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dc.contributor.advisorspivak, gregory
dc.contributor.authorbeach, michael t.
dc.date.accessioned2012-11-11t03:21:22z
dc.date.available2012-11-11t03:21:22z
dc.date.created2011-12
dc.date.issued2012-11-10
dc.identifier.urihttp://knowledgecommons.lakeheadu.ca/handle/2453/297
dc.description.abstractconventional phosphine ligands (i.e., those typically bearing alkyl and/or aryl substituents) have played a crucial role in the development of transition metal coordination chemistry. many structural and electronic variants have been explored, including the class of bis(n-pyrrolidinyl)alkylphosphines. these phosphines generally possess moderate steric properties, yet exhibit exceptional electron-donating properties. the greater lewis basicity of bis(n-pyrrolidinyl)alkylphosphines likely can be attributed to the additional electron density provided by the lone pair of the planar nitrogen atoms through a dative interaction with the phosphorus donor atom.en_us
dc.language.isoen_usen_us
dc.subjectruthenium piano-stool complexesen_us
dc.subjectphosphine ligandsen_us
dc.titleruthenium piano stool complexes incorporating novel bis(pyrrolidinyl)alkylphosphinesen_us
dc.typethesisen_us
etd.degree.namem.sc.en_us
etd.degree.levelmasteren_us
etd.degree.disciplinechemistryen_us
etd.degree.grantor阿根廷vs墨西哥竞猜 en_us


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