Synthesis and optical properties of new conjugated polymers composed of 1,3,4‐thiadiazole and 2,5‐dialkoxybenzene rings

Intramolecular cyclization of precursor polyhydrazides derived from hydrazine and four 2,5‐dialkoxyterephthalic acids by direct polycondensation with Lawesson's reagent afforded new conjugated polymers constituted of 1,3,4‐thiadiazole and 2,5‐dialkoxybenzene units. The polymers emitted bluish green light in solution and green light in solid state in spite of the coexistence of non‐cyclized hydrazide linkage in the backbones, the Stokes shifts being 91–138 nm in the solid state. It was suggested that these polymers have appropriate lengths of conjugation backbones based on the 1,3,4‐thiadiazole moiety.