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Article: Cyclophanes with self-recognising components

TitleCyclophanes with self-recognising components
Authors
Issue Date1995
Citation
Journal of the Chemical Society, Chemical Communications, 1995, n. 24, p. 2541-2545 How to Cite?
AbstractHigh dilution techniques have been employed to construct a series of charged flexible cyclophanes comprised of π-electron-rich hydroquinone and π-electron-deficient bipyridinium residues linked by polyether spacer units of varying length: significant conformational changes, leading to intramolecular and intermolecular interactions between the π-donors and π-acceptors, have been observed-as evidenced by X-ray crystallographic and variable temperature 1H NMR and 2D ROESY spectroscopic investigations-within the series of the cyclophanes both in the solid and solution states as a result of increasing the lengths of the polyether spacer units.
Persistent Identifierhttp://hdl.handle.net/10722/332766
ISSN
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorAnelli, Pier Lucio-
dc.contributor.authorAsakawa, Masumi-
dc.contributor.authorAshton, Peter R.-
dc.contributor.authorBrown, George R.-
dc.contributor.authorHayes, Wayne-
dc.contributor.authorKocian, Oldrich-
dc.contributor.authorPastor, Santiago Rodríguez-
dc.contributor.authorStoddart, J. Fraser-
dc.contributor.authorTolley, Malcolm S.-
dc.contributor.authorWhite, Andrew J.P.-
dc.contributor.authorWilliams, David J.-
dc.date.accessioned2023-10-06T05:14:06Z-
dc.date.available2023-10-06T05:14:06Z-
dc.date.issued1995-
dc.identifier.citationJournal of the Chemical Society, Chemical Communications, 1995, n. 24, p. 2541-2545-
dc.identifier.issn0022-4936-
dc.identifier.urihttp://hdl.handle.net/10722/332766-
dc.description.abstractHigh dilution techniques have been employed to construct a series of charged flexible cyclophanes comprised of π-electron-rich hydroquinone and π-electron-deficient bipyridinium residues linked by polyether spacer units of varying length: significant conformational changes, leading to intramolecular and intermolecular interactions between the π-donors and π-acceptors, have been observed-as evidenced by X-ray crystallographic and variable temperature 1H NMR and 2D ROESY spectroscopic investigations-within the series of the cyclophanes both in the solid and solution states as a result of increasing the lengths of the polyether spacer units.-
dc.languageeng-
dc.relation.ispartofJournal of the Chemical Society, Chemical Communications-
dc.titleCyclophanes with self-recognising components-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/C39950002541-
dc.identifier.scopuseid_2-s2.0-37049078478-
dc.identifier.issue24-
dc.identifier.spage2541-
dc.identifier.epage2545-
dc.identifier.isiWOS:A1995TN66900034-

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