Proton-Coupled Electron Transfer Enhances the Electrocatalytic Reduction of Nitrite to NO in a Bioinspired Copper Complex
Author(s) -
Giacomo Cioncoloni,
Isolda Roger,
Paul Wheatley,
Claire Wilson,
Russell E. Morris,
Stephen Sproules,
Mark D. Symes
Publication year - 2018
Publication title -
acs catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.898
H-Index - 198
ISSN - 2155-5435
DOI - 10.1021/acscatal.8b00361
Subject(s) - nitrite , electrocatalyst , chemistry , electron transfer , proton coupled electron transfer , reactivity (psychology) , catalysis , electrochemistry , carboxylate , copper , redox , combinatorial chemistry , inorganic chemistry , ligand (biochemistry) , photochemistry , stereochemistry , organic chemistry , nitrate , electrode , medicine , biochemistry , alternative medicine , receptor , pathology
The selective and efficient electrocatalytic reduction of nitrite to nitric oxide (NO) is of tremendous importance, both for the development of NO-release systems for biomedical applications and for the removal of nitrogen oxide pollutants from the environment. In nature, this transformation is mediated by (among others) enzymes known as the copper-containing nitrite reductases. The development of synthetic copper complexes that can reduce nitrite to NO has therefore attracted considerable interest. However, there are no studies describing the crucial role of proton-coupled electron transfer during nitrite reduction when such synthetic complexes are used. Herein, we describe the synthesis and characterization of two previously unreported Cu complexes (3 and 4) for the electrocatalytic reduction of nitrite to NO, in which the role of proton-relaying units in the secondary coordination sphere of the metal can be probed. Complex 4 bears a pendant carboxylate group in close proximity to the copper center, whi...
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