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dc.contributor.authorShay, Daniel Travis-
dc.date.accessioned2008-01-17T01:15:25Z-
dc.date.available2008-01-17T01:15:25Z-
dc.date.issued2006-
dc.identifier.urihttp://ir.vnulib.edu.vn/handle/123456789/1809-
dc.description.abstractThe synthesis and structural characterization of imido ligated cobalt complexes that employ the sterically hindered hydrotris(3-`Bu-5-Me-pyrazolyl)borate ligand, i. e., TptBu,MeCoNR (R = Me, Et, `Bu, Ad) have been accomplished. These terminal imido complexes possess relatively short Co-N bond distances in the range of 1.64-1.67 A, indicating a multiple bond to the metal. Reactivity studies have been undertaken with a variety of substrate ranging from protonation using acids such as HC1 and lutidinium-BARF (BARF = tetrakis(3,5-bis(trifluoromethyl)phenyl)borate) to ligand transfer of the imido fragment to carbon monoxide. Kinetic studies of the thermal decomposition of Tp'Bu,MeCoNAd which undergoes C-H activation of the Tp ligand yielding BptBu,Me(Me-pz-CMe2CH22N(Ad)H)Co, have been closely monitored by 1H NMR spectroscopy. Determination of the rate of C-H insertion of the imido ligand of Tp'Bu,MeCoNAd at a variety of temperatures led to the generation of an Erying Plot which showed curvature. Kinetic isotope measurements were also conducted showing a temperature dependent kinetic isotope effect indicating that breaking of the C-H bond was involved in the rate determining step.
dc.language.isoen_US
dc.publisherUniversity of Delaware
dc.relation.ispartofseriesDoctor of Philosophy
dc.subjectThesis
dc.titleSynthesis, structure, and reactivity of terminal cobalt imido complexes
dc.typeThesis
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