Journal
MOLECULAR CRYSTALS AND LIQUID CRYSTALS
Volume 344, Issue -, Pages 83-88Publisher
GORDON BREACH SCI PUBL LTD
DOI: 10.1080/10587250008023818
Keywords
diarylethene; terthiophene; femtosecond transient absorption spectroscopy; Woodward-Hoffmann rule
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Photochromic ring-closure reactions of diarylethene derivatives with terthiophene (T3H, T3Me) have been examined by femtosecond transient absorption spectroscopy. The rate of the ring-closure reaction of T3H in n-hexane was estimated to be similar to 2.5 ps, which is very similar to that of T3Me in the same solvent. It was suggested that the ring-closure reaction proceeds through a concerted mechanism without any intermediates but not a two-step mechanism. The rate of ring-closure reaction was also dependent on the solvent polarity, suggesting that the charge transfer state in the excited singlet state plays an important role in the photochromic reaction.
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