Polymerisable LC medium and polymer film with flat optical dispersion
US-12031079-B2 · Jul 9, 2024 · US
US9862886B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9862886-B2 |
| Application number | US-201615184212-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 16, 2016 |
| Priority date | Jun 22, 2015 |
| Publication date | Jan 9, 2018 |
| Grant date | Jan 9, 2018 |
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An exemplary embodiment of the present invention provides a compound represented by Chemical Formula 1: wherein, in Chemical Formula 1, n is 0, 1, or 2, and a substituent represented by X is F, Cl, CF 3 , CF 2 CF 3 CHF 2 , CH 2 F, OCF 3 , CN, NCS, or a C1 to C5 alkyl including 1 to 3 fluoro substituents and a CH 2 group independently substituted with one or more oxygen atoms; (R 1 ) is hydrogen or a C1 to C15 alkyl, at least one CH 2 group being independently replaced with —C≡C—, —CF 2 O—, —CH═CH—, —O—, —CO—O—, —O—CO—, or —O—CO—O— in a way that oxygen atoms are directly connected to each other, and 1 to 3 hydrogen atoms of the C1 to C15 alkyl being replaced with halogen; (F) indicates that a fluoro is optionally substituted in place of a hydrogen, and each of is independently
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What is claimed is: 1. A compound represented by Chemical Formula 1: wherein, in Chemical Formula 1, n is 0, 1, or 2, and a substituent represented by “X” is F, Cl, CF 3 , CF 2 CF 3 , CHF 2 , CH 2 F, OCF 3 , CN, NCS, or a C1 to C5 alkyl including 1 to 3 fluoro substituents and a CH 2 group independently substituted with one or more oxygen atoms; (R 1 ) is hydrogen or a C1 to C15 alkyl, at least one CH 2 group being independently replaced with —C≡C—, —CF 2 O—, —CH═CH—, —O—, —CO—O—, —O—CO—, or —O—CO—O— in a way that oxygen atoms are directly connected to each other, and 1 to 3 hydrogen atoms of the C1 to C15 alkyl being replaced with a halogen; (F) indicates that a fluoro is optionally substituted in place of a hydrogen; and each of are independently 2. The compound of claim 1 , wherein the compound represented by Chemical Formula 1 comprises one or more compound represented by Chemical Formula 1-1 to Chemical Formula 1-14: 3. A liquid crystal composition comprising a compound represented by Chemical Formula 1: wherein, in Chemical Formula 1, n is 0, 1, or 2, and a substituent represented by X is F, Cl, CF 3 , CF 2 CF 3 , CHF 2 , CH 2 F, OCF 3 , CN, NCS, or a C1 to C5 alkyl including 1 to 3 fluoro substituents and a CH 2 group independently substituted with one or more oxygen atoms; (R 1 ) is hydrogen or a C1 to C15 alkyl, at least one CH 2 group being independently replaced with —C≡C—, —CF 2 O—, —CH═CH—, —O—, —CO—O—, —O—CO—, or —O—CO—O— in a way that oxygen atoms are directly connected to each other, and 1 to 3 hydrogen atoms of the C1 to C15 alkyl being replaced with halogen; (F) indicates that a fluoro is optionally substituted in place of hydrogen; and each of is independently wherein (F) indicates that a fluoro is optionally substituted in place of a hydrogen. 4. The liquid crystal composition of claim 3 , wherein the compound represented by Chemical Formula 1 comprises one or more compounds represented by Chemical Formula 1-1 to Chemical Formula 1-14: 5. The liquid crystal composition of claim 3 , wherein a content of the compound represented by Chemical Formula 1 is in a range of about 1 wt % to about 30 wt % of the total weight of the liquid crystal composition. 6. The liquid crystal composition of claim 3 , wherein the liquid crystal composition further comprises one or more of the compound represented by Chemical Formula 2: wherein, in Chemical Formula 2, R 1 and R 2 independently indicate C1 to C12 alkyl, C1 to C12 alkoxy, or C2 to C12 alkenyl. 7. The liquid crystal composition of claim 6 , wherein a content of the compound represented by Chemical Formula 2 is in a range of about 5 wt % to about 60 wt % of the total weight of the liquid crystal composition. 8. The liquid crystal composition of claim 3 , wherein the liquid crystal composition further comprises one or more of the compound represented by Chemical Formula 3: wherein each of is independently wherein (F) indicates that a fluoro is optionally substituted in place of a hydrogen, and R 3 and R 4 independently indicate C1 to C12 alkyl, C1 to C12 alkoxy, or C2 to C12 alkenyl. 9. The liquid crystal composition of claim 8 , wherein a content of the compound represented by Chemical Formula 3 is in a range of about 1 wt % to about 40 wt % of the total weight of the liquid crystal composition. 10. The liquid crystal composition of claim 3 , wherein the liquid crystal composition further comprises one or more of the compound represented by Chemical Formula 4: wherein each of is independently R 5 indicates C1 to C12 alkyl, C1 to C12 alkoxy, or C2 to C12 alkenyl, and (F) indicates that a fluoro is optionally substituted in place of a hydrogen. 11. The liquid crystal composition of claim 10 , wherein a content of the compound represented by Chemical Formula 4 is in a range of about 1 wt % to about 40 wt % of the total weight of the liquid crystal composition. 12. The liquid crystal composition of claim 3 , wherein the liquid crystal composition further comprises one or more of the compound represented by Chemical Formula 5: wherein R 6 indicates C1 to C12 alkyl, C1 to C12 alkoxy, or C2 to C12 alkenyl. 13. The liquid crystal composition of claim 12 , wherein a content of the compound represented by Chemical Formula 5 is in a range of about 1 wt % to about 15 wt % of the total weight of the liquid crystal composition. 14. A liquid crystal display comprising: a first insulation substrate; a thin film transistor disposed on the first insulation substrate; a first electrode connected to the thin film transistor; a second electrode disposed on the first insulation substrate while being insulated from the first electrode; a second insulation substrate configured to face the first insulation substrate; and a liquid crystal layer disposed between the first insulation substrate and the second insulation substrate, wherein the liquid crystal layer comprises a liquid crystal composition comprising a compound represented by Chemical Formula 1: wherein, in Chemical Formula 1, n is 0, 1, or 2, and a substituent represented by X is F, Cl, CF 3 , CF 2 CF 3 , CHF 2 , CH 2 F, OCF 3 , CN, NCS, or a C1 to C5 alkyl including 1 to 3 fluoro substituents and a CH 2 group independently substituted with one or more oxygen atoms; (R 1 ) is hydrogen or a C1 to C15 alkyl, at least one CH 2 group being independently replaced with —C≡C—, —CF 2 O—, —CH—CH—, —O—, —CO—O—, —O—CO—, or —O—CO—O— in a way that oxygen atoms are directly connected to each other, and 1 to 3 hydrogen atoms of the C1 to C15 alky
Cy-Cy-Ph · CPC title
the linking chain being a -CF2O- chain · CPC title
containing halogen · CPC title
at least two benzene rings directly linked, e.g. biphenyls · CPC title
in which the rings are linked by a chain containing carbon and oxygen atoms, e.g. esters or ethers · CPC title
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