Design of new Schiff base polymers containing thiadiazole rings and study of their liquid crystalline behavior

New liquid crystalline thiadiazole dibenzaldehyde monomers labeled as THDB1-THDB3 were successfully synthesized by alkylation of thiadiazole's potassium salt with 4-(bromomethyl) benzaldehyde. A number of polymers consisting of thiadiazole and azomethine coded PTDAZ1-PTDAZ5 were synthesized via condensation reaction of the presynthesized monomers THDB1-THDB3 with aromatic diamines. The chemical structures of the prepared materials were confirmed using Fourier-transform infrared spectroscopy and proton nuclear magnetic resonance techniques. The liquid crystalline behavior of the studied monomers and polymers was examined by differential scanning calorimetry and hot stage polarized optical microscopy (POM) techniques. All these compounds were found to demonstrate mesomorphic transitions belonging to smectic and nematic liquid crystals. The studied monomers exhibited fan-like texture of smectic mesophase under POM cooling investigation. Fan-like texture of smectic and nematic mesophases was observed under POM for PTDAZ1 and PTDAZ2, while PTDAZ3 and PTDAZ4 revealed clay and schlieren textures of the smectic and nematic mesophases, respectively, and nematic texture has been found for the polymer PTDAZ5.