还原胺化
胺化
生物量(生态学)
选择性
纳米颗粒
碳纤维
化学
热解
产量(工程)
材料科学
有机化学
催化作用
组合化学
纳米技术
海洋学
冶金
复合材料
复合数
地质学
作者
Zhengyi Pan,Qian Zhang,Wenquan Wang,Lulin Wang,Guanghui Wang
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2022-03-11
卷期号:10 (11): 3777-3786
被引量:13
标识
DOI:10.1021/acssuschemeng.2c00800
摘要
Reductive aminations of biomass-derived carbonyl compounds, an industrially important class of reactions applied for green and sustainable production of valuable amines/imines, often suffer from problems of selectivity toward the target product and reusability of the catalyst. Herein, we develop a facile strategy to synthesize two carbon-doped Ni catalysts with particle sizes of 7.5 and 47.5 nm, respectively, over which the selectivity in the reductive amination of biomass-derived carbonyl compounds is completely switched between primary amines (>96% yield, 7.5 nm) and secondary imines (>97% yield, 47.5 nm). The synthesis is derived from the confined pyrolysis of Ni-Al layered double hydroxides (NiAl-LDH) grafted on hollow polymer nanospheres (HPS), in which the HPS play four roles (i.e., template, reductant, carbon resource, and Ni size controller). The two catalysts exhibit excellent stability due to the existence of surface Ni-Cx species. Reductive aminations over these two catalysts have a broad substrate scope and can be scaled up to the gram level, indicating the potential for industrial applications.
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