Matthews, S. E. ORCID: https://orcid.org/0000-0001-8821-0851, Felix, V., Drew, M. G. B. and Beer, P. D. (2003) Halo-derivatised calix[4]tubes. Organic & Biomolecular Chemistry, 1 (7). pp. 1232-1239. ISSN 1477-0520
Full text not available from this repository. (Request a copy)Abstract
Halo functionalisation of calix[4] tubes has been investigated through both derivatisation of individual calix[4]arenes and calix[4] tubes, using classical synthetic methods, to allow preparation of a series of novel derivatives. The solution and solid state properties are in accordance with the constituent calix[4] arenes adopting flattened cone arrangements which on complexation with potassium simplify to a regular cone. Electrospray and H-1 NMR studies, combined with molecular modelling have been used to ascertain the metal binding of this new series of cryptand like ionophores, demonstrating their retained selectivity for binding potassium over other Group 1 metals and the dependence on counter anion in the weak binding of silver.
Item Type: | Article |
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Uncontrolled Keywords: | capsules,calix<4>arenes,rim,calixarenes,selectivity |
Faculty \ School: | Faculty of Science > School of Pharmacy |
UEA Research Groups: | Faculty of Science > Research Groups > Medicinal Chemistry (former - to 2017) Faculty of Science > Research Groups > Chemical Biology and Medicinal Chemistry (former - to 2021) |
Depositing User: | Rachel Smith |
Date Deposited: | 26 May 2011 11:03 |
Last Modified: | 05 May 2024 00:43 |
URI: | https://ueaeprints.uea.ac.uk/id/eprint/31447 |
DOI: | 10.1039/b211303a |
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