Compound, binder resin, negative-type photosensitive resin composition, and display device comprising black bank formed using same

US2022348716A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2022348716-A1
Application numberUS-202017640710-A
CountryUS
Kind codeA1
Filing dateNov 4, 2020
Priority dateNov 8, 2019
Publication dateNov 3, 2022
Grant date

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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 application relates to a compound of Formula 1, a binder resin, a negative-type photosensitive resin composition, and a display device comprising a black bank formed using same.

First claim

Opening claim text (preview).

1 . A compound represented by the following Formula 1: wherein, in the Formula 1, R1 and R2 are the same as or different from each other, and are each independently hydrogen; —CO-L-R; or —CONR′R″, L is a substituted or unsubstituted alkenylene group; a substituted or unsubstituted cycloalkenylene group; or a substituted or unsubstituted arylene group, R, R′, and R″ are the same as or different from each other, and are each independently hydrogen; —COOH; or a substituted or unsubstituted alkyl group, R3 and R4 are the same as or different from each other, and are each independently hydrogen; or a substituted or unsubstituted alkyl group, r3 and r4 are an integer from 0 to 4, and when r3 is 2 or higher, R3s are the same as or different from each other, and when r4 is 2 or higher, R4s are the same as or different from each other, L1 and L2 are the same as or different from each other, and are each independently a substituted or unsubstituted alkylene group, M1 and M2 are -M1′-M2′-M3′-, M1′, M2′ and M3′ are the same as or different from each other, and are each independently a direct bond; —SO 2 —; a substituted or unsubstituted alkylene group; or a substituted or unsubstituted arylene group, and n is an integer from 1 to 30. 2 . The compound of claim 1 , wherein M1′ and M3′ are the same as or different from each other, and are each independently a direct bond; or a substituted or unsubstituted arylene group, and M2′ is a direct bond; —SO 2 —; or a substituted or unsubstituted arylene group. 3 . The compound of claim 1 , wherein M1 and M2 are each represented by the following Formula 2: in the Formula 2, means a moiety linked to the Formula 1, M2′ is as defined in claim 1 , R13 and R14 are the same as or different from each other, and are each independently hydrogen; a hydroxyl group; or a substituted or unsubstituted alkyl group, and r13 and r14 are an integer from 1 to 4, and when r13 is 2 or higher, R13s are the same as or different from each other, and when r14 is 2 or higher, R14s are the same as or different from each other. 4 . The compound of claim 1 , wherein R1 and R2 are hydrogen. 5 . The compound of claim 1 , wherein R1 is —CO-L-R; or —CONR′R″, and L, R, R′, and R″ are as defined in claim 1 . 6 . The compound of claim 1 , wherein the compound has a weight average molecular weight of 3,000 g/mol to 8,000 g/mol. 7 . A binder resin comprising the compound of claim 1 . 8 . A negative-type photosensitive resin composition comprising: the binder resin of claim 7 ; a pigment dispersion; a polyfunctional monomer; a photoinitiator; and a solvent. 9 . The negative-type photosensitive resin composition of claim 8 , further comprising a surfactant. 10 . The negative-type photosensitive resin composition of claim 8 , wherein the pigment dispersion comprises a black organic pigment. 11 . The negative-type photosensitive resin composition of claim 8 , wherein based on 100 parts by weight of the negative-type photosensitive resin composition, the negative-type photosensitive resin composition comprises: 10 to 40 parts by weight of the binder resin; 20 to 40 parts by weight of the pigment dispersion; 0.1 to 10 parts by weight of the polyfunctional monomer; 0.1 to 5 parts by weight of the photoinitiator; and 20 to 50 parts by weight of the solvent. 12 . The negative-type photosensitive resin composition of claim 8 , wherein a coating film formed from the negative-type photosensitive resin composition has a taper angle of 150 or more and 300 or less when tested with the coating film has a thickness of 1.5 μm. 13 . A display device comprising a black bank formed from the negative-type photosensitive resin composition of claim 8 .

Assignees

Inventors

Classifications

  • C08G73/024Primary

    Polyamines containing oxygen in the form of ether bonds in the main chain · CPC title

  • Polyamines containing other atoms than carbon, hydrogen, nitrogen or oxygen in the main chain · CPC title

  • C08G73/02Primary

    Polyamines · CPC title

  • Macromolecular compounds which are rendered insoluble or differentially wettable (G03F7/075 takes precedence; macromolecular azides G03F7/012; macromolecular diazonium compounds G03F7/021) · CPC title

  • C07C217/80Primary

    having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings · CPC title

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Frequently asked questions

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What does patent US2022348716A1 cover?
The present application relates to a compound of Formula 1, a binder resin, a negative-type photosensitive resin composition, and a display device comprising a black bank formed using same.
Who is the assignee on this patent?
Lg Chemical Ltd
What technology area does this patent fall under?
Primary CPC classification C08G73/024. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Nov 03 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 3 related publications on this page (citations in our corpus or others sharing the same primary CPC).