催化作用
化学
肉桂醛
肉桂醇
选择性
吸附
Atom(片上系统)
光化学
转移加氢
反应机理
无机化学
有机化学
计算机科学
钌
嵌入式系统
作者
Jiawen Chen,Yongming Xia,Yuxuan Ling,Xuehui Liu,Shuyuan Li,Xiong Yin,Lipeng Zhang,Minghui Liang,Yi‐Ming Yan,Qiang Zheng,Wenxing Chen,Yanjun Guo,En‐Hui Yuan,Gaofei Hu,Xiao‐Le Zhou,Leyu Wang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-04-18
卷期号:24 (17): 5197-5205
被引量:2
标识
DOI:10.1021/acs.nanolett.4c00512
摘要
Highly active nonprecious-metal single-atom catalysts (SACs) toward catalytic transfer hydrogenation (CTH) of α,β-unsaturated aldehydes are of great significance but still are deficient. Herein, we report that Zn–N–C SACs containing Zn–N3 moieties can catalyze the conversion of cinnamaldehyde to cinnamyl alcohol with a conversion of 95.5% and selectivity of 95.4% under a mild temperature and atmospheric pressure, which is the first case of Zn-species-based heterogeneous catalysts for the CTH reaction. Isotopic labeling, in situ FT-IR spectroscopy, and DFT calculations indicate that reactants, coabsorbed at the Zn sites, proceed CTH via a "Meerwein–Ponndorf–Verley" mechanism. DFT calculations also reveal that the high activity over Zn–N3 moieties stems from the suitable adsorption energy and favorable reaction energy of the rate-determining step at the Zn active sites. Our findings demonstrate that Zn–N–C SACs hold extraordinary activity toward CTH reactions and thus provide a promising approach to explore the advanced SACs for high-value-added chemicals.
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