Boothe R, Oppelt J, Franke A, Moore JL, Squarcina A, Zahl A, Senft L, Kellner I, Awalah AL, Bradford A, Obisesan SV, Schwartz DD, Ivanović-Burmazović I, Goldsmith CR (2025)
Publication Type: Journal article
Publication year: 2025
DOI: 10.1039/d4dt03331k
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.
APA:
Boothe, R., Oppelt, J., Franke, A., Moore, J.L., Squarcina, A., Zahl, A.,... Goldsmith, C.R. (2025). Nickel(ii) complexes with covalently attached quinols rely on ligand-derived redox couples to catalyze superoxide dismutation. Dalton Transactions. https://doi.org/10.1039/d4dt03331k
MLA:
Boothe, Robert, et al. "Nickel(ii) complexes with covalently attached quinols rely on ligand-derived redox couples to catalyze superoxide dismutation." Dalton Transactions (2025).
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