Bioorthogonal Turn-on Probes
US-2016121002-A1 · May 5, 2016 · US
US10112959B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10112959-B2 |
| Application number | US-201515529046-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 26, 2015 |
| Priority date | Dec 29, 2014 |
| Publication date | Oct 30, 2018 |
| Grant date | Oct 30, 2018 |
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The present disclosure relates to a novel compound, a color conversion film, a backlight unit and a display device comprising the same.
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The invention claimed is: 1. A compound of the following Chemical Formula 1: wherein, in Chemical Formula 1, at least one of R 1 to R 5 is selected from among the following structural formulae; R 6 is hydrogen; a nitrile group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted aryl group; a substituted or unsubstituted alkylaryl group; or a substituted or unsubstituted aromatic or aliphatic heterocyclic group; X 1 and X 2 are the same as or different from each other, and each independently F; a nitrile group; a substituted or unsubstituted alkynyl group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted aryloxy group; a substituted or unsubstituted arylalkoxy group; a substituted or unsubstituted aryl group; or a substituted or unsubstituted aromatic or aliphatic heterocyclic group, or bond to each other to form an aromatic or aliphatic ring; X 3 is a halogen group; a nitrile group; a carbonyl group; an ester group; an amide group; a sulfonate group; a substituted or unsubstituted alkyl group; a fluoroalkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted alkylsulfoxy group; a substituted or unsubstituted silyl group; a substituted or unsubstituted phosphine oxide group; or a substituted or unsubstituted alkylaryl group; Y 1 is CR 101 or N, Y 2 is CR 102 or N, Y 3 is CR 103 or N and Y 4 is CR 104 or N; and groups of R 1 to R 5 that are not the above-mentioned structural formulae, R 8 to R 13 and R 101 to R 104 are the same as or different from each other, and each independently hydrogen; deuterium; a halogen group; a nitrile group; a nitro group; a carbonyl group; an ester group; an imide group; an amide group; a sulfonate group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; 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 boron group; a substituted or unsubstituted arylphosphine group; a substituted or unsubstituted phosphine oxide group; a substituted or unsubstituted arylalkyl group; a substituted or unsubstituted alkylaryl group; a substituted or unsubstituted aryl group; or a substituted or unsubstituted aromatic or aliphatic heterocyclic group, and R 9 and R 10 bond to each other to form an aliphatic or aromatic ring, and R 12 and R 13 bond to each other to form an aliphatic or aromatic ring. 2. The compound of claim 1 , wherein R 1 to R 4 are the same as or different from each other, and each independently hydrogen, deuterium, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkylaryl group, a substituted or unsubstituted arylalkyl group, a substituted or unsubstituted aryl group, or one of the following structural formulae: wherein definitions of R 8 to R 13 are the same as those described above. 3. The compound of claim 1 , wherein R 5 is hydrogen, deuterium, or one of the following structural formulae: wherein definitions of R 8 to R 13 are the same as those described above. 4. The compound of claim 1 , wherein Y 1 to Y 4 are the same as or different from each other, and each independently CH, CF or N. 5. The compound of claim 1 , wherein the compound of Chemical Formula 1 has a maximum light emission peak present in 520 nm to 550 nm in a film state. 6. The compound of claim 1 , wherein the compound of Chemical Formula 1 has a maximum light emission peak present in 520 nm to 550 nm in a film state, and a half-width of the light emission peak is 50 nm or less. 7. The compound of claim 1 , wherein the compound of Chemical Formula 1 has a maximum light emission peak present in 610 nm to 650 nm in a film state. 8. The compound of claim 1 , wherein the compound of Chemical Formula 1 has a maximum light emission peak present in 610 nm to 650 nm in a film state, and a half-width of the light emission peak is 60 nm or less. 9. The compound of claim 1 , wherein the compound of Chemical Formula 1 has quantum efficiency of 0.9 or more. 10. The compound of claim 1 , wherein Chemical Formula 1 is selected from among the following structural formulae: 11. A color conversion film comprising: a resin matrix; and the compound of Chemical Formula 1 of claim 1 dispersed into the resin matrix. 12. A backlight unit comprising the color conversion film of claim 11 . 13. A display device comprising the backlight unit of claim 12 .
without C-boron linkages · CPC title
Boron compounds · CPC title
Boron-containing compounds {(C08K5/0091 takes precedence)} · CPC title
using wavelength conversion means distinct or spaced from the light-generating element, e.g. a remote phosphor layer · CPC title
Elements containing photoluminescent material distinct from or spaced from the light source (shades F21V1/17; globes, bowls or cover glasses F21V3/08, F21V3/12; refractors F21V5/10; reflectors F21V7/26, F21V7/30; elements with provision for controlling the spectral properties or intensity F21V9/40) · CPC title
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