Liquid crystal composition, optical element, and light guide element

US2023124399A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2023124399-A1
Application numberUS-202218065339-A
CountryUS
Kind codeA1
Filing dateDec 13, 2022
Priority dateJun 19, 2020
Publication dateApr 20, 2023
Grant date

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

A liquid crystal composition includes: at least one of a compound represented by Formula (I) or a compound represented by Formula (II); and a rod-like liquid crystal compound having a polymerizable group that does not correspond to both of Formula (I) and Formula (II)

First claim

Opening claim text (preview).

What is claimed is: 1 . A liquid crystal composition comprising: at least one of a compound represented by Formula (I) or a compound represented by Formula (II); and a rod-like liquid crystal compound having a polymerizable group that does not correspond to both of Formula (I) and Formula (II), in Formula (I), P 1 and P 2 each independently represent a hydrogen atom or a substituent, S 1 and S 2 each independently represent a single bond or a divalent linking group, A 1 , A 2 , A 3 , and A 4 each independently represent a non-aromatic ring, an aromatic ring, or an aromatic heterocycle which may have a substituent, in a case where a plurality of A 1 's are present, the plurality of A 1 's may be the same as or different from each other, and in a case where a plurality of A 4 's are present, the plurality of A 4 's may be the same as or different from each other, Y 1 and Y 2 each independently represent —O—, —S—, —OCH 2 —, —CH 2 O—, —CH 2 CH 2 —, —CO—, —COO—, —OCO—, —CO—S—, —S—CO—, —O—CO—O—, —CO—NH—, —NH—CO—, —SCH 2 —, —CH 2 S—, —CF 2 O—, —OCF 2 —, —CF 2 S—, —SCF 2 —, —CH═CH—COO—, —CH═CH—OCO—, —COO—CH═CH—, —OCO—CH═CH—, —CH═CH—, —N═N—, —CH═N—N═CH—, —CF═CF—, —C≡C—, or a single bond, in a case where a plurality of Y 1 's are present, the plurality of Y 1 's may be the same as or different from each other, and in a case where a plurality of Y 2 's are present, the plurality of Y 2 's may be the same as or different from each other, m1 and m2 each independently represent an integer of 0 to 5, Z represents a linear or branched alkylene group, the number of atoms in a bond where A 2 and A 3 are bonded by a shortest distance is 3 or 5 or more, and one —CH 2 — or two or more non-adjacent —CH 2 —'s that form the alkylene group may be substituted with —O—, —COO—, —OCO—, —OCOO—, —NRCO—, —CONR—, —NRCOO—, —OCONR—, —CO—, —S—, —SO 2 —, —NR—, —NRSO 2 —, or —SO 2 NR—, and R represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, in Formula (II), P 3 and P 4 each independently represent a hydrogen atom or a substituent, S 3 and S 4 each independently represent a single bond or a divalent linking group, A 5 and A 6 each independently represent a non-aromatic ring, an aromatic ring, or an aromatic heterocycle which may have a substituent, in a case where a plurality of A 5 's are present, the plurality of A 5 's may be the same as or different from each other, and in a case where a plurality of A 6 's are present, the plurality of A 6 's may be the same as or different from each other, Y 3 and Y 4 each independently represent —O—, —S—, —OCH 2 —, —CH 2 O—, —CH 2 CH 2 —, —CO—, —COO—, —OCO—, —CO—S—, —S—CO—, —O—CO—O—, —CO—NH—, —NH—CO—, —SCH 2 —, —CH 2 S—, —CF 2 O—, —OCF 2 —, —CF 2 S—, —SCF 2 —, —CH═CH—COO—, —CH═CH—OCO—, —COO—CH═CH—, —OCO—CH═CH—, —COO—CH 2 CH 2 —, —OCO—CH 2 CH 2 —, —CH 2 CH 2 —COO—, —CH 2 CH 2 —OCO—, —COO—CH 2 —, —OCO—CH 2 —, —CH 2 —COO—, —CH 2 —OCO—, —CH═CH—, —N═N—, —CH═N—N═CH—, —CF═CF—, —C≡C—, or a single bond, in a case where a plurality of Y 3 's are present, the plurality of Y 3 's may be the same as or different from each other, and in a case where a plurality of Y 4 's are present, the plurality of Y 4 's may be the same as or different from each other, m3 and m4 each independently represent an integer of 1 to 5, and B represents any one of groups represented by Formulas (B-1) to (B-11) which may have a substituent, a carbon atom in Formulas (B-1) to (B-11) may be substituted with a nitrogen atom, an oxygen atom, or a sulfur atom, X in Formulas (B-4) to (B-8), (B-10), and (B-11) represents a nitrogen atom, an oxygen atom, or a sulfur atom, two X's in Formula (B-5) may each independently represent the same atom or different atoms, and two X's in Formula (B-6) may each independently represent the same atom or different atoms, and in a case where B represents a group represented by Formula (B-11), both Y 3 and Y 4 bonded to B represent a single bond. 2 . The liquid crystal composition according to claim 1 , wherein at least one of P 1 or P 2 in Formula (I) represents a polymerizable group. 3 . The liquid crystal composition according to claim 1 , wherein at least one of P 3 or P 4 in Formula (II) represents a polymerizable group. 4 . The liquid crystal composition according to claim 1 , wherein a total content of the compound represented by Formula (I) and the compound represented by Formula (II) is 50 mass % or less with respect to the mass of the rod-like liquid crystal compound. 5 . The liquid crystal composition according to claim 1 , wherein a difference Δn 550 in refractive index generated by refractive index anisotropy of the liquid crystal composition is 0.2 or more. 6 . The liquid crystal composition according to claim 1 , wherein a phase transition temperature between a liquid crystal phase and an isotropic phase is 50° C. or higher. 7 . An optical element comprising: an optically-anisotropic layer that is formed of the liquid crystal composition according to claim 1 , wherein the optically-anisotropic layer has a liquid crystal alignment pattern in which a direction of an optical axis derived from a rod-like liquid crystal compound in the liquid crystal composition changes while continuously rotating in at least one in-plane direction. 8 . The optical element according to claim 7 , wherein the directions of the optical axes in the optically-anisotropic layer match each other in a thickness direction. 9 . The optical element according to claim 7 , wherein the optically-anisotropic layer has a region where the direction of the optical axis is twisted in the thickness direction and rotates. 10 . The optical element according to claim 7 , wherein in a case where a length over which the direction of the optical axis rotates by 180° in a plane is set as a single period, the optically-anisotropic layer has regions having different lengths of the single periods in the liquid crystal alignment pattern. 11 . The optical element according to claim 7 , wherein the single period in the liquid crystal alignment pattern gradually decreases in the one in-plane direction in which the direction of the optical axis changes while continuously rotating in the liquid crystal alignment pattern. 12 . The optical element according to claim 7 , wherein the liquid crystal alignment pattern of the optically-anisotropic layer is a concentric circular pattern having a concentric circular shape where the one in-plane direction in which the direction of the optical axis changes while continuously rotating moves from an inner side toward an outer side. 13 . A light guide element comprising: the optical element according to claim 7 ; and a light guide plate.

Assignees

Inventors

Classifications

  • C08F20/30Primary

    containing aromatic rings in the alcohol moiety · CPC title

  • Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids · CPC title

  • Polyvinyl alcohol {; Vinyl alcohol} · CPC title

  • G02B5/3016Primary

    involving passive liquid crystal elements (optical properties of liquid crystals G02F1/0063; polarising elements associated with active liquid crystal devices G02F1/133528) · CPC title

  • Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US2023124399A1 cover?
A liquid crystal composition includes: at least one of a compound represented by Formula (I) or a compound represented by Formula (II); and a rod-like liquid crystal compound having a polymerizable group that does not correspond to both of Formula (I) and Formula (II)
Who is the assignee on this patent?
Fujifilm Corp
What technology area does this patent fall under?
Primary CPC classification C08F20/30. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Apr 20 2023 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 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).