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Coordination chemistry of Sb (III) and Sb (V) cations

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dc.contributor.author Frazee, Chris
dc.date.accessioned 2018-08-30T22:42:38Z
dc.date.copyright 2018 en_US
dc.date.issued 2018-08-30
dc.identifier.uri https://dspace.library.uvic.ca//handle/1828/9995
dc.description.abstract The coordination chemistry of antimony(III) and antimony(V) have been investigated to reveal fundamental structural and electronic features. The limited scope of known cationic antimony(V) complexes was greatly expanded, including the first examples of pnictogen(V) trications. The systematic nature of these investigations led to the observation of redox chemistry, determined to be the result of reductive elimination of chlorobenzene and biphenyl from an antimony center. The reactivity of [Ph2Sb(OPyrMe)4][OTf]3 was investigated and it was found that the OPyrMe ligands are sufficiently labile to perform ligand substitution chemistry. However, when exposed to phosphines, ligand-centered reactivity prevails and phosphonium salts of the form [R3P(2-4-methylpyridine)][OTf] which may be useful reagents in the field of medicinal chemistry and drug design. While attempts were made to synthesise antimony(V) tetra- and penta- cations have been unsuccessful, the methodologies reported here will serve as a foundation to future endeavors. en_US
dc.language English eng
dc.language.iso en en_US
dc.rights Available to the World Wide Web en_US
dc.subject coordination chemistry en_US
dc.subject main group en_US
dc.subject cations en_US
dc.subject antimony en_US
dc.subject inorganic en_US
dc.subject phosphorus en_US
dc.title Coordination chemistry of Sb (III) and Sb (V) cations en_US
dc.type Thesis en_US
dc.contributor.supervisor Burford, Neil
dc.degree.department Department of Chemistry en_US
dc.degree.level Doctor of Philosophy Ph.D. en_US
dc.description.scholarlevel Graduate en_US
dc.description.embargo 2019-08-31


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