Bu Faxiang, Deng Yuqi, Lu Lijun, Li Yan, Song Wenxu, Yang Zhaoliang, Luo Xu, Dong Xin, Yi Ruijie, Yang Dali, Wang Shengchun, Lei Aiwen, Li Wu
College of Chemistry and Molecular Sciences, Institute for Advanced Studies (IAS), Wuhan University, Wuhan 430072, P. R. China.
J Am Chem Soc. 2025 Feb 19;147(7):5785-5795. doi: 10.1021/jacs.4c14320. Epub 2025 Feb 4.
Traditional reductions of alkenes, such as using stoichiometric reductants with waste generation and catalytic hydrogenation with high-pressure H, are accompanied by environmental or safety issues. Herein, we demonstrated a universal method for the electrocatalytic hydrogenation and deuteration of alkenes with modified electrodes under ambient temperature. The key M-H/M-D species for alkene reduction were generated from the electrolysis of HO/DO on modified electrodes, which avoided the usage of H and D. Mono-, di-, tri-, and tetra-substituted alkenes were successfully reduced in this electrocatalytic system using HO and DO as hydrogen and deuterium sources. Electron-donating/-withdrawing alkenes, alkenes with other easily reducible functional groups, and complicated natural products and drugs were all reductive hydrogenated and deuterated with excellent yields (85 examples, yields up to 99%). Faraday efficiency of this efficient method could reach 84%. Moreover, the catalytic amount of metal could decrease to less than 0.01 mol %.
传统的烯烃还原方法,如使用化学计量还原剂会产生废物以及使用高压氢气进行催化氢化,都伴随着环境或安全问题。在此,我们展示了一种在室温下用修饰电极对烯烃进行电催化氢化和氘化的通用方法。用于烯烃还原的关键M-H/M-D物种是通过在修饰电极上电解H₂O/D₂O产生的,避免了使用H₂和D₂。在该电催化体系中,使用H₂O和D₂O作为氢源和氘源,单取代、二取代、三取代和四取代烯烃均成功实现了还原。具有供电子/吸电子基团的烯烃、带有其他易于还原官能团的烯烃以及复杂的天然产物和药物都能以优异的产率(85个例子,产率高达99%)进行还原氢化和氘化。这种高效方法的法拉第效率可达84%。此外,金属的催化用量可降至小于0.01 mol%。