Toward Chemically Controlled Nanoscale Molecular Machinery

Mechanical displacement of the ring by around 40 % along the approximately 9‐nm long dumbbell‐shaped component has been seen in a bistable redox‐controllable [2]rotaxane. Chemical oxidation of the tetrathiafulvalene recognition station (green, see scheme) in the dumbbell‐shaped component, which also...

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Veröffentlicht in:Angewandte Chemie International Edition 2003-04, Vol.42 (13), p.1491-1495
Hauptverfasser: Tseng, Hsian-Rong, Vignon, Scott A., Stoddart, J. Fraser
Format: Artikel
Sprache:eng
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Zusammenfassung:Mechanical displacement of the ring by around 40 % along the approximately 9‐nm long dumbbell‐shaped component has been seen in a bistable redox‐controllable [2]rotaxane. Chemical oxidation of the tetrathiafulvalene recognition station (green, see scheme) in the dumbbell‐shaped component, which also contains a 1,5‐dioxynaphthalene recognition station (red), results in the cyclobis(paraquat‐p‐phenylene) tetracation (blue) undergoing translation from the much preferred green station to the second‐choice, red station.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.200250453