Constructing Pd and Cu Crowding Single Atoms by Protein Confinement to Promote Sonogashira Reaction

Author:

Zhao Qinying1,Zhao Xudong2,Liu Zhiyi1,Ge Yi1,Ruan Jiaxiong1,Cai Hongyi1,Zhang Shasha1,Ye Chenliang3,Xiong Yu4,Chen Wei1,Meng Ge1,Liu Zhiliang2,Zhang Jian1ORCID

Affiliation:

1. Key Laboratory of Carbon Materials of Zhejiang Province Key Lab of Biohealth Materials and Chemistry of Wenzhou College of Chemistry and Materials Engineering Wenzhou University Wenzhou Zhejiang 325035 China

2. College of Material Sciences and Chemical Engineering Harbin Engineering University Harbin Heilongjiang 150001 China

3. Department of Power Engineering North China Electric Power University Baoding Hebei 071003 China

4. Department of Chemistry and Chemical Engineering Central South University Changsha Hunan 410083 China

Abstract

AbstractFor multicenter‐catalyzed reactions, it is important to accurately construct heterogeneous catalysts containing multiple active centers with high activity and low cost, which is more challenging compared to homogeneous catalysts because of the low activity and spatial confinement of active centers in the loaded state. Herein, a convenient protein confinement strategy is reported to locate Pd and Cu single atoms in crowding state on carbon coated alumina for promoting Sonogashira reaction, the most powerful method for constructing the acetylenic moiety in molecules. The single‐atomic Pd and Cu centers take advantage in not only the maximized atomic utilization for low cost, but also the much‐enhanced performance by facilitating the activation of aryl halides and alkynes. Their locally crowded dispersion brings them closer to each other, which facilitates the transmetallation process of acetylide intermediates between them. Thus, the Sonogashira reaction is drove smoothly by the obtained catalyst with a turnover frequency value of 313 h−1, much more efficiently than that by commercial Pd/C and CuI catalyst, conventional Pd and Cu nanocatalysts, and mixed Pd and Cu single‐atom catalyst. The obtained catalyst also exhibits the outstanding durability in the recycling test.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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