The preparation, characterization, and switching mechanism of a unique single-station mechanically switchable hetero[2]catenane are reported. The facile synthesis utilizing a “threading-followed-by-clipping” protocol features Cu2+-catalyzed Eglinton coupling as a mild and efficient route to the tetrathiafulvalene-based catenane in high yield. The resulting mechanically interlocked molecule operates as a perfect molecular switch, most readily described as a “push-button” switch, whereby two discrete and fully occupied translational states are toggled electrochemically at incredibly high rates. This mechanical switching was probed using a wide variety of experimental techniques as well as quantum-mechanical investigations. The fundamental distinctions between this single-station [2]catenane and other more traditional bi- and multistation molecular switches are significant.
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Spruell, Jason M.; Paxton, Walter F.; Olsen, John-Carl; Benítez, Diego; Tkatchouk, Ekaterina; Stern, Charlotte L.; et al. (2016). A Push-Button Molecular Switch. ACS Publications. Collection. https://doi.org/10.1021/ja904104c