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dc.contributor.authorCameron, Lee
dc.contributor.authorRajagopalan, Aswin
dc.contributor.authorAbad Galan, Laura
dc.contributor.authorPhe, Rene
dc.contributor.authorSkelton, B.W.
dc.contributor.authorMassi, Max
dc.contributor.authorOgden, Mark
dc.date.accessioned2019-10-18T05:14:55Z
dc.date.available2019-10-18T05:14:55Z
dc.date.issued2019
dc.identifier.citationCameron, L. and Rajagopalan, A. and Abad Galan, L. and Phe, R.Z.H. and Skelton, B.W. and Massi, M. and Ogden, M.I. 2019. Lanthanoid coordination with a tetrazole-substituted calix[4]diquinone and calix[4]dihydroquinone. Supramolecular Chemistry. 31 (7): pp. 466-472.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/76621
dc.identifier.doi10.1080/10610278.2019.1625357
dc.description.abstract

© 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group. The tetrazole-functionalised calixdiquinone 5,17-di-tert-butyl-26,28-bis-(1H-tetrazole-5-ylmethoxy)-calix[4]-25,27-diquinone Q was synthesised by chemical oxidation of the bis-tetrazole calix[4]arene precursor using PbO2/HClO4. The single crystal X-ray structure determination of Q confirmed the structure and showed binding of a water molecule in the solid state. Chemical reduction of Q to the dihydroquinone QR was achieved using N,N-diethylhydroxylamine. Comparison of the solution phase photophysical properties of Q or QR in the presence of terbium ions showed significant excitation only with QR, suggesting redox switching of the photophysical response may be possible with this or similar receptor.

dc.languageEnglish
dc.publisherTAYLOR & FRANCIS LTD
dc.subjectScience & Technology
dc.subjectPhysical Sciences
dc.subjectChemistry, Multidisciplinary
dc.subjectChemistry
dc.subjectCalixarene
dc.subjectlanthanide
dc.subjectquinone
dc.subjectION-PAIR RECOGNITION
dc.subjectOXIDATION
dc.titleLanthanoid coordination with a tetrazole-substituted calix[4]diquinone and calix[4]dihydroquinone
dc.typeJournal Article
dcterms.source.volume31
dcterms.source.number7
dcterms.source.startPage466
dcterms.source.endPage472
dcterms.source.issn1061-0278
dcterms.source.titleSupramolecular Chemistry
dc.date.updated2019-10-18T05:14:55Z
curtin.note

This is an Accepted Manuscript of an article published by Taylor & Francis in Supramolecular Chemistry on 09/06/2019 available online at http://www.tandfonline.com/10.1080/10610278.2019.1625357

curtin.departmentSchool of Molecular and Life Sciences (MLS)
curtin.accessStatusOpen access
curtin.facultyFaculty of Science and Engineering
curtin.contributor.orcidMassi, Max [0000-0001-6949-4019]
curtin.contributor.orcidOgden, Mark [0000-0001-5317-1637]
dcterms.source.eissn1029-0478
curtin.contributor.scopusauthoridMassi, Max [7102368846]
curtin.contributor.scopusauthoridOgden, Mark [7005364420]


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