化学选择性
化学
催化作用
醛
氢溢流
分子
组合化学
氢
光化学
有机化学
小分子
过氧化氢
烷基
金属
质子
多相催化
纳米技术
氢分子
过渡金属
溢出效应
电子
作者
Yan Liang,Zhiwei Chen,Hongru Zhou,Hu Jin,Qianshuo Wang,Zhaolin Dou,M H Wang
摘要
molecules for being activated into electrons and protons. In such a process, proton and electron transiently bind with O species and Pd via the hydrogen spillover pathway, respectively, and participate in aldehyde hydrogenation via a consecutive transfer. Meanwhile, the PVP sheath redirects the movement of alcohols away from the metal to inhibit hydrodeoxygenation, thereby achieving the selective hydrogenation of aromatic aldehyde. This noncontact hydrogenation mechanism based on MOF breaks away from conventional substrate-modulation paradigms, providing a new tool for fabricating catalysts with superior chemoselectivity and activity.
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