共价键
催化作用
化学
配体(生物化学)
Atom(片上系统)
金属
色散(光学)
多孔性
无定形固体
过氧化物酶
化学工程
组合化学
光化学
结晶学
有机化学
酶
嵌入式系统
工程类
受体
物理
光学
生物化学
计算机科学
作者
Tiantian Feng,Qing Hao,Bing Sun,Dong Wang
标识
DOI:10.1021/acs.jpcc.2c07887
摘要
Metal–covalent organic frameworks (MCOFs) feature regular structures, adjustable pore channels, designable structures, and abundant tunable metal-catalytic active sites and are promising candidates for advanced single-atom enzymes. Here, we constructed porous and crystalline Fe-COFTAPB-BPA linked with Fe-iminopyridine moieties from the corresponding building blocks under ambient conditions in the time scale of minutes. Fe-COFTAPB-BPA with single-atom Fe dispersion could react with H2O2 to catalyze the oxidation of tetramethylbenzidine (TMB), demonstrating that an MCOF with a well-defined metallo ligand structure can function as a single-atom enzyme. Steady-state kinetic analysis showed that crystalline Fe-COFTAPB-BPA revealed a higher affinity to TMB than amorphous Fe-PolyTAPB-BPA at a similar Fe content attributed to its regular pore structure, higher specific surface area, and uniform distribution of catalytically active sites. As a peroxidase mimetic, Fe-COFTAPB-BPA exhibits the advantages of easy preparation, good stability, and higher catalytic efficiency.
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