IP Library › Granted Patent US 9,929,353
Granted Patent B2
US 9,929,353 · App. 14/636,310 · Granted Mar 27, 2018

Organic electroluminescent materials and devices

Inventors: Gregg Kottas (Ewing, NJ); Zeinab Elshenawy (Holland, PA); Chuanjun Xia (Lawrenceville, NJ); Lichang Zeng (Lawrenceville, NJ)
Assignee: Universal Display Corporation
H01L51/0072C07D487/06H01L51/0085H01L51/5016H01L51/5024H01L51/5072H01L51/5096
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Quick Facts
Patent No.
US 9,929,353
App. No.
14/636,310
Granted
Mar 27, 2018
Kind
B2
Abstract

Novel host compounds containing indolo[3,2,1-jk]carbazole moiety are disclosed. These compounds are useful in phosphorescent OLEDs and particularly as hosts and/or electron-blocking layer materials.

Claims (67)

1. A compound having a structure according to a formula G 1 -G 2 -G 3 -G 4 -G 5 , Formula I;

wherein G 1 has the structure:

wherein R 1 and R 3 each independently represent mono, di, tri, or tetra substitutions, or no substitution,

wherein R 2 represents mono, di, or tri substitutions, or no substitution,

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

wherein G 2 and G 4 are each independently selected from the group consisting of a direct bond, an aryl group having from 6-30 carbon atoms, a heteroaryl group having from 3-30 carbon atoms, and combinations thereof, wherein the aryl group and the heteroaryl group are optionally further substituted with one or more groups selected from 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;

wherein G 3 and G 5 are each independently a carbazole or a carbazole that is substituted with one or more groups selected from 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

wherein the structure according to Formula I is further defined according to at least one of:

wherein R 6 , and R 7 each independently represents mono, di, tri, or tetra substitutions, or no substitution;

wherein R 6 , and R 7 are each 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;

wherein R 4 represents mono, di, or tri substitutions, or no substitution;

wherein R 5 represents mono, di, tri, or tetra substitutions, or no substitution;

wherein R 4 , R 5 , and R 8 are each 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

wherein R 4 represents mono, di, or tri substitutions, or no substitution;

wherein R 5 represents mono, di, tri, or tetra substitutions, or no substitution;

wherein R 4 , R 5 , and R 8 are each 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.

2. The compound of claim 1 , wherein G 1 connects to G 2 at the ring having R 2 substituent.

3. The compound of claim 1 , wherein G 1 connects to G 2 at the ring having R 3 substituent.

4. The compound of claim 1 , wherein G 2 and G 4 are each a direct bond.

5. The compound of claim 1 , wherein the compound has a structure selected from the group consisting of:

wherein R 4 , R 6 , and R 7 each independently represents mono, di, tri, or tetra substitutions, or no substitution;

wherein R 5 represents mono, di, or tri, substitutions, or no substitution;

wherein R 4 , R 5 , R 6 , R 7 , R 8 , and R 9 are each 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.

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

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

8. A formulation comprising the compound in claim 1 .

9. A device comprising one or more organic light emitting devices, at least one of the organic light emitting devices comprising:

an anode;

a cathode; and

an organic layer, disposed between the anode and the cathode, comprising a compound having a structure according to the formula G 1 -G 2 -G 3 -G 4 -G 5 , Formula I;

wherein G 1 has the structure:

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

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

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

wherein G 2 and G 4 are each independently selected from the group consisting of a direct bond, an aryl group having from 6-30 carbon atoms, a heteroaryl group having from 3-30 carbon atoms, and combinations thereof; wherein the aryl group and the heteroaryl group are optionally further substituted with one or more groups selected from 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;

wherein G 3 and G 5 are each independently a carbazole or a carbazole that is substituted with one or more groups selected from 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

wherein the organic layer is an electron transporting layer and the compound having Formula I is an electron transporting material in the organic layer.

10. The device of claim 9 , wherein the device is selected from the group consisting of a consumer product, an electronic component module, an organic light-emitting device, and a lighting panel.

11. The device of claim 9 , wherein the organic layer further comprises a phosphorescent emissive dopant.

12. The device of claim 11 , wherein the phosphorescent 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 R a , R b , R c , and R d may represent mono, di, tri, or tetra substitution, or no substitution;

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

13. The device of claim 12 , wherein the phosphorescent emissive dopant is selected from the group consisting of:

14. A device comprising one or more organic light emitting devices, at least one of the organic light emitting devices comprising:

an anode;

a cathode; and

an organic layer, disposed between the anode and the cathode, comprising a compound having a structure according to the formula G 1 -G 2 -G 3 -G 4 -G 5 , Formula I;

wherein G 1 has the structure:

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

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

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

wherein G 2 and G 4 are each independently selected from the group consisting of a direct bond, an aryl group having from 6-30 carbon atoms, a heteroaryl group having from 3-30 carbon atoms, and combinations thereof; wherein the aryl group and the heteroaryl group are optionally further substituted with one or more groups selected from 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;

wherein G 3 and G 5 are each independently a carbazole or a carbazole that is substituted with one or more groups selected from 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

wherein the structure according to Formula I, is further defined according to at least one of:

wherein R 6 , and R 7 each independently represents mono, di, tri, or tetra substitutions, or no substitution;

wherein R 6 , and R 7 are each 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; or

wherein R 4 represents mono, di, or tri substitutions, or no substitution;

wherein R 5 represents mono, di, tri, or tetra substitutions, or no substitution;

wherein R 4 , R 5 , and R 8 are each 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

wherein R 4 represents mono, di, or tri substitutions, or no substitution;

wherein R 5 represents mono, di, tri, or tetra substitutions, or no substitution;

wherein R 4 , R 5 , and R 8 are each 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.

15. The device of claim 14 , wherein the organic layer is an emissive layer and the compound is a host.

16. The device of claim 14 , wherein the organic layer is an electron blocking layer and the compound having Formula I is an electron blocking material in the organic layer.

17. The device of claim 14 , wherein the organic layer further comprises a phosphorescent emissive dopant.

18. The device of claim 14 , wherein the device is selected from the group consisting of a consumer product, an electronic component module, an organic light-emitting device, and a lighting panel.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 3, 2015
From: KOTTAS, GREGG; ELSHENAWY, ZEINAB; XIA, CHUANJUN; ZENG, LICHANG
To: UNIVERSAL DISPLAY CORPORATION
Reel/Frame 035072/0978 →
Continuity (2)
Provisional Application 61974057 · Apr 2, 2014
Related Publication 20150287933A1 · Oct 8, 2015