Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/4380
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Type: Journal article
Title: Enantiomerization of Pendant-Arm Triaza Macrocyclic Lithium(I) and Sodium(I) Complex Ions
Author: Whitbread, S.
Weeks, J.
Valente, P.
Buntine, M.
Lincoln, S.
Wainwright, K.
Citation: Australian Journal of Chemistry: an international journal for chemical science, 1997; 50(1):853-856
Publisher: CSIRO Publishing
Issue Date: 1997
ISSN: 0004-9425
1445-0038
Statement of
Responsibility: 
Sonya L. Whitbread, Jennifer M. Weeks, Peter Valente, Mark A. Buntine, Stephen F. Lincoln and Kevin P. Wainwright
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>
DOI: 10.1071/C97068_CO
Published version: http://www.publish.csiro.au/?act=view_file&file_id=C97068_CO.pdf
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