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X-WR-CALNAME;VALUE=TEXT:Sharon Hammes-Schiffer
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SUMMARY:Sharon Hammes-Schiffer
DESCRIPTION:<p>Professor Sharon Hammes-Schiffer, University of Illinois at Urbana-Champaign.  "Proton-Coupled Electron Transfer:  Theory and Application."  Theoretical Chemistry Seminar.<!--break--></p><p align="LEFT"><strong>Proton-Coupled Electron Transfer: Theory and Applications</strong></p><p align="LEFT"><font face="LiberationSerif">Sharon Hammes-Schiffer</font></p><p align="LEFT"><font face="LiberationSerif">Department of Chemistry, University of Illinois at Urbana-Champaign, </font><font face="LiberationSerif">Urbana, IL 61801; shs3@illinois.edu</font></p><p align="LEFT"><font face="LiberationSerif">Proton-coupled electron transfer (PCET) reactions play a vital role in a wide range of </font><font face="LiberationSerif">chemical and biological processes. This talk will present a general theory for PCET </font><font face="LiberationSerif">reactions. The quantum mechanical effects of the active electrons and transferring </font><font face="LiberationSerif">proton(s), as well as the motions of the proton donor-acceptor mode and solvent or </font><font face="LiberationSerif">protein environment, are included in this theory. This formulation enables the calculation </font><font face="LiberationSerif">of rate constants and kinetic isotope effects for comparison to experiment. This theory </font><font face="LiberationSerif">has also been extended to electrochemical processes. Applications to PCET reactions in </font><font face="LiberationSerif">solution, enzymes, and electrochemical systems will be presented. Studies of the enzyme </font><font face="LiberationSerif">soybean lipoxygenase provide a physical explanation for the experimental observation of </font><font face="LiberationSerif">unusually high kinetic isotope effects for C-H bond activation at room temperature.  </font><font face="LiberationSerif">Investigations of molecular electrocatalysts for hydrogen production identify the </font><font face="LiberationSerif">thermodynamically and kinetically favorable mechanisms and guide the theoretical </font><font face="LiberationSerif">design of more effective molecular electrocatalysts. In addition, recent developments of </font><font face="LiberationSerif">theoretical approaches for simulating the ultrafast nonequilibrium dynamics of </font><font face="LiberationSerif">photoinduced PCET processes will be presented. Quantum mechanical/molecular </font><font face="LiberationSerif">mechanical nonadiabatic dynamics simulations enable the investigation of the relaxation </font><font face="LiberationSerif">pathways following photoexcitation. These calculations provide insights into the roles of </font><font face="LiberationSerif">proton vibrational relaxation and nonequilibrium solvent dynamics in photoinduced </font><font face="LiberationSerif">PCET processes in solution and photoreceptor proteins.</font></p><p> </p>
LOCATION:MIT, Room 4-237
STATUS:CONFIRMED
DTSTART:20170308T211500Z
DTEND:20170308T231500Z
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