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Zirconium Phosphate Supported Copper Catalyst for Selective Oxidation of Phenol to CIS, Cis-Muconic Acid  ( EI收录)  

文献类型:期刊文献

英文题名:Zirconium Phosphate Supported Copper Catalyst for Selective Oxidation of Phenol to CIS, Cis-Muconic Acid

作者:Hou, Zhenshan[1,3]; He, Jingjing[1]; Jiang, Yongjun[2]; Ding, Bingjie[1]; Wang, Yajun[1]; Qiu, Hewen[3]; Dai, Sheng[2]; Zhao, Xiuge[1]

机构:[1] State Key Laboratory of Green Chemical Engineering and Industrial Catalysis, Research Institute of Industrial Catalysis, School of Chemistry & Molecular Engineering, East China University of Science and Technology, Shanghai, 200237, China; [2] Key Laboratory for Advanced Materials and Feringa Nobel Prize Scientist Joint Research Center, Institute of Fine Chemicals, School of Chemistry & Molecular Engineering East China University of Science and Technology, Shanghai, 200237, China; [3] Shanghai Key Laboratory of Green Chemistry and Chemical Processes, East China Normal University, School of Chemistry and Molecular Engineering, Shanghai, 200062, China

年份:2023

外文期刊名:SSRN

收录:EI(收录号:20230177068)

语种:英文

外文关键词:Catalyst supports - Copper compounds - Hydroxylation - Oxidation - Phosphates - Zirconium compounds

摘要:The selective oxidation of phenol into cis, cis-muconic acid was carried out with α-zirconium phosphate supported-copper catalysts. It has been found that a sole α-zirconium phosphate exhibited a preferential selectivity (up to 80%) towards dihydroxybenzene (Catechol/Hydroquinone=1.4:1). Moreover, the further studies indicated that α-zirconium phosphate-supported copper catalysts enable to catalyze the oxidative cleavage of catechol into high-added valuable platform molecule cis,cis-muconic acid (ccMA) by in-situ generating performic acid. A 66% conversion of phenol and 60% selectivity towards cis, cis-muconic acid were obtained under mild reaction condition. The detailed characterization demonstrated that copper(II) species were highly dispersed on α-zirconium phosphate, and could be bonded with the phosphate group. The forming Cu(II)-O-P linkage was proved to be catalytically active species and endowed the supported-copper catalysts with a superior recyclability. The reaction pathway involved hydroxylation of phenol, followed by the formation of a metal-catechol complex which was oxidized into cis, cis-muconic acid. ? 2023, The Authors. All rights reserved.

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