详细信息
Boosting the catalysis of cesium phosphomolybdate encapsulated in hierarchical porous UiO-66 by microenvironment modulation for epoxidation of alkenes ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:Boosting the catalysis of cesium phosphomolybdate encapsulated in hierarchical porous UiO-66 by microenvironment modulation for epoxidation of alkenes
作者:Hu, Dianwen[1,2];Miao, Songsong[3];Zhang, Pengfei[4];Wu, Siyuan[5];He, Yu-Peng[1,2];Meng, Qingwei[1,2]
机构:[1]Dalian Univ Technol, Ningbo Inst, Ningbo 315016, Peoples R China;[2]Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China;[3]Chinese Acad Sci, Changchun Inst Appl Chem, Changchun 130022, Peoples R China;[4]Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China;[5]East China Univ Sci & Technol, Sch Chem & Mol Engn, Shanghai 200237, Peoples R China
年份:2023
卷号:52
期号:40
起止页码:14676
外文期刊名:DALTON TRANSACTIONS
收录:;EI(收录号:20234314946946);WOS:【SCI-EXPANDED(收录号:WOS:001074889600001)】;
基金:Financial support from the Postdoctoral Research Foundation of Ningbo Institution of Dalian University of Technology (No. 03030001) is gratefully acknowledged.
语种:英文
外文关键词:Catalyst activity - Cesium - Olefins - Styrene
摘要:The chemical microenvironment of polyoxometalates (POMs) encapsulated in metal-organic frameworks (MOFs) presents a significant influence on their catalytic performance, which can be easily regulated by the linker functional group alteration or metal substitution in MOFs. Herein, a series of cesium phosphomolybdate (CsPM) encapsulated in hierarchical porous UiO-66-X composites (CsPM@HP-UiO-66-X, X = H, 2CH3, or 2OH, where X represents the alterable group grafted onto the linker benzene ring) were successfully synthesized through a one pot modulated solvothermal method. The catalytic performances of the obtained materials were explored in alkene epoxidation reaction with tert-butyl hydroperoxide (t-BuOOH). CsPM@HP-UiO-66-2CH3 showed relatively high catalytic activity, stability, and epoxidation selectivity in cyclooctene epoxidation among the CsPM@HP-UiO-66-X composites. Moreover, CsPM@HP-UiO-66-2CH3 was effective in the epoxidation of numerous alkenes, especially cyclic alkenes. The superior catalytic activity of CsPM@HP-UiO-66-2CH3 is mainly attributed to the modulation of the microenvironment surrounding CsPM active sites by introducing a hydrophobic methyl group. Meanwhile, the size-matched effect, the introduction of cesium cations, and the strong metal-support interactions (SMSIs) between CsPM and HP-UiO-66-2CH3 play a crucial role in the stability of CsPM@HP-UiO-66-2CH3. CsPM@HP-UiO-66-2CH3 showed preferable catalytic performance in alkene epoxidation reaction among CsPM@HP-UiO-66-X composites, which is mainly attributed to the modulation of the microenvironment surrounding CsPM active sites with a methyl group.
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