Chemically and electrochemically induced expansion and contraction of a ferrocene rotor

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Abstract

A 2,2′-bipyridine-appended ferrocene rotor, 1,1′-di(5-yl-ethynyl-2,2′-bipyridine)ferrocene, can be switched from a folded/stacked (syn) conformation to an extended/unstacked (anti) conformation by the addition of [Cu(CH3CN)4](PF6) and 6,6′-dimesityl-2,2′-bipyridine. This extension and contraction process was completely reversible and could be triggered either chemically or electrochemically.

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Scottwell, S. O., Elliott, A. B. S., Shaffer, K. J., Nafady, A., McAdam, C. J., Gordon, K. C., & Crowley, J. D. (2015). Chemically and electrochemically induced expansion and contraction of a ferrocene rotor. Chemical Communications, 51(38), 8161–8164. https://doi.org/10.1039/c5cc01973g

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