Stable frustrated phases in chiral liquid crystals derived from optically active (R)- and (S)-3-ethylmercapto-2-methylpropionic acids
Highly optically pure (R)- and (S)-3-ethylmercapto-2-methylpropionic acids were synthesized by using optically active (D)- and (L)-2,10-camphorsultams as chiral auxiliaries, respectively. Their derivatives, (R)- and (S)-EMMPNmB (m=6-12), were prepared for investigation. Microscopic texture observations demonstrated that the materials possess three stable frustrated phases: BP, TGBA* and TGBC* phases. Interestingly, it was found that the N* phase behaves as an intermediary phase between BP and TGBA* phases in a rather narrow temperature range (calc. 0.5-1.4°C). A study of the racemic mixture, (±)-EMMPNmB (m=10), indicated that the chirality of the molecule could suppress the formation of smectic phases in the heating process. An increase of alkyl chain length favoured the formation of the TGB phases particularly, in accompaniment with a change of TGB phases from monotropic to enantiotropic. Moderate maximum PS values (calc. 14-19 nC cm-2) and apparent tilt angle (calc. 20°) were obtained for the TGBC* phase in a surface stabilized ferroelectric liquid crystal geometry.
Document Type: Research Article
Affiliations: 1: Department of Chemical Engineering, Tatung University, 40 Chunghan N. Rd., 3rd Sec., Taipei, Taiwan 104, ROC 2: Department of Chemistry, National Tsinhua University, Hsinchu, Taiwan ROC
Publication date: 01 January 2001
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