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dc.contributor.advisorDarensbourg, Donald J.
dc.creatorFlatt, Brenton Todd
dc.date.accessioned2022-04-01T16:03:55Z
dc.date.available2022-04-01T16:03:55Z
dc.date.issued1990
dc.identifier.urihttps://hdl.handle.net/1969.1/CAPSTONE-CarthelC_1985
dc.descriptionProgram year: 1989/1990en
dc.descriptionDigitized from print original stored in HDRen
dc.description.abstractGroup 6 metal anionic complexes, (CO)₅M(O₂CR)⁻ (M = Cr, Mo, W; R = Me, OPh , were investigated for potential catalytic properties that would mediate a copolymer synthesis. Copolymers made of alternating carbon dioxide and epoxides have been activated by various reported organozinc complexes. A similar group 6 metal species was sought as a probe for the mechanistic features of a proposed catalytic cycle. At present, details about the mechanisms that facilitate carbon dioxide and epoxide copolymerization are poorly understood. In a proposed mechanistic scheme for a copolymer synthesis of CO₂ and epoxides, the activation of the CO₂ by group 6 metal complexes represents a very well-documented and important step, applicable in the chain propagation. The epoxide insertion, however, remains an elusive detail to the complete copolymer cycle. Two group 6 anionic species, (CO)₅M(O₂CCH₃)⁻, 1, and (CO)₅M(O₂COPh)⁻, 5, represent CO₂ insertion products that were investigated for potential catalytic activity toward propylene oxide.en
dc.format.extent31 pagesen
dc.format.mediumelectronicen
dc.format.mimetypeapplication/pdf
dc.subjectGroup 6 metal anionic complexesen
dc.subjectcatalytic propertiesen
dc.subjectcopolymer synthesisen
dc.subjectepoxidesen
dc.subjectCO₂en
dc.titleActivation Of Carbon Dioxide By Transition Metal Complexesen
dc.title.alternativeACTIVATION OF CARBON DIOXIDE BY TRANSITION METAL COMPLEXESen
dc.typeThesisen
thesis.degree.departmentChemistryen
thesis.degree.grantorUniversity Undergraduate Fellowen
thesis.degree.levelUndergraduateen
dc.type.materialtexten


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