Abstract
Two new series of chiral aliphatic and aromatic esters of 7-decyl[1]benzothieno[3,2-b][1]benzothiophene-2-carboxylic acid were synthesized and their mesomorphic behaviour studied. While the chiral aliphatic esters exhibited only the SmA phase, the antiferroelectric SmCA* phase was found for esters with chiral 4-hydroxybenzoates; for one homologue a ferroelectric SmC* phase was also observed. Introduction of lateral substituents in the 3-position of the 4-hydroxybenzoic acids (methoxy, fluoro, chloro, and bromo) led to a reduction of the polymorphism and only the SmA phase remained.