Liquid crystal system and liquid crystal display

US9567522B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9567522-B2
Application numberUS-201313801403-A
CountryUS
Kind codeB2
Filing dateMar 13, 2013
Priority dateDec 17, 2004
Publication dateFeb 14, 2017
Grant dateFeb 14, 2017

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  1. Title

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  2. Abstract

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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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Abstract

Official abstract text for this publication.

The instant invention relates to mesogenic systems comprising a) a polymeric component, component A, obtained or obtainable from polymerisation of a precursor comprising one or more mesogenic mono-reactive compounds, one or more di-reactive compounds, which optionally are also mesogenic compounds and optionally a photo-initiator and a low molecular weight component, component B, comprising one or more mono-reactive, mesogenic compounds, one or more mesogenic compounds and one or more chiral dopants, exhibiting a Blue Phase, as well as to the use of these systems in deices and to these devices.

First claim

Opening claim text (preview).

The invention claimed is: 1. A mesogenic system comprising a) a polymeric component, component A, obtained from polymerization of a precursor comprising one or more mesogenic mono-reactive compounds of formula IA wherein R 11 is H, F, Cl, Br, I, CN, NO 2 , NCS, SF 5 , SO 2 CF 3 or alkyl which is straight chain or branched, is unsubstituted, mono- or poly-substituted by F, Cl, Br, I or CN, and in which one or more non-adjacent CH 2 groups are optionally replaced, in each case independently from one another, by —O—, —S—, —NH—, —NR 01 —, —SiR 01 R 02 —, —CO—, —COO—, —OCO—, —OCO—O—, —S—CO—, —CO—S—, —CY 1 ═CY 2 —or —C≡C—in such a manner that O and/or S atoms are not linked directly to one another, R 01 and R 02 are, independently of each other, H or alkyl with 1 to 12 C— atoms,  is a mesogenic moiety, PG 11 is a polymerizable or reactive group, Sp 11 is a spacer group or a single bond, and X 11 is —O—, —S—, —CO—, —CO—O—, —O—CO—, S—CO—, —CO—S—, —O—CO—O—, —CO—NR 01 —, —NR 01 —CO—, —OCH 2 —, —CH 2 O—, —SCH 2 —, —CH 2 S—, —CF 2 O—, —OCF 2 —, —CF 2 S—, —SCF—, —CH 2 CH 2 —, —CF 2 CH 2 —, —CH 2 CF 2 —, —CF 2 CF 2 —, —CH═N—, —N═CH—, —N═N—, —CH═CR 01 —, —CY 01 ═CY 02 —, —C≡C—, —(CH 2 ) 4 —, —CH═CH—CO—O—, —O—CO—CH═CH— or a single bond, and Y 01 and Y 02 are, independently of each other, F, Cl or CN, and alternatively one of them may be H, one or more di-reactive compounds, which optionally are also mesogenic compounds and optionally a photo-initiator and b) a low molecular weight component, component B, comprising one or more mesogenic compounds and one or more chiral dopants, exhibiting a Blue Phase. 2. The system according to claim 1 , wherein the precursor of component A comprises one or more mesogenic di-reactive compounds. 3. The system according to claim 1 , wherein the precursor of component A comprises one or more non-mesogenic (isotropic) mono-reactive compounds. 4. The system according to claim 1 , wherein the precursor of component A comprises one or more compounds, which lead to an increase of the characteristic temperatures during and/or upon its polymerization and one or more compounds which on their own lead or would lead to a decrease of the characteristic temperatures during and/or upon its polymerization. 5. The system according to claim 1 , having a Blue Phase extending at least over a temperature range from −10° C. or below to +50° C. or above. 6. A light modulation element, comprising a system according to claim 1 . 7. In a light modulation medium comprising a mesogenic system, the improvement wherein the system is one according to claim 1 . 8. An electro-optical display, comprising a system according to claim 1 . 9. They system according to claim 2 , wherein the mesogenic di-reactive compound is wherein has the meaning given for under formula I above, PG 12 and PG 13 independently of each other, have one of the meanings given for PG 11 in formula I, SP 12 and SP 13 independently of each other, have one of the meanings given for SP 11 in formula I, and X 12 and X 13 independently of each other, have one of the meanings given for X 11 in formula I.

Assignees

Inventors

Classifications

  • Optically active dopants; chiral dopants · CPC title

  • Heterocyclic compounds · CPC title

  • C09K19/38Primary

    Polymers · CPC title

  • Cross-Sectional Technologies · mapped topic

  • Cross-Sectional Technologies · mapped topic

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Frequently asked questions

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What does patent US9567522B2 cover?
The instant invention relates to mesogenic systems comprising a) a polymeric component, component A, obtained or obtainable from polymerisation of a precursor comprising one or more mesogenic mono-reactive compounds, one or more di-reactive compounds, which optionally are also mesogenic compounds and optionally a photo-initiator and a low molecular weight component, component B, comprising one …
Who is the assignee on this patent?
Merck Patent Gmbh
What technology area does this patent fall under?
Primary CPC classification C09K19/38. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Feb 14 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).