Liquid Crystal compound containing cyclobutyl group and difluoromethyleneoxy linking group, and preparation method and use thereof
US-9481828-B2 · Nov 1, 2016 · US
US9957213B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9957213-B2 |
| Application number | US-201414330012-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 14, 2014 |
| Priority date | Jul 30, 2013 |
| Publication date | May 1, 2018 |
| Grant date | May 1, 2018 |
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A novel organic compound that can be used in a variety of liquid crystal devices or a liquid crystal composition containing the novel organic compound is provided. An organic compound represented by General Formula (G1) is provided. A novel liquid crystal composition containing the organic compound is provided. In General Formula (G1), Ar 1 and Ar 2 separately represent a substituted or unsubstituted arylene group having 6 to 12 carbon atoms, a substituted or unsubstituted cycloalkylene group having 3 to 12 carbon atoms, or a substituted or unsubstituted cycloalkenylene group having 3 to 12 carbon atoms. In addition, m and n separately represent 0 or 1. R 1 and R 2 separately represent a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 11 carbon atoms, or a substituted or unsubstituted alkoxy group having 1 to 11 carbon atoms.
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What is claimed is: 1. An organic compound represented by Formula (G1): wherein Ar 1 and Ar 2 separately represent a substituted or unsubstituted cycloalkylene group having 3 to 12 carbon atoms, or a substituted or unsubstituted cycloalkenylene group having 3 to 12 carbon atoms, wherein m represents 1, wherein n represents 0 or 1 1, and wherein R 1 and R 2 separately represent a hydrogen atom or a substituted or unsubstituted alkyl group having 1 to 11 carbon atoms. 2. The organic compound according to claim 1 , wherein a substituent of the substituted cycloalkylene group or the substituted cycloalkenylene group of Ar 1 or Ar 2 is one selected from the group consisting of fluorine (F), bromine (Br), chlorine (Cl), iodine (I), a cyano group (CN), a trifluoromethyl group (CF 3 ), a trifluoromethylsulfonyl group (SO 2 CF 3 ), a nitro group (NO 2 ), an isothiocyanate group (NCS), a thiocyanate group (SCN), and a pentafluorosulfanyl group (SF 5 ), and wherein a substituent of the substituted alkyl group of R 1 or R 2 is one selected from the group consisting of fluorine (F), bromine (Br), chlorine (Cl), iodine (I), a cyano group (CN), a trifluoromethyl group (CF 3 ), a trifluoromethylsulfonyl group (SO 2 CF 3 ), a nitro group (NO 2 ), an isothiocyanate group (NCS), a thiocyanate group (SCN), and a pentafluorosulfanyl group (SF 5 ). 3. An organic compound represented by Formula (110): 4. A liquid crystal composition comprising: a liquid crystal compound; and an organic compound represented by Formula (G1): wherein Ar 1 and Ar 2 separately represent a substituted or unsubstituted cycloalkylene group having 3 to 12 carbon atoms, or a substituted or unsubstituted cycloalkenylene group having 3 to 12 carbon atoms, wherein m represents 1, wherein n represents 0 or 1, and wherein R 1 and R 2 separately represent a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 11 carbon atoms, or a substituted or unsubstituted alkoxy group having 1 to 11 carbon atoms. 5. The liquid crystal composition according to claim 4 , wherein a substituent of the substituted cycloalkylene group or the substituted cycloalkenylene group of Ar 1 or Ar 2 is one selected from the group consisting of fluorine (F), bromine (Br), chlorine (CO, iodine (I), a cyano group (CN), atrifluoromethyl group (CF 3 ), a trifluoromethylsulfonyl group (SO 2 CF 3 ), a nitro group (NO 2 ), an isothiocyanate group (NCS), a thiocyanate group (SCN), or a pentafluorosulfanyl group (SF 5 ), and wherein a substituent of the substituted alkyl group of R 1 or R 2 is one selected from the group consisting of fluorine (F), bromine (Br), chlorine (Cl), iodine (I), a cyano group (CN), a trifluoromethyl group (CF 3 ), a trifluoromethylsulfonyl group (SO 2 CF 3 ), a nitro group (NO 2 ), an isothiocyanate group (NCS), a thiocyanate group (SCN), and a pentafluorosulfanyl group (SF 5 ). 6. A liquid crystal composition comprising: a liquid crystal compound; and an organic compound represented by Formula (110): 7. A liquid crystal element comprising the liquid crystal composition according to claim 4 . 8. A liquid crystal display device comprising the liquid crystal element according to claim 7 . 9. The liquid crystal element according to claim 7 , wherein the liquid crystal element has a high voltage holding ratio.
the aromatic ring being a non-condensed ring · CPC title
in which the rings are linked by a chain containing carbon and oxygen atoms, e.g. esters or ethers · CPC title
Optically active dopants; chiral dopants · CPC title
linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters {or ethers} · CPC title
The ring being saturated · CPC title
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