文摘
The cycloreversion (ring-opening) process of one of the photochromic diarylethene derivatives,bis(2-methyl-5-phenylthiophen-3-yl)perfluorocyclopentene, was investigated by means of picosecond andfemtosecond laser photolysis methods. The drastic enhancement of the reaction yield was observed onlyby the picosecond laser exposure. The excitation intensity effect of the reaction profiles revealed that thesuccessive multiphoton absorption process leading to higher excited states opened the efficient cycloreversion process with a reaction yield of (50 ± 10)%, while the one-photon absorption directly pumped toa higher excited state did not lead to the efficient cycloreversion reaction. These results indicate that notthe energy of the excitation but the character of the electronic state takes an important role in theenhancement of the cycloreversion reaction.