Organic compound and light emitting diode and organic light emitting diode display device using the same
US-2017346012-A1 · Nov 30, 2017 · US
US11005047B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11005047-B2 |
| Application number | US-201815976879-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 11, 2018 |
| Priority date | May 11, 2018 |
| Publication date | May 11, 2021 |
| Grant date | May 11, 2021 |
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A heteroaromatic compound which can be used as the fluorescent guest material in the light emitting layer of the organic electroluminescence device is disclosed. The organic electroluminescence device employing the heteroaromatic compound of the present invention shows lower power consumption, higher efficiency, and longer half-life time than the existed organic electroluminescence devices.
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What is claimed is: 1. A heteroaromatic compound of formula (1) below: wherein Ar 1 and Ar 2 are independently an aryl group or a heteroaryl group having 4 to 6 ring carbon atoms; Ar 3 is a cycloalkyl group, a cycloalkenyl group, or an aryl group having 5 to 6 ring carbon atoms; R 1 and R 2 are independently a hydrogen atom, a unsubstituted alkyl group having 1 to 36 carbon atoms, a unsubstituted aryl group having 6 to 36 carbon atoms, or a unsubstituted aralkyl group having 6 to 36 carbon atoms; W represents a divalent bridge selected from the group consisting of O, S, CR 3 R 4 , NR 5 , and SiR 6 R 7 , and R 3 to R 7 are independently a hydrogen atom or a unsubstituted alkyl group having 1 to 20 carbon atoms; X is absent or a divalent bridge selected from the group consisting of O, S, CR 8 R 9 , NR 10 , and SiR 11 R 12 ; A is absent or represents formula (2) below: wherein Y represents a divalent bridge selected from the group consisting of O, S, CR 13 R 14 , NR 15 , and SiR 16 R 17 ; and R 8 to R 17 are independently a hydrogen atom, a unsubstituted alkyl group having 1 to 36 carbon atoms, a unsubstituted aryl group having 6 to 36 carbon atoms, a unsubstituted aralkyl group having 6 to 36 carbon atoms, or a unsubstituted heteroaryl group having 3 to 36 carbon atoms. 2. The heteroaromatic compound according to claim 1 , wherein Ar 1 and Ar 2 are independently 3. The heteroaromatic compound according to claim 1 , wherein Ar 3 is 4. A heteroaromatic compound selected from the group consisting of following compounds: 5. An organic electroluminescence device, comprising a pair of electrodes composed of a cathode and an anode, and a light emitting layer between the pair of electrodes, wherein the light emitting layer comprises the heteroaromatic compound according to claim 4 . 6. The organic electroluminescence device according to claim 5 , wherein the heteroaromatic compound of formula (1) is a fluorescent dopant material. 7. The organic electroluminescence device according to claim 5 , wherein the light emitting layer emits blue fluorescence. 8. The organic electroluminescence device according to claim 5 , wherein the organic electroluminescence device is a lighting panel. 9. The organic electroluminescence device according to claim 5 , wherein the organic electroluminescence device is a backlight panel.
Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00 · CPC title
spiro-condensed with carbocyclic rings or ring systems, e.g. griseofulvins · CPC title
bridged by heteroatoms, e.g. N, P, Si or B · CPC title
Spiro-condensed systems · CPC title
directly linked by a ring-member-to-ring-member bond · CPC title
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