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SUMMARY:Enabling Tandem Catalysis with Cooperative Ligand-Centered Reactivi
 ty
LOCATION:Chemistry A101
TZID:America/Denver
DTSTART:20230328T160000
UID:2026-04-22-19-06-48@natsci.colostate.edu
DTSTAMP:20260422T190648
Description:About the Seminar\n\nTandem catalysts that catalyze two differe
 nt organic transformations in a single pot are highly desirable because th
 ey enable atom-efficient\, multi-component assembly of complex molecules f
 rom simple building blocks. Tandem one-pot reactions collapse the synthesi
 s timeline\, limit material loss\, and can reduce operational costs becaus
 e they do not require workup and purification after each reaction step. Ma
 ny examples of tandem catalysis rely on metal-catalyzed reactions involvin
 g one or more metal complexes. In contrast\, and despite remarkable advanc
 es in the development of reactive ligand platforms\, there are few example
 s of metal complexes that contain reactive ligands capable of performing i
 ndependent catalytic reactions in tandem with separate reactions at the me
 tal.\n\nIn this talk\, I will describe the first examples of tandem metal-
 ligand catalysis using a class of reactive ligands called TBDPhos. These d
 iphosphorus ligands contain a triaminoborane subunit derived from 1\,8\,10
 \,9-triazaboradecalin (TBD) that can undergo cooperative ligand-centered r
 eactions. I will discuss chemical factors that control ligand-centered rea
 ctivity in TBDPhos complexes and show how this reactivity proceeds via for
 mation of highly Lewis-acidic borenium ions (three-coordinate boron cation
 s) while TBDPhos is bound to different transition metals. I will then desc
 ribe how Pd TBDPhos complexes were used successfully to access borenium-ca
 talyzed cycloaddition reactions at the ligand in tandem with Pd-catalyzed 
 cross-coupling reactions at the metal. The potential advantages and limita
 tions of this approach will be discussed with respect to more traditional 
 examples of tandem catalysis.\n\nAbout the Speaker\n\nScott attended colle
 ge after completing three years of active-duty service in the U.S. Army. H
 e earned his B.S. degree in chemistry from North Central College\, a small
  liberal arts college in Naperville\, IL. In 2006\, he entered the PhD che
 mistry program at the University of Illinois at Urbana-Champaign and perfo
 rmed research under the guidance of Gregory Girolami. Scott’s research f
 ocused on the synthesis and characterization of chelating borohydride liga
 nds and their use in the preparation of volatile transition metal\, lantha
 nide\, and actinide complexes for chemical vapor deposition applications. 
 After receiving his PhD in spring 2010\, he began working as a Seaborg Pos
 tdoctoral Fellow with Stosh Kozimor and David Clark at Los Alamos National
  Lab in Los Alamos\, NM. His research there focused on ligand K-edge X-ray
  absorption spectroscopy (XAS) studies to understand structure-function re
 lationships in effective minor actinide extractants. In 2012\, Scott accep
 ted a faculty position at George Washington University in Washington\, DC.
  In 2014\, he moved his research group to the University of Iowa where he 
 is currently an Associate Professor of Chemistry. His research interests f
 ocus primarily on coordination chemistry and reactive ligand design to add
 ress chemical challenges related to nuclear energy\, CO2 mitigation\, and 
 catalysis. 4:00 pm
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