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Photocatalytic CO₂ Reduction Using Manganese and Rhenium Catalysts Containing Bidentate Phosphinoaminopyridine Ligands

dc.contributor.authorOsterholm, Sarah
dc.contributor.supervisorRicheson, Darrin
dc.date.accessioned2021-09-15T17:29:23Z
dc.date.available2021-09-15T17:29:23Z
dc.date.issued2021-09-15en_US
dc.description.abstractCO2 is generally regarded as a waste product. However, the efficient catalytic reduction of CO2 means that this concept can change to viewing this molecule as a feedstock to produce chemically valuable products. The catalytic reduction of CO2 is a challenge because of its stability, and its reduction into chemically valuable products requires an appropriate catalyst and accessible energy source. While second and third row transition metals have shown considerable promise as photocatalysts for the reduction of CO2 to CO, one of our goals is to elaborate on the metal centers and the ligand environments in order to discover new catalysts and processes. These efforts have revealed new photocatalysts based on manganese and rhenium supported by κ2-PN phosphinoaminopyridine ligands. This thesis will describe the synthesis and characterization of these catalysts and their CO2 reduction parameters. The selectivity of these catalysts for either CO or HCOOH will be explored. Furthermore, ligand modifications and their effects on the catalyst behaviour will also be presented.en_US
dc.identifier.urihttp://hdl.handle.net/10393/42669
dc.identifier.urihttp://dx.doi.org/10.20381/ruor-26889
dc.language.isoenen_US
dc.publisherUniversité d'Ottawa / University of Ottawaen_US
dc.subjectcatalysisen_US
dc.subjectphotochemistryen_US
dc.subjectcarbon dioxideen_US
dc.subjectphosphinoaminopyridineen_US
dc.titlePhotocatalytic CO₂ Reduction Using Manganese and Rhenium Catalysts Containing Bidentate Phosphinoaminopyridine Ligandsen_US
dc.typeThesisen_US
thesis.degree.disciplineSciences / Scienceen_US
thesis.degree.levelMastersen_US
thesis.degree.nameMScen_US
uottawa.departmentChimie et sciences biomoléculaires / Chemistry and Biomolecular Sciencesen_US

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