Mitsumoto Taichi, Nishibayashi Yoshiaki
Department of Applied Chemistry, School of Engineering, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo, Japan.
Angew Chem Int Ed Engl. 2025 May;64(19):e202423858. doi: 10.1002/anie.202423858. Epub 2025 Mar 22.
We have recently achieved a highly effective ammonia formation from dinitrogen using samarium diiodide and water under ambient reaction conditions. However, further research is needed to establish a carbon-free green ammonia production route without carbon dioxide emissions. In this study, we have developed a novel molybdenum-catalyzed nitrogen fixation method using a combination of zero-valent metal powders as reductants and alcohols or HO as a proton source under ambient reaction conditions. In this reaction system, samarium compounds serve as crucial electron mediators for the molybdenum complexes. Remarkably, the combination of zinc powder and water in the presence of samarium triiodide facilitates highly selective ammonia production over dihydrogen under ambient reaction conditions, yielding up to 900 equiv of ammonia per Mo atom in the catalyst. Intriguingly, using magnesium powder, known for its potent reducing capability, reduces the requisite amount of samarium compounds to catalytic levels. We believe that the novel insights gained from this reaction system represent a substantial step toward achieving green ammonia production.
我们最近在环境反应条件下,使用二碘化钐和水从氮气中实现了高效的氨合成。然而,需要进一步研究以建立一条无二氧化碳排放的无碳绿色氨生产路线。在本研究中,我们开发了一种新型钼催化固氮方法,在环境反应条件下使用零价金属粉末作为还原剂与醇类或HO作为质子源相结合。在该反应体系中,钐化合物作为钼配合物的关键电子介质。值得注意的是,在三碘化钐存在下锌粉与水的组合在环境反应条件下促进了比二氢更具选择性的氨生产,催化剂中每个钼原子可产生高达900当量的氨。有趣的是,使用以其强大还原能力而闻名的镁粉,可将所需的钐化合物量降低到催化水平。我们相信,从该反应体系中获得的新见解代表了朝着实现绿色氨生产迈出的重要一步。