生物正交化学
催化作用
化学
合理设计
钯
组合化学
磷
纳米技术
黑磷
生物化学
材料科学
有机化学
点击化学
光电子学
作者
Mingjie Rong,Jian Liu,Zhen Sun,Tong Li,Yang Li,Chunhuan Jiang,Lehui Lu
标识
DOI:10.1002/anie.202216822
摘要
Abstract Pd‐catalyzed chemistry has played a significant role in the growing subfield of bioorthogonal catalysis. However, rationally designing Pd nanocatalysts that show outstanding catalytic activity and good biocompatibility poses a great challenge. Herein, we propose an innovative strategy through exploiting black phosphorous nanosheets (BPNSs) to enhance Pd‐mediated bioorthogonal catalytic activity. Firstly, the electron‐donor properties of BPNSs enable in situ growth of Pd nanoparticles (PdNPs) on it. Meanwhile, due to the superb capability of reducing Pd II , BPNSs can act as hard nucleophiles to accelerate the transmetallation in the decaging reaction process. Secondly, the lone pair electrons of BPNSs can firmly anchor PdNPs on their surface via Pd−P bonds. This design endows Pd/BP with the capability to retard tumor growth by activating prodrugs. This work proposes new insights into the design of heterogeneous transition‐metal catalysts (TMCs) for bioorthogonal catalysis.
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