Liquid crystal cell
US-2016115389-A1 · Apr 28, 2016 · US
US10954444B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10954444-B2 |
| Application number | US-201716068471-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 23, 2017 |
| Priority date | May 23, 2016 |
| Publication date | Mar 23, 2021 |
| Grant date | Mar 23, 2021 |
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The present application relates to a novel liquid crystal compound and a use thereof. The novel liquid crystal compounds of the present application can exhibit a smectic A phase over a wide temperature range. The novel liquid crystal compounds of the present application can be usefully used in the technical fields to which smectic A liquid crystals can be applied, for example, bistable devices.
Opening claim text (preview).
The invention claimed is: 1. A liquid crystal compound of the following Formula 1: in said Formula 1, R 1 to R 4 are each independently an alkyl group having 1 to 3 carbon atoms, R 5 is —F, —Cl, —Br, —OF 3 , —NCS, —CN or —OCH 3 , X is —CH 2 — or —O—, k is an integer of 0 to 9, l is an integer of 0 to 2, m is an integer of 2 to 13, Y 1 to Y 8 are each independently CH, CF or N, where CF of Y 1 to Y 8 is not more than 2, A is the following Formula 2, or a single bond, —O—, —S—, —CO—, —COO—, —OCO—, —S—CO—, —CO—S—, —O—COO, —CO—NR 0 —, —NR 0 —CO—, —NR 0 —CO—NR 00 —, —NR 0 —CO—O—, —O—CO—NR 0 —, OCH 2 —, —OCH 2 —, —SCH 2 —, —CH 2 S—, —CF 2 O—, —OCF 2 —, —CF 2 S—, —SCF 2 —, —CH 2 CH 2 —, —(CH 2 ) 4 —, —CF 2 CH 2 —, —CH 2 CHF 2 —, —CH═N—, —N═CH—, —NH—NH—, —N═N—, —CH—CR 0 —, —CY 1 ═CY 2 —, —C═C—, —CH═CH—COO— or —OCO—CH═CH—, where R 0 , R 00 , Y 1 and Y 2 are each independently H or CH 3 ; in said Formula 2, Z 1 and Z 2 are each independently CH or N, and when said Z 1 and Z 2 are each CH, at least one of Y 1 to Y 8 is N, and wherein when A is not a heterocyclic structure then at least one of Y 1 to Y 8 is N. 2. The liquid crystal compound according to claim 1 , wherein in said Formula 1, R 1 to R 4 are a methyl group. 3. The liquid crystal compound according to claim 1 , wherein in said Formula 1, R 5 is —CN. 4. The liquid crystal compound according to claim 1 , wherein in said Formula 1, k is an integer of 0 to 3. 5. The liquid crystal compound according to claim 1 , wherein in said Formula 1, l is 0 or 1. 6. The liquid crystal compound according to claim 1 , wherein in said Formula 1, m is an integer of 7 to 9. 7. The liquid crystal compound according to claim 1 , wherein in said Formula 1, A is a single bond, any one of Y 1 to Y 8 is N and the remainder are CH. 8. The liquid crystal compound according to claim 1 , wherein in said Formula 1, A is Formula 2, Z 1 and Z 2 are CH, any one of Y 1 to Y 8 is N and the remainder are CH. 9. The liquid crystal compound according to claim 1 , wherein in said Formula 1, A is Formula 2, Z 1 and Z 2 are N, and Y 1 to Y 8 are each CH. 10. The liquid crystal compound according to claim 1 , wherein said liquid crystal compound of Formula 1 has a structure represented by the following formulas a-1 to a-18: 11. The liquid crystal compound according to claim 1 , wherein the liquid crystal compound exhibits a smectic A phase in a temperature range of −20° C. to 100° C. 12. The liquid crystal compound according to claim 1 , wherein the liquid crystal compound has a dielectric anisotropy of −1.0 to 20. 13. A bistable device comprising the liquid crystal compound of claim 1 . 14. The bistable device according to claim 13 , comprising two electrode substrates disposed opposite to each other and a liquid crystal layer containing the liquid crystal compound of claim 1 and a charging substance between said two electrode substrates.
Polysiloxanes · CPC title
the heterocyclic ring being a six-membered aromatic ring containing one nitrogen atom, e.g. pyridine · CPC title
based on liquid crystals, e.g. single liquid crystal display cells · CPC title
the heterocyclic ring being a non-aromatic ring · CPC title
comprising a heterocyclic ring · CPC title
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