Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/4380
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dc.contributor.authorWhitbread, S.-
dc.contributor.authorWeeks, J.-
dc.contributor.authorValente, P.-
dc.contributor.authorBuntine, M.-
dc.contributor.authorLincoln, S.-
dc.contributor.authorWainwright, K.-
dc.date.issued1997-
dc.identifier.citationAustralian Journal of Chemistry: an international journal for chemical science, 1997; 50(1):853-856-
dc.identifier.issn0004-9425-
dc.identifier.issn1445-0038-
dc.identifier.urihttp://hdl.handle.net/2440/4380-
dc.description.abstract<jats:p>The first reported enantiomerization of six-coordinate alkali metal complex ions, represented by 1,4,7-tris(2-hydroxyethyl)-1,4,7-triazacyclononanelithium(I) and its sodium(I) analogue in methanol, has been characterized by variable-temperature 13C{1H} n.m.r. spectroscopy. The respective kinetic parameters are: k = (1·11 ± 0·05) × 106 and (2·27 ± 0·09) × 105 s-1 at 298·2 K, ΔH = 27·2 ± 0·3 and 21·7±0·2 kJ mol-1, and ΔS = –36·3 ± 1·3 and –69·6±1·2 J K-1 mol-1. Molecular orbital calculations show that these enantiomers have distorted trigonal prismatic structures consistent with the interpretation of the n.m.r. spectra. For the Li+, Na+, K+, Rb+ and Cs+ complex ions log(K/dm3 mol−1) = 3·13±0·09, 3·52±0·05, 3·23±0·05, 2·78±0·10 and 2·47±0·08, respectively, at 298·2 K and I = 0·05 mol dm-3 (NEt4 ClO4) in methanol, where K is the complex ion stability constant.</jats:p>-
dc.description.statementofresponsibilitySonya L. Whitbread, Jennifer M. Weeks, Peter Valente, Mark A. Buntine, Stephen F. Lincoln and Kevin P. Wainwright-
dc.language.isoen-
dc.publisherCSIRO Publishing-
dc.source.urihttp://www.publish.csiro.au/?act=view_file&file_id=C97068_CO.pdf-
dc.titleEnantiomerization of Pendant-Arm Triaza Macrocyclic Lithium(I) and Sodium(I) Complex Ions-
dc.typeJournal article-
dc.identifier.doi10.1071/C97068_CO-
pubs.publication-statusPublished-
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