Analyzing Structure–Activity Variations for Mn–Carbonyl Complexes in the Reduction of CO2 to CO
Author:
Affiliation:
1. Cavendish Laboratory, University of Cambridge, J.J. Thomson Avenue, Cambridge CB3 0HE, U.K.
2. ISIS Neutron and Muon Source, STFC Rutherford Appleton Laboratory, Harwell Campus for Science and Innovation, Didcot OX11 0QX, U.K.
Funder
Royal Academy of Engineering
Basic Energy Sciences
Science and Technology Facilities Council
Winston Churchill Foundation of the United States
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.inorgchem.2c03391
Reference59 articles.
1. CO2 Reduction: From Homogeneous to Heterogeneous Electrocatalysis
2. Carbon nanosheets supporting Ni–N3S single-atom sites for efficient electrocatalytic CO2 reduction
3. Homogeneously Catalyzed Electroreduction of Carbon Dioxide—Methods, Mechanisms, and Catalysts
4. From non-innocent to guilty: on the role of redox-active ligands in the electro-assisted reduction of CO2 mediated by a cobalt(ii)-polypyridyl complex
5. Electrocatalytic reduction of carbon dioxide with Mn(terpyridine) carbonyl complexes
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1. Mechanistic insights of electrocatalytic CO2 reduction by Mn complexes: synergistic effects of the ligands;Dalton Transactions;2024
2. Electronic Effect Promoted Visible-Light-Driven CO2-to-CO Conversion in a Water-Containing System;Inorganic Chemistry;2023-12-07
3. Manganese(I) Diamine Electrocatalysts: Electrochemical Carbon Dioxide Reduction to Carbon Monoxide;Inorganics;2023-09-21
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