Liquid crystal composition and liquid crystal display device
US-10100252-B2 · Oct 16, 2018 · US
US10385272B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10385272-B2 |
| Application number | US-201515521303-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 10, 2015 |
| Priority date | Oct 24, 2014 |
| Publication date | Aug 20, 2019 |
| Grant date | Aug 20, 2019 |
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Provided is a liquid crystal composition satisfying at least one or having suitable balance regarding at least two of characteristics such as high maximum or low minimum temperature of a nematic phase, large optical anisotropy, large positive dielectric anisotropy and high stability to ultraviolet light, and a liquid crystal display device including such a composition, particularly an encapsulated liquid crystal display device, and a liquid crystal display device serving as a constituent of 3D lenses. The liquid crystal composition contains a specific compound having large optical anisotropy as a first component, and a specific compound having large optical anisotropy and large positive dielectric anisotropy as a second component; a specific compound having large positive dielectric anisotropy as a third component; and a specific compound having large optical anisotropy and further having high maximum or low minimum temperature as a fourth component, and the liquid crystal display device includes the composition.
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What is claimed is: 1. A liquid crystal composition having positive dielectric anisotropy, containing at least one compound selected from the group of compounds represented by formula (1) as a first component, and at least one compound selected from the group of compounds represented by formula (2-1) or formula (2-2) as a second component, and a compound having cyano, and dielectric anisotropy as an optional component, wherein the compound having cyano is a compound other than the compounds of the first component and the second component, and when the compound having cyano is included in the liquid crystal composition, a proportion of the compound having cyano is less than 3% by weight based on a total of the liquid crystal composition: wherein, in formula (1), formula (2-1) and formula (2-2), R 11 , R 12 , R 21 and R 22 are independently alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons or alkenyl having 2 to 12 carbons; ring A 11 is 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,5-difluoro-1,4-phenylene or 2,6-difluoro-1,4-phenylene; ring A 21 and ring A 24 are independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene, pyridine-2,5-diyl, pyrimidine-2,5-diyl, 1,3-dioxane-2,5-diyl or tetrahydropyran-2,5-diyl; ring A 22 , ring A 23 , ring A 25 and ring A 26 are independently 1,4-phenylene, 2-fluoro-1,4-phenylene or 2,6-difluoro-1,4-phenylene; Z 11 , Z 21 , Z 22 , Z 23 and Z 24 are independently a single bond, ethylene, vinylene, methyleneoxy, carbonyloxy, difluoromethyleneoxy, ethynylene or tetrafluoroethylene, in which at least one of Z 21 and Z 22 is ethynylene, and at least one of Z 23 and Z 24 is ethynylene; X 11 , X 21 , X 22 , X 23 and X 24 are independently hydrogen or fluorine; Y 21 and Y 22 are independently fluorine, chlorine, alkyl having 1 to 12 carbons in which at least one piece of hydrogen may be replaced by halogen, alkoxy having 1 to 12 carbons in which at least one piece of hydrogen may be replaced by halogen, or alkenyl having 2 to 12 carbons in which at least one piece of hydrogen may be replaced by halogen; and m 21 and m 22 are independently 0, 1 or 2, and when m 21 or m 22 represents 2, a plurality of ring A 21 , Z 21 , ring A 24 and Z 23 may be identical or different, respectively. 2. The liquid crystal composition according to claim 1 , containing at least one compound selected from the group of compounds represented by formula (1-1) to formula (1-13) as the first component: wherein, in the formulas, R 11 and R 12 are independently alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons or alkenyl having 2 to 12 carbons. 3. The liquid crystal composition according to claim 1 , wherein a proportion of a compound represented by formula (1) described in claim 1 is in the range of 10% by weight to 50% by weight based on the weight of the liquid crystal composition. 4. The liquid crystal composition according to claim 1 , containing at least one compound selected from the group of compounds represented by formula (2-1-1) to formula (2-1-14) and formula (2-2-1) to formula (2-2-2) as the second component: wherein, in the formulas, R 21 and R 22 are independently alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons or alkenyl having 2 to 12 carbons. 5. The liquid crystal composition according to claim 1 , wherein a proportion of a compound represented by formula (2-1) and formula (2-2) described in claim 1 is in the range of 5% by weight to 60% by weight based on the weight of the liquid crystal composition. 6. The liquid crystal composition according to claim 1 , further containing at least one compound selected from the group of compounds represented by formula (3) as a third component: wherein, in formula (3), R 31 is alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons or alkenyl having 2 to 12 carbons; ring A 31 is 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene, pyridine-2,5-diyl, pyrimidine-2,5-diyl, 1,3-dioxane-2,5-diyl or tetrahydropyran-2,5-diyl; ring A 32 and ring A 33 are independently 1,4-phenylene, 2-fluoro-1,4-phenylene, 1,3-dioxane-2,5-diyl or 2,6-difluoro-1,4-phenylene; Z 31 , Z 32 and Z 33 are independently a single bond, ethylene, vinylene, methyleneoxy, carbonyloxy, difluoromethyleneoxy or tetrafluoroethylene; X 31 and X 32 are independently hydrogen or fluorine; Y 31 is fluorine, chlorine, alkyl having 1 to 12 carbons in which at least one piece of hydrogen may be replaced by halogen, alkoxy having 1 to 12 carbons in which at least one piece of hydrogen may be replaced by halogen, or alkenyl having 2 to 12 carbons in which at least one piece of hydrogen may be replaced by halogen; and m 3 is 0, 1 or 2, and when m 3 represents 2, a plurality of ring A 31 and Z 31 may be identical or different, respectively. 7. The liquid crystal composition according to claim 1 , containing at least one compound selected from the group of compounds represented by formula (3-1) to formula (3-15) as the third component: wherein, in the formulas, R 31 is alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons or alkenyl having 2 to 12 carbons. 8. The liquid crystal composition according to claim 6 , wherein a proportion of the third component is in the range of 1% by weight to 50% by weight based on the weight of the liquid crystal composition. 9. The liquid crystal composition according to claim 1 , further containing at least one compound selected from the group of compounds represented by formula (4): wherein, in formula (4), R 41 and R 42 are independently alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons or alkenyl having 2 to 12 carbons; ring A 41 and ring A 42 are independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,5-difluoro- 1,4-phenylene or 2,6-difluoro-1,4-phenylene; Z 41 is a single bond, ethylene, vinylene, methyleneoxy, carbonyloxy, difluoromethyleneoxy, ethynylene or tetrafluoroethylene; Z 42 is a single bond, ethylene, vinylene, methyleneoxy, carbonyloxy, difluoromethyleneoxy or tetrafluoroethylene; and m 4 is 0, 1 or 2, and when m 4 represents 2, a plurality of ring A 42 and Z 42 may be identical or different, respectively. 10. The liquid crystal composition according to claim 1 , containing at least one compound selected from the group of compounds represented by formula (4-1) to formula (4-13): wherein, in the formulas, R 41 and R 42 are independently alkyl having 1 to 12 carbons, alkoxy having 1 to 12 carbons or alkenyl having 2 to 12 carbons. 11. The liquid crystal composition according to claim 9 , wherein a proportion of the compounds represented by fo
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