Please use this identifier to cite or link to this item: http://hdl.handle.net/10267/33454
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dc.contributor.advisorEckenhoff, William T. (Will)-
dc.contributor.authorHutchison, Phillips S.-
dc.contributor.authorKiker, Meghan T.-
dc.contributor.authorTinker, Cameron W.-
dc.date.accessioned2018-05-09T15:13:19Z-
dc.date.available2018-05-09T15:13:19Z-
dc.date.issued2018-04-27-
dc.identifier.urihttp://hdl.handle.net/10267/33454-
dc.descriptionPresentation by Phillips Hutchison ('19), Meghan Kiker ('19), and Cameron Tinker ('19) delivered at the Rhodes College Undergraduate Research and Creative Activity Symposium (URCAS).-
dc.description.abstractAs the world's population increases, developing new energy sources, such as artificial photosynthetic hydrogen production, is becoming a priority. Recent studies have shown the effectiveness of cobalt complexes with polypyridine ligands acting as catalysts for light driven hydrogen production. 1,1-(pyridine-2,6-diyl)bis(2-(2-pyridinyl)ethyl)ethanimine is a promising ligand because of its electronic similarity to ligands previously used for cobalt catalyzed hydrogen production. Ligands were synthesized following procedures in available literature and subsequently complexed to cobalt using a Co(BF4)3 salt. Recent work has focused on further purification of the ligand to eliminate impurities in the complex. Electrochemical analysis shows redox waves at -0.725V and -2.147V vs Fc/Fc+. In the presence of acetic acid, a catalytic wave, indicative of hydrogen formation, was observed at -2.147 V vs Fc/Fc+. These results suggest that this complex might be suitable in light driven artificial photosiynthetic systems.-
dc.subjectClass of 2019-
dc.subjectURCAS-
dc.subjectStudent research-
dc.subject2018 Spring-
dc.subjectChemistry, Department of-
dc.titleHydrogen Production Catalyzed by a Cobalt Schiff Base Complex-
dc.date.graduation2019-
Appears in Collections:Undergraduate Research and Creative Activity Symposium

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