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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.identifier.citationCordes , D B , Hua , G , Slawin , A M Z & Woollins , J D 2011 , ' 2-Phenyl-5-(p-tolyl)-1,3,4-oxadiazole ' , Acta Crystallographica. Section E, Structure reports online , vol. 67 , pp. o1757 .
dc.identifier.otherPURE: 14284006
dc.identifier.otherPURE UUID: 4d1bb65e-a103-4408-bb86-219097eaa5d7
dc.identifier.otherWOS: 000294663200112
dc.identifier.otherScopus: 79960041395
dc.identifier.otherORCID: /0000-0002-5366-9168/work/28024053
dc.identifier.otherORCID: /0000-0002-9527-6418/work/56861566
dc.identifier.otherORCID: /0000-0002-1498-9652/work/31779232
dc.descriptionFunding: University of St. Andrews and the Engineering and Physical Science Research Council (EPSRC, UK).en
dc.description.abstractThe title compound, C15H12N2O, adopts the expected near-planar geometry, the phenyl and tolyl rings being inclined relative to the oxadiazole ring by 3.8 (3) and 8.3 (2)degrees, respectively. This allows adjacent molecules to pack in a parallel fashion and form stacking along [010] via pi-pi interactions [centroid-centroid distances = 3.629 (2) and 3.723 (2) angstrom]. Further intermolecular interactions include C-H center dot center dot center dot pi interactions and weak C-H center dot center dot center dot N hydrogen bonds, giving rise to a crossed herringbone packing motif.
dc.relation.ispartofActa Crystallographica. Section E, Structure reports onlineen
dc.rights(c) The Author(s) 2011.en
dc.subjectQD Chemistryen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.description.statusPeer revieweden

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