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- W2941483238 endingPage "4332" @default.
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- W2941483238 abstract "By introducing an oleyl group at the end of the straight rodlike molecule, the effect of the tail shape on the liquid crystallinity, biaxiality, and lateral switching behavior of the smectic A phase was investigated. Three types of molecules possessing a fluorinated phenyl (pentafluorophenyl, 2,3,4-trifluorophenyl, or 2,3-difluorophenyl) group and a cis-octadec-9-enyl group were synthesized, and their liquid crystallinities were compared with the corresponding molecules with a straight alkyl (trans-octadec-9-enyl or n-octadecanyl) group. In switching experiments, the molecules with a bent terminal chain showed higher spontaneous polarization (Ps) values than those with a straight terminal chain. Further, the directional changes of the long molecular axes were suppressed for the molecules possessing a bent terminal chain. These results show that the introduction of a bent terminal chain is highly effective for stabilizing ferroelectric switching behaviors." @default.
- W2941483238 created "2019-05-03" @default.
- W2941483238 creator A5007435252 @default.
- W2941483238 creator A5008202506 @default.
- W2941483238 creator A5022892968 @default.
- W2941483238 creator A5072790141 @default.
- W2941483238 date "2019-04-24" @default.
- W2941483238 modified "2023-10-07" @default.
- W2941483238 title "Does Introduction of a Bent Tail Stabilize Biaxiality and Lateral Switching Behavior of Smectic A Liquid Crystal Phases of Rodlike Molecules?" @default.
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- W2941483238 doi "https://doi.org/10.1021/acs.jpcb.9b00589" @default.
- W2941483238 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31017436" @default.
- W2941483238 hasPublicationYear "2019" @default.
- W2941483238 type Work @default.