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2,2 '-o-Phenylenediacetonitrile

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dc.contributor.authorLi, Yang
dc.contributor.authorHua, Guoxiong
dc.contributor.authorSlawin, Alexandra M. Z.
dc.contributor.authorWoollins, J. Derek
dc.date.accessioned2011-04-04T10:04:47Z
dc.date.available2011-04-04T10:04:47Z
dc.date.issued2009-11
dc.identifier.citationLi , Y , Hua , G , Slawin , A M Z & Woollins , J D 2009 , ' 2,2 '-o-Phenylenediacetonitrile ' , Acta Crystallographica. Section E, Structure reports online , vol. 65 , no. 11 , pp. O2757-U830 . https://doi.org/10.1107/S1600536809041506en
dc.identifier.issn1600-5368
dc.identifier.otherPURE: 4637300
dc.identifier.otherPURE UUID: 42d548f9-9ab9-43aa-b4b6-6c201d99f2ae
dc.identifier.otherWOS: 000271977700068
dc.identifier.otherScopus: 70449396011
dc.identifier.otherORCID: /0000-0002-9527-6418/work/56861794
dc.identifier.otherORCID: /0000-0002-1498-9652/work/31779268
dc.identifier.urihttps://hdl.handle.net/10023/1781
dc.descriptionThis work is funded by EPSRC UK.en
dc.description.abstractIn the title compound, NCCH2C6H4CH2CN, the bond lengths and angles are within normal ranges. The benzene ring makes dihedral angles of 4.94 (8) and 77.04 (8)degrees with the C-C-C-N mean planes. Weak non-conventional C-H center dot center dot center dot N hydrogen bonds are effective in the stabilization of the crystal structure. The weak C-H center dot center dot center dot N contacts form antiparallel chains running in the a + c direction, and ring systems with two N-atom acceptors and four H-atom donors.
dc.format.extent8
dc.language.isoeng
dc.relation.ispartofActa Crystallographica. Section E, Structure reports onlineen
dc.rightsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en
dc.subjectWoollins reagenten
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.title2,2 '-o-Phenylenediacetonitrileen
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/S1600536809041506
dc.description.statusPeer revieweden


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