Synthesis, phase transitions and birefringence of novel liquid crystalline 1,4-phenylene bis(4-alkylthio benzoates) and insights into the cybotactic nematic behaviour

<p>We synthesised a novel family of liquid crystalline 1,4-phenylene bis(4-alkylthio benzoates), of which homologues with different alkyl chain lengths of 1–8 were designed, to investigate the structure–property relationship. The mesogenic incidence and tendency were found to be strongly dependent on the carbon numbers in the terminal alkyl chains. Even members formed widely monotropic or enantiotropic nematic (N) phases compared to odd members that showed either none or monotropic-narrower ones. The temperature dependence of birefringence (Δ<i>n</i>) for the hexylthio homologue was evaluated and compared to that for a hexyloxy counterpart. It was found that the hexylthio homologue exhibited higher Δ<i>n</i> values than the hexyloxy counterpart over the entire range of near <i>T</i>_IN–<i>T</i>. In addition, wide-angle X-ray diffraction measurements, using magnetically aligned specimens, found enhanced cybotactic nematic tendency with smectic (Sm) A-like temperature dependence for the hexylthio analogue, due to the intermolecular attractive S···S interaction, in comparison with the hexyloxy analogue exhibiting N phase with clear Sm C-type clusters. We revealed the actual benefits of alkylthio groups in the fluid N phase.