Electrochemical Aerobic Epoxidation of Styrenes Catalyzed by Manganese Tetraphenylporphyrin

Oxygen atom transfer (OAT) is a useful reaction in chemical synthesis, but because of the low reactivity of O<sub>2</sub> with organic substrates, harsh oxidants are often required. In contrast, metalloenzymes such as Cytochrome P450 catalyze a wide range of OAT reactions under mild conditions with O<sub>2</sub> as the source of the O atoms. In this work, we use a synthetic manganese porphyrin catalyst to mimic this reactivity. Our method enables electrochemical epoxidation of styrenes using O<sub>2</sub> through the generation of a Mn-superoxo intermediate. We report the reactivity of 12 styrene derivatives, with yields impacted by the position and electronic properties of the substituents. Spectroelectrochemical analyses indicate the generation of high-valent intermediates that enable epoxidation under these mild conditions.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-01-26
DOI
https://doi.org/10.1021/acs.joc.5c02884
Primary Topic
Metal-Catalyzed Oxygenation Mechanisms
Type
article
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article

Electrochemical Aerobic Epoxidation of Styrenes Catalyzed by Manganese Tetraphenylporphyrin

Steven Oppenheim, Anna C. Brezny, Elizabeth Scholer, Pauline E. Iwerks et al.
The Journal of Organic Chemistry
Metal-Catalyzed Oxygenation Mechanisms
article

Electrochemical Aerobic Epoxidation of Styrenes Catalyzed by Manganese Tetraphenylporphyrin

Steven Oppenheim, Anna C. Brezny, Elizabeth Scholer, Pauline E. Iwerks, Eva R. McKinney, Tashani M. Williams
article en

Abstract

Oxygen atom transfer (OAT) is a useful reaction in chemical synthesis, but because of the low reactivity of O<sub>2</sub> with organic substrates, harsh oxidants are often required. In contrast, metalloenzymes such as Cytochrome P450 catalyze a wide range of OAT reactions under mild conditions with O<sub>2</sub> as the source of the O atoms. In this work, we use a synthetic manganese porphyrin catalyst to mimic this reactivity. Our method enables electrochemical epoxidation of styrenes using O<sub>2</sub> through the generation of a Mn-superoxo intermediate. We report the reactivity of 12 styrene derivatives, with yields impacted by the position and electronic properties of the substituents. Spectroelectrochemical analyses indicate the generation of high-valent intermediates that enable epoxidation under these mild conditions.

The Journal of Organic ChemistryVol. 91(5)
Skidmore College (US), St. Olaf College (US)
Clean water and sanitation
Openalex Percentile: Top 79%
Metal-Catalyzed Oxygenation Mechanisms
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