Dihydroimidazo pyrimido pyrimidinone compound
US-2024010655-A1 · Jan 11, 2024 · US
US9728730B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9728730-B2 |
| Application number | US-201514602974-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 22, 2015 |
| Priority date | Apr 22, 2014 |
| Publication date | Aug 8, 2017 |
| Grant date | Aug 8, 2017 |
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Provided are a compound, a composition, a light emitting material including the same, an organic optoelectric device and a display device including the organic optoelectric device, and the compound is represented by the following Chemical Formula I, in the Chemical Formula I, X 1 to X 8 , L and R 1 to R 5 are the same as defined in the specification.
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What is claimed is: 1. A compound for an organic optoelectric device represented by the following Chemical Formula I: wherein, in the Chemical Formula I, X 1 to X 8 are independently N, C or CR a , L is a single bond, a substituted or unsubstituted C6 to C30 arylene group, or a substituted or unsubstituted C2 to C30 heteroarylene group, R 1 is a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heteroaryl group, or a combination thereof, R 2 to R 5 and R a are independently hydrogen, deuterium, a substituted or unsubstituted C6 to C30 aryl group, or a substituted or unsubstituted C2 to C30 heteroaryl group, and the R 2 and R 3 , or R 4 and R 5 are independently present, or are fused to each other to provide a ring. 2. The compound for an organic optoelectric device of claim 1 , wherein the Chemical Formula I is represented by one of the following Chemical Formulae 1 to 4: wherein, in the Chemical Formulae 1 to 4, L is a single bond, a substituted or unsubstituted C6 to C30 arylene group, or a substituted or unsubstituted C2 to C30 heteroarylene group, R 1 is a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heteroaryl group, or a combination thereof, and R 2 to R 5 are independently hydrogen, deuterium, a substituted or unsubstituted C6 to C30 aryl group, or a substituted or unsubstituted C2 to C30 heteroaryl group. 3. The compound for an organic optoelectric device of claim 1 , wherein the Chemical Formula I is represented by one of the following Chemical Formulae 5 to 8: wherein, in the Chemical Formulae 5 to 8, L is a single bond, a substituted or unsubstituted C6 to C30 arylene group, or a substituted or unsubstituted C2 to C30 heteroarylene group, R 1 is a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C2 to C30 heteroaryl group, or a combination thereof, and R 2 is hydrogen, deuterium, a substituted or unsubstituted C6 to C30 aryl group, or a substituted or unsubstituted C2 to C30 heteroaryl group. 4. The compound for an organic optoelectric device of claim 1 , wherein the R 1 is a heteroaryl-containing moiety selected from moieties in the following Group I: [Group I] wherein, in the Group I, Z are independently N or CR b , at least one of Z is N, W is NR c , O, S, SO, SO 2 , CR d R e , or SiR f R g , wherein R b to R g are independently hydrogen, deuterium, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C3 to C30 cycloalkyl group, a substituted or unsubstituted C3 to C30 heterocycloalkyl group, a substituted or unsubstituted C6 to C30 aryl group, or a substituted or unsubstituted C2 to C30 heteroaryl group, and * is a linking point and may be positioned at one of element consisting of the functional groups. 5. The compound for an organic optoelectric device of claim 4 , wherein the moieties listed in the Group I is represented by one of moieties listed in the following Group I-1: [Group I-1] wherein, in the Group I-1, * is a linking point. 6. The compound for an organic optoelectric device of claim 1 , wherein the R 1 is selected from moieties in the following Group II: [Group II] wherein, in the Group II, R 101 to R 104 are independently hydrogen, deuterium, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C1 to C30 silyl group, a substituted or unsubstituted C6 to C30 aryl group, or a combination thereof, Y is O, S, SO, or SO 2 , and * is a linking point and may be positioned at one of element consisting of the functional groups. 7. The compound for an organic optoelectric device of claim 6 , wherein the moieties listed in the Group II are represented by one of moieties listed in the following Group II-1: [Group II-1] wherein, in the Group II-1, * is a linking point. 8. The compound for an organic optoelectric device of claim 1 , wherein the substituted or unsubstituted C6 to C30 arylene group, or a substituted or unsubstituted C2 to C30 heteroarylene group is a substituted or unsubstituted phenylene group, a substituted or unsubstituted biphenylene group, a substituted or unsubstituted terphenylene group, a substituted or unsubstituted pyridylene group, or a combination thereof. 9. The compound for an organic optoelectric device of claim 8 , wherein the substituted or unsubstituted phenylene group, or the substituted or unsubstituted pyridylene group are one of moieties of the following Group III: [Group III] wherein, in the Group III, * is a linking point. 10. The composition for an organic optoelectric device comprising the first compound for an organic optoelectric device of claim 4 and a second compound for an organic optoelectric device of claim 6 . 11. The composition for an organic optoelectric device of claim 10 , wherein the first compound for an organic optoelectric device is selected from compounds listed in the following Group I-2: [Group I-2] 12. The composition for an organic optoelectric device of claim 10 , wherein the second compound for an organic optoelectric device is selected from compounds listed in the following Group II-2: [Group II-2]
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