Abstract
Repeatable PET-driven rotational isomerization is described. I demonstrated the conversion of light stimuli into electrochemical potential via reversibly working artificial molecular rotation, using two strategies, DMFc+ system and partial oxidation system. In both systems, photoinduced electron transfer from copper complex to electron acceptor plays a key role for the photo- and heat-driven rotation.
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Nishikawa, M. (2014). Repeatable Copper(II)/(I) Redox Potential Switching Driven Visible Light-Induced Coordinated Ring Rotation. In: Photofunctionalization of Molecular Switch Based on Pyrimidine Ring Rotation in Copper Complexes. Springer Theses. Springer, Tokyo. https://doi.org/10.1007/978-4-431-54625-2_4
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DOI: https://doi.org/10.1007/978-4-431-54625-2_4
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