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dc.contributor.authorCordes, David B.
dc.contributor.authorHua, Guoxiong
dc.contributor.authorSlawin, Alexandra M. Z.
dc.contributor.authorWoollins, J. Derek
dc.date.accessioned2014-05-06T11:31:00Z
dc.date.available2014-05-06T11:31:00Z
dc.date.issued2011-07
dc.identifier.citationCordes , D B , Hua , G , Slawin , A M Z & Woollins , J D 2011 , ' 2,4,5-Triphenyl-1,3,2-dioxaphospholan-2-one ' Acta Crystallographica. Section E, Structure reports online , vol. 67 , o1790 . https://doi.org/10.1107/S1600536811024202en
dc.identifier.issn1600-5368
dc.identifier.otherPURE: 14284037
dc.identifier.otherPURE UUID: 1a01d2b7-9561-404f-9b1c-52bbf31b83bd
dc.identifier.otherWOS: 000294663200136
dc.identifier.otherScopus: 79960047838
dc.identifier.otherORCID: /0000-0002-5366-9168/work/28024055
dc.identifier.otherORCID: /0000-0002-9527-6418/work/56861950
dc.identifier.urihttp://hdl.handle.net/10023/4705
dc.descriptionFunding: University of St Andrews and the EPSRC, UK.en
dc.description.abstractThe dioxaphospholane ring in the title compound, C20H17O3P, adopts an envelope conformation about one of the ring carbons. The benzene rings of the compound do not form face-to-face pi-pi interactions, instead weak C-H center dot center dot center dot pi interactions occur between adjacent molecules. The methine H atoms on the dioxaphospholane ring form weak C-H center dot center dot center dot O hydrogen bonds to the oxide group of an adjacent molecule.
dc.format.extent1
dc.language.isoeng
dc.relation.ispartofActa Crystallographica. Section E, Structure reports onlineen
dc.rights(c) The Author(s) 2011.en
dc.subjectAcidsen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.title2,4,5-Triphenyl-1,3,2-dioxaphospholan-2-oneen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews.School of Chemistryen
dc.contributor.institutionUniversity of St Andrews.EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1107/S1600536811024202
dc.description.statusPeer revieweden


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