Thermal circuits built in liquid crystal elastomers
US-2024084183-A1 · Mar 14, 2024 · US
US9567522B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9567522-B2 |
| Application number | US-201313801403-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 13, 2013 |
| Priority date | Dec 17, 2004 |
| Publication date | Feb 14, 2017 |
| Grant date | Feb 14, 2017 |
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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.
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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.
Optically active dopants; chiral dopants · CPC title
Heterocyclic compounds · CPC title
Polymers · CPC title
Cross-Sectional Technologies · mapped topic
Cross-Sectional Technologies · mapped topic
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