Light-emitting element, light-emitting device, electronic device, and lighting device
US-9761812-B2 · Sep 12, 2017 · US
US12127474B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12127474-B2 |
| Application number | US-201916973867-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 26, 2019 |
| Priority date | Jun 15, 2018 |
| Publication date | Oct 22, 2024 |
| Grant date | Oct 22, 2024 |
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The present invention is related to a first compound for an organic optoelectronic device represented by Chemical Formula 1, a composition for an organic optoelectronic device including the same, an organic optoelectronic device, and a display device. In Chemical Formula 1, definitions of each substituent are the same as defined in the specification.
Opening claim text (preview).
The invention claimed is: 1. A compound for an organic optoelectronic device represented by Chemical Formula 1: wherein, in Chemical Formula 1, Ar 1 is an unsubstituted C6 aryl group or a substituted or unsubstituted C7 to C12 aryl group, Ar 2 is a substituted or unsubstituted C6 to C12 aryl group, Ar 3 and Ar 4 are independently a substituted or unsubstituted C6 to C30 aryl group, L 1 is a single bond or a phenylene group, L 2 to L 4 are independently a single bond or a substituted or unsubstituted C6 to C12 arylene group, and R 1 and R 2 are independently hydrogen, deuterium, a cyano group, or a substituted or unsubstituted C1 to C10 alkyl group. 2. The compound for an organic optoelectronic device of claim 1 , wherein Chemical Formula 1 is represented by Chemical Formula 1A: wherein, in Chemical Formula 1A, Ar 1 is an unsubstituted C6 aryl group or a substituted or unsubstituted C7 to C12 aryl group, Ar 2 is a substituted or unsubstituted C6 to C12 aryl group, Ar 3 and Ar 4 are independently a substituted or unsubstituted C6 to C30 aryl group, L 1 is a single bond or a phenylene group, and L 2 to L 4 are independently a single bond or a substituted or unsubstituted C6 to C12 arylene group. 3. The compound for an organic optoelectronic device of claim 1 , wherein: Ar 1 is an unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, or a substituted or unsubstituted naphthyl group, and Ar 2 is a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, or a substituted or unsubstituted naphthyl group. 4. The compound for an organic optoelectronic device of claim 1 , wherein Ar 3 and Ar 4 are independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted anthracenyl group, or a substituted or unsubstituted phenanthrenyl group. 5. The compound for an organic optoelectronic device of claim 1 , wherein the compound is a compound of Group 1: 6. A composition for an organic optoelectronic device, comprising: a first compound, the first compound being the compound for an organic optoelectronic device of claim 1 , and a second compound for an organic optoelectronic device represented by Chemical Formula 2: wherein, in Chemical Formula 2, Z 1 to Z 3 are independently N or CR a , at least two of Z 1 to Z 3 are N, R a is hydrogen, deuterium, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heterocyclic group, a substituted or unsubstituted silyl group, a substituted or unsubstituted amine group, a halogen, a cyano group, or a combination thereof, L 5 to L 7 are independently a single bond, a substituted or unsubstituted C6 to C20 arylene group, a substituted or unsubstituted C2 to C20 heterocyclic group, or a combination thereof, R 3 to R 5 are independently substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof, at least one of R 3 to R 5 is a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted benzocarbazolyl group, a substituted or unsubstituted dibenzocarbazolyl group, or a substituted or unsubstituted triphenylene group, and R a and R 3 to R 5 are independently present or adjacent groups thereof are linked with each other to form a substituted or unsubstituted aliphatic, aromatic, or heteroaromatic monocyclic or polycyclic ring. 7. The composition for an organic optoelectronic device of claim 6 , wherein the second compound for an organic optoelectronic device is represented by one of Chemical Formula 2B-1 to Chemical Formula 2B-4: wherein, in Chemical Formulae 2B-1 to 2B-4, Z 1 to Z 3 are independently N or CR a , at least two of Z 1 to Z 3 are N, R a is hydrogen, deuterium, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heterocyclic group, a substituted or unsubstituted silyl group, a substituted or unsubstituted amine group, a halogen, a cyano group, or a combination thereof, R 4 and R 5 are independently substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof, L 5 to L 7 are independently a single bond, a substituted or unsubstituted C6 to C20 arylene group, a substituted or unsubstituted C2 to C20 heterocyclic group, or a combination thereof, X 1 to X 4 are independently O or S, and R b1 to R b3 , R c1 to R c3 , R d1 to R d3 , and R e1 to R e3 , R s , and R t are independently hydrogen, deuterium, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, a substituted or unsubstituted silyl group, a substituted or unsubstituted amine group, a halogen, a cyano group, or a combination thereof. 8. The composition for an organic optoelectronic device of claim 6 , wherein the second compound for an organic optoelectronic device is represented by one of Chemical Formula 2C-1 to Chemical Formula 2C-12: wherein, in Chemical Formula 2C-1 to Chemical Fo
Triplet emission · CPC title
Hole transporting layers · CPC title
characterised by the electroluminescent [EL] layers · CPC title
comprising only oxygen in the heteroaromatic polycondensed ring system, e.g. cumarine dyes · CPC title
comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole · CPC title
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