Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/17920
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Type: Journal article
Title: Installation of a ratchet tooth and pawl to restrict rotation in a cyclodextrin rotaxane
Author: Onagi, H.
Blake, C.
Easton, C.
Lincoln, S.
Citation: Chemistry: A European Journal, 2003; 9(24):5978-5988
Publisher: Wiley-V C H Verlag GMBH
Issue Date: 2003
ISSN: 0947-6539
1521-3765
Statement of
Responsibility: 
Hideki Onagi, Christopher J. Blake, Christopher J. Easton, Stephen F. Lincoln
Abstract: Eight new [2]rotaxanes have been prepared, incorporating an -cyclodextrin as the rotor, a stilbene as the axle, and trinitrophenyl substituents as capping groups. Strategies have been devised to elaborate these by linking the rotor to the axle, to produce two new [1]rotaxanes. Rotational motion in a selection of these rotaxanes has been investigated through the application of two-dimensional NMR spectroscopy by performing TOCSY, DQF-COSY, ROESY and HMQC experiments. This has shown that a methoxyl group incorporated on the stilbene and a succinamide joining the stilbene and the cyclodextrin behave analogously to a ratchet tooth and pawl, respectively, to restrict rotation.
Keywords: Cyclodextrins
molecular devices
molecular dynamics
NMR spectroscopy
rotaxanes
Description: The definitive version may be found at www.wiley.com
DOI: 10.1002/chem.200305280
Published version: http://www3.interscience.wiley.com/cgi-bin/abstract/106571055/ABSTRACT
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