Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/4297
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dc.contributor.authorDavies, P.-
dc.contributor.authorLincoln, S.-
dc.contributor.authorSmith, C.-
dc.contributor.authorTaylor, M.-
dc.contributor.authorWainwright, K.-
dc.contributor.authorWallwork, K.-
dc.date.issued2000-
dc.identifier.citationActa Crystallographica Section C: Crystal Structure Communications, 2000; C56(1):28-30-
dc.identifier.issn0108-2701-
dc.identifier.issn1600-5759-
dc.identifier.urihttp://hdl.handle.net/2440/4297-
dc.descriptionCopyright © 2008 International Union of Crystallography-
dc.description.abstractCrystallization of [Cd(S-thpc12)](ClO4)2·H2O {S-thpc12 is 1,4,7,10-tetrakis[(S)-2-hydroxypropyl]-1,4,7,10-tetraazacyclododecane} in the presence of sodium p-nitrophenolate forms the title complex, [Cd(C20H44N4O4)](C6H 4NO3)(ClO4)·H2O. in which p-nitrophenolate and water separately hydrogen bond to a different pair of cis-related pendant hydroxyl groups which, together with the four N atoms, are themselves hound to CdII in an approximately square antiprismatic arrangement. The diastereoselectivity of the complex-forming process is apparent from the fact that both different disymmetric cations in the asymmetric unit have the same Δ helicity.-
dc.description.statementofresponsibilityPhilip. J. Davies, Stephen F. Lincoln, Christopher B. Smith, Max R. Taylor, Kevin P. Wainwright and Kia S. Wallwork-
dc.language.isoen-
dc.publisherBlackwell Munksgaard-
dc.source.urihttp://dx.doi.org/10.1107/s0108270199012391-
dc.title{D-1,4,7,10 -Tetrakis[(S)-2-hydroxy-propyl-kO]-1,4,7,10-tetraazacyclododecane-k4N}cadmium(II) 4-nitro-phenolate hydrate-
dc.typeJournal article-
dc.identifier.doi10.1107/S0108270199012391-
pubs.publication-statusPublished-
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