Organic molecules, in particular for use in optoelectronic devices
US-2019019960-A1 · Jan 17, 2019 · US
US12098156B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12098156-B2 |
| Application number | US-201917278406-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 15, 2019 |
| Priority date | Nov 27, 2018 |
| Publication date | Sep 24, 2024 |
| Grant date | Sep 24, 2024 |
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Provided is a compound of Chemical Formula 1: wherein: X 1 to X 6 are each independently CH or N, provided that at least one of X 1 to X 6 is N; Ar 1 to Ar 4 are each independently a substituted or unsubstituted: C 6-60 aryl or C 2-60 heteroaryl containing one or more of N, O, and S, provided that at least one of Ar 1 to Ar 4 is any one of: R 2 is hydrogen, deuterium, or a substituted or unsubstituted: C 6-60 aryl or C 2-60 heteroaryl containing one or more of N, O and S; each R 3 is independently hydrogen, deuterium, or a substituted or unsubstituted: C 6-60 aryl or C 2-60 heteroaryl containing one or more of N, O, and S; each R 1 is independently hydrogen, deuterium, or a substituted or unsubstituted: C 6-60 aryl or C 2-60 heteroaryl containing one or more of N, O and S; and n is an integer of 0 to 8, and organic light emitting devices including the same.
Opening claim text (preview).
The invention claimed is: 1. A compound of Chemical Formula 1: wherein, in Chemical Formula 1: X 1 to X 6 are each independently CH or N, with the proviso that at least one of X 1 to X 6 is N; Ar 1 to Ar 4 are each independently a substituted or unsubstituted C 6-60 aryl or a substituted or unsubstituted C 2-60 heteroaryl containing any one or more heteroatoms selected from the group consisting of N, O, and S, with the proviso that at least one of Ar 1 to Ar 4 is any one substituent selected from the group consisting of the following substituents: wherein: R 2 is hydrogen, deuterium, a substituted or unsubstituted C 6-60 aryl, or a substituted or unsubstituted C 2-60 heteroaryl containing any one or more selected from the group consisting of N, O and S; each R 3 is independently hydrogen, deuterium, a substituted or unsubstituted C 6-60 aryl, or a substituted or unsubstituted C 2-60 heteroaryl containing any one or more selected from the group consisting of N, O and S; a is an integer of 0 to 8; each R 1 is independently hydrogen, deuterium, a substituted or unsubstituted C 6-60 aryl, or a substituted or unsubstituted C 2-60 heteroaryl containing any one or more selected from the group consisting of N, O and S; and n is an integer of 0 to 8. 2. The compound of claim 1 , wherein X 1 to X 6 are each independently CH or N, with the proviso that at least one of X 1 to X 3 is N and at least one of X 4 to X 6 is N. 3. The compound of claim 1 , wherein R 2 and R 3 are each independently hydrogen, deuterium, phenyl, or phenyl substituted with 5 deuteriums. 4. The compound of claim 1 , wherein: Ar 1 to Ar 4 are each independently a phenyl, biphenylyl, naphthyl, phenanthrenyl, triphenylenyl, dibenzofuranyl, dibenzothiophenyl, dimethylfluorenyl, carbazolyl, phenyl carbazolyl, phenyl substituted with five deuteriums, carbazolyl substituted with phenyl substituted with 5 deuteriums, or with the proviso that at least one of Ar 1 to Ar 4 is any one substituent selected from the group consisting of the following substituents: 5. The compound of claim 1 , wherein R 1 is hydrogen, phenyl or phenyl substituted with 1 to 5 deuteriums. 6. The compound of claim 1 , wherein n is 0 or 1. 7. The compound of claim 1 , wherein: the compound of Chemical Formula 1 is any one compound selected from the group consisting of the following compounds: 8. An organic light emitting device, comprising: a first electrode; a second electrode that is disposed opposite to the first electrode; and one or more organic material layers that are disposed between the first electrode and the second electrode, wherein one or more layers of the one or more organic material layers comprise the compound of claim 1 .
Multiple hosts in the emissive layer · CPC title
Interrelation of parameters between multiple constituent active layers or sublayers, e.g. HOMO values in adjacent layers · CPC title
Triplet emission · CPC title
characterised by the electroluminescent [EL] layers · CPC title
comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene · CPC title
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