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dc.contributor.authorHua, Guoxiong
dc.contributor.authorFuller, Amy L.
dc.contributor.authorSlawin, Alexandra M. Z.
dc.contributor.authorWoollins, J. Derek
dc.date.accessioned2011-04-04T09:34:43Z
dc.date.available2011-04-04T09:34:43Z
dc.date.issued2010-10
dc.identifier.citationHua , G , Fuller , A L , Slawin , A M Z & Woollins , J D 2010 , ' 1,2-Bis(2-bromobenzyl)diselane ' , Acta Crystallographica. Section E, Structure reports online , vol. 66 , no. 10 , pp. O2579-U623 . https://doi.org/10.1107/S1600536810036676en
dc.identifier.issn1600-5368
dc.identifier.otherPURE: 4638679
dc.identifier.otherPURE UUID: a0793eb8-b157-4a36-9391-bc1bc801e224
dc.identifier.otherWOS: 000282558000056
dc.identifier.otherScopus: 77957842957
dc.identifier.otherORCID: /0000-0002-9527-6418/work/56861903
dc.identifier.otherORCID: /0000-0002-1498-9652/work/31779244
dc.identifier.urihttps://hdl.handle.net/10023/1775
dc.description.abstractIn the title compound, C14H12Br2Se2, the Se-Se bond length [2.3034 (9) angstrom] is similar to those in diphenyl diselenide [2.3066 (7) and 2.3073 (10) angstrom] and shorter than that in 1,8-diselenonaphthalene [2.0879 (8) angstrom]. The molecule adopts a classical gauche conformation.
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.subjectQD Chemistryen
dc.subject.lccQDen
dc.title1,2-Bis(2-bromobenzyl)diselaneen
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/S1600536810036676
dc.description.statusPeer revieweden


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