| Literature DB >> 29740926 |
Maciej Krzeszewski1,2,3, Eli M Espinoza4, Ctirad Červinka4,5, James B Derr6, John A Clark1, Dan Borchardt4, Gregory J O Beran4, Daniel T Gryko2, Valentine I Vullev1,4,6.
Abstract
Molecular dipoles present important, but underutilized, methods for guiding electron transfer (ET) processes. While dipoles generate fields of Gigavolts per meter in their vicinity, reported differences between rates of ET along versus against dipoles are often small or undetectable. Herein we show unprecedentedly large dipole effects on ET. Depending on their orientation, dipoles either ensure picosecond ET, or turn ET completely off. Furthermore, favorable dipole orientation makes ET possible even in lipophilic medium, which appears counterintuitive for non-charged donor-acceptor systems. Our analysis reveals that dipoles can substantially alter the ET driving force for low solvent polarity, which accounts for these unique trends. This discovery opens doors for guiding forward ET processes while suppressing undesired backward electron transduction, which is one of the holy grails of photophysics and energy science.Entities:
Keywords: Rehm-Weller equation; charge transfer; dipoles; electron transfer; kinetics
Year: 2018 PMID: 29740926 DOI: 10.1002/anie.201802637
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336