Fast Cyclohexane Oxidation Under Mild Reaction Conditions Through a Controlled Creation of Redox-Active Fe(II/III) Sites in a Metal-Organic Framework

被引:24
作者
Kim, Ah-Reum [1 ]
Ahn, Sol [2 ]
Yoon, Tae-Ung [1 ]
Notestein, Justin M. [2 ]
Farha, Omar K. [2 ,3 ,4 ]
Bae, Youn-Sang [1 ]
机构
[1] Yonsei Univ, Dept Chem & Biomol Engn, Seoul 03722, South Korea
[2] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60208 USA
[3] Northwestern Univ, Int Inst Nanotechnol, Evanston, IL 60208 USA
[4] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
基金
新加坡国家研究基金会;
关键词
Metal-organic frameworks (MOFs); Redox-active sites; Oxidation; Cyclohexane; SELECTIVE OXIDATION; CATALYTIC-ACTIVITY; HIGHLY EFFICIENT; LOW-TEMPERATURE; II COMPLEX; SEPARATION; HYDROGEN; DEGRADATION; CU(I); CO2;
D O I
10.1002/cctc.201901050
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
MIL-100(Fe), a metal-organic framework containing coordinatively unsaturated iron sites, was prepared by a solvothermal method and utilized in cyclohexane oxidation. Interestingly, the composition and fraction of redox-active Fe(II/III) sites in MIL-100(Fe) could be tuned by using different pretreatment temperatures. The obtained materials were characterized by means of field-emission scanning electron microscopy (FE-SEM), powder X-ray diffraction (PXRD), N-2 adsorption-desorption isotherms, and X-ray photoelectron spectroscopy (XPS). Due to the presence of redox-active coordinatively unsaturated sites (CUS) at the iron atoms, MIL-100(Fe) exhibited good performance for cyclohexane oxidation under mild reaction conditions. Oxidation rates were significantly enhanced when reduced Fe-II sites were generated by high-temperature pretreatments. In either high-temperature or low-temperature pretreatment, the isolated Fe(II/III) sites in MIL-100 were far more reactive in cyclohexane oxidation than were bulk iron oxide materials. Finally, possible reaction pathways were proposed based on radical, Haber-Weiss routes.
引用
收藏
页码:5650 / 5656
页数:7
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