Amine-based compound and organic light-emitting device including the same
US-2015364705-A1 · Dec 17, 2015 · US
US2017237014A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2017237014-A1 |
| Application number | US-201715586997-A |
| Country | US |
| Kind code | A1 |
| Filing date | May 4, 2017 |
| Priority date | Dec 7, 2012 |
| Publication date | Aug 17, 2017 |
| Grant date | — |
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Devices containing novel carbazole-containing compounds are provided. The novel compounds also contain electron donor groups, aryl linkers, and at least one nitrogen heterocycle. These novel organic compounds can exhibit delayed fluorescence in the devices.
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1 . A first device comprising a 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 compound having the formula: wherein Z 1 , Z 2 , Z 3 , Z 4 and Z 5 are each independently selected from group consisting of CR 9 and N; wherein any adjacent R 9 are optionally joined to form a fused ring; wherein at least one of Z 1 , Z 2 , Z 3 , Z 4 and Z 5 is N; wherein L 1 is selected from the group consisting of: and combinations thereof; wherein X 1 is O, S, or CRR′; wherein R, R′ are optionally joined to form a ring; wherein n 1 is an integer from 1 to 20; wherein L 1 can be further substituted by a substituent selected from the group consisting of alkyl, aryl, and heteroaryl; wherein at least one of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 comprises at least one electron donor group selected from the group consisting of: wherein X and Y is selected from the group consisting of O, S, NR 14 ; and wherein R 11 , R 12 , R 13 and R 14 are selected from the group consisting of aryl and heteroaryl. wherein any two adjacent R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 are not joined to form a ring; wherein m is an integer from 1 to 20; wherein n 2 is an integer from 1 to 20; wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 do not contain an electron acceptor group; wherein R 9 does not contain an electron donor group; wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 are independently selected from the group consisting of hydrogen, deuterium, alkyl, cycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, and combinations thereof; wherein R 9 , R, and R′ are independently selected from the group consisting of hydrogen, deuterium, alkyl, cycloalkyl, heteroalkyl, arylalkyl, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, and combinations thereof; and wherein at least one of Z′, Z 2 , Z 3 , Z 4 and Z 5 is CR 9 wherein R 9 is selected from aryl and heteroaryl, and can be further substituted. 2 . The first device of claim 1 , wherein at least one of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 comprises the electron donor group selected from the group consisting of: 3 . The first device of claim 1 , wherein the compound has the formula: and wherein R 91 and R 92 are independently selected from aryl or heteroaryl, and can be further substituted. 4 . The first device of claim 1 , wherein the electron donor group is selected from the group consisting of: 5 . The first device of claim 1 , wherein the compound is selected from the group consisting of:
the oxygen-containing ring being five-membered · CPC title
Ortho-condensed systems · CPC title
linked by a carbon chain containing aromatic rings · CPC title
containing one nitrogen atom as the heteroatom · CPC title
Electricity · mapped topic
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