Nathaniel Szymczak

Department of Chemistry
University of Michigan
Thursday, May. 18, 2017 4:30pm
Frick Chemistry Laboratory, Taylor Auditorium
Brad Carrow
Add to Calendar2017-05-18 16:30:002017-05-18 16:30:00Brad CarrowFrick Chemistry Laboratory, Taylor Auditorium 15YYYY-MM-DD

Moving Beyond the Metal: Assisted Small Molecule Activation

The design of reagents and catalysts that are capable of selective bond activation of small molecules has been a longstanding target of the synthetic community. The current paradigm for the development of new homogenous catalysts primarily focuses on a single active metal site with ligands that impart steric and electronic tunability to achieve substrate binding and activation, with limited attention paid to the secondary interactions of appended groups. Taking inspiration from biological systems, our group is working to develop strategies to exploit acidic and basic groups (hydrogen bond donors, Lewis acids/bases) to promote cooperative interactions. In addition to ground-state stabilization, the acidic/basic groups can also participate to bias catalytic reactivity. This presentation will emphasize how ligand design principles that include secondary sphere groups can be used to regulate the reactivity of polar bonds and delineate key contributors that are required for efficient catalysis/reactivity. Specific examples will be described that include cases where the mechanism of a given catalytic reduction reaction (hydrogenation, hydroboration, etc.) is changed, resulting in concommitant differences in chemoselectivity. Additional emphasis will be placed systems where an appropriately selected Lewis acid serves a primary role for substrate activation/transfer.