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Docking Site Modulation of Isostructural Covalent Organic Frameworks for CO2 Fixation
Authors:Fan Yang  Yusen Li  Ting Zhang  Ziqiang Zhao  Guolong Xing  Prof Long Chen
Institution:Department of Chemistry, Institute of Molecular Plus, and, Tianjin Key Laboratory of Molecular Optoelectronic Science, Tianjin University, Tianjin, 300072 P. R. China
Abstract:Three isostructural covalent organic frameworks (COFs) with either methoxyl, hydroxyl, or both groups on the channel wall, are synthesized and served as metal-free heterogeneous catalysts for chemical fixation of CO2. Among them, the COF decorated with both hydroxyl and methoxyl groups named OMe-OH-TPBP-COF exhibits the highest catalytic activity and efficiency for CO2 cycloaddition under mild conditions.
Keywords:covalent organic frameworks  cycloaddition of CO2  docking site modulation
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