Probing the structure and solvation of catalytic reaction intermediates
Seminar | November 28 | 4-5 p.m. | 120 Latimer Hall
Understanding reaction pathways and mechanisms is vitally important for the rational design of catalysts. Towards that end, we developed a method based on a unique combination of mass spectrometry and cryogenic ion vibrational spectroscopy to capture and characterize the reaction complexes formed during homogeneous catalytic processes. In our approach, an in-line electrochemical flow cell is incorporated into an electrospray ionization source, thereby allowing us to controllably form, and mass spectrometrically isolate, the product of each catalytic step. Moreover, the structures of these isolated ions can be directly probed in detail using infrared predissociation spectroscopy. In addition to experimental considerations, this talk will present the application of our approach to model systems as well as to the study of homogeneous catalytic water oxidation by the single metal center [Ru(tpy)(bpy)(H2O)]2+ complex. This talk will also present recent technical developments that gave us the capability to perform controlled gas-phase chemistry and clustering in a separate temperature controlled ion trap. This allows us to access unstable reactive species via controlled ion-molecule reactions as well as microsolvated complexes.
Light refreshments will be served at 3:50 at The Coffee Lab