化学计量学
光催化
四苯乙烯
共价键
单体
接受者
电子受体
表面改性
材料科学
三嗪
光化学
化学
高分子化学
组合化学
催化作用
有机化学
聚合物
物理化学
物理
聚集诱导发射
荧光
量子力学
凝聚态物理
作者
Qiaobo Liao,Wentao Xu,Xin Huang,Can Ke,Qi Zhang,Kai Xi,Jin Xie
标识
DOI:10.1007/s11426-019-9696-3
摘要
Three unprecedented 2D [4+3] covalent organic frameworks (TTCOF-1, TTCOF-2, and TTCOF-3) have been prepared by sub-stoichiometric condensation of tetratopic and tritopic monomers, overcoming the limitations of the design rules of conventional topologies. By reticulating the tetraphenylethylene (TPE)-based and triazine-based moieties into COF frameworks, novel electron donor-acceptor (D-A) type structures were obtained. These TTCOFs have good photocatalytic activity in aerobic C(sp3)–H bond functionalization and arylboronic acid oxidation driven by visible light, with yields up to 94%. This can expedite possibilities of COFs with new structural and topological complexities and can also expand the application of COF-based photocatalysis in synthetic chemistry.
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