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Article: Speed-controlled molecular shuttles

TitleSpeed-controlled molecular shuttles
Authors
KeywordsBipyridinium salts
Crown ethers
Dynamic NMR spectroscopy
Molecular machines
Molecular recognition
Molecular shuttle
Post-assembly covalent modification
Rotaxanes
Issue Date2002
Citation
Collection of Czechoslovak Chemical Communications, 2002, v. 67, n. 11, p. 1719-1728 How to Cite?
AbstractFive potential molecular shuttles based on degenerate [2]rotaxanes - wherein the ring component is a bis-1,4-phenylene[34]crown-10 and the dumbbell components are terminated by tetraarylmethane (slippage) stoppers and contain two identical bipyridinium recognition sites and a central 1,3-phenylene unit carrying a CH2OR (R = Me, Et, Ph, i-Pr, and t-Bu) substituent on its C-5 position - have been prepared by acylating the parent hydroxymethyl derivative with the appropriate reagents. Dynamic 1H NMR spectroscopy, carried out on these five potential molecular shuttles in CD3CN solutions, has revealed average Gibbs energy barriers to shuttling of 11.5, 12.0, 14.6, and 14.8 kcal mol-1 for the [2]rotaxanes where R = Me, Et, i-Pr, and Ph, respectively. For the [2]rotaxane where R = t-Bu, the Gibbs energy barrier to shuttling must exceed 17.2 kcal mol-1.
Persistent Identifierhttp://hdl.handle.net/10722/332510
ISSN
2013 Impact Factor: 1.137
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorBělohradský, Martin-
dc.contributor.authorElizarov, Arkadij M.-
dc.contributor.authorStoddart, J. Fraser-
dc.date.accessioned2023-10-06T05:12:05Z-
dc.date.available2023-10-06T05:12:05Z-
dc.date.issued2002-
dc.identifier.citationCollection of Czechoslovak Chemical Communications, 2002, v. 67, n. 11, p. 1719-1728-
dc.identifier.issn0010-0765-
dc.identifier.urihttp://hdl.handle.net/10722/332510-
dc.description.abstractFive potential molecular shuttles based on degenerate [2]rotaxanes - wherein the ring component is a bis-1,4-phenylene[34]crown-10 and the dumbbell components are terminated by tetraarylmethane (slippage) stoppers and contain two identical bipyridinium recognition sites and a central 1,3-phenylene unit carrying a CH2OR (R = Me, Et, Ph, i-Pr, and t-Bu) substituent on its C-5 position - have been prepared by acylating the parent hydroxymethyl derivative with the appropriate reagents. Dynamic 1H NMR spectroscopy, carried out on these five potential molecular shuttles in CD3CN solutions, has revealed average Gibbs energy barriers to shuttling of 11.5, 12.0, 14.6, and 14.8 kcal mol-1 for the [2]rotaxanes where R = Me, Et, i-Pr, and Ph, respectively. For the [2]rotaxane where R = t-Bu, the Gibbs energy barrier to shuttling must exceed 17.2 kcal mol-1.-
dc.languageeng-
dc.relation.ispartofCollection of Czechoslovak Chemical Communications-
dc.subjectBipyridinium salts-
dc.subjectCrown ethers-
dc.subjectDynamic NMR spectroscopy-
dc.subjectMolecular machines-
dc.subjectMolecular recognition-
dc.subjectMolecular shuttle-
dc.subjectPost-assembly covalent modification-
dc.subjectRotaxanes-
dc.titleSpeed-controlled molecular shuttles-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1135/cccc20021719-
dc.identifier.scopuseid_2-s2.0-0036881064-
dc.identifier.volume67-
dc.identifier.issue11-
dc.identifier.spage1719-
dc.identifier.epage1728-
dc.identifier.isiWOS:000179586000015-

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