Conductive catalysis by subsurface transition metals

Author:

Deng Xin1,Zheng Caiyan2,Li Yangsheng3,Zhou Zeyu3,Wang Jiamin4,Ran Yihua3,Hu Zhenpeng2ORCID,Yang Fan3ORCID,Li Landong145ORCID

Affiliation:

1. Frontiers Science Center for New Organic Matter, College of Chemistry, Nankai University , Tianjin 300071 , China

2. School of Physics, Nankai University , Tianjin 300071 , China

3. School of Physical Science and Technology, ShanghaiTech University , Shanghai 201210 , China

4. School of Materials Science and Engineering, Nankai University , Tianjin 300350 , China

5. Haihe Laboratory of Sustainable Chemical Transformations , Tianjin 300192 , China

Abstract

Abstract The nature of catalysis is being hotly pursued for over a century, and current research is focused on understanding active centers and their electronic structures. Herein, the concept of conductive catalysis is proposed and verified by theoretical simulations and experimental observations. Metallic systems containing buried catalytically active transitional metals and exposed catalytically inert main group metals are constructed, and the electronic interaction between them via metallic bonding is disclosed. Through the electronic interaction, the catalytic properties of subsurface transitional metals (Pd or Rh) can be transferred to outermost main group metals (Al or Mg) for several important transformations like semi-hydrogenation, Suzuki-coupling and hydroformylation. The catalytic force is conductive, in analogy with the magnetic force and electrostatic force. The traditional definition of active centers is challenged by the concept of conductive catalysis and the electronic nature of catalysis is more easily understood. It might provide new opportunities for shielding traditional active centers against poisoning or leaching and allow for precise regulation of their catalytic properties by the conductive layer.

Publisher

Oxford University Press (OUP)

Subject

Multidisciplinary

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