Investigation of the Scope and Reaction Properties of Metal Promoted Reactions with Nitriles to form Triazines

carrollscholars.legacy.contextkey11208882
carrollscholars.legacy.itemurlhttps://scholars.carroll.edu/chemphys_theses/20
carrollscholars.object.degreeBachelor's
carrollscholars.object.departmentChemistry & Physics
carrollscholars.object.disciplinesChemistry; Inorganic Chemistry
carrollscholars.object.seasonSpring
dc.contributor.advisorColin Thomas
dc.contributor.advisorKelly Cline
dc.contributor.advisorDaniel Gretch
dc.contributor.authorGill, Zach
dc.date.accessioned2020-04-30T09:39:07Z
dc.date.available2020-04-30T09:39:07Z
dc.date.embargo12/31/1899 0:00
dc.date.issued2010-04-01
dc.description.abstractThe reaction properties of copper acetylacetonate, Cu(acac)2, toward nitrile activation to generate triazine-containing species are being examined. Results indicate necessity of a nitrogen containing base for the reaction to result in the desired species. Studies are aimed at determining the role of the base and assessing the scope of tolerable nitriles. Copper dimer species containing triazine rings have been confirmed by x-ray crystallography
dc.identifier.urihttps://scholars.carroll.edu/handle/20.500.12647/169
dc.titleInvestigation of the Scope and Reaction Properties of Metal Promoted Reactions with Nitriles to form Triazines
dc.typethesis
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