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作 者:Zepeng Lei Francisco W.S.Lucas Enrique Canales Moya Shaofeng Huang Yicheng Rong Aaron Wesche Patrick Li Lauren Bodkin Yinghua Jin Adam Holewinski Wei Zhang
机构地区:[1]Department of Chemistry,University of Colorado Boulder,Boulder,CO 80309,United States [2]Renewable and Sustainable Energy Institute,and Department of Chemical and Biological Engineering,University of Colorado Boulder,Boulder,CO 80309,United States
出 处:《Chinese Chemical Letters》2021年第12期3799-3802,共4页中国化学快报(英文版)
基 金:supported by University of Colorado Boulder and K. C. Wong Education Foundation;financial support by the Koch Graduate fellowship。
摘 要:We report a series of highly stable metallophthalocyanine-based covalent organic frameworks(MPc-dxCOFs) linked by robust 1,4-dioxin bonds constructed through nucleophilic aromatic substitution(SNAr)reaction. The chemical structures and crystallinity of the COFs largely remain unchanged even after treating with boiling water(90°C), concentrated acids(12 mol/L HCl) or bases(12 mol/L Na OH), oxidizing(30% H_(2)O_(2)) or reducing agents(1 mol/L NaBH;) for three days due to their stable M-Pc building blocks and resilient dioxin linkers. With metallated phthalocyanine active sites regularly arranged in the stable framework structures, MPc-dx-COFs can be directly used as efficient electrocatalysts for the oxygen reduction reaction(ORR) without pyrolysis treatment that has commonly been used in previous studies.
关 键 词:Covalent organic framework METALLOPHTHALOCYANINE Nucleophilic aromatic substitution Dioxin linkage ELECTROCATALYSIS Oxygen reduction reaction
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