Liquid crystal compound, liquid crystal composition and liquid crystal display device

US10023799B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10023799-B2
Application numberUS-201414769444-A
CountryUS
Kind codeB2
Filing dateJan 27, 2014
Priority dateFeb 20, 2013
Publication dateJul 17, 2018
Grant dateJul 17, 2018

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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.

To provide a liquid crystal compound satisfying at least one of physical properties such as high stability to light, a high clearing point, a low minimum temperature of a liquid crystal phase, small viscosity, suitable optical anisotropy, large dielectric anisotropy, a large dielectric constant in a minor axis direction, a suitable elastic constant and excellent compatibility; a liquid crystal composition containing the compound; and a liquid crystal display device including the composition. The compound is represented by formula (1):

First claim

Opening claim text (preview).

What is claimed is: 1. A compound represented by formula (1): wherein, in formula (1), R 1 is alkyl having 1 to 15 carbons, in the alkyl, at least one of —CH 2 — may be replaced by —O— or —S—, at least one of —(CH 2 ) 2 — may be replaced by —CH═CH—, and in the groups, at least one of hydrogen may be replaced by halogen; ring A 1 , ring A 2 , ring A 3 and ring A 4 are independently 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene, 2-chloro-1,4-phenylene, 2,6-dichloro-1,4-phenylene, 2-chloro-6-fluoro-1,4-phenylene, tetrahydropyran-2,5-diyl, 1,3-dioxane-2,5-diyl, 2,6,7-trioxabicyclo[2.2.2]octane-1,4-diyl, pyrimidine-2,5-diyl or pyridine-2,5-diyl; X 1 is fluorine, chlorine, —C≡N, —CF 3 , —CHF 2 , —OCF 3 , —OCHF 2 , —CH═CHCF 3 , —CF═CHCF 3 or —CF═CFCF 3 ; L 1 and L 2 are independently hydrogen or fluorine; Y 1 and Y 2 are independently fluorine or chlorine; W 1 is a single bond, —(CH 2 ) 2 —, —CH═CH—, —C≡C—, —COO—, —OCO—, —CH 2 O—, —OCH 2 — or —CF═CF—; Z 1 , Z 2 , Z 3 and Z 4 are independently a single bond, —(CH 2 ) 2 —, —CH═CH—, —C≡C—, —COO—, —OCO—, —CF 2 O—, —CH 2 O—, —OCH 2 — or —CF═CF—; a, b, c and d are independently 0 or 1, a sum of a, b, c and d is 1, 2 or 3; and at least one of Z 1 when a is 1, Z 2 when b is 1, Z 3 when c is 1, and Z 4 when d is 1 is —CF 2 O—. 2. The compound according to claim 1 , wherein, in formula (1) described in claim 1 , R 1 is alkyl having 1 to 15 carbons, alkenyl having 2 to 15 carbons, alkoxy having 1 to 14 carbons or alkenyloxy having 2 to 14 carbons; and X 1 is fluorine, chlorine, —C≡N, —CF 3 , —CHF 2 , —OCF 3 , —OCHF 2 , —CH═CHCF 3 , —CF═CHCF 3 or —CF═CFCF 3 . 3. The compound according to claim 1 , wherein, in formula (1) described in claim 1 , R 1 is alkyl having 1 to 10 carbons, alkenyl having 2 to 10 carbons, alkoxy having 1 to 9 carbons or alkenyloxy having 2 to 9 carbons; and X 1 is fluorine, chlorine, —C≡N, —CF 3 , —CHF 2 , —OCF 3 , —OCHF 2 , —CH═CHCF 3 , —CF═CHCF 3 or —CF═CFCF 3 . 4. The compound according to claim 1 , represented by any one of formulas (1-1) to (1-7): wherein, in formulas (1-1) to (1-7), R 1 is alkyl having 1 to 10 carbons, alkenyl having 2 to 10 carbons or alkoxy having 1 to 9 carbons; ring A 1 , ring A 2 , ring A 3 and ring A 4 are independently 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene, tetrahydropyran-2,5-diyl or 1,3-dioxane-2,5-diyl; Z 1 , Z 2 , Z 3 and Z 4 are independently a single bond, —(CH 2 ) 2 —, —COO—, —CF 2 O—, —CH 2 O— or —OCH 2 —; W 1 is a single bond, —(CH 2 ) 2 — or —OCH 2 —; X 1 is fluorine, —CF 3 or —OCF 3 ; L 1 and L 2 are independently hydrogen or fluorine; Y 1 and Y 2 are independently fluorine or chlorine; in formula (1-3), any one of Z 1 and Z 2 is —CF 2 O—; in formula (1-4), any one of Z 1 and Z 3 is —CF 2 O—; in formula (1-5), any one of Z 3 and Z 4 is —CF 2 O—; in formula (1-6), any one of Z 1 , Z 2 and Z 3 is —CF 2 O—; and in formula (1-7), any one of Z 1 , Z 3 and Z 4 is —CF 2 O—. 5. The compound according to claim 1 , represented by any one of formulas (1-8) to (1-12): wherein, in formulas (1-8) to (1-12), R 1 is alkyl having 1 to 10 carbons, alkenyl having 2 to 10 carbons or alkoxy having 1 to 9 carbons; ring A 1 , ring A 2 , ring A 3 and ring A 4 are independently 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene, tetrahydropyran-2,5-diyl or 1,3-dioxane-2,5-diyl; X 1 is fluorine, —CF 3 or —OCF 3 ; and L 1 and L 2 are independently hydrogen or fluorine. 6. The compound according to claim 1 , represented by any one of formulas (1-13) to (1-22): wherein, in formulas (1-13) to (1-22), R 1 is alkyl having 1 to 10 carbons, alkenyl having 2 to 10 carbons or alkoxy having 1 to 9 carbons; X 1 is fluorine, —CF 3 or —OCF 3 ; and L 1 , L 2 , L 3 , L 4 , L 5 and L 6 are independently hydrogen or fluorine. 7. The compound according to claim 1 , represented by any one of formulas (1-23) to (1-25): wherein, in formulas (1-23) to (1-25), R 1 is alkyl having 1 to 10 carbons, alkenyl having 2 to 10 carbons or alkoxy having 1 to 9 carbons; X 1 is fluorine, —CF 3 or —OCF 3 ; and L 1 , L 2 and L 3 are independently hydrogen or fluorine. 8. A liquid crystal composition, containing at least one compound according to claim 1 . 9. The liquid crystal composition according to claim 8 , further containing at least one compound selected from the group of compounds represented by formulas (2) to (4): wherein, in formulas (2) to (4), R 11 is alkyl having 1 to 10 carbons or alkenyl having 2 to 10 carbons, and in the alkyl and the alkenyl, at least one of hydrogen may be replaced by fluorine, and at least one of —CH 2 — may be replaced by —O—; X 11 is fluorine, chlorine, —OCF 3 , —OCHF 2 , —CF 3 , —CHF 2 , —CH 2 F, —OCF 2 CHF 2 or —OCF 2 CHFCF 3 ; ring B 1 , ring B 2 and ring B 3 are independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene, tetrahydropyran-2,5-diyl, 1,3-dioxane-2,5-diyl or pyrimidine-2,5-diyl; Z 11 , Z 12 and Z 13 are independently a single bond, —CH 2 CH 2 —, —CH═CH—, —C≡C—, —COO—, —CF 2 O—, —OCF 2 —, —CH 2 O— or —(CH 2 ) 4 —; and L 11 and L 12 are independently hydrogen or fluorine. 10. The liquid crystal composition according to claim 8 , further containing at least one compound selected from the group of compounds represented by formula (5): wherein, in formula (5), R 12 is alkyl having 1 to 10 carbons or alkenyl having 2 to 10 carbons, and in the alkyl and the alkenyl, at least one of hydrogen may be replaced by fluorine, and at least one of —CH 2 — may be replaced by —O—; X 12 is —C≡N or —C≡C—C≡N; ring C 1 is 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene, tetrahydropyran-2,5-diyl, 1,3-dioxane-2,5-diyl or pyrimidine-2,5-diyl; Z 14 is a single bond, —CH 2 CH 2 —, —C≡C—, —COO—, —CF 2 O—, —OCF 2 — or —CH 2 O—; L 13 and L 14 are independently hydrogen or fluorine; and i is 1, 2, 3 or 4. 11. The liquid crystal composition according to claim 8 , further containing at least one compound selected from the group of compounds represented by formulas (6) to (12): wherein, in formulas (6) to (12), R 13 and R 14 are independently alkyl having 1 to 10 carbons or alkenyl having 2 to 10 carbons, and in the alkyl and the alkenyl, at least one of —CH 2 — may be replaced by —O—; R 15 is hydrogen, fluorine, alkyl having 1 to 10 carbons or alkenyl having 2 to 10 carbons, and in the alkyl and the alkenyl, at least one of —CH 2 — may be replaced by —

Assignees

Inventors

Classifications

  • Cy-Ph-COO-Ph · CPC title

  • Cy-Cy-COO-Ph · CPC title

  • to carbon atoms of non-condensed six-membered aromatic rings · CPC title

  • C07D309/06Primary

    Radicals substituted by oxygen atoms · CPC title

  • containing a carbocyclic ring, e.g. dicyano-benzene, chlorofluoro-benzene or cyclohexanone · CPC title

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What does patent US10023799B2 cover?
To provide a liquid crystal compound satisfying at least one of physical properties such as high stability to light, a high clearing point, a low minimum temperature of a liquid crystal phase, small viscosity, suitable optical anisotropy, large dielectric anisotropy, a large dielectric constant in a minor axis direction, a suitable elastic constant and excellent compatibility; a liquid crystal …
Who is the assignee on this patent?
Jnc Corp, Jnc Petrochemical Corp
What technology area does this patent fall under?
Primary CPC classification C07D309/06. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jul 17 2018 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 5 related publications on this page (citations in our corpus or others sharing the same primary CPC).