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New developments in the coordination chemistry of Gold(I), Gold(II) and Gold(III) with C-, N- , P-and S-donor ligands

dc.contributor.advisorCronje, S.
dc.contributor.advisorRaubenheimer, H. G.
dc.contributor.authorCoetzee, Jacorienen_ZA
dc.contributor.otherUniversity of Stellenbosch. Faculty of Science. Dept. of Chemistry and Polymer Science.
dc.date.accessioned2007-11-27T11:02:06Zen_ZA
dc.date.accessioned2010-06-01T08:31:05Z
dc.date.available2007-11-27T11:02:06Zen_ZA
dc.date.available2010-06-01T08:31:05Z
dc.date.issued2007-03en_ZA
dc.identifier.urihttp://hdl.handle.net/10019.1/1702
dc.descriptionThesis (MSc (Chemistry and Polymer Science))--University of Stellenbosch, 2007.
dc.description.abstractA comprehensive, comparative structural study of gold(I), gold(II) and gold(III) compounds with the general formula [Aux(C6F5)y(tht)z] (tht = tetrahydrothiophene) was performed. The series of compounds included the unprecedented dinucleur gold(II) compound, tetrakis(pentafluorophenyl)bis(tetrahydrothiophene)digold(II), which could be prepared in a rational manner. This very unique compound represents the first example of an unbridged dinucleur gold(II) compound in which the gold(II) centres are not stabilised by chelating ligands. Formation of this compound was postulated to have taken place by radical pentafluorophenyl (pfp) ligand migration along with AuII–AuII bond formation. It may therefore be regarded as a rare example of labile behaviour by a generally inert pfp ligand. In addition to this compound, the crystal and molecular structures of the wellknown gold(I) and gold(III) precursor compounds, (pentafluorophenyl)(tetrahydrothiophene) gold(I) and tris(pentafluorophenyl)(tetrahydrothiophene)gold(III) were carried out and are described for the first time. The latter underwent a unique mononuclear ligand rearrangement (metathesis or disproportionation) reaction in solution to yield the novel rearrangement product, bis(pentafluorophenyl)bis(tetrahydrothiophene)gold(III)tetrakis- (pentafluorophenyl)gold(III). In all the complexes, the Au–C and Au–S bond lengths displayed a variation which appears to be dependent on the oxidation state of the central gold atom. Both of these bond types were found to descrease in the order Au(II) > Au(III) > Au(I)...en_ZA
dc.format.extent2443802 bytesen_ZA
dc.format.mimetypeapplication/pdfen_ZA
dc.publisherStellenbosch : University of Stellenbosch
dc.subjectLigandsen_ZA
dc.subjectCoordination compoundsen_ZA
dc.subjectGold compoundsen_ZA
dc.subjectDissertations -- Chemistryen_ZA
dc.subjectTheses -- Chemistryen_ZA
dc.subject.otherChemistry and Polymer Scienceen_ZA
dc.titleNew developments in the coordination chemistry of Gold(I), Gold(II) and Gold(III) with C-, N- , P-and S-donor ligandsen_ZA
dc.typeThesisen_ZA
dc.rights.holderUniversity of Stellenbosch


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