Organic electroluminescent materials and devices
US-2019140193-A1 · May 9, 2019 · US
US12108657B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12108657-B2 |
| Application number | US-202017023666-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 17, 2020 |
| Priority date | Sep 30, 2019 |
| Publication date | Oct 1, 2024 |
| Grant date | Oct 1, 2024 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A compound for an organic optoelectronic device, a composition, an organic optoelectronic device, and a display device, the compound being represented by Chemical Formula 1A or Chemical Formula 1B.
Opening claim text (preview).
What is claimed is: 1. A compound for an organic optoelectronic device, the compound being represented by Chemical Formula 1A or Chemical Formula 1B: wherein, in Chemical Formula 1A and Chemical Formula 1B, Z 1 to Z 3 are independently N or CR a , at least two of Z 1 to Z 3 being N, R a and R 1 to R 10 are independently hydrogen, deuterium, a substituted or unsubstituted C1 to C10 alkyl group, or a substituted or unsubstituted C6 to C20 aryl group, and R b and R c are independently a substituted or unsubstituted C6 to C20 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group. 2. The compound as claimed in claim 1 , wherein: Chemical Formula 1A is represented by Chemical Formula 1A-1 and Chemical Formula 1B is represented by Chemical Formula 1B-1: in Chemical Formula 1A-1 and Chemical Formula 1B-1, R 1 to R 10 , R b , and R c are defined the same as those of Chemical Formulae 1A and 1B. 3. The compound as claimed in claim 1 , wherein: the compound is represented by Chemical Formula 1A, Chemical Formula 1A is represented by Chemical Formula 1A-1-a: in Chemical Formula 1A-1-a, R 1 to R 10 , R b , and R c are defined the same as those of Chemical Formula 1A. 4. The compound as claimed in claim 1 , wherein R b and R c are independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, a substituted or unsubstituted carbazolyl group, or a combination thereof. 5. The compound as claimed in claim 1 , wherein: R b and R c are independently a group of Group I: in Group I, * is a linking point. 6. The compound as claimed in claim 1 , wherein the compound is a compound of Group 1: 7. A composition for an organic optoelectronic device, the composition comprising: a first compound and a second compound, wherein: the first compound includes the compound for an organic optoelectronic device as claimed in claim 1 , the second compound is represented by Chemical Formula 2: in Chemical Formula 2, Y 1 and Y 2 are independently a single bond or a substituted or unsubstituted C6 to C20 arylene group, Ar 1 and Ar 2 are independently a substituted or unsubstituted C6 to C20 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group, and R 11 to R 16 are independently hydrogen, deuterium, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C6 to C20 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, a cyano group, or a combination thereof. 8. The composition as claimed in claim 7 , wherein: moieties *—Y 1 —Ar 1 and *—Y 2 —Ar 2 of Chemical Formula 2 are each independently a moiety of Group II: in Group II, * is a linking point. 9. An organic optoelectronic device, comprising an anode and a cathode facing each other, and at least one organic layer between the anode and the cathode wherein the at least one organic layer includes the compound for an organic optoelectronic device as claimed in claim 1 . 10. The organic optoelectronic device as claimed in claim 9 , wherein: the at least one organic layer includes a light emitting layer, and the light emitting layer includes the compound for an organic optoelectronic device. 11. A display device comprising the organic optoelectronic device as claimed in claim 9 . 12. An organic optoelectronic device, comprising an anode and a cathode facing each other, and at least one organic layer between the anode and the cathode, wherein the at least one organic layer includes the composition for an organic optoelectronic device as claimed in claim 7 . 13. The organic optoelectronic device as claimed in claim 12 , wherein the at least one organic layer includes a light emitting layer, and the light emitting layer includes the composition for an organic optoelectronic device. 14. A display device comprising the organic optoelectronic device as claimed in claim 12 .
containing four rings, e.g. pyrene · CPC title
Polycyclic condensed aromatic hydrocarbons, e.g. anthracene · CPC title
Organic light-emitting devices (integrated devices or assemblies of multiple devices H10K59/00, H10K65/00; organic semiconductor lasers H01S5/36) · CPC title
comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene · CPC title
comprising only oxygen in the heteroaromatic polycondensed ring system, e.g. cumarine dyes · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.