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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.identifier4637430
dc.identifier4f75efb9-a6af-4e04-aa08-274ad471eeb5
dc.identifier000270593400003
dc.identifier74249112692
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.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.format.extent480072
dc.language.isoeng
dc.relation.ispartofDalton Transactionsen
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.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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