Dr. Jeffrey Johnson, Chemistry
The kinetics involved in the reaction pathways of transition metal-catalyzed carbon-carbon bond activation reactions can provide key insights into the mechanism. Previous work has shown that pyridyl ketones undergo rhodium-catalyzed decarbonylation reactions. The determination of the mechanistic pathway of this reaction could allow for the knowledge necessary for exploring alternative reactivity. Utilizing in situ Fourier Transform Infrared Spectroscopy (FTIR) and Nuclear Magnetic Resonance Spectroscopy (NMR), kinetic analysis of the decarbonylation reaction is being performed with various substituted pyridyl ketones. Initial rate constants will be used to compare the electronic effects of substituents, providing insight of the intermediates involved.
Repository citation: Loula, Julia and Schoonover, Erik, "Mechanistic Survey of Rhodium-Catalyzed Decarbonylation Reactions: A Kinetics Study" (2020). 19th Annual Celebration of Undergraduate Research and Creative Activity (2020). Paper 17.
April 17, 2020. Copyright © 2020 Hope College, Holland, Michigan.