Fused heterocyclic aromatic derivative, organic electroluminescence element material, and organic electroluminescence element using same
US-9978952-B2 · May 22, 2018 · US
Compound for organic optoelectronic device, composition for organic optoelectronic device, organic optoelectronic device, and display device
US11459316B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11459316-B2 |
| Application number | US-202016887114-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 29, 2020 |
| Priority date | May 30, 2019 |
| Publication date | Oct 4, 2022 |
| Grant date | Oct 4, 2022 |
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- Title
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Abstract
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A compound for an organic optoelectronic device, a composition for an organic optoelectronic device including the same, an organic optoelectronic device, and a display device, the being represented by Chemical Formula 1:
First claim
Opening claim text (preview).
What is claimed is: 1. A compound for an organic optoelectronic device, the compound being represented by Chemical Formula 1: wherein, in Chemical Formula 1, X 1 and X 2 are independently O or S, R 1 to R 13 are independently hydrogen, deuterium, a cyano group, a halogen, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C6 to C12 aryl group, a substituted or unsubstituted C2 to C20 heterocyclic group, or a combination thereof, R 10 to R 13 are separate or adjacent groups are linked to each other to provide a substituted or unsubstituted aliphatic, aromatic, or heteroaromatic monocyclic ring or a substituted or unsubstituted aliphatic, aromatic, or heteroaromatic polycyclic ring, and n is 0 or 1. 2. The compound as claimed in claim 1 , wherein the compound represented by Chemical Formula 1 is represented by one of Chemical Formula 1-1 to Chemical Formula 1-4: wherein, in Chemical Formula 1-1 to Chemical Formula 1-4, X 1 and X 2 are independently O or S, R 1 to R 13 are independently hydrogen, deuterium, a cyano group, a halogen, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C6 to C12 aryl group, a substituted or unsubstituted C2 to C20 heterocyclic group, or a combination thereof, R 10 to R 13 are separate or adjacent groups are linked to each other to provide a substituted or unsubstituted aliphatic, aromatic, or heteroaromatic monocyclic ring or a substituted or unsubstituted aliphatic, aromatic, or heteroaromatic polycyclic ring, and n is 0 or 1. 3. The compound as claimed in claim 2 , wherein: the compound represented by Chemical Formula 1 is represented by Chemical Formula 1-1, and Chemical Formula 1-1 is represented by one of Chemical Formula 1-1a to Chemical Formula 1-1d: wherein, in Chemical Formula 1-1a to Chemical Formula 1-1d, X 1 and X 2 are independently O or S, R 1 to R 13 are independently hydrogen, deuterium, a cyano group, a halogen, a substituted or unsubstituted C1 to C10 alkyl group, a C6 to C12 aryl group, a C2 to C20 heterocyclic group, or a combination thereof, R 10 to R 13 are separate or adjacent groups are linked to each other to provide a substituted or unsubstituted aliphatic, aromatic, or heteroaromatic monocyclic ring or a substituted or unsubstituted aliphatic, aromatic, or heteroaromatic polycyclic ring, and n is 0 or 1. 4. The compound as claimed in claim 2 , wherein: the compound represented by Chemical Formula 1 is represented by Chemical Formula 1-2, and Chemical Formula 1-2 is represented by one of Chemical Formula 1-2a to Chemical Formula 1-2d: wherein, in Chemical Formula 1-2a to Chemical Formula 1-2d, X 1 and X 2 are independently O or S, R 1 to R 13 are independently hydrogen, deuterium, a cyano group, a halogen, a substituted or unsubstituted C1 to C10 alkyl group, a C6 to C12 aryl group, a C2 to C20 heterocyclic group, or a combination thereof, R 10 to R 13 are separate or adjacent groups are linked to each other to provide a substituted or unsubstituted aliphatic, aromatic, or heteroaromatic monocyclic ring or a substituted or unsubstituted aliphatic, aromatic, or heteroaromatic polycyclic ring, and n is 0 or 1. 5. The compound as claimed in claim 2 , wherein: the compound represented by Chemical Formula 1 is represented by Chemical Formula 1-3, and Chemical Formula 1-3 is represented by one of Chemical Formula 1-3a to Chemical Formula 1-3d: wherein, in Chemical Formula 1-3a to Chemical Formula 1-3d, X 1 and X 2 are independently O or S, R 1 to R 13 are independently hydrogen, deuterium, a cyano group, a halogen, a substituted or unsubstituted C1 to C10 alkyl group, a C6 to C12 aryl group, a C2 to C20 heterocyclic group, or a combination thereof, R 10 to R 13 are separate or adjacent groups are linked to each other to provide a substituted or unsubstituted aliphatic, aromatic, or heteroaromatic monocyclic ring or a substituted or unsubstituted aliphatic, aromatic, or heteroaromatic polycyclic ring, and n is 0 or 1. 6. The compound as claimed in claim 2 , wherein: the compound represented by Chemical Formula 1 is represented by Chemical Formula 1-4, and Chemical Formula 1-4 is represented by one of Chemical Formula 1-4a to Chemical Formula 1-4d: wherein, in Chemical Formula 1-4a to Chemical Formula 1-4d, X 1 and X 2 are independently O or S, R 1 to R 13 are independently hydrogen, deuterium, a cyano group, a halogen, a substituted or unsubstituted C1 to C10 alkyl group, a C6 to C12 aryl group, a C2 to C20 heterocyclic group, or a combination thereof, R 10 to R 13 are separate or adjacent groups are linked to each other to provide a substituted or unsubstituted aliphatic, aromatic, or heteroaromatic monocyclic ring or a substituted or unsubstituted aliphatic, aromatic, or heteroaromatic polycyclic ring, and n is 0 or 1. 7. The compound as claimed in claim 1 , wherein the compound represented by Chemical Formula 1 is represented by one of Chemical Formula 1A to Chemical Formula 1G: wherein, in Chemical Formula 1A to Chemical Formula 1G, X 1 and X 2 are independently O or S, and R 1 to R 13 are independently hydrogen, deuterium, a cyano group, a halogen, a substituted or unsubstituted C1 to C10 alkyl group, a C6 to C12 aryl group, a C2 to C20 heterocyclic group, or a combination thereof. 8. The compound as claimed in claim 1 , wherein the compound represented by Chemical Formula 1 is represented by Chemical Formula 1-1a-IV, Chemical Formula 1-2b-IV, Chemical Formula 1-3c-III, Chemical Formula 1-4c-I, Chemical Formula 1-4c-III, Chemical Formula 1-4c-IV, Chemical Formula 1-4d-II, or Chemical Formula 1-4d-IV: wherein, in Chemical Formula 1-1a-IV, Chemical Formula 1-2b-IV, Chemical Formula 1-3c-III, Chemical Formula 1-4c-I, Chemical Formula 1-4c-III, Chemical Formula 1-4c-IV, Chemical Formula 1-4d-II, and
Assignees
Inventors
Classifications
- C07D409/14Primary
containing three or more hetero rings · CPC title
- C07D407/14Primary
containing three or more hetero rings · CPC title
- C07D405/14Primary
containing three or more hetero rings · CPC title
Electricity · mapped topic
Electricity · mapped topic
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Frequently asked questions
Answers are generated from the same data shown on this page.
- What does patent US11459316B2 cover?
- A compound for an organic optoelectronic device, a composition for an organic optoelectronic device including the same, an organic optoelectronic device, and a display device, the being represented by Chemical Formula 1:
- Who is the assignee on this patent?
- Samsung Sdi Co Ltd
- What technology area does this patent fall under?
- Primary CPC classification C07D409/14. Mapped technology areas include Chemistry & Metallurgy.
- When was this patent published?
- Publication date Tue Oct 04 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
- What related patents are in patentsdb?
- We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).