Ii(pi)-conjugated compound, organic electroluminescence element material, light-emitting material, light-emitting thin film, organic electroluminescence element, display device, and illumination device
US-2018170914-A1 · Jun 21, 2018 · US
US2018051007A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2018051007-A1 |
| Application number | US-201615556465-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jun 3, 2016 |
| Priority date | Jun 3, 2015 |
| Publication date | Feb 22, 2018 |
| Grant date | — |
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 relates to a hetero-cyclic compound and an organic light emitting device comprising the same.
Opening claim text (preview).
1 . A hetero-cyclic compound represented by the following Chemical Formula 1: in Chemical Formula 1, X 1 to X 3 are the same as or different from each other, and are each independently N or C—CN, two of X 1 to X 3 are N, and R 1 to R 3 are the same as or different from each other, and are each independently selected from the group consisting of hydrogen; a substituted or unsubstituted straight-chained or branched alkyl group having 1 to 30 carbon atoms; a substituted or unsubstituted monocyclic or polycyclic cycloalkyl group having 3 to 30 carbon atoms; 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 arylphosphine group; a substituted or unsubstituted phosphine oxide group; a substituted or unsubstituted monocyclic or polycyclic aryl group having 6 to 30 carbon atoms; and a substituted or unsubstituted monocyclic or polycyclic hetero-cyclic group having 2 to 30 carbon atoms. 2 . The hetero-cyclic compound of claim 1 , wherein the hetero-cyclic compound represented by Chemical Formula 1 is represented by the following Chemical Formula 2 or 3: in Chemical Formulae 2 and 3, the definitions of R 1 to R 3 are the same as those in Chemical Formula 1. 3 . The hetero-cyclic compound of claim 1 , wherein R 1 to R 3 are the same as or different from each other, and are each independently selected from the group consisting of a substituted or unsubstituted phenyl group; a substituted or unsubstituted biphenyl group; a substituted or unsubstituted terphenyl group; and a substituted or unsubstituted fluorenyl group. 4 . The hetero-cyclic compound of claim 1 , wherein the compound represented by Chemical Formula 1 is any one of the following compounds 1 to 9: 5 . An organic light emitting device, comprising: a first electrode; a second electrode provided to face the first electrode; and one or more organic material layers provided between the first electrode and the second electrode, wherein one or more layers of the organic material layers comprise the hetero-cyclic compound of claim 1 . 6 . The organic light emitting device of claim 5 , wherein the organic material layer comprises a light emitting layer, and the light emitting layer comprises the hetero-cyclic compound. 7 . The organic light emitting device of claim 5 , wherein the organic material layer comprises an electron transporting layer, an electron injection layer, or a layer which simultaneously transports and injects electrons, and the electron transporting layer, the electron injection layer, or the layer which simultaneously transports and injects electrons comprises the hetero-cyclic compound. 8 . The organic light emitting device of claim 5 , wherein the organic material layer further comprises one or more selected from the group consisting of a hole injection layer, a hole transporting layer, a light emitting layer, an electron transporting layer, and an electron injection layer. 9 . The organic light emitting device of claim 5 , wherein the organic material layer comprises a light emitting layer, and the light emitting layer comprises a compound represented by the following Chemical Formula 1-A: in Chemical Formula 1-A, n1 is an integer of 1 or more, Ar3 is a substituted or unsubstituted monovalent or more benzofluorene group; a substituted or unsubstituted monovalent or more fluoranthene group; a substituted or unsubstituted monovalent or more pyrene group; or a substituted or unsubstituted monovalent or more chrysene group, L1 is a direct bond; a substituted or unsubstituted arylene group; or a substituted or unsubstituted heteroarylene group, Ar4 and Ar5 are the same as or different from each other, and are each independently a substituted or unsubstituted aryl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted arylalkyl group; or a substituted or unsubstituted heteroaryl group, or combine with each other to form a substituted or unsubstituted ring, and when n1 is 2 or more, two or more structures in the parenthesis are the same as or different from each other. 10 . The organic light emitting device of claim 9 , wherein L1 is a direct bond, Ar3 is a divalent pyrene group, Ar4 and Ar5 are the same as or different from each other, and are each independently an aryl group which is unsubstituted or substituted with a silyl group which is substituted with an alkyl group, and n1 is 2. 11 . The organic light emitting device of claim 5 , wherein the organic material layer comprises a light emitting layer, and the light emitting layer comprises a compound represented by the following Chemical Formula 2-A: in Chemical Formula 2-A, Ar11 and Ar12 are the same as or different from each other, and are each independently a substituted or unsubstituted monocyclic aryl group; or a substituted or unsubstituted polycyclic aryl group, and G1 to G8 are the same as or different from each other, and are each independently hydrogen; a substituted or unsubstituted monocyclic aryl group; or a substituted or unsubstituted polycyclic aryl group. 12 . The organic light emitting device of claim 11 , wherein Ar11 and Ar12 are a 1-naphthyl group, and G1 to G8 are hydrogen. 13 . The organic light emitting device of claim 9 , wherein the light emitting layer comprises a compound represented by the following Chemical Formula 2-A: in Chemical Formula 2-A, Ar11 and Ar12 are the same as or different from each other, and are each independently a substituted or unsubstituted monocyclic aryl group; or a substituted or unsubstituted polycyclic aryl group, and G1 to G8 are the same as or different from each other, and are each independently hydrogen; a substituted or unsubstituted monocyclic aryl group; or a substituted or unsubstituted polycyclic aryl group.
Non-condensed systems · CPC title
containing organic luminescent materials · CPC title
with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms · CPC title
having three or more double bonds between ring members or between ring members and non-ring members · CPC title
containing oxygen as the only heteroatom · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.