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 |
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Hauptverfasser: | , , |
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. |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.200250453 |