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.

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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
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article
Field-Weighted Citation Impact
15.47
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article

Mononuclear Non-Heme Iron(III)-Peroxo Complexes in Oxidative N -Demethylation Reaction as a Chemical Model Study of Rieske Oxygenases

Xiaoyan Lu, Vandana Kardam, Wenjuan Zhu, Anran Zhou et al.
1 citations
Journal of the American Chemical Society
Metal-Catalyzed Oxygenation Mechanisms
15.47
article

Mononuclear Non-Heme Iron(III)-Peroxo Complexes in Oxidative N -Demethylation Reaction as a Chemical Model Study of Rieske Oxygenases

Xiaoyan Lu, Vandana Kardam, Wenjuan Zhu, Anran Zhou, Kallol Ray, Kyung‐Bin Cho, S. Fukuzumi, Wonwoo Nam, Akhilesh Kumar
article en
1 citations

Abstract

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.

Journal of the American Chemical SocietyVol. 148(4)
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)
Clean water and sanitation
Openalex Percentile: Top 3%
Metal-Catalyzed Oxygenation Mechanisms
15.47
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