Heterocyclic compounds comprising dibenzofuran and/or dibenzothiophene structures
US-2019165282-A1 · May 30, 2019 · US
US12209083B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12209083-B2 |
| Application number | US-201917054687-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 4, 2019 |
| Priority date | Jul 5, 2018 |
| Publication date | Jan 28, 2025 |
| Grant date | Jan 28, 2025 |
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.
The present specification provides a compound represented by Formula 1 and an organic light emitting device including the same. The compound is used for an organic material layer of the organic light emitting device.
Opening claim text (preview).
What is claimed is: 1. An organic light emitting device comprising: a first electrode; a second electrode provided to face the first electrode; and an organic material layer having one or more layers provided between the first electrode and the second electrode, wherein the organic material layer comprises a light emitting layer, and the light emitting layer comprises a combination including a compound represented by Formula 1 and a dopant, wherein the dopant is a green light emitting material: wherein in Formula 1: at least two of X1 to X3 are N, and any remaining is CR; R is hydrogen, deuterium, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group; Ar1 and Ar2 are each independently a substituted or unsubstituted aryl group or a substituted or unsubstituted heterocyclic group; Y is O or S; L is a phenylene group; a is 1 or 2; and Ls in the parenthesis are the same as or different from each other when a is 2. 2. The organic light emitting device of claim 1 , wherein Ar1 and Ar2 are each 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 anthracenyl group; a substituted or unsubstituted phenanthrenyl group; a substituted or unsubstituted pyrenyl group; a substituted or unsubstituted perylenyl group; a substituted or unsubstituted triphenylene group; a substituted or unsubstituted chrysenyl group; a substituted or unsubstituted fluorenyl group; a substituted or unsubstituted dibenzothiophene group; or a substituted or unsubstituted dibenzofuran group. 3. The organic light emitting device of claim 1 , wherein the compound of Formula 1 is any one of the following compounds: 4. An organic light emitting device, comprising: a first electrode; a second electrode provided to face the first electrode; and an organic material layer having one or more layers provided between the first electrode and the second electrode, wherein one of the one or more layers of the organic material layer is a light emitting layer comprising a combination including a compound of Formula 1, a fluorescent host or a phosphorescent host, and an iridium (Ir)-based dopant: wherein in Formula 1: at least two of X1 to X3 are N, and any remaining is CR; R is hydrogen, deuterium, a substituted or unsubstituted alkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group; Ar1 and Ar2 are each independently a substituted or unsubstituted aryl group or a substituted or unsubstituted heterocyclic group; Y is O or S; L is a substituted or unsubstituted arylene group; a is 1 or 2; and Ls in the parenthesis are the same as or different from each other when a is 2. 5. The organic light emitting device of claim 4 , wherein the compound of Formula 1 is any one of the following compounds: 6. The organic light emitting device of clai
Electron injection layers · CPC title
Electron transporting layers · CPC title
comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole · CPC title
comprising two or more different heteroatoms per ring (H10K85/652 takes precedence) · CPC title
containing three or more hetero rings · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.