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Single-Site Nickel-Anchored Photosensitive Covalent Organic Framework for Metallaphotocatalytic C─S/C─N
Yang-Yang Xiong1, Songlin Deng1, Haiping Wang2
1GBRCE For Functional Molecular Engineering, Lehn Institute of Functional Materials, IGCME, School of Chemistry, Sun Yat-Sen University, Guangzhou, China.
None:
The development of multifunctionally heterogeneous catalysts, simultaneously bearing photosensitizer and nonnoble metal catalyst in close spatial proximity, represents a promising solution for promoting metallaphotoredox-mediated catalysis, albeit it remains challenging. Herein, a single-site Ni-functionalized photosensitive covalent organic framework (COF), TTA-BPyDA(Ni)-COF, has been constructed by implementing a postsynthetic metallization strategy in a triazine-based COF scaffold. The precise integration of photosensitizer and Ni-catalytic active centers within TTA-BPyDA(Ni)-COF not only dramatically improves the metallaphotocatalytic (MPC) performance in C─S/C─N cross-coupling reaction between diverse thiols/amines and aryl iodides with electron-rich/neutral/deficient groups but also confers TTA-BPyDA(Ni)-COF with outstanding recyclability and durability compared with its homogeneous counterpart. Importantly, the MPC C─S/C─N reaction mechanisms have been well established by comprehensive experimental and theoretical simulations. This work offers valuable insights for developing single-site nonnoble metal-functionalized COF catalytic platforms that integrate photoredox centers with catalytic transition-metal cores.
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