肉桂醛
选择性
转移加氢
化学
醛
钴
纳米囊
硫化钴
电化学
吸附
硫化物
催化作用
无机化学
光化学
材料科学
有机化学
纳米颗粒
电极
纳米技术
钌
物理化学
作者
Shuhe Han,Yanmei Shi,Changhong Wang,Cuibo Liu,Bin Zhang
标识
DOI:10.1016/j.xcrp.2021.100337
摘要
Designing nanostructured electrocatalysts for selective transfer hydrogenation of α, β-unsaturated aldehydes with water as the hydrogen source is highly desirable. Here, a facile self-templating strategy is designed for the synthesis of CoS2 and CoS2-x nanocapsules (NCs) as efficient cathodes for selective transfer hydrogenation of cinnamaldehyde, a model α, β-unsaturated aldehyde. The hollow porous structures of NCs are rich in active sites and improve mass transfer, resulting in high turnover frequency. The specific adsorption of the styryl block on pristine CoS2 NCs is conducive to the selective formation of half-hydrogenated hydrocinnamaldehyde with 91.7% selectivity, and the preferential adsorption of the C = O group induced by sulfur vacancies on defective CoS2-x NCs leads to the full-hydrogenated hydrocinnamyl alcohol with 92.1% selectivity. A cross-coupling of carbon and hydrogen radicals may be involved in this electrochemical hydrogenation reaction. Furthermore, this selective hydrogenation method is also effective for other α, β-unsaturated aldehydes, illustrating the universality of the method.
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