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Updated: May 30, 2025

Preparation of SNS CobaltII Pincer Model Complexes of Liver Alcohol Dehydrogenase
Published on: March 19, 2020
Nickel(II) complexes with covalently attached quinols rely on ligand-derived redox couples to catalyze superoxide
Robert Boothe1, Julian Oppelt2,3, Alicja Franke2,3
1Department of Chemistry and Biochemistry, Auburn University, Auburn, AL 36849, USA. Ivana.Ivanovic-Burmazovic@cup.uni-muenchen.de.
Abstract:
Although nickel is found in the active sites of a class of superoxide dismutase (SOD), nickel complexes with non-peptidic ligands normally do not catalyze superoxide degradation, and none has displayed activity comparable to those of the best manganese-containing SOD mimics. Here, we find that nickel complexes with polydentate quinol-containing ligands can exhibit catalytic activity comparable to those of the most efficient manganese-containing SOD mimics. The nickel complexes retain a significant portion of their activity in phosphate buffer and under operando conditions and rely on ligand-centered redox processes for catalysis. Although nickel SODs are known to cycle through Ni(II) and Ni(III) species during catalysis, cryo-mass spectrometry studies indicate that the nickel atoms in our catalysts remain in the +2 oxidation state throughout SOD mimicry.
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