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Please use this identifier to cite or link to this item: https://doi.org/10.1039/c2cc31009k
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dc.titleTrifluoromethyl acting as stopper in [2]rotaxane
dc.contributor.authorDasgupta, S.
dc.contributor.authorHuang, K.-W.
dc.contributor.authorWu, J.
dc.date.accessioned2014-06-23T05:53:30Z
dc.date.available2014-06-23T05:53:30Z
dc.date.issued2012-05-18
dc.identifier.citationDasgupta, S., Huang, K.-W., Wu, J. (2012-05-18). Trifluoromethyl acting as stopper in [2]rotaxane. Chemical Communications 48 (40) : 4821-4823. ScholarBank@NUS Repository. https://doi.org/10.1039/c2cc31009k
dc.identifier.issn13597345
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/77315
dc.description.abstractA modified dumbbell obtained by replacing one of the phenyl groups of the dibenzylammonium with a strong electron-withdrawing trifluoromethyl group templated the synthesis of the smallest [2]rotaxane reported so far. The trifluoromethyl group not only enhances the templating effect of the dumbbell but also acts as the stopper to prevent dethreading of a [20]crown ether macrocycle. © 2012 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c2cc31009k
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c2cc31009k
dc.description.sourcetitleChemical Communications
dc.description.volume48
dc.description.issue40
dc.description.page4821-4823
dc.description.codenCHCOF
dc.identifier.isiut000303125600007
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