Heteroaromatic isothiocyanates
US-2024124779-A1 · Apr 18, 2024 · US
US2016348002A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016348002-A1 |
| Application number | US-201615091371-A |
| Country | US |
| Kind code | A1 |
| Filing date | Apr 5, 2016 |
| Priority date | May 29, 2015 |
| Publication date | Dec 1, 2016 |
| Grant date | — |
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A liquid crystal composition includes one or more compounds represented by Chemical Formula 1. In Chemical Formula 1, are a cyclohexane or tetrahydropyran, and R1 and R2 are each independently hydrogen, a C1 to C8 alkyl group, a C2 to C8 alkenyl group, or a C1 to C8 alkoxy group.
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What is claimed is: 1 . A liquid crystal composition comprising one or more compound represented by Chemical Formula 1: wherein, are independently a cyclohexane or tetrahydropyran, and R1 and R2 are independently a hydrogen, a C1 to C8 alkyl group, a C2 to C8 alkenyl group, or a C1 to C8 alkoxy group. 2 . The liquid crystal composition of claim 1 , wherein: in the compound of Chemical Formula 1, one or more hydrogen in R1 and R2 is substituted with F, one or more —CH 2 — group in R1 and R2 is substituted with —OCH 2 —, or —OCF 2 —, or one or more —CH 3 group in R1 and R2 is substituted with —CF 3 or —OCF 3 . 3 . The liquid crystal composition of claim 1 , wherein: in the compound of Chemical Formula 1, one or more hydrogen in is substituted with F, or one or more —CH 2 — group in is substituted with —O— or —CF 2 —. 4 . The liquid crystal composition of claim 1 , wherein: the compound represented by Chemical Formula 1 is at least one compound selected from Chemical Formulas 1-1 to 1-9: 5 . The liquid crystal composition of claim 1 , wherein: the compound represented by Chemical Formula 1 is present in an amount of about 1 wt % to about 40 wt % based on the entire weight of the liquid crystal composition. 6 . The liquid crystal composition of claim 1 , wherein: the liquid crystal composition further comprises at least one compound selected from Chemical Formulas 2-1 to 2-8: wherein, R3 and R4 are independently hydrogen, a C1 to C8 alkyl group, a C2 to C8 alkenyl group, or a C1 to C8 alkoxy group. 7 . The liquid crystal composition of claim 6 , wherein: one or more hydrogen in R3 and R4 is substituted with F, one or more —CH 2 — group in R3 and R4 is substituted with —OCH 2 —, —CF 2 —, or —OCF 2 —, or one or more —CH 3 group in R3 and R4 is substituted with —CF 3 or —OCF 3 . 8 . The liquid crystal composition of claim 6 , wherein: the compound selected from Chemical Formulas 2-1 to 2-8 is present in an amount of about 2 wt % to about 40 wt %, based upon the entire weight of the liquid crystal composition. 9 . The liquid crystal composition of claim 1 , wherein: the liquid crystal composition further comprises at least one compound selected from Chemical Formulas 3-1 to 3-12: wherein, R5 and R6 are independently hydrogen, a C1 to C8 alkyl group, a C2 to C8 alkenyl group, or a C1 to C8 alkoxy group. 10 . The liquid crystal composition of claim 9 , wherein: at least one hydrogen in R5 and R6 is substituted with fluorine. 11 . The liquid crystal composition of claim 9 , wherein: the compound selected from Chemical Formulas 3-1 to 3-12 is present in an amount of about 2 wt % to about 30 wt % based upon the entire liquid crystal composition. 12 . A liquid crystal display comprising: a first insulation substrate comprising a pixel electrode; a second insulation substrate facing the first insulation substrate and comprising a common electrode; and a liquid crystal layer positioned between the first insulation substrate and the second insulation substrate, wherein the liquid crystal layer comprises one or more compound represented by Chemical Formula 1: wherein, are independently a cyclohexane or tetrahydropyran, and R1 and R2 are independently hydrogen, a C1 to C8 alkyl group, a C2 to C8 alkenyl group, or a C1 to C8 alkoxy group. 13 . The liquid crystal display of claim 12 , wherein: in the compound of Chemical Formula 1, one or more hydrogen in R1 and R2 is substituted with F, one or more —CH 2 — group in R1 and R2 is substituted —OCH 2 —, —CF 2 —, or —OCF 2 —, or one or more —CH 3 group in R1 and R2 is substituted with —CF 3 or —OCF 3 . 14 . The liquid crystal display of claim 12 , wherein: in the compound of Chemical Formula 1, one or more hydrogen in is substituted with F, or one or more —CH 2 — group in is substituted with —O— or —CF 2 —. 15 . The liquid crystal display of claim 12 , wherein: the compound represented by Chemical Formula 1 is at least one compound selected from Chemical Formulas 1-1 to 1-9: 16 . The liquid crystal display of claim 12 , wherein: the compound represented by Chemical Formula 1 is present in an amount of about 1 wt % to about 40 wt % based upon the entire weight of the liquid crystal composition. 17 . The liquid crystal display of claim 12 , wherein: the liquid crystal layer further comprises at least one compound selected from Chemical Formulas 2-1 to 2-8: wherein, R3 and R4 are independently hydrogen, a C1 to C8 alkyl group, a C2 to C8 alkenyl group, or a C1 to C8 alkoxy group. 18 . The liquid crystal display of claim 17 , wherein: one or more hydrogen in R3 and R4 is substituted with F, one or more —CH 2 — group in R3 and R4 is substituted with one among —OCH 2 —, —CF 2 —, or —OCF 2 —, or one or more —CH 3 group in R3 and R4 is substituted with —CF 3 or —OCF 3 . 19 . The liquid crystal display of claim 17 , wherein: the compound selected from Chemical Formulas 2-1 to 2-8 is present in an amount of about 2 wt % to about 40 wt % based on the entire weight of the liquid crystal composition. 20 . The liquid crystal display of claim 12 , wherein: the liquid crystal layer further comprises at least one compound selected from Chemical Formulas 3-1 to 3-12: wherein, R5 and R6 are independently hydrogen, a C1 to C8 alkyl group, a C2 to C8 alkenyl group, or a C1 to C8 alkoxy group. 21 . The liquid crystal display of claim 20 , wherein: at least one hydrogen in R5 and R6 is substituted with fluorine. 22 . The liquid crystal display of claim 20 , wherein: the compound of Chemical Formula 3-1 to 3-12 is present in an amount of about 2 wt % to about 30 wt % based upon the entire weight of the liquid crystal composition. 23 . The liquid cry
Ph-Ph · CPC title
containing one non-condensed benzene ring · CPC title
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Compounds containing at least two rings in which the different rings are directly linked (covalent bond) · CPC title
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