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Transition Metal Complexes as Catalysts for the Electroconversion of CO2: An Organometallic Perspective

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 60, Issue 21, Pages 11628-11686

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202006988

Keywords

carbon dioxide; electrocatalysis; homogeneous (molecular) catalysis; reduction; transition metals

Funding

  1. Max Planck Society
  2. RWTH Aachen University
  3. Ruhr University Bochum
  4. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany's Excellence Strategy [2186, 390919832]
  5. Kopernikus Project P2X: Flexible use of renewable resources-exploration, validation, and implementation of Power-to-X concepts - German Federal Ministry of Education and Research (BMBF) [FKZ: 03SFK2A0-2]
  6. Projekt DEAL

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The electrocatalytic transformation of carbon dioxide has long been a topic of interest, with recent focus on it as an alternative strategy for CO2 reduction. Studies have increasingly looked at direct electron transfer and molecular transition metal complexes as catalysts. This can lead to the production of C-1 compounds as well as more complex transformations.
The electrocatalytic transformation of carbon dioxide has been a topic of interest in the field of CO2 utilization for a long time. Recently, the area has seen increasing dynamics as an alternative strategy to catalytic hydrogenation for CO2 reduction. While many studies focus on the direct electron transfer to the CO2 molecule at the electrode material, molecular transition metal complexes in solution offer the possibility to act as catalysts for the electron transfer. C-1 compounds such as carbon monoxide, formate, and methanol are often targeted as the main products, but more elaborate transformations are also possible within the coordination sphere of the metal center. This perspective article will cover selected examples to illustrate and categorize the currently favored mechanisms for the electrochemically induced transformation of CO2 promoted by homogeneous transition metal complexes. The insights will be corroborated with the concepts and elementary steps of organometallic catalysis to derive potential strategies to broaden the molecular diversity of possible products.

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