Kazutoshi Miyazawa

Chiral smectic C liquid crystals having an electronegative substituent ortho to the chiral tail group - a study of a factor determining the magnitude of spontaneous polarization

Abstract Chiral smectic C compounds having an ester group in the central core, an optically active tail group (alkoxy or alkoxycarbonyl), and an electronegative substituent (halogen or cyano) ortho to the chiral tail were synthesized. The effect of the ortho substitution on the characteristics, especially on spontaneous polarization (Ps), was examined. When the chiral tail is a 1-methylheptyloxy group the lateral substituent increases Ps relative to the unsubstituted analogue. In the case of 1-methylheptyloxycarbonyl tail group, however, the lateral substituent decreases Ps relative to the unsubstituted. These effects of lateral substituents are explained in terms of chemical structure of a single molecule, i. e., by taking statistical weight of conformers and the associated electric dipole moments into account.

Novel optically active compounds having 2-alkanoyloxypropyl moiety as chiral dopants

Abstract Novel optically active compounds having 2-alkanoyloxypropyl moiety were synthesized. By use of these compounds as chiral dopants in an achiral smectic C mixtures, Sc* mixtures exhibiting quick response and a long N* pitch suitable for the SSFLC displays could be obtained.