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Tris(ethylenediamine)zinc(II) hexafluoridosilicate

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dc.contributor.authorLi, Yang
dc.contributor.authorShi, Qi
dc.contributor.authorSlawin, Alexandra M. Z.
dc.contributor.authorWoollins, J. Derek
dc.contributor.authorDong, Jinxiang
dc.date.accessioned2011-04-04T10:04:38Z
dc.date.available2011-04-04T10:04:38Z
dc.date.issued2009-12
dc.identifier.citationLi , Y , Shi , Q , Slawin , A M Z , Woollins , J D & Dong , J 2009 , ' Tris(ethylenediamine)zinc(II) hexafluoridosilicate ' , Acta Crystallographica. Section E, Structure reports online , vol. 65 , no. 12 , pp. M1522-U277 . https://doi.org/10.1107/S1600536809045693en
dc.identifier.issn1600-5368
dc.identifier.otherPURE: 4637064
dc.identifier.otherPURE UUID: 98c7c71a-60f8-40df-80ac-60a85f68a98f
dc.identifier.otherWOS: 000272244600029
dc.identifier.otherScopus: 72049092662
dc.identifier.otherORCID: /0000-0002-9527-6418/work/56861398
dc.identifier.otherORCID: /0000-0002-1498-9652/work/31779264
dc.identifier.urihttps://hdl.handle.net/10023/1777
dc.description.abstractThe title compound, [Zn(C2H8N2)(3)](SiF6), was synthesized ionothermally using choline chloride-imidazolidone as solvent and template provider. In the crystal structure, the anions and cations are located on special positions of site symmetry 3.2 and show a typical octahedral geometry. The Zn-II ion is coordinated by six N atoms from three ethylenediamine molecules. The crystal structure displays weak hydrogen bonding between [SiF6](2-) anions and the ethylenediamine NH hydrogen atoms.
dc.format.extent7
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.subjectCrystalen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleTris(ethylenediamine)zinc(II) hexafluoridosilicateen
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/S1600536809045693
dc.description.statusPeer revieweden


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