Aromatic heterocyclic derivative, material for organic electroluminescent element, and organic electroluminescent element
US-2018102485-A1 · Apr 12, 2018 · US
US10538510B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10538510-B2 |
| Application number | US-201715788136-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 19, 2017 |
| Priority date | Dec 2, 2016 |
| Publication date | Jan 21, 2020 |
| Grant date | Jan 21, 2020 |
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Disclosed are a compound for an organic optoelectronic device represented by Chemical Formula 1, a composition for an organic optoelectronic device, an organic optoelectronic device including the same, and a display device. Details of Chemical Formula 1 are the same as defined in the specification.
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What is claimed is: 1. A composition for an organic optoelectronic device, comprising: a first compound represented by Chemical Formula 1; and a second compound represented by Chemical Formula 2, wherein, in Chemical Formula 1, R 1 to R 7 are independently hydrogen, deuterium, a substituted or unsubstituted C1 to C5 alkyl group, or a substituted or unsubstituted C6 to C18 aryl group, L is a single bond, a substituted or unsubstituted C6 to C20 arylene group, or a substituted or unsubstituted C2 to C30 heteroarylene group, and ET is a substituted or unsubstituted C2 to C30 heterocyclic group including at least two N's, wherein, in Chemical Formula 1, the “substituted” refers to replacement of at least one hydrogen by deuterium, a cyano group, a C1 to C20 alkyl group, a C6 to C30 aryl group, or a C2 to C30 heteroaryl group; wherein, in Chemical Formula 2, Y 1 and Y 2 are independently a single bond, a substituted or unsubstituted C6 to C30 arylene group, a substituted or unsubstituted C2 to C30 heteroarylene group, or a combination thereof, A 1 and A 2 are independently substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof, R 8 to R 13 are independently hydrogen, deuterium, a substituted or unsubstituted C1 to C20 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heterocyclic group, or a combination thereof, and l is an integer of 0 to 2; wherein the “substituted” refers to replacement of at least one hydrogen by deuterium, a C1 to C4 alkyl group, a C6 to C18 aryl group, or a C2 to C30 heteroaryl group. 2. The composition for an organic optoelectronic device as claimed in claim 1 , wherein ET of Chemical Formula 1 is a substituted or unsubstituted pyrimidinyl group, a substituted or unsubstituted triazinyl group, a substituted or unsubstituted quinazolinyl group, a substituted or unsubstituted benzoquinazolinyl group, a substituted or unsubstituted benzothieno[3,2-d]pyrimidinyl group, a substituted or unsubstituted benzothieno[2,3-d]pyrimidinyl group, a substituted or unsubstituted benzofuro[3,2-d]pyrimidinyl group, or a substituted or unsubstituted benzofuro[2,3-d]pyrimidinyl group. 3. The composition for an organic optoelectronic device as claimed in claim 1 , wherein the first compound represented by Chemical Formula 1 is represented by one of Chemical Formula 1-I, Chemical Formula 1-II, Chemical Formula 1-III, Chemical Formula 1-IV, Chemical Formula 1-V and Chemical Formula 1-VI: wherein, in Chemical Formula 1-I, Chemical Formula 1-II, Chemical Formula 1-III, Chemical Formula 1-IV, Chemical Formula 1-V, and Chemical Formula 1-VI, Z 1 , Z 3 , Z 5 , and Z 6 to Z 5 are independently N or CR a , m and n are independently an integer of 0 to 2, X is O or S, at least two of Z 1 , Z 3 and Z 5 of Chemical Formula 1-I to Chemical Formula 1-V are N, at least two of Z 11 to Z 14 of Chemical Formula 1-VI are N, R a and R 1 to R 7 are independently hydrogen, deuterium, a substituted or unsubstituted C1 to C5 alkyl group, or a substituted or unsubstituted C6 to C18 aryl group, and L is a single bond, a substituted or unsubstituted C6 to C20 arylene group, or a substituted or unsubstituted C2 to C30 heteroarylene group. 4. The composition for an organic optoelectronic device as claimed in claim 1 , wherein ET of Chemical Formula 1 is selected from substituents of Group I: wherein, in Group I, is a linking point with “L” of Chemical Formula 1. 5. The composition for an organic optoelectronic device as claimed in claim 1 , wherein L of Chemical Formula 1 is a single bond, a substituted or unsubstituted phenylene group, a substituted or unsubstituted biphenylene group, a substituted or unsubstituted terphenylene group, or a substituted or unsubstituted naphthylene group. 6. The composition for an organic optoelectronic device as claimed in claim 1 , wherein the first compound represented by Chemical Formula 1 is selected from compounds of Group 1: 7. The composition for an organic optoelectronic device as claimed in claim 1 , wherein A 1 and A 2 of Chemical Formula 2 are independently a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted quaterphenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthracenyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted pyridinyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or un
Ortho-condensed systems · CPC title
linked by a carbon chain containing aromatic rings · CPC title
the oxygen-containing ring being five-membered · CPC title
directly linked by a ring-member-to-ring-member bond · CPC title
containing two nitrogen atoms as heteroatoms · CPC title
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