Metal complex and color conversion film comprising same

US10112959B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10112959-B2
Application numberUS-201515529046-A
CountryUS
Kind codeB2
Filing dateOct 26, 2015
Priority dateDec 29, 2014
Publication dateOct 30, 2018
Grant dateOct 30, 2018

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present disclosure relates to a novel compound, a color conversion film, a backlight unit and a display device comprising the same.

First claim

Opening claim text (preview).

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 .

Assignees

Inventors

Classifications

  • C07F5/022Primary

    without C-boron linkages · CPC title

  • C07F5/02Primary

    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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Frequently asked questions

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What does patent US10112959B2 cover?
The present disclosure relates to a novel compound, a color conversion film, a backlight unit and a display device comprising the same.
Who is the assignee on this patent?
Lg Chemical Ltd
What technology area does this patent fall under?
Primary CPC classification C07F5/022. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 30 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).