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dc.contributor.authorFang, Zeguo
dc.contributor.authorAl-Maharik, Nawaf
dc.contributor.authorSlawin, Alexandra M. Z.
dc.contributor.authorBuehl, Michael
dc.contributor.authorO'Hagan, David
dc.identifier.citationFang , Z , Al-Maharik , N , Slawin , A M Z , Buehl , M & O'Hagan , D 2016 , ' Polar alicyclic rings: synthesis and structure of all cis -1,2,3,4-tetrafluorocyclopentane ' , Chemical Communications , vol. 52 , no. 29 , pp. 5116-5119 .
dc.identifier.otherPURE: 241567442
dc.identifier.otherPURE UUID: 9793468c-20db-4383-a03b-de80d83083ab
dc.identifier.otherScopus: 84963762499
dc.identifier.otherORCID: /0000-0002-1095-7143/work/48131794
dc.identifier.otherORCID: /0000-0002-9527-6418/work/56862116
dc.identifier.otherWOS: 000373629800007
dc.identifier.otherORCID: /0000-0002-0510-5552/work/68281313
dc.descriptionThe authors are grateful to the Chinese Scholarship Council for Studentship support (ZF), to EPSRC for financial support and to the EPSRC National Mass Spectrometry Service at Swansea for analytical support. DO’H thanks the Royal Society for a Wolfson Research Merit Award.en
dc.description.abstractThe all-cis isomer of 1,2,3,4-tetrafluorocyclopentane is prepared and characterised by NMR and X-ray crystallography and the experimental structure compared with theory. The structure has a similarly high polarity to all-cis tetrafluorocyclohexanes despite the increased conformational flexibility of a cyclopentane.
dc.relation.ispartofChemical Communicationsen
dc.rightsCopyright 2016 the Authors. This work is made available online in accordance with the publisher’s policies. This is the author created, accepted version manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at
dc.subjectQD Chemistryen
dc.titlePolar alicyclic rings: synthesis and structure of all cis-1,2,3,4-tetrafluorocyclopentaneen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews.School of Chemistryen
dc.contributor.institutionUniversity of St Andrews.EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews.Biomedical Sciences Research Complexen
dc.description.statusPeer revieweden

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