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dc.contributor.authorKnight, Fergus Ross
dc.contributor.authorRandall, Rebecca Amy Michele
dc.contributor.authorWakefield, Lucy
dc.contributor.authorSlawin, Alexandra Martha Zoya
dc.contributor.authorWoollins, J Derek
dc.date.accessioned2012-12-14T15:01:05Z
dc.date.available2012-12-14T15:01:05Z
dc.date.issued2012-11-08
dc.identifier.citationKnight , F R , Randall , R A M , Wakefield , L , Slawin , A M Z & Woollins , J D 2012 , ' Investigating silver coordination to mixed chalcogen ligands ' Molecules , vol. 17 , no. 11 , pp. 13307-13329 . https://doi.org/10.3390/molecules171113307en
dc.identifier.issn1420-3049
dc.identifier.otherPURE: 41270032
dc.identifier.otherPURE UUID: 4de4ff0b-64ab-47ed-8e88-c511f650cb8c
dc.identifier.otherWOS: 000311428400063
dc.identifier.otherScopus: 84870184929
dc.identifier.otherORCID: /0000-0002-9527-6418/work/56861425
dc.identifier.urihttp://hdl.handle.net/10023/3299
dc.descriptionThe work in this project was supported by the Engineering and Physical Sciences Research Council (EPSRC).en
dc.description.abstractSix silver(I) coordination complexes have been prepared and structurally characterised. Mixed chalcogen-donor acenaphthene ligands L1–L3 [Acenap(EPh)(E'Ph)] (Acenap = acenaphthene-5,6-diyl; E/E' = S, Se, Te) were independently treated with silver(I) salts (AgBF4/AgOTf). In order to keep the number of variables to a minimum, all reactions were carried out using a 1:1 ratio of Ag/L and run in dichloromethane. The nature of the donor atoms, the coordinating ability of the respective counter-anion and the type of solvent used in recrystallisation, all affect the structural architecture of the final silver(I) complex, generating monomeric, silver(I) complexes {[AgBF4(L)2] (1 L = L1; 2 L = L2; 3 L = L3), [AgOTf(L)3] (4 L = L1; 5 L = L3), [AgBF4(L)3] (2a L = L1; 3a L = L3)} and a 1D polymeric chain {[AgOTf(L3)]n 6}. The organic acenaphthene ligands L1-L3 adopt a number of ligation modes (bis-monodentate μ2-η2-bridging, quasi-chelating combining monodentate and η6-E(phenyl)-Ag(I) and classical monodentate coordination) with the central silver atom at the centre of a tetrahedral or trigonal planar coordination geometry in each case. The importance of weak interactions in the formation of metal-organic structures is also highlighted by the number of short non-covalent contacts present within each complex.
dc.format.extent23
dc.language.isoeng
dc.relation.ispartofMoleculesen
dc.rights© 2012 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).en
dc.subjectSilver(I) complexesen
dc.subjectChalcogen-donoren
dc.subjectCoordination networksen
dc.subjectHelical chain polymeren
dc.subjectAcenaphthene ligandsen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleInvestigating silver coordination to mixed chalcogen ligandsen
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/10.3390/molecules171113307
dc.description.statusPeer revieweden


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