A Push-Button Molecular Switch

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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 Cu(2+)-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.
Publisher
AMER CHEMICAL SOC
Issue Date
2009-08
Language
English
Article Type
Article
Keywords

TEMPLATE-DIRECTED SYNTHESIS; DENSITY FUNCTIONALS; INTERLOCKED MOLECULES; CLICK CHEMISTRY; ROTAXANES; ELECTRONICS; CYCLOBIS(PARAQUAT-P-PHENYLENE); TETRATHIAFULVALENE; CATENANES; MACHINES

Citation

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.131, no.32, pp.11571 - 11580

ISSN
0002-7863
DOI
10.1021/ja904104c
URI
http://hdl.handle.net/10203/94429
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