Hard-hard and soft-soft coordination in complexes of Group 6 and Group 10 & 11 metals respectively

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dc.contributor.advisorLuckay, Robert C.en_ZA
dc.contributor.advisorRaubenheimer, H. G.
dc.contributor.authorLe Roux, Adeleen_ZA
dc.contributor.otherUniversity of Stellenbosch. Faculty of Science. Dept. of Chemistry and Polymer Science.
dc.date.accessioned2008-06-18T10:56:13Zen_ZA
dc.date.accessioned2010-06-01T09:06:34Z
dc.date.available2008-06-18T10:56:13Zen_ZA
dc.date.available2010-06-01T09:06:34Z
dc.date.issued2008-03en_ZA
dc.descriptionThesis (MSc (Chemistry and Polymer Science))--University of Stellenbosch, 2008.
dc.description.abstractIn this study, the coordination of certain Group 6 and Group 10 & 11 metals to Odonor and S-donor ligands were investigated. For the most part, this involved the isolation of new Mo(VI) and W(VI) complexes. By using a distribution diagram that shows the dependence of the type of species in solution with pH, we attempted to crystallize new polyoxoanion species of the two metals. It was found that the products that crystallize are not necessarily dependant upon the relative concentrations of the species in solution, but rather on the effective packing of the crystal types that are prepared. During this study a unique W(VI) polyanion, [(CH3CH2)4N]2[W6O19] (4), was isolated. The Mo(VI) analogue of this compound as well as the dinuclear Mo(VI)-W(VI) complex have been reported previously, but a pure W(VI) compound of this type has not been successfully isolated yet. A new polymorph of a known dimolybdate, K2Mo2O7·H2O (1), was also crystallized, even though dimolybdate species do not generally occur in solution. This structure, although previously reported, shows some differences with the one in the literature, in particular large deviations in unit cell dimensions. Subsequently, as a second component of this study, a variety of carboxylates were coordinated to Mo(VI) and W(VI) species in an acidic medium. Two new complexes of Mo(VI) with these carboxylate ligands were isolated: [(CH3CH2)4N][MoO3(mal)]·H2O (5) (mal = malate) and Na6[Mo2O5(cit)2] (6) (cit = citrate). The ligands are two- and threefold deprotonated respectively and coordinate in a polydentate manner to the metal centra. The formation of compound 5 in solution has been known for many years, but the structure of this complex has not been determined in the solid state until now. Also, the tungsten analogue of compound 6 was reported years ago, but the Mo(VI) complex has not been crystallized before. Compounds 5 and 6 exhibit a 1:1 and 2:2 metal to ligand ratio respectively, and these ratios are quite rare in Mo(VI) crystal chemistry. Finally, the dimolybdate complex, [CH3)3N(CH2)6N(CH3)3][Mo2O7(cit)] (7), was isolated, and its structure determined and compared to the one in the literature. In the third part of this study, our attention shifted to the group 10 and 11 metals, platinum and gold. Attempts were made to coordinate unusual ligands with donor atoms P, Se and/or S to these metal centers. During this investigation, we isolated a unique Pt(IV) complex, PtCl2(S3C8H7)2 (9). The structure of this compound that was determined crystallographically involves the coordination of two identical R-SCS2 fragments to the metal ion forming four-membered chelate rings. No compounds of Pt and Au with the P-Se ligand, P3Se3(C(C6H5)3)3, could be isolated. However, a mixed valence compound of Au(I,III), [Au(I)Cl(S(CH2C6H5)2)][Au(III)Cl3(S(CH2C6H5)2] (8), could be isolated and characterized. In this compound Au exhibits two oxidation states, +1 and +3. Although the complex has been reported previously, the structure was not described fully, and we now unequivocally determined its crystal structure. The extended structure shows the formation of chains of alternating Au(I) and Au(III) centers with a separation of 5.610 Å.en_ZA
dc.identifier.urihttp://hdl.handle.net/10019.1/3111
dc.language.isoen_ZAen_ZA
dc.subjectPolyoxometalatesen_ZA
dc.subjectMetal complexesen_ZA
dc.subjectLigandsen_ZA
dc.subjectSulphur-complexesen_ZA
dc.subjectDissertations -- Chemistryen_ZA
dc.subjectTheses -- Chemistryen_ZA
dc.subject.otherChemistry and Polymer Scienceen_ZA
dc.titleHard-hard and soft-soft coordination in complexes of Group 6 and Group 10 & 11 metals respectivelyen_ZA
dc.typeThesisen_ZA
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