Cluster Control in Oligouranyl Complexes of p-t-Butylcalix[8]arene

Formation of uranyl ion complexes of p-t-butylcalix[8]arene by reaction of the calixarene with [UO2(dmso)5]2+ in the presence of various bases leads to the crystallisation of solids with interestingly different stoichiometry, involving both di- and tri-uranate oligomers bound to the calixarene in an...

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Main Authors: Harrowfield, J., Ogden, Mark, Skelton, B., White, A.
Format: Journal Article
Published: The Royal Society of Chemistry 2010
Online Access:http://hdl.handle.net/20.500.11937/29459
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author Harrowfield, J.
Ogden, Mark
Skelton, B.
White, A.
author_facet Harrowfield, J.
Ogden, Mark
Skelton, B.
White, A.
author_sort Harrowfield, J.
building Curtin Institutional Repository
collection Online Access
description Formation of uranyl ion complexes of p-t-butylcalix[8]arene by reaction of the calixarene with [UO2(dmso)5]2+ in the presence of various bases leads to the crystallisation of solids with interestingly different stoichiometry, involving both di- and tri-uranate oligomers bound to the calixarene in anionic species. In all, the calixarene hexa-anion is present in a virtually identical conformation, suggesting that conformational preferences of the ligand must be a major factor controlling the form of the bound oxo-metal complex. Hydrogen bonding to the anions does not appear to be prominent even in the presence of protonated amines and this may explain the formation of some remarkable cation/solvent/simple anion clusters found within the lattices.
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spelling curtin-20.500.11937-294592017-09-13T15:52:27Z Cluster Control in Oligouranyl Complexes of p-t-Butylcalix[8]arene Harrowfield, J. Ogden, Mark Skelton, B. White, A. Formation of uranyl ion complexes of p-t-butylcalix[8]arene by reaction of the calixarene with [UO2(dmso)5]2+ in the presence of various bases leads to the crystallisation of solids with interestingly different stoichiometry, involving both di- and tri-uranate oligomers bound to the calixarene in anionic species. In all, the calixarene hexa-anion is present in a virtually identical conformation, suggesting that conformational preferences of the ligand must be a major factor controlling the form of the bound oxo-metal complex. Hydrogen bonding to the anions does not appear to be prominent even in the presence of protonated amines and this may explain the formation of some remarkable cation/solvent/simple anion clusters found within the lattices. 2010 Journal Article http://hdl.handle.net/20.500.11937/29459 10.1039/c0dt00667j The Royal Society of Chemistry fulltext
spellingShingle Harrowfield, J.
Ogden, Mark
Skelton, B.
White, A.
Cluster Control in Oligouranyl Complexes of p-t-Butylcalix[8]arene
title Cluster Control in Oligouranyl Complexes of p-t-Butylcalix[8]arene
title_full Cluster Control in Oligouranyl Complexes of p-t-Butylcalix[8]arene
title_fullStr Cluster Control in Oligouranyl Complexes of p-t-Butylcalix[8]arene
title_full_unstemmed Cluster Control in Oligouranyl Complexes of p-t-Butylcalix[8]arene
title_short Cluster Control in Oligouranyl Complexes of p-t-Butylcalix[8]arene
title_sort cluster control in oligouranyl complexes of p-t-butylcalix[8]arene
url http://hdl.handle.net/20.500.11937/29459