Compound and organic light-emitting device including the same
US-2016118599-A1 · Apr 28, 2016 · US
US11094889B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11094889-B2 |
| Application number | US-201715777811-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 22, 2017 |
| Priority date | Feb 23, 2016 |
| Publication date | Aug 17, 2021 |
| Grant date | Aug 17, 2021 |
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The present specification relates to a hetero-cyclic compound and an organic light emitting device comprising the same.
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The invention claimed is: 1. A hetero-cyclic compound represented by the following Chemical Formula 1: wherein, in Chemical Formula 1, R1 is deuterium; a nitrile group; a nitro group; a hydroxyl group; a carbonyl group; an ester group; an imide group; an amide group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted aryloxy group; a substituted or unsubstituted alkylthioxy group; a substituted or unsubstituted arylthioxy group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted boron group; a substituted or unsubstituted amine group; a substituted or unsubstituted arylphosphine group; a substituted or unsubstituted aryl group; or a substituted or unsubstituted heteroaryl group; L1 is a direct bond; a substituted or unsubstituted arylene group; or a substituted or unsubstituted heteroarylene group; Ar1 is a structure represented by the following Chemical Formula 3; m is an integer of 1 to 4; n is an integer of 0 to 3; 1≤n+m≤4; and when m and n are each 2 or greater, each of L1-Ar1, and R1 is the same as or different from each other, respectively, wherein, in Chemical Formula 3, X1 is N or CR11, X2 is N or CR12 and X3 is N or CR13; at least one of X1 to X3 is N; and any one of G2 to G4 and R11 to R13 is a site bonding to L1 of Chemical Formula 1, and the rest are the same as or different from each other and each independently hydrogen; deuterium; a nitrile group; a nitro group; a hydroxyl group; a carbonyl group; an ester group; an imide group; an amide group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted aryloxy group; a substituted or unsubstituted alkylthioxy group; a substituted or unsubstituted arylthioxy group; a substituted or unsubstituted alkylsulfoxy group; a substituted or unsubstituted arylsulfoxy group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted boron group; a substituted or unsubstituted amine group; a substituted or unsubstituted arylphosphine group; a substituted or unsubstituted aryl group; or a substituted or unsubstituted heteroaryl group, with the proviso that when R1, L1 and/or Ar1 contain a carbazolyl group, the carbazolyl group is not substituted with a nitrile group. 2. The hetero-cyclic compound of claim 1 , wherein Chemical Formula 1 is represented by any one of the following Chemical Formulae 1-1 to 1-4: wherein, in Chemical Formulae 1-1 to 1-4, definitions of L1, Ar1, R1 and n are the same as in Chemical Formula 1. 3. The hetero-cyclic compound of claim 1 , wherein Chemical Formula 1 is selected as any one of the following compounds:
comprising only nitrogen as heteroatom (H10K85/652 takes precedence) · CPC title
linked by a carbon chain containing aromatic rings · CPC title
Interrelation of parameters between multiple constituent active layers or sublayers, e.g. HOMO values in adjacent layers · CPC title
spiro-condensed with carbocyclic rings or ring systems · CPC title
Ring systems having three or more relevant rings · CPC title
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