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DOI 10.1021/jacs.4c06840

Медицинская библиотека · Journal of the American Chemical Society · 2024

Electrocatalytic Coupling of Nitrate and Formaldehyde for Hexamethylenetetramine Synthesis via C-N Bond Construction and Ring Formation.

Pan Yuping, Zou Yuqin, Ma Chongyang, Nga Ta Thi Thuy, An Qizheng, Miao Rong, Xia Zhongcheng, Fan Yun, Dong Chung-Li, Liu Qinghua, Wang Shuangyin

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Аннотация

Hexamethylenetetramine (HMTA) is extensively used in the defense industry, medicines, food, plastics, rubber, and other applications. Traditional organic synthesis of HMTA relies on ammonia derived from the Haber process at high temperatures and pressures. In contrast, electrochemical methods enable a safe and green one-pot synthesis of HMTA from waste NO3-. However, HMTA synthesis through the electrochemical method is challenging owing to the complex reaction pathways involving C-N bond construction and ring formation. In this study, HMTA was efficiently synthesized over electrochemical oxidation-derived copper (e-OD-Cu), with a yield of 76.8% and a Faradaic efficiency of 74.9% at -0.30 VRHE. The catalytic mechanism and reaction pathway of HMTA synthesis on e-OD-Cu were investigated through a series of in situ characterization methods and density-functional theory calculations. The results demonstrated that the electrocatalytic synthesis of HMTA involved a tandem electrochemical-chemical reaction. Additionally, the results indicated that the presence of Cu vacancies enhanced substrate adsorption and inhibited the further hydrogenation of C═N. Overall, this study provides an electrocatalytic method for HMTA synthesis and an electrochemical strategy for constructing multiple C-N bonds.

Для цитирования: Pan Yuping, Zou Yuqin, Ma Chongyang, Nga Ta Thi Thuy, An Qizheng, Miao Rong, Xia Zhongcheng, Fan Yun, Dong Chung-Li, Liu Qinghua, Wang Shuangyin. Electrocatalytic Coupling of Nitrate and Formaldehyde for Hexamethylenetetramine Synthesis via C-N Bond Construction and Ring Formation.. Journal of the American Chemical Society. 2024. DOI: 10.1021/jacs.4c06840.
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