New ferroelectric liquid crystal having 2-methylalkanoyl group
- 1 February 1991
- journal article
- research article
- Published by Taylor & Francis in Ferroelectrics
- Vol. 114 (1) , 251-257
- https://doi.org/10.1080/00150199108221587
Abstract
A relationship between molecular structure and physical properties of newly prepared ferroelectric liquid crystals having 2-methylalkanoyl group is investigated by observing the phase transition temperatures, the spontaneous polarization, and the bistability. Carbon chain length is proved to play an important role not only in the thermal stability of the SC phase but also in the magnitude of the spontaneous polarization in this phase. A lateral fluoro substituent is efficient at producing more stable SC* phase and reducing the occurrence of higher ordered phases. Especially the lateral fluoro substitution at the ortho position to the chiral tail favors the uniform state and contributes to the bistability.Keywords
This publication has 5 references indexed in Scilit:
- 13C NMR Analysis of Molecular Motions of a Ferroelectric Liquid CrystalJapanese Journal of Applied Physics, 1989
- New Ferroelectric Liquid Crystal with Large Spontaneous PolarizationJapanese Journal of Applied Physics, 1989
- 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 polarizationFerroelectrics, 1988
- Rotational damping and the spontaneous polarization in ferroelectric liquid crystalsThe Journal of Physical Chemistry, 1987
- The effect of lateral substitution on smectic C formationLiquid Crystals, 1987