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dc.contributor.authorD'Alessio, Daniel
dc.contributor.authorSkelton, B.
dc.contributor.authorLengkeek, N.
dc.contributor.authorFraser, B.
dc.contributor.authorKrause-Heuer, A.
dc.contributor.authorMuzzioli, S.
dc.contributor.authorStagni, S.
dc.contributor.authorMassi, Max
dc.contributor.authorOgden, Mark
dc.date.accessioned2017-01-30T14:42:25Z
dc.date.available2017-01-30T14:42:25Z
dc.date.created2015-12-17T20:00:16Z
dc.date.issued2015
dc.identifier.citationD'Alessio, D. and Skelton, B. and Lengkeek, N. and Fraser, B. and Krause-Heuer, A. and Muzzioli, S. and Stagni, S. et al. 2015. Ionophoric properties of a tetra-tetrazole functionalised calix[4]arene. Supramolecular Chemistry. 27 (11-12): pp. 787-791.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/40409
dc.identifier.doi10.1080/10610278.2015.1075536
dc.description.abstract

© 2015 Taylor & Francis. The synthesis and characterisation of p-t-butylcalix[4]arene functionalised at the lower rim with four tetrazole moieties is reported. The macrocycle is found to be a poorer ionophore for lanthanoid cations than the bis-tetrazole-substituted analogue. Solution-phase photophysical studies strongly suggested that the cations interacted only weakly with the calixarene ligand. A mixed sodium/triethylammonium salt of the calixarene ligand was crystallised in the presence of lanthanoid cations and structurally characterised. Strong intramolecular interactions are hypothesised to be the cause of the observed behaviour.

dc.titleIonophoric properties of a tetra-tetrazole functionalised calix[4]arene
dc.typeJournal Article
dcterms.source.volume27
dcterms.source.number11-12
dcterms.source.startPage787
dcterms.source.endPage791
dcterms.source.issn1061-0278
dcterms.source.titleSupramolecular Chemistry
curtin.note

This is an Author's Original Manuscript of an article published by Taylor & Francis in Supramolecular Chemistry on 23/10/2015, available online at <a href="http://www.tandfonline.com/10.1080/10610278.2015.1075536">http://www.tandfonline.com/10.1080/10610278.2015.1075536</a>

curtin.departmentDepartment of Chemistry
curtin.accessStatusOpen access


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