邻接
劈理(地质)
键裂
兴奋剂
碳纤维
无氧运动
化学
生物量(生态学)
材料科学
立体化学
化学工程
有机化学
催化作用
光电子学
复合材料
复合数
生物
生态学
工程类
断裂(地质)
生理学
作者
Fei-Feng Mao,Yian Wang,Yan Zhou,Ming-Shuai Sun,Haijun Wang,Duan‐Jian Tao
标识
DOI:10.1021/acsanm.4c03304
摘要
The efficient and selective conversion of biomass-derived vicinal diols into high-value-added chemicals represents a pivotal area of research that has garnered substantial interest within the scientific community. In this work, three ultralow loading Fe supports on N-doped carbon nanosphere catalysts (Fe@NC-T) were successfully prepared using the hard template method with acid etching. The selective conversion of vicinal diols into aldehydes, ketones, and amines over the Fe@NC-800 nanosphere catalyst was achieved through an anaerobic cleavage of C–C bonds and successfully utilized autologous hydrogen resources. The exceptional catalytic activity of the Fe@NC-800 nanosphere catalyst may be credited to the presence of highly dispersed Fe species at the active sites, which has been verified through several characterization techniques, control tests, and density functional theory calculations. In addition, the Fe@NC-800 nanosphere catalyst also demonstrated its wide applicability and excellent reusability under the operating conditions. We believe that this study presents an auspicious scheme for the highly selective conversion of vicinal diols into high value-added carbonyl compounds and amine products.
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