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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/17920
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dc.contributor.authorOnagi, H.-
dc.contributor.authorBlake, C.-
dc.contributor.authorEaston, C.-
dc.contributor.authorLincoln, S.-
dc.date.issued2003-
dc.identifier.citationChemistry: A European Journal, 2003; 9(24):5978-5988-
dc.identifier.issn0947-6539-
dc.identifier.issn1521-3765-
dc.identifier.urihttp://hdl.handle.net/2440/17920-
dc.descriptionThe definitive version may be found at www.wiley.com-
dc.description.abstractEight 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.-
dc.description.statementofresponsibilityHideki Onagi, Christopher J. Blake, Christopher J. Easton, Stephen F. Lincoln-
dc.language.isoen-
dc.publisherWiley-V C H Verlag GMBH-
dc.source.urihttp://www3.interscience.wiley.com/cgi-bin/abstract/106571055/ABSTRACT-
dc.subjectCyclodextrins-
dc.subjectmolecular devices-
dc.subjectmolecular dynamics-
dc.subjectNMR spectroscopy-
dc.subjectrotaxanes-
dc.titleInstallation of a ratchet tooth and pawl to restrict rotation in a cyclodextrin rotaxane-
dc.typeJournal article-
dc.identifier.doi10.1002/chem.200305280-
pubs.publication-statusPublished-
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