Liquid crystal compound and liquid crystal composition

US2017101581A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2017101581-A1
Application numberUS-201615161010-A
CountryUS
Kind codeA1
Filing dateMay 20, 2016
Priority dateOct 13, 2015
Publication dateApr 13, 2017
Grant date

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

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 Δε, 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).

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. 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 the definitions of R 1 and are identical to the definition of R 1 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 being composed 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 is composed of at least one of the compounds as represented by formula II; and said component C is composed 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, or 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; and X 4 is F, Cl or —OCF 3 . 6 . The liquid crystal mixture according to claim 5 , wherein said liquid crystal mixture is composed 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 is composed 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 is composed 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 is composed 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. 9 . The liquid crystal mixture according to claim 8 , wherein the mass parts of the components in said liquid crystal mixture are as follows, respectively: component A: 5-25 parts; component B: 15-45 parts; component C: 5-45 parts; component D: 5-25 parts; component E: 5-25 parts: and component F: 5-25 parts. 10 . A liquid crystal display element or liquid crystal display containing the compound as represented by formula I of claim 1 ; and said liquid crystal display element or liquid crystal display is an active matrix-addressing liquid crystal display element or an active matrix-addressing liquid crystal display; wherein said active matrix display element is a TN-TFT, IPS-TFT, or FFS-TFT liquid crystal display element; and said active-matrix addressing liquid crystal display is a TN-TFT, IPS-TFT, or FFS-TFT liquid crystal display.

Assignees

Inventors

Classifications

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

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

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

  • Chemistry & Metallurgy · mapped topic

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

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US2017101581A1 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 Δε, 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 C09K19/3066. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Apr 13 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). 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).