Mononuclear Non-Heme Iron(III)-Peroxo Complexes in Oxidative <i>N</i> -Demethylation Reaction as a Chemical Model Study of Rieske Oxygenases
Mononuclear nonheme iron(III)-peroxo complexes bearing <i>N</i>-tetramethylated cyclam (<i>n</i>-TMC) ligands, [Fe<sup>III</sup>(O<sub>2</sub>)(<i>n</i>-TMC)]<sup>+</sup> (<i>n</i> = 12, 13, and 14), have recently shown highly intriguing reactivities in various oxidation reactions, such as the <i>cis</i>-dihydroxylation and C-H functionalization reactions, which were previously associated only with high-valent iron-oxo intermediates in heme and nonheme iron enzymes. Herein, we extend our study to report [Fe<sup>III</sup>(O<sub>2</sub>)(<i>n</i>-TMC)]<sup>+</sup> mediated <i>N</i>-demethylation of <i>N</i>,<i>N</i>-dimethylanilines (DMAs), another reaction that was previously associated only with high-valent iron-oxo cores. Most importantly, we provide definitive evidence of the occurrence of electron transfer from DMAs to [Fe<sup>III</sup>(O<sub>2</sub>)(<i>n</i>-TMC)]<sup>+</sup>, thereby establishing an electron-transfer (ET) pathway for the <i>N</i>-demethylation reaction. Investigation of the ET reactivity of [Fe<sup>III</sup>(O<sub>2</sub>)(<i>n</i>-TMC)]<sup>+</sup> in light of the Marcus theory of ET, and a comparison of the <i>N</i>-demethylation and the ET rate constants corroborate a mechanism, whereby <i>N</i>-demethylation of DMAs by [Fe<sup>III</sup>(O<sub>2</sub>)(<i>n</i>-TMC)]<sup>+</sup> proceeds via the peroxide O-O bond cleavage of [Fe<sup>III</sup>(O<sub>2</sub>)(<i>n</i>-TMC)]<sup>+</sup> to form a transient [Fe<sup>IV</sup>(O<sup>2-</sup>)(O<sup>• -</sup>)(<i>n</i>-TMC)]<sup>+</sup> species, which undergoes a proton-coupled electron-transfer (PCET) or an uncoupled electron transfer-proton transfer (ET/PT) in the presence of DMAs. Saturation kinetics support the rate-determining formation of [Fe<sup>IV</sup>(O<sup>2-</sup>)(O<sup>• -</sup>)(<i>n</i>-TMC)]<sup>+</sup> in a pre-equilibrium step with the same values of the O-O bond cleavage rate constants irrespective of the substrates, such as DMAs and one-electron oxidants. The present study corroborates that mononuclear nonheme iron(III)-peroxo cores are not mere pass-through points en route to high-valent metal-oxo intermediates, but they can play an important role in the diverse oxidation reactions of Rieske oxygenases, such as in the <i>N</i>-demethylation reaction.
Authors
- Xiaoyan Lu (ORCID: https://orcid.org/0000-0001-5710-4968)
- Vandana Kardam (ORCID: https://orcid.org/0000-0002-3542-5178)
- Wenjuan Zhu (ORCID: https://orcid.org/0000-0003-4316-370X)
- Anran Zhou (ORCID: https://orcid.org/0009-0000-9170-086X)
- Kallol Ray
- Kyung‐Bin Cho (ORCID: https://orcid.org/0000-0001-6586-983X)
- S. Fukuzumi
- Wonwoo Nam
- Akhilesh Kumar
Institutions
- Humboldt-Universität zu Berlin (DE)
- Energy Research Institute (CN)
- NanoSD (United States) (US)
- Luoyang Normal University (CN)
- Ewha Womans University Medical Center (KR)
- Convergence (US)
- Jeonbuk National University (KR)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-01-20
- DOI
- https://doi.org/10.1021/jacs.5c18643
- Citations
- 1
- Primary Topic
- Metal-Catalyzed Oxygenation Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 15.47