Organic electroluminescent materials and devices
US-2015243893-A1 · Aug 27, 2015 · US
US9331288B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9331288-B2 |
| Application number | US-201514722870-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 27, 2015 |
| Priority date | May 28, 2014 |
| Publication date | May 3, 2016 |
| Grant date | May 3, 2016 |
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A compound represented by Formula 1. An organic electric element includes a first electrode, a second electrode, and an organic material layer between the first electrode and the second electrode. The organic material layer includes the compound represented by Formula 1. When the organic electric element includes the compound in the organic material layer, driving voltage, luminous efficiency, color purity, stability, and life span can be improved.
Opening claim text (preview).
The invention claimed is: 1. A compound represented by Formula 1 below: in Formula 1 above, S ring is a C 4 -C 8 heterocyclic group containing S (sulfer), N ring is a C 4 -C 8 heterocyclic group containing N (nitrogen), l, m, and n are each an integer from 0 to 4, R 1 to R 3 are independently selected from the group consisting of halogen, deuterium, a cyano group, a C 6 -C 60 aryl group, a C 2 -C 60 heterocyclic group containing at least one heteroatom selected from O, N, S, Si, and P, a C 1 -C 30 alkoxy group, a C 1 -C 60 alkyl group, a C 2 -C 60 alkenyl group, and -L 1 -N(R′)(R″), and any two adjacent groups of R 1 s to R 3 s are optionally linked together to form a fused ring, L and L 1 are independently selected from the group consisting of a single bond, a C 6 -C 60 arylene group, and a C 2 -C 60 heteroarylene group containing at least one heteroatom selected from O, N, S, Si, and P, wherein, the arylene group, and the heteroarylene group are optionally substituted by one or more substituents selected from the group consisting of deuterium, halogen, a silane group, a siloxane group, a boron group, a germanium group, a cyano group, a nitro group, a C 1 -C 20 alkylthio group, a C 1 -C 20 alkoxy group, a C 1 -C 20 alkyl group, a C 2 -C 20 alkenyl group, a C 2 -C 20 alkynyl group, a C 6 -C 20 aryl group, a C 6 -C 20 aryl group substituted by deuterium, a C 2 -C 60 heterocyclic group containing at least one heteroatom selected from O, N, S, Si, and P, a C 3 -C 20 cycloalkyl group, a C 7 -C 20 arylalkyl group, and a C 8 -C 20 arylalkenyl group, Ar is an unsubstituted C 6 -C 60 aryl group, a C 6 -C 60 aryl group substituted with deuterium, or a C 6 -C 60 aryl group substituted with a C6-C20 aryl group, R′ and R″ are independently selected from the group consisting of a C 6 -C 60 aryl group, and a C 2 -C 60 heterocyclic group containing at least one heteroatom selected from O, N, S, Si, and P, X and Y are independently selected from the group consisting of a single bond, C(R 4 )(R 5 ), N(R 4 ), O, S, Se, and Si(R 4 )(R 5 ), R 4 and R 5 are independently selected from the group consisting of hydrogen, deuterium, a C 6 -C 60 aryl group, a C 2 -C 60 heterocyclic group containing at least one heteroatom selected from O, N, S, Si, and P, a C 1 -C 30 alkoxy group, a C 1 -C 60 alkyl group, and a C 2 -C 60 alkenyl group, when Ar, R 1 to R 5 , R′, and R″ are an aryl group, or a heterocyclic group, Ar, R 1 to R 5 , R′, and R″ are optionally substituted by one or more substituents selected from the group consisting of deuterium, halogen, a silane group, a siloxane group, a boron group, a germanium group, a cyano group, a nitro group, a C 1 -C 20 alkylthio group, a C 1 -C 20 alkoxy group, a C 1 -C 20 alkyl group, a C 2 -C 20 alkenyl group, a C 2 -C 20 alkynyl group, a C 6 -C 20 aryl group, a C 6 -C 20 aryl group substituted by deuterium, a C 2 -C 60 heterocyclic group containing at least one heteroatom selected from O, N, S, Si, and P, a C 3 -C 20 cycloalkyl group, a C 7 -C 20 arylalkyl group, and a C 8 -C 20 arylalkenyl group, and when R 1 to R 5 are an alkyl group, alkenyl group or alkoxy, R 1 to R 5 are optionally substituted by one or more substituents selected from the group consisting of deuterium, halogen, a silane group, a siloxane group, a boron group, a germanium group, a cyano group, a nitro group, a C 1 -C 20 alkylthio group, a C 1 -C 20 alkoxy group, a C 1 -C 20 alkyl group, a C 2 -C 20 alkenyl group, a C 2 -C 20 alkynyl group, a C 6 -C 20 aryl group, a C 6 -C 20 aryl group substituted by deuterium, a C 2 -C 60 heterocyclic group containing at least one heteroatom selected from O, N, S, Si, and P, a C 3 -C 20 cycloalkyl group, a C 7 -C 20 arylalkyl group, and a C 8 -C 20 arylalkenyl group. 2. The compound as claimed in claim 1 , wherein the compound is represented by one of Formulas below: in Formulas above, Ar, R 1 to R 3 , l, m, n, X and Y are as defined in Formula 1 of claim 1 . 3. The compound as claimed in claim 1 , wherein Z is any one of groups below: in Formulas above, Ar, X and Y are as defined in Formula 1 of claim 1 . 4. The compound as claimed in claim 1 , wherein the compound is represented by any one of Formulas below: in Formulas above, Ar, R 1 to R 3 , l, m and n are as defined in Formula 1 of claim 1 . 5. The compound as claimed in claim 1 , wherein Ar is any one of groups below: 6. The compound as claimed in claim 1 , being any one of compounds below:
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