Azo compounds and Schiff 's bases derived from 5-(4-pyridyl)-2-amino-1,3,4-thiadiazole: synthesis, mesomorphic properties and structural study by semi-empirical calculations

Abstract

The synthesis and liquid crystalline properties of new Schiff 's bases (series 3a-f) and azo compounds (4a-f) incorporating pyridine and 1,3,4-thiadiazole rings are reported. The first homologues in the series of Schiff's bases (3a-c) show a monotropic mesophase and the homologues 3d-f display an enantiotropic SmA phase. The only azo compounds to exhibit liquid crystalline properties are the homologues 4e, f which show a monotropic nematic phase. These series are compared with Schiff's bases and azo compounds analogues (series 5 and 6), previously reported by us and an AM1 study of the structure/mesomorphic property relationship is described.