Liquid crystal compound and liquid crystal composition

US9803140B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9803140-B2
Application numberUS-201615161010-A
CountryUS
Kind codeB2
Filing dateMay 20, 2016
Priority dateOct 13, 2015
Publication dateOct 31, 2017
Grant dateOct 31, 2017

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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 disclosure discloses a liquid crystal compound and a liquid crystal composition. The liquid crystal compound has a general structural formula as represented by formula I. The liquid crystal composition provided by the present disclosure has a lower rotary viscosity γ 1 , can achieve a quick response, and further has an appropriate dielectric anisotropy Δ∈, an appropriate optical anisotropy Δn, a high stability to heat and light, a high VHR numerical value especially in the case where the liquid crystal is under harsh conditions, and a stability to electric field and electromagnetic radiation. As a liquid crystal material for use in thin film transistor techniques (TFT-LCD), the material further has the properties of a wider nematic phase temperature range, an appropriate birefringence anisotropy, a very high electrical resistivity, a good anti-ultraviolet performance, a high charge holding rate, a low vapor pressure etc.

First claim

Opening claim text (preview).

The invention claimed is: 1. A compound as represented by formula I, in said formula I, R 1 represents an alkyl having a carbon atom number of 1-9, a fluoro-substituted alkyl having a carbon atom number of 1-9, an alkoxy having a carbon atom number of 1-9, a fluoro-substituted alkoxy having a carbon atom number of 1-9, an alkenyl having a carbon atom number of 2-9, a fluoro-substituted alkenyl having a carbon atom number of 2-9, an alkenyloxy having a carbon atom number of 3-8, or an alkenyloxy having a carbon atom number of 3-8; represents 1,4-phenylene, fluoro-substituted 1,4-phenylene, 1,4-cyclohexylidene, 1,4-cyclohexenylene, or 1,4-cyclohexylidene with one or two —CH 2 -being substituted by oxygen atoms; X 1 and X 3 each independently represent hydrogen or fluorine; and X 2 represents hydrogen, fluorine, an alkyl having a carbon atom number of 1-9, an alkoxy having a carbon atom number of 1-9, a fluoro-substituted alkyl having a carbon atom number of 1-9, a fluoro-substituted alkoxy having a carbon atom number of 1-9, or an alkenyl having a carbon atom number of 2-9; wherein said fluoro-substituted 1,4-phenylene in said and wherein said 1,4-cyclohexylidene with one or two —CH 2 — being substituted by oxygen atoms in said 2. The compound according to claim 1 , wherein said compound as represented by formula I is a compound of formula IA in said formula IA, both definitions of R 1 and are identical to the definitions of R 1 and in claim 1 . 3. The compound according to claim 2 , wherein said compound as represented by formula I is any one of the compounds as represented by formulae I1 to I12: in said formulae I1 to I12, R 11 represents an alkyl having a carbon atom number of 1-5; and X 21 represents an alkyl having a carbon atom number of 1-5, an alkoxy having a carbon atom number of 1-5, an alkenyl having a carbon atom number of 2-5, a fluoro-substituted alkyl having a carbon atom number of 1-5, or a fluoro-substituted alkoxy having a carbon atom number of 1-5. 4. A liquid crystal mixture containing component A; said component A consisting of at least one of the compounds as represented by formula I of claim 1 . 5. The liquid crystal mixture according to claim 4 , wherein said liquid crystal mixture further comprises components B and C; said component B consisting of at least one of the compounds as represented by formula II; and said component C consisting of at least one of the compounds as represented by formula III; in said formulae II and III, R 2 , R 3 , and R 4 are each selected from a C1-C6 alkyl, a C2-C6 alkenyl, or a C1-C6 alkoxy; each independently represent 1,4-cyclohexylidene, 1,4-cyclohexenylene, or 1,4-phenylene; is selected from at least one of 1,4-cyclohexylidene, 1,4-cyclohexenylene, 1,4-phenylene, and fluoro-substituted 1,4-phenylene; p is 2 or 3; (F) represents H or F; X 4 is F, Cl, or —OCF 3 ; and wherein said fluoro-substituted 1,4-phenylene in said represents 6. The liquid crystal mixture according to claim 5 , wherein said liquid crystal mixture consists of components A, B, and C. 7. The liquid crystal mixture according to claim 5 , wherein said compound as represented by formula II is any one of the compounds as represented by formulae II1 to II13: said compound as represented by formula III is any one of the compounds as represented by formulae III1 to III22: in said formulae III1 to III22, R 4 is selected from at least one of a C1-C6 alkyl, a C2-C6 alkenyl, and a C1-C6 alkoxy. 8. The liquid crystal mixture according to claim 5 , wherein said liquid crystal mixture further comprises at least one of components D, E and F; said component D consists of at least one of the compounds as represented by formula IV; in said formula IV, R 51 and R 52 are each selected from any one of a C1-C6 alkyl, a C2-C6 alkenyl, and a C1-C6 alkoxy; m is 1 or 2; and are each selected from at least one of 1,4-cyclohexylidene, 1,4-cyclohexenylene, 1,4-phenylene, and fluoro-substituted 1,4-phenylene; said component E consists of at least one of the compounds as represented by formula V; in said formula V, R 61 and R 62 are each selected from any one of a C1-C6 alkyl, a C2-C6 alkenyl, and a C1-C6 alkoxy; n is 1 or 2; is selected from at least one of 1,4-cyclohexylidene, 1,4-cyclohexenylene, 1,4-phenylene, and fluoro-substituted 1,4-phenylene; Z is a single bond, —CH 2 O—, —COO—, or —CH 2 CH 2 —; and said component F consists of at least one of the compounds as represented by formula VI; in said formula VI, R 71 and R 72 are each selected from any one of a C1-C6 alkyl, a C2-C6 alkenyl, and a C1-C6 alkoxy; and wherein said fluoro-substituted 1,4-phenylene in said and represents 9. The liquid crystal mixture according to claim

Assignees

Inventors

Classifications

  • having oxygen as hetero atom (sugars C09K19/0422) · CPC title

  • C07C43/225Primary

    containing halogen · CPC title

  • in which the rings are linked by a chain containing carbon and oxygen atoms, e.g. esters or ethers · CPC title

  • the heterocyclic ring being a six-membered ring · CPC title

  • Twisted Nematic (T.N.); Super Twisted Nematic (S.T.N.); Optical Mode Interference (O.M.I.) · CPC title

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What does patent US9803140B2 cover?
The present disclosure discloses a liquid crystal compound and a liquid crystal composition. The liquid crystal compound has a general structural formula as represented by formula I. The liquid crystal composition provided by the present disclosure has a lower rotary viscosity γ 1 , can achieve a quick response, and further has an appropriate dielectric anisotropy Δ∈, an appropriate optical ani…
Who is the assignee on this patent?
Shijiazhuang Chengzhi Yonghua Display Materials Co Ltd
What technology area does this patent fall under?
Primary CPC classification C07C43/225. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 31 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).