Liquid crystal composition and liquid crystal display device
US-9512360-B2 · Dec 6, 2016 · US
US10023799B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10023799-B2 |
| Application number | US-201414769444-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 27, 2014 |
| Priority date | Feb 20, 2013 |
| Publication date | Jul 17, 2018 |
| Grant date | Jul 17, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
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):
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 —
Cy-Ph-COO-Ph · CPC title
Cy-Cy-COO-Ph · CPC title
to carbon atoms of non-condensed six-membered aromatic rings · CPC title
Radicals substituted by oxygen atoms · CPC title
containing a carbocyclic ring, e.g. dicyano-benzene, chlorofluoro-benzene or cyclohexanone · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.