US2020044163A1PendingUtilityA1
Organic electroluminescent materials and devices
Est. expiryJun 3, 2034(~7.8 yrs left)· nominal 20-yr term from priority
C07D 405/14C07D 401/14C09K 2211/1088C09K 2211/1092C07D 403/10C09K 11/06C07D 403/04C07D 409/14C07D 487/06C09K 2211/1007C07D 403/14C09K 2211/1059H01L 51/0072H01L 51/0067H01L 51/0061H01L 51/5016H10K 85/6576H10K 85/6574H10K 85/654H10K 85/6572H10K 50/11H10K 2101/10H10K 2101/20H10K 2101/27H10K 2102/103H10K 85/636H10K 50/125
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Claims
Abstract
A luminescent materials including donor-acceptor compounds with a nitrogen containing donor connected to the 1-position of a carbazole and triazene acceptor connected at the 9-position is disclosed.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A compound having a structure according to Formula 1:
wherein R a to R g , R 1 and R 2 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 Ar 1 to Ar 3 are independently substituted or unsubstituted aryl or heteroaryl and can connect to one another to form fused ring(s) and,
wherein L is a direct bond or a linker.
2 . The compound of claim 1 , wherein R a to R g are H.
3 . The compound of claim 1 , wherein Ar 1 is
4 . The compound of claim 3 , wherein Ar 2 and Ar 3 are phenyl.
5 . The compound of claim 4 , wherein L is a direct bond.
6 . The compound of claim 1 , wherein Ar 1 and L are
and Ar 2 and Ar 3 are phenyl.
7 . The compound of claim 1 , wherein said compound is selected from the group consisting of
8 . The compound of claim 1 , wherein Ar 1 and Ar 2 are connected to form a carbazole moiety.
9 . The compound of claim 8 , wherein said compound is selected from the group consisting of
10 . The compound of claim 1 , wherein Ar 2 and Ar 3 are connected to form a carbazole moiety.
11 . The compound of claim 10 , wherein said compound is selected from the group consisting of
12 . The compound of claim 1 , wherein said compound is selected from the group consisting of
13 . A first device comprising a first organic light emitting device, the first organic light emitting device comprising:
an anode; a cathode; and an emissive layer, disposed between the anode and the cathode, wherein the emissive layer comprises a first emitting compound having a structure according to Formula 1:
wherein R a to R g , R 1 and R 2 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 Ar 1 to Ar 3 are independently substituted or unsubstituted aryl or heteroaryl and can connect to one another to form fused ring(s) and,
wherein L is a direct bond or a linker.
14 . The first device of claim 13 , wherein the first emitting compound is selected from the group consisting of
15 . The first device of claim 13 , wherein the first device emits a luminescent radiation at room temperature when a voltage is applied across the organic light emitting device;
wherein the luminescent radiation comprises a delayed fluorescence process.
16 . The first device of claim 13 , wherein the emissive layer further comprises a first phosphorescent emitting material.
17 . The first device of claim 16 , wherein the emissive layer further comprises a second phosphorescent emitting material.
18 . The first device of claim 13 , wherein the emissive layer further comprises a host material.
19 . The first device of claim 16 , wherein the first device emits a white light at room temperature when a voltage is applied across the organic light emitting device.
20 . A formulation comprising a compound having a structure according to Formula 1:
wherein R a to R g , R 1 and R 2 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 Ar 1 to Ar 3 are independently substituted or unsubstituted aryl or heteroaryl and can connect to one another to form fused ring(s) and,
wherein L is a direct bond or a linker.Join the waitlist — get patent alerts
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