Abstract

Covalent organic frameworks (COFs) were ideal carriers for noble metal catalysts due to their rich pore structure, pre-designable monomers, and high stability. Herein, a series of novel thiourea-based COFs (Tx-COFs) enriched with heteroatoms were constructed to provide abundant and powerful anchoring sites for metal. The successful preparation of Pd@COFs with high metal dispersion and substantial active sites was confirmed by XPS and STEM-EDX element mapping. These catalysts exhibited excellent catalytic activity and stability for the Suzuki-Miyaura coupling reaction. Especially for Pd@TU-COF, the catalyst still catalyzed the reaction at room temperature to afford the product in a yield of 99 % after 10 reuses, while the palladium load only decreased from 5.78 % to 5.66 %. The structure-activity relationships between the metal loading mode, the structure of Tx-COF, and its catalytic performance were also investigated in this study, which provided a feasible strategy for the preparation of efficient and stable heterogeneous catalysts.

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