化学
催化作用
双金属片
微型多孔材料
反应性(心理学)
沸石
胺化
偶联反应
多相催化
无机化学
有机化学
医学
替代医学
病理
作者
Tianxiang Chen,Wenhua Yu,Ching Kit Tommy Wun,Tai‐Sing Wu,Mingzi Sun,Sarah J. Day,Zehao Li,Bo Yuan,Yong Wang,Mingjie Li,Zi Wang,Yung‐Kang Peng,Wing‐Yiu Yu,Kwok‐Yin Wong,Bolong Huang,Taoyuan Liang,Tsz Woon Benedict Lo
摘要
A cross-coupling reaction via the dehydrogenative route over heterogeneous solid atomic catalysts offers practical solutions toward an economical and sustainable elaboration of simple organic substrates. The current utilization of this technology is, however, hampered by limited molecular definition of many solid catalysts. Here, we report the development of Cu-M dual-atom catalysts (where M = Co, Ni, Cu, and Zn) supported on a hierarchical USY zeolite to mediate efficient dehydrogenative cross-coupling of unprotected phenols with amine partners. Over 80% isolated yields have been attained over Cu-Co-USY, which shows much superior reactivity when compared with our Cu1 and other Cu-M analogues. This amination reaction has hence involved simple and non-forceful reaction condition requirements. The superior reactivity can be attributed to (1) the specifically designed bimetallic Cu-Co active sites within the micropore for "co-adsorption-co-activation" of the reaction substrates and (2) the facile intracrystalline (meso/micropore) diffusion of the heterocyclic organic substrates. This study offers critical insights into the engineering of next-generation solid atomic catalysts with complex reaction steps.
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