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.
