脱氢
催化作用
化学
镍
纳米颗粒
冷凝
氢键
光化学
有机化学
材料科学
纳米技术
分子
物理
热力学
作者
Jian Zhang,Zhe An,Yanru Zhu,Xin Shu,Hongyan Song,Yitao Jiang,Wenlong Wang,Xu Xiang,Linlin Xu,Jing He
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2019-11-05
卷期号:9 (12): 11438-11446
被引量:57
标识
DOI:10.1021/acscatal.9b03245
摘要
Simultaneous formation of C–C/C–N bonds provides insight into the bottom-up synthesis of N-heterocycles. This work reports Ni0/Niδ+ synergistic catalysis on the surface of Ni nanoparticles for the highly efficient one-pot formation of C–C/C–N bonds, affording 1,2,3,4-tetrahydroquinoline and its derivatives from 2-amino benzyl alcohol and ethanol without any addition of liquor base or external hydrogen. Ni0/Niδ+ synergistic catalysis has been achieved by regulating the Ni particle size or activating the Ni surface with O2. In the dehydrogenation of −CH2–OH to −CH═O, the formation of C══C and C═N bonds via concurrent cross-condensation, and the transformation of C═C/C═N to C–C/C–N via hydrogen transfer, ethanol dehydrogenation has been found to be the rate-determining step. Reducing the Ni particle size effectively increases the number of surface Niδ+ sites, which accelerates catalytic dehydrogenation through synergistic catalysis between surface Niδ+ and Ni0 sites. The number of surface Niδ+ sites can be further increased by appropriately activating the Ni surface with O2.
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