氨氧化
催化作用
生物量(生态学)
化学
碳纤维
氮气
无机化学
溶剂
有机化学
丙烯腈
材料科学
农学
复合数
共聚物
复合材料
生物
聚合物
作者
Qingqing Pu,Yongqiang Yao,Longfei Wang,Dan Fan,Yuqi Yao,Yong Guo,Zhenyu Sun,Yongsheng Li,Zhengang Ke
标识
DOI:10.1021/acssuschemeng.5c04497
摘要
Nitriles are high-value chemicals with wide applications, and alcohol ammoxidation is a green route to them. However, solvents are widely used and suffer from increasing cost and energy consumption, inevitable solvent volatilization, and separation problems. Herein, a solvent-free ammoxidation of biomass alcohols to nitriles was realized over the FeNC-700 catalyst, and a series of nitriles including benzonitriles, 2-furonitrile, 2-thiophenecarbonitrile, 4-cyanopyridine, naphthonitriles, cinnamonitrile, and 3-phenylpropanenitrile were obtained in good to excellent yields. Mechanism investigation indicated that the •O2– radical was the active oxygen species. The unique structure of iron- and nitrogen-doped carbon is key for the reaction, and the Fe–Nx site is the possible catalytically active site.
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