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Article: Exploring dynamics and stereochemistry in mechanically-interlocked compounds

TitleExploring dynamics and stereochemistry in mechanically-interlocked compounds
Authors
KeywordsCatenanes
Donor-acceptor
Dynamic stereochemistry
Macrocycles
Molecular machines
NMR dynamics
Pretzelanes
Rotaxanes
Self-complexing
Tetrathiafulvalenes
Issue Date2005
Citation
Collection of Czechoslovak Chemical Communications, 2005, v. 70, n. 10, p. 1493-1576 How to Cite?
AbstractThe advent of self-assembly and template-directed synthetic protocols has led to a tremendous surge in the number of mechanically-interlocked compounds being prepared and studied. As these investigations are being carried out, it is becoming increasingly apparent that many of these compounds, known as catenanes and rotaxanes, possess unique dynamic and stereochemical properties. In addition, the drive to create molecular switches and machines for nanotechnological applications has generated a need to understand how to control those properties in condensed phases. Here, we present an overview of the field with regard to the solution dynamics and stereochemistry of mechanically-interlocked compounds - as well as to some related structural types - and review the recent results from our own research in some detail. 1H NMR spectroscopy has proven to be a powerful tool for probing both degenerate and nondegenerate dynamic processes in these compounds, as well as for identifying stereoisomers if they are present in solution. The results of several variable temperature NMR investigations on the effects of structural changes upon the dynamic processes and stimulated relative motions of components in catenanes and rotaxanes, as well as in some self-complexes and pretzelanes, are discussed. A review with 90 references.
Persistent Identifierhttp://hdl.handle.net/10722/333597
ISSN
2013 Impact Factor: 1.137
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorVignon, Scott A.-
dc.contributor.authorStoddart, J. Fraser-
dc.date.accessioned2023-10-06T05:20:54Z-
dc.date.available2023-10-06T05:20:54Z-
dc.date.issued2005-
dc.identifier.citationCollection of Czechoslovak Chemical Communications, 2005, v. 70, n. 10, p. 1493-1576-
dc.identifier.issn0010-0765-
dc.identifier.urihttp://hdl.handle.net/10722/333597-
dc.description.abstractThe advent of self-assembly and template-directed synthetic protocols has led to a tremendous surge in the number of mechanically-interlocked compounds being prepared and studied. As these investigations are being carried out, it is becoming increasingly apparent that many of these compounds, known as catenanes and rotaxanes, possess unique dynamic and stereochemical properties. In addition, the drive to create molecular switches and machines for nanotechnological applications has generated a need to understand how to control those properties in condensed phases. Here, we present an overview of the field with regard to the solution dynamics and stereochemistry of mechanically-interlocked compounds - as well as to some related structural types - and review the recent results from our own research in some detail. 1H NMR spectroscopy has proven to be a powerful tool for probing both degenerate and nondegenerate dynamic processes in these compounds, as well as for identifying stereoisomers if they are present in solution. The results of several variable temperature NMR investigations on the effects of structural changes upon the dynamic processes and stimulated relative motions of components in catenanes and rotaxanes, as well as in some self-complexes and pretzelanes, are discussed. A review with 90 references.-
dc.languageeng-
dc.relation.ispartofCollection of Czechoslovak Chemical Communications-
dc.subjectCatenanes-
dc.subjectDonor-acceptor-
dc.subjectDynamic stereochemistry-
dc.subjectMacrocycles-
dc.subjectMolecular machines-
dc.subjectNMR dynamics-
dc.subjectPretzelanes-
dc.subjectRotaxanes-
dc.subjectSelf-complexing-
dc.subjectTetrathiafulvalenes-
dc.titleExploring dynamics and stereochemistry in mechanically-interlocked compounds-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1135/cccc20051493-
dc.identifier.scopuseid_2-s2.0-30344457892-
dc.identifier.volume70-
dc.identifier.issue10-
dc.identifier.spage1493-
dc.identifier.epage1576-
dc.identifier.isiWOS:000233617400001-

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