卟啉
光催化
共价键
共轭体系
化学
光化学
共价有机骨架
催化作用
组合化学
材料科学
聚合物
有机化学
作者
Ji‐Long Shi,Rufan Chen,Huimin Hao,Cheng Wang,Xianjun Lang
标识
DOI:10.1002/anie.202000723
摘要
Abstract 2D covalent organic frameworks (COFs) are receiving ongoing attention in semiconductor photocatalysis. Herein, we present a photocatalytic selective chemical transformation by combining sp 2 carbon‐conjugated porphyrin‐based covalent organic framework (Por‐sp 2 c‐COF) photocatalysis with TEMPO catalysis illuminated by 623 nm red light‐emitting diodes (LEDs). Highly selective conversion of amines into imines was swiftly afforded in minutes. Specifically, the π‐conjugation of porphyrin linker leads to extensive absorption of red light; the sp 2 −C=C− double bonds linkage ensures the stability of Por‐sp 2 c‐COF under high concentrations of amine. Most importantly, we found that crystalline framework of Por‐sp 2 c‐COF is pivotal for cooperative photocatalysis with (2,2,6,6‐tetramethylpiperidin‐1‐yl)oxyl (TEMPO). This work foreshadows that the outstanding hallmarks of COFs, particularly crystallinity, could be exploited to address energy and environmental challenges by cooperative photocatalysis.
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