Palladium nanoparticles-confined pore-engineered urethane-linked thiol-functionalized covalent organic frameworks: a...

Covalent organic frameworks (COFs) are potential templates for the synthesis of nanomaterials owing to the versatility of their structure. Most of the reported COFs comprise imine linkages. Herein, we report for the first time the synthesis of a urethane-linked COF (UCOF) using monoformylphloroglucinol and 1,4-phenylene diisocyanate as monomers. Furthermore, the UCOF was functionalized with cysteamine to introduce free dangling thiol groups into the cavity. The latter played a critical role in fixing the active metal efficiently and facilitating the confined growth of small metal nanoparticles (∼4-6 nm) with a high surface area leading to a pore-engineered heterogeneous Pd catalyst (PdNPs@UCOF-SH). The COF and Pd catalyst were characterized using various analytical techniques such as CP-MAS NMR, FTIR, PXRD, BET, FEG-SEM, HRTEM, XPS, TGA, and ICP-AES. The as-prepared UCOF-SH-supported Pd nanoparticles showed excellent catalytic activity in the Suzuki Miyaura cross-coupling reaction under mild conditions with low catalyst loading and eco-friendly solvents. The scope was extended to various aryl boronic acids and aryl halides (I, Br, and Cl). The halo-substituted and non-halo biaryl derivatives were obtained in good to excellent yields, within a shorter reaction time, avoiding the homocoupling of aryl boronic acid. The pore-engineered COF-derived catalyst is selective and easily recycled up to 10 runs without significant loss of catalytic activity. This reveals the robust nature of the PdNPs@UCOF-SH catalyst and the sustainability of the process which opens a new frontier for several catalytic applications.