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Pulsed‐EPR Evidence of a Manganese(II) Hydroxycarbonyl Intermediate in the Electrocatalytic Reduction of Carbon Dioxide by a Manganese Bipyridyl Derivative
Author(s) -
Bourrez Marc,
Orio Maylis,
Molton Florian,
Vezin Hervé,
Duboc Carole,
Deronzier Alain,
ChardonNoblat Sylvie
Publication year - 2014
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201306750
Subject(s) - manganese , chemistry , adduct , carbon monoxide , catalysis , electron paramagnetic resonance , dimer , photochemistry , catalytic cycle , derivative (finance) , electrochemical reduction of carbon dioxide , carbon dioxide , inorganic chemistry , metal , organic chemistry , nuclear magnetic resonance , physics , financial economics , economics
A key intermediate in the electroconversion of carbon dioxide to carbon monoxide, catalyzed by a manganese tris(carbonyl) complex, is characterized. Different catalytic pathways and their potential reaction mechanisms are investigated using a large range of experimental and computational techniques. Sophisticated spectroscopic methods including UV/Vis absorption and pulsed‐EPR techniques (2P‐ESEEM and HYSCORE) were combined together with DFT calculations to successfully identify a key intermediate in the catalytic cycle of CO 2 reduction. The results directly show the formation of a metal–carboxylic acid–CO 2 adduct after oxidative addition of CO 2 and H + to a Mn 0 carbonyl dimer, an unexpected intermediate.
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