Controlling product selectivity during dioxygen reduction with Mn complexes using pendent proton donor relays and added base
Author:
Affiliation:
1. Department of Chemistry University of Virginia, PO Box 400319 McCormick Rd, Charlottesville, VA 22904-4319, USA
Abstract
Funder
Division of Chemistry
Jefferson Scholars Foundation
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/2024/SC/D3SC02611F
Reference50 articles.
1. Bioinspired mononuclear Mn complexes for O2 activation and biologically relevant reactions
2. Homogeneous catalysis of dioxygen reduction by molecular Mn complexes
3. Oxygen Reduction by Homogeneous Molecular Catalysts and Electrocatalysts
4. Advances in the Molecular Catalysis of Dioxygen Reduction
5. O2 Activation by Non-Heme Iron Enzymes
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1. Acid Strength Effects on Dimerization during Metal-Free Catalytic Dioxygen Reduction;Journal of the American Chemical Society;2024-08-29
2. Design of Cr-Based Molecular Electrocatalyst Systems for the CO2 Reduction Reaction;Accounts of Chemical Research;2024-08-06
3. Installing Quinol Proton/Electron Mediators onto Non-Heme Iron Complexes Enables Them to Electrocatalytically Reduce O2 to H2O at High Rates and Low Overpotentials;Inorganic Chemistry;2024-07-15
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