Electrochemical Oxidation of Methane to Methylamine

The electrochemical methane (CH<sub>4</sub>) oxidation reaction under ambient conditions is a promising approach for natural gas utilization. However, the highly stable nature of CH<sub>4</sub> restrains efficient cleavage of the C-H bond without overoxidation. To this end, we proposed a coupled oxidative strategy for converting CH<sub>4</sub> to value-added products via NH<sub>2</sub> intermediates. The ammonia-oxidation-driven anodic reaction facilitates the formation of NH<sub>2</sub> species and activates CH<sub>4</sub> through nucleophilic attack to achieve C-N bond formation. Further the generated methylamine could be protected from overoxidation in the ammonia-based anolyte. Under such conditions, a methylamine productivity of 3.8 mmol g<sup>-1</sup><sub>cat</sub> h<sup>-1</sup> at 1.55 V vs a reversible hydrogen electrode is reported. This work provides new insights into electrocatalytic C-N coupling based on the ammonia oxidation reaction, which could extend to other alkane or alkene conversions.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-04-25
DOI
https://doi.org/10.1021/jacs.5c04802
Citations
4
Primary Topic
Catalysis and Oxidation Reactions
Type
article
Field-Weighted Citation Impact
1.56

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article

Electrochemical Oxidation of Methane to Methylamine

Qiang Song, Patrick J. Cullen, Jungmi Hong, Wanping Xu et al.
4 citations
Journal of the American Chemical Society
Catalysis and Oxidation Reactions
1.56
article

Electrochemical Oxidation of Methane to Methylamine

Qiang Song, Patrick J. Cullen, Jungmi Hong, Wanping Xu, Tianqi Zhang, Xin Zeng
article en
4 citations

Abstract

The electrochemical methane (CH<sub>4</sub>) oxidation reaction under ambient conditions is a promising approach for natural gas utilization. However, the highly stable nature of CH<sub>4</sub> restrains efficient cleavage of the C-H bond without overoxidation. To this end, we proposed a coupled oxidative strategy for converting CH<sub>4</sub> to value-added products via NH<sub>2</sub> intermediates. The ammonia-oxidation-driven anodic reaction facilitates the formation of NH<sub>2</sub> species and activates CH<sub>4</sub> through nucleophilic attack to achieve C-N bond formation. Further the generated methylamine could be protected from overoxidation in the ammonia-based anolyte. Under such conditions, a methylamine productivity of 3.8 mmol g<sup>-1</sup><sub>cat</sub> h<sup>-1</sup> at 1.55 V vs a reversible hydrogen electrode is reported. This work provides new insights into electrocatalytic C-N coupling based on the ammonia oxidation reaction, which could extend to other alkane or alkene conversions.

Journal of the American Chemical SocietyVol. 147(18)
The University of Sydney (AU)
Australian Research Council
Clean water and sanitation
Openalex Percentile: Top 18%
Catalysis and Oxidation Reactions
1.56
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Electrochemical Oxidation of Methane to Methylamine — Qiang Song, Patrick J. Cullen, et al. · Journal of the American Chemical Society (2025) | TGRS Research Map | TGRS