R 3 is hydrogen.

6. The compound of claim 1 , wherein R 4 and R 5 are each independently a phenyl.

7. The compound of claim 1 , wherein R 2 is hydrogen.

8. A compound selected from the group consisting of:

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 of Formula I:

wherein R 1 represents mono, di, tri, or tetra substitution;

wherein R 2 represents mono, di, tri, or tetra substition, or no substution;

wherein R 3 represents mono, or di substitution, or no substitution;

wherein R 1 is selected from the group consisting of biphenyl, terphenyl, tetraphenyl, triphenylene, naphthalene, phenanthrene, 9,9-dialkylfluorene, indole, benzofuran, benzothiophene, benzoselenophene, dibenzofuran, dibenzothiophene, dibenzoselenophene, pyrimidine, pyrazine, triazine, aza-carbazole, aza-dibenzofuran, aza-dibenzothiophene, aza-dibenzoselenophene, aza-triphenylene, aza-fluorene, quinoline, isoquinoline, quinoxaline, quinazoline, silyl, halogen, and combinations thereof;

wherein R 1 may be further substituted with a substituent 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 each R 2 , R 3 , R 4 , and R 5 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;

wherein R 4 and R 5 are not thiophene, thiazole, thiadiazole, furan, oxazole, or oxadiazole.

10. The OLED of claim 9 , wherein the organic layer is an emissive layer and the compound of Formula I is a host.

11. The OLED of claim 9 , wherein the organic layer further comprises 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 substituents 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 selected from the group consisting of a consumer product, an electronic component module, and a lighting panel.

15. A formulation comprising a compound of claim 1 .

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

an anode;

a cathode; and

an organic layer, disposed between the anode and the cathode, comprising the compound of claim 8 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 8, 2025
From: JI, ZHIQIANG; ZENG, LICHANG; DYATKIN, ALEXEY BORISOVICH; XIA, CHUANJUN
To: UNIVERSAL DISPLAY CORPORATION
Reel/Frame 071629/0608 →
Continuity (6)
Continuation 15064041 · Mar 8, 2016
Provisional Application 62274520 · Jan 4, 2016
Provisional Application 62254299 · Nov 12, 2015
Provisional Application 62245578 · Oct 23, 2015
Provisional Application 62143370 · Apr 6, 2015
Related Publication 20200266363A1 · Aug 20, 2020