Liquid-crystal medium

US11781069B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11781069-B2
Application numberUS-201816225508-A
CountryUS
Kind codeB2
Filing dateDec 19, 2018
Priority dateDec 20, 2017
Publication dateOct 10, 2023
Grant dateOct 10, 2023

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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 invention relates to an LC medium comprising and a liquid-crystalline host consisting of an LC component H) comprising one or more mesogenic or liquid-crystalline compounds and an optically active component D) and optionally a polymerizable component P) comprising one or more polymerizable compounds; and to the use of the polymerizable compounds and LC media for optical, electro-optical and electronic purposes, in particular in LC displays, especially in LC displays of the polymer sustained alignment type.

First claim

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The invention claimed is: 1. A liquid crystal display comprising: two substrates, at least one which is transparent to light; an electrode provided on each substrate or two electrodes provided on only one of the substrates; and located between the substrates a layer of a liquid-crystal medium; the liquid-crystal medium comprising: a liquid-crystalline host containing a liquid crystal component, and an optically active component, wherein the liquid crystal component comprises one or more compounds of formula CPY-n-Om, one or more compounds of formula PY-n-Om and one or more compounds of formula PYP-n-m in a total concentration in the range of from 45 to 70%: wherein m and n are each, independently of each other, an integer from 1 to 12, wherein the liquid crystal medium has negative dielectric anisotropy and the molecules in the layer of the liquid crystal medium in the switched-off state are aligned perpendicular to the electrode surfaces or have a tilted homeotropic alignment, the liquid-crystalline host has a chiral pitch, p, in the range of from 8 to 30 μm, the liquid crystal component has a birefringence Δn in the range of from 0.110 to 0.150; wherein the display has a cell gap and the thickness, d, of the cell gap is in the range of from 3 μm to 5 μm; and wherein the ratio d/p between the thickness of the cell gap d and the chiral pitch p is 0.1 to 1. 2. The liquid crystal display according to claim 1 , wherein the optically active component comprises one or more compounds selected from the formulae in which R a11 , R a12 and R b12 , independently of one another, denote alkyl having 1 to 15 C atoms, in which, in addition, one or more non-adjacent CH 2 groups may each be replaced, independently of one another, by —C(R z )═C(R z )—, —C≡C—, —O—, —S—, —CO—, —CO—O—, —O—CO— or —O—CO—O— in such a way that O and/or S atoms are not linked directly to one another, and in which, in addition, one or more H atoms may each be replaced by F, Cl, Br, I or CN, with the proviso that R a12 is different from R b12 , R a21 and R a22 , independently of one another, denote alkyl having 1 to 15 C atoms, in which, in addition, one or more non-adjacent CH 2 groups may each be replaced, independently of one another, by —C(R z )═C(R z )—, —C≡C—, —O—, —S—, —CO—, —CO—O—, —O—CO— or —O—CO—O— in such a way that O and/or S atoms are not linked directly to one another, and in which, in addition, one or more H atoms may each be replaced by F, Cl, Br, I or CN, R a31 , R a31 and R b32 , independently of one another, denote straight-chain alkyl having 1 to 15 C atoms or branched alkyl having 3 to 15 C atoms, in which, in addition, one or more non-adjacent CH 2 groups may each be replaced, independently of one another, by —C(R z )═C(R z )—, —C≡C—, —O—, —S—, —CO—, —CO—O—, —O—CO— or —O—CO—O— in such a way that O and/or S atoms are not linked directly to one another, and in which, in addition, one or more H atoms may each be replaced by F, Cl, Br, I or CN, with the proviso that R a32 is different from R b32 , R z denotes H, CH 3 , F, Cl, or CN, R 8 denotes alkyl having 1 to 15 C atoms, in which, in addition, one or more non-adjacent CH 2 groups may each be replaced, independently of one another, by —C(R z )═C(R z )—, —C≡C—, —O—, —S—, —CO—, —CO—O—, —O—CO— or —O—CO—O— in such a way that O and/or S atoms are not linked directly to one another, and in which, in addition, one or more H atoms may each be replaced by F, Cl, Br, I or CN, Z 8 denotes —C(O)O—, —CH 2 O—, —CF 2 O— or a single bond, A 11 is defined as A 12 below, or alternatively denotes A 12 denotes L 11 denotes F, Cl, —CN, P-Sp-, or straight chain alkyl having 1 to 25 C atoms, branched alkyl having 3 to 25 C atoms, or cyclic alkyl having 3 to 25 C atoms, wherein in said alkyl groups one or more non-adjacent CH 2 — groups are each optionally replaced by —O—, —S—, —CO—, —CO—O—, —O—CO—, or —O—CO—O— in such a manner that O- and/or S-atoms are not directly connected with each other, and wherein one or more H atoms are each optionally replaced by P-Sp-, F or Cl, A 21 denotes A 22 has one of the meanings given for A 12 A 31 has one of the meanings given for A 11 , alternatively denotes A 32 has one of the meanings given for A 12 , n2 on each occurrence, identically or differently, is 0, 1 or 2, and n3 is 1, 2 or 3. 3. The liquid crystal display according to claim 1 , wherein the liquid-crystalline host further comprises one or more compounds of the formulae in which R 11 and R 12 each, independently of one another, denote alkyl having 1 to 12 C atoms, where one or two non-adjacent CH 2 groups may each be replaced by —O—, —CH═CH—, —CO—, —OCO— or —COO— in such a way that O atoms are not linked directly to one another, L denotes F, b denotes 0 or 1, and r denotes 1, 2 or 3. 4. The liquid crystal display according to claim 1 , wherein the liquid-crystalline host additionally comprises one or more compounds of the following formulae: in which alkyl and alkyl* each, independently of one another, denote a straight-chain alkyl radical having 1-6 C atoms, and alkenyl and alkenyl* each, independently of one another, denote a straight-chain alkenyl radical having 2-6 C atoms. 5. The liquid crystal display according to claim 1 , wherein the liquid-crystalline host additionally comprises one or more compounds of the following formula: in which R 5 and R 6 each, independently of one another, denote alkyl having 1 to 12 C atoms, where, in addition, one or two non-adjacent CH 2 groups may each be replaced by —O—, —CH═CH—, —CO—, —OCO— or —COO— in such a way that O atoms are not linked directly to one another, each, independently of one another, denote in which L 5 denotes F or Cl, and L 6 denotes F, Cl, OCF 3 , CF 3 , CH 3 , CH 2 F or CHF 2 . 6. The liquid crystal display according to claim 1 , wherein the liquid-crystalline host further comprises one or more compounds of the following formula: in which the individual radicals have the following meanings: R 3 and R 4 each, independently of one another, denote alkyl having 1 to 12 C atoms, in which, in addition, one or two non-adjacent CH 2 groups may each be replaced by —O—, —CH═CH—, —CO—, —O—CO— or —CO—O— in such a way that O atoms are not

Assignees

Inventors

Classifications

  • the end chain group being a polymerizable end group, e.g. -Sp-P or acrylate · CPC title

  • Constructional arrangements; {Manufacturing methods}(G02F1/135, G02F1/136 take precedence) · CPC title

  • Optically active dopants; chiral dopants · CPC title

  • containing esters · CPC title

  • C09K19/44Primary

    containing compounds with benzene rings directly linked · CPC title

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What does patent US11781069B2 cover?
The present invention relates to an LC medium comprising and a liquid-crystalline host consisting of an LC component H) comprising one or more mesogenic or liquid-crystalline compounds and an optically active component D) and optionally a polymerizable component P) comprising one or more polymerizable compounds; and to the use of the polymerizable compounds and LC media for optical, electro-opt…
Who is the assignee on this patent?
Merck Patent Gmbh
What technology area does this patent fall under?
Primary CPC classification C09K19/44. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 10 2023 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 6 related publications on this page (citations in our corpus or others sharing the same primary CPC).