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dc.contributor.authorKnight, Fergus R.
dc.contributor.authorFuller, Amy L.
dc.contributor.authorSlawin, Alexandra M. Z.
dc.contributor.authorWoollins, J. Derek
dc.date.accessioned2011-04-01T11:01:03Z
dc.date.available2011-04-01T11:01:03Z
dc.date.issued2009
dc.identifier.citationKnight , F R , Fuller , A L , Slawin , A M Z & Woollins , J D 2009 , ' Controlling Cu•••Cu distances using halides: (8-phenylthionaphth-1-yl)diphenylphosphine copper halide dimers ' , Dalton Transactions , no. 40 , pp. 8476-8478 . https://doi.org/10.1039/b916692ken
dc.identifier.issn1477-9226
dc.identifier.otherPURE: 4637430
dc.identifier.otherPURE UUID: 4f75efb9-a6af-4e04-aa08-274ad471eeb5
dc.identifier.otherWOS: 000270593400003
dc.identifier.otherScopus: 74249112692
dc.identifier.otherORCID: /0000-0002-9527-6418/work/56861795
dc.identifier.otherORCID: /0000-0002-1498-9652/work/31779271
dc.identifier.urihttps://hdl.handle.net/10023/1762
dc.description.abstractIn the isomorphous binuclear Cu2X2L2 systems (L = (8-phenylthionaphth-1-yl)diphenylphosphine the Cu center dot center dot center dot Cu separation is reduced as the halide size increases.
dc.format.extent3
dc.language.isoeng
dc.relation.ispartofDalton Transactionsen
dc.rightsThis is the author's version of an article in Dalton Transactions. The published version (c)Royal society of Chemistry is available from DOI: 10.1039/B916692Ken
dc.subjectPolyaromatic hydrocarbon ligandsen
dc.subjectCrystal-structureen
dc.subjectSpectroscopic characterizationen
dc.subjectSubstituted naphthalenesen
dc.subjectHeterocyclic thionesen
dc.subjectPlatinum complexesen
dc.subjectC-2 carbonen
dc.subjectThiosemicarbazonesen
dc.subjectMononuclearen
dc.subjectChlorideen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleControlling Cu•••Cu distances using halides: (8-phenylthionaphth-1-yl)diphenylphosphine copper halide dimersen
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.description.versionPostprinten
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1039/b916692k
dc.description.statusPeer revieweden
dc.identifier.grantnumberEP/D061768/1en


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