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Mechanistic Study of the Activation and the Electrocatalytic Reduction of Hydrogen Peroxide by Cu‐tmpa in Neutral Aqueous Solution
Author(s) -
Langerman Michiel,
Hetterscheid Dennis G. H.
Publication year - 2021
Publication title -
chemelectrochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.182
H-Index - 59
ISSN - 2196-0216
DOI - 10.1002/celc.202100436
Subject(s) - chemistry , hydrogen peroxide , copper , aqueous solution , catalysis , inorganic chemistry , electrochemistry , reaction rate constant , kinetic isotope effect , amine gas treating , photochemistry , reaction mechanism , kinetics , organic chemistry , electrode , quantum mechanics , physics , deuterium
Hydrogen peroxide plays an important role as an intermediate and product in the reduction of dioxygen by copper enzymes and mononuclear copper complexes. The copper(II) tris(2‐pyridylmethyl)amine complex (Cu‐tmpa) has been shown to produce H 2 O 2 as an intermediate during the electrochemical 4‐electron reduction of O 2 . We investigated the electrochemical hydrogen peroxide reduction reaction (HPRR) by Cu‐tmpa in a neutral aqueous solution. The catalytic rate constant of the reaction was shown to be one order of magnitude lower than the reduction of dioxygen. A significant solvent kinetic isotope effect (KIE) of 1.4 to 1.7 was determined for the reduction of H 2 O 2 , pointing to a Fenton‐like reaction pathway as the likely catalytic mechanism, involving a single copper site that produces an intermediate copper(II) hydroxo species and a free hydroxyl radical anion in the process.