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2-Phenyl-5-(p-tolyl)-1,3,4-oxadiazole

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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.accessioned2014-05-02T15:01:01Z
dc.date.available2014-05-02T15:01:01Z
dc.date.issued2011-07
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 . https://doi.org/10.1107/S1600536811023579en
dc.identifier.issn1600-5368
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.identifier.urihttps://hdl.handle.net/10023/4701
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.format.extent1
dc.language.isoeng
dc.relation.ispartofActa Crystallographica. Section E, Structure reports onlineen
dc.rights(c) The Author(s) 2011.en
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.title2-Phenyl-5-(p-tolyl)-1,3,4-oxadiazoleen
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/S1600536811023579
dc.description.statusPeer revieweden
dc.identifier.urlhttp://scripts.iucr.org/cgi-bin/paper?S1600536811023579en


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