Heterocyclic compound, organic light-emitting device including the same, and electronic apparatus including the organic light-emitting device
US-2024373662-A1 · Nov 7, 2024 · US
US2024237519A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2024237519-A1 |
| Application number | US-202318489717-A |
| Country | US |
| Kind code | A1 |
| Filing date | Oct 18, 2023 |
| Priority date | Dec 22, 2022 |
| Publication date | Jul 11, 2024 |
| Grant date | — |
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The present disclosure relates to an organic compound including at least one fused hetero aromatic moiety with at least one nitrogen atom linked to a triazine moiety directly or through a linking group and a benzothiazole moiety linked to the triazine moiety, an organic light emitting diode and an organic light emitting device having the organic compound. The organic light emitting diode and the organic light emitting device where an emissive layer includes the organic compound have beneficial luminous efficiency and luminous lifespan.
Opening claim text (preview).
What is claimed is: 1 . An organic compound having the following structure of Chemical Formula 1: wherein, in the Chemical Formula 1, each of R 1 and R 2 is independently an unsubstituted or substituted C 6 -C 30 aryl group or an unsubstituted or substituted C 3 -C 30 hetero aryl group; R 3 is independently an unsubstituted or substituted C 1 -C 20 alkyl group, an unsubstituted or substituted C 6 -C 30 aryl group or an unsubstituted or substituted C 3 -C 30 hetero aryl group, where each R 3 is identical to or different from each other when m is 2, 3, or 4; Z is CR 4 or a carbon atom linked to a triazine moiety, where R 4 is hydrogen, an unsubstituted or substituted C 1 -C 20 alkyl group, an unsubstituted or substituted C 6 -C 30 aryl group, or an unsubstituted or substituted C 3 -C 30 hetero aryl group, wherein at least one of R 1 , R 2 , R 3 and R 4 is an unsubstituted or substituted C 10 -C 30 fused hetero aryl group with at least one nitrogen atom; each of L 1 and L 2 is independently a single bond or an unsubstituted or substituted C 6 -C 30 arylene group; and m is 0, 1, 2, or 3 when Z is CR 4 and m is 0, 1, 2, 3 or 4 when Z is the carbon atom linked to the triazine moiety. 2 . The organic compound of claim 1 , wherein the organic compound has the following structure of Chemical Formula 2: wherein, in the Chemical Formula 2, each of R 1 , R 2 , R 3 , L 1 , and L 2 is a same as defined in Chemical Formula 1; Z 1 is CR 4 , where R 4 is a same as defined in Chemical Formula 1; and n is 0, 1, 2, or 3. 3 . The organic compound of claim 1 , wherein the organic compound has the following structure of Chemical Formula 3A, Chemical Formula 3B, Chemical Formula 3C, or Chemical Formula 3D: wherein, in the Chemical Formulae 3A, 3B, 3C and 3D, each of R 1 , R 2 , R 3 , R 4 , L 1 , and L 2 is a same as defined in Chemical Formula 1; and n is 0, 1, 2, or 3. 4 . The organic compound of claim 1 , wherein the organic compound has the following structure of Chemical Formula 4: wherein, in the Chemical Formula 4, each of R 1 , R 2 , R 3 , L 1 , and L 2 is a same as defined in Chemical Formula 1; and p is 0, 1, 2, 3, or 4. 5 . The organic compound of claim 1 , wherein one of R 1 and R 2 in Chemical Formula 1 is a carbazolyl group unsubstituted or substituted with a C 1 -C 20 alkyl group and the other of R 1 and R 2 in Chemical Formula 1 is selected from the group consisting of phenyl, biphenyl, pyrenyl, fluorenyl, dibenzofuranyl, dibenzothiophenyl and carbazolyl each of which is independently unsubstituted or substituted with at least one of a C 1 -C 20 alkyl group and a C 6 -C 30 aryl group, R 4 in Chemical Formula 1 is hydrogen or phenyl unsubstituted or substituted with a C 1 -C 20 alkyl group, and m is 0. 6 . The organic compound of claim 1 , wherein the organic compound is at least one of the following compounds: 7 . The organic compound of claim 1 , wherein the organic compound is at least one of the following compounds: 8 . An organic light emitting diode, including: a first electrode; a second electrode facing the first electrode; and an emissive layer disposed between the first electrode and the second electrode, wherein the emissive layer includes an organic compound having the following structure of Chemical Formula 1: wherein, in the Chemical Formula 1, each of R 1 and R 2 is independently an unsubstituted or substituted C 6 -C 30 aryl group or an unsubstituted or substituted C 3 -C 30 hetero aryl group; R 3 is independently an unsubstituted or substituted C 1 -C 20 alkyl group, an unsubstituted or substituted C 6 -C 30 aryl group or an unsubstituted or substituted C 3 -C 30 hetero aryl group, where each R 3 is identical to or different from each other when m is 2, 3, or 4; Z is CR 4 or a carbon atom linked to a triazine moiety, where R 4 is hydrogen, an unsubstituted or substituted C 1 -C 20 alkyl group, an unsubstituted or substituted C 6 -C 30 aryl group, or an unsubstituted or substituted C 3 -C 30 hetero aryl group, wherein at least one of R 1 , R 2 , R 3 and R 4 is an unsubstituted or substituted C 10 -C 30 fused hetero aryl group with at least one nitrogen atom; each of L 1 and L 2 is independently a single bond or an unsubstituted or substituted C 6 -C 30 arylene group; and m is 0, 1, 2, or 3 when Z is CR 4 and m is 0, 1, 2, 3, or 4 when Z is the carbon atom linked to the triazine moiety. 9 . The organic ligh
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