A conducting polymer, poly(isothianaphthene) (PITN) was prepared by di
rect photopolymerization in solution of 1,3-dihydroisothianaphthene (D
HITN) which was more stable in air than isothianaphthene (ITN). This p
hotopolymerization was initiated with electron transfer from DHITN to
an acceptor such as carbon tetrachloride or oxygen. It proceeded by bo
th UV irradiation and cationic polymerization under light exclusion. T
he polymerization rate was accelerated by the addition of salts. The r
ate of the PITN fraction of the product composition was governed by th
e nucleophilicity of the anion species of added salts. The features of
this polymerization were seen in electrochemical polymerization and p
hotopolymerization of ITN.1