Liquid Crystal composition

US9644148B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9644148-B2
Application numberUS-201514719854-A
CountryUS
Kind codeB2
Filing dateMay 22, 2015
Priority dateMay 26, 2014
Publication dateMay 9, 2017
Grant dateMay 9, 2017

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

Provided is a composition that can form a polarizing film with high dichroic ratio, which contains a compound having a function as a dichroic dye and having a local maximum absorption in a wavelength range of 350 to 550 nm. The composition contains a compound represented by the formula (1) and a polymerizable liquid crystal compound: wherein Y represents a group represented by the formula (Y1) or the formula (Y2)

First claim

Opening claim text (preview).

What is claimed is: 1. A composition comprising a compound represented by the formula (1) and a polymerizable liquid crystal compound: wherein Y represents a group represented by the formula (Y1) or the formula (Y2); R 1 represents an alkyl group having 1 to 20 carbon atoms, an alkoxy group having 1 to 20 carbon atoms, or —N(R)(R 0 ); wherein R and R 0 each independently represent a hydrogen atom or an alkyl group having 1 to 10 carbon atoms, or R and R 0 are bonded together to form a ring together with the nitrogen atom to which R and R 0 are bonded; one or more hydrogen atoms constituting the alkyl group having 1 to 20 carbon atoms, the alkoxy group having 1 to 20 carbon atoms, or the alkyl group having 1 to 10 carbon atoms are independently optionally substituted with an atom or a group selected from the group consisting of a halogen atom, a hydroxyl group and an optionally substituted amino group; the alkyl group having 1 to 20 carbon atoms, the alkoxy group having 1 to 20 carbon atoms, and the alkyl group having 1 to 10 carbon atoms each optionally have an ether linkage (—O—) between carbon atoms constituting them; R 7 and R 8 are substituents other than a hydrogen atom and are each independently an alkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, a halogen atom, or a cyano group; one or more hydrogen atoms constituting the alkyl group having 1 to 4 carbon atoms or the alkoxy group having 1 to 4 carbon atoms are independently optionally substituted with a halogen atom or a hydroxyl group; p and q are each independently an integer of 0 to 2; R 2 and R 3 each independently represent a hydrogen atom or an alkyl group having 1 to 10 carbon atoms, or R 2 and R 3 are bonded together to form a ring together with the nitrogen atom to which R 2 and R 3 are bonded; one or more hydrogen atoms constituting the alkyl group having 1 to 10 carbon atoms are independently optionally substituted with an atom or a group selected from the group consisting of a halogen atom, a hydroxyl group and an optionally substituted amino group; and the alkyl group having 1 to 10 carbon atoms optionally have an ether linkage (—O—) between carbon atoms constituting it; wherein * shows a bonding site to N; P 1 and P 2 each independently represent a sulfur atom, an oxygen atom or —NR 10 — wherein R 10 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms; Q 1 and Q 2 each independently represent a nitrogen atom or ═CH—. 2. The composition according to claim 1 , wherein the compound represented by the formula (1) is a compound represented by the formula (1a): wherein Y and R 1 to R 3 respectively represent as defined in claim 1 . 3. The composition according to claim 1 , wherein the polymerizable liquid crystal compound exhibits a smectic liquid crystal phase. 4. The composition according to claim 1 , wherein the composition further comprises a polymerization initiator. 5. A polarizing film formed from the composition according to claim 1 . 6. The polarizing film according to claim 5 , wherein a local maximum absorption wavelength (λmax1) of the polarizing film according to claim 5 is longer than a local maximum absorption wavelength (λmax2) of the compound represented by the formula (1) contained in the polarizing film. 7. The polarizing film according to claim 6 , wherein a difference between λmax 1 and λmax 2 is 15 nm or longer. 8. The polarizing film according to claim 5 , wherein the polarizing film exhibits a Bragg peak in x-diffraction measurement. 9. A liquid crystal display device comprising the polarizing film according to claim 5 . 10. A liquid crystal cell comprising a substrate, a liquid crystal layer, and the polarizing film according to claim 5 . 11. The liquid crystal cell according to claim 10 , wherein the polarizing film is disposed between the substrate and the liquid crystal layer. 12. The liquid crystal cell according to claim 11 , further comprising a color filter disposed between the substrate and the liquid crystal layer. 13. A circularly polarizing plate comprising the polarizing film according to claim 5 and a ¼ wavelength plate. 14. An organic EL display device comprising the circularly polarizing plate according to claim 13 and an organic EL element.

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Classifications

  • Ortho-condensed systems · CPC title

  • Ortho-condensed systems · CPC title

  • in the form of a thin sheet or foil, e.g. Polaroid · CPC title

  • the chain containing -COO- or -OCO- groups · CPC title

  • Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond {; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16} · CPC title

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What does patent US9644148B2 cover?
Provided is a composition that can form a polarizing film with high dichroic ratio, which contains a compound having a function as a dichroic dye and having a local maximum absorption in a wavelength range of 350 to 550 nm. The composition contains a compound represented by the formula (1) and a polymerizable liquid crystal compound: …
Who is the assignee on this patent?
Sumitomo Chemical Co
What technology area does this patent fall under?
Primary CPC classification C07C245/08. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 09 2017 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 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).