Abstract
Abstract 3,4-Bis[5-(2′-thiophene)-2-methylthien-3-yl]-2,5-dihydrothiophene 1a was synthesized and underwent excellent ring-opening and ring-closing photoisomerization in solution with UV/Vis light irradiation. Both ring-open isomer and ring-closed isomer of diarylethene showed electrochemical behavior, and the oxidation/reduction potential was reversible based on the ring-opening and ring-closing photoisomerization of diarylethene with UV/Vis light irradiation. Besides, a combination of photochromism and electrochromism of 1a was also observed.
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