Acylation of benzo[c][1,2,5]thiadiazole-4,7-diamine
and 2-hexyl-2H-benzo[d][1,2,3]triazole-4,7-diamine
with aromatic acid halides furnished the corresponding N,N′-diamides, which were converted into N,N′-dithioamides by reacting with
Lawesson’s reagent. A method was developed for the preparation
of previously unknown fused systems, dithiazolobenzo[1,2-c][1,2,5]thiadiazoles and dithiazolobenzo[1,2-d][1,2,3]triazoles,
by oxidative photochemical cyclization of N,N′-dithioamides. The photophysical and (spectro)electrochemical
properties of the obtained compounds and their polymer films electrochemically
deposited on ITO were studied. The optical contrast and response time
of the synthesized oligomers were determined. The results obtained
allow us to consider these substances as promising candidates for
electrochromic devices.