Search for: All records

Metal‐encapsulated covalent organic frameworks (metal/COFs) represent an emerging paradigm in heterogeneous catalysis. However, the time‐intensive (usually 4 or more days) and tedious multi‐step synthesis of metal/COFs remains a significant stumbling block for their broad application. To address this challenge, we introduce a facile microwave‐assistedin situmetal encapsulation strategy to cooperatively combine COF formation andin situpalladium(II) encapsulation in one step. With this unprecedented approach, we synthesize a diverse range of palladium(II)‐encapsulated COFs (termed Mw‐Pd/COF) in the air within just an hour. Notably, this strategy is scalable for large‐scale production (~0.5 g). Leveraging the high crystallinity, porosity, and structural stability, one representative Mw‐Pd/COF exhibits remarkable activity, functional group tolerance, and recyclability for the Suzuki‐Miyaura coupling reaction at room temperature, surpassing most previously reported Pd(II)/COF catalysts with respect to catalytic performance, preparation time, and synthetic ease. This microwave‐assistedin situmetal encapsulation strategy opens a facile and rapid avenue to construct metal/COF hybrids, which hold enormous potential in a multitude of applications including heterogeneous catalysis, sensing, and energy storage.