Aerobic Epoxidation of Olefins Catalyzed by the Cobalt-Based Metal-Organic Framework STA-12(Co)

被引:106
作者
Beier, Matthias J. [1 ,2 ]
Kleist, Wolfgang [1 ,3 ]
Wharmby, Michael T. [4 ]
Kissner, Reinhard [1 ]
Kimmerle, Bertram [1 ]
Wright, Paul A. [4 ]
Grunwaldt, Jan-Dierk [2 ,3 ]
Baiker, Alfons [1 ]
机构
[1] ETH, Dept Chem & Appl Biosci, HCI, CH-8093 Zurich, Switzerland
[2] Tech Univ Denmark, Dept Chem & Biochem Engn, DK-2800 Lyngby, Denmark
[3] Karlsruhe Inst Technol KIT, Inst Catalysis Res & Technol, D-76344 Eggenstein Leopoldshafen, Germany
[4] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
基金
英国工程与自然科学研究理事会;
关键词
cobalt; epoxidation; heterogeneous catalysis; metal-organic frameworks; stilbene oxides; COBALT(II)-EXCHANGED ZEOLITE-X; MOLECULAR-OXYGEN; HETEROGENEOUS CATALYSTS; OXIDATION REACTIONS; RAPID INTERACTION; ALPHA-PINENE; STYRENE; COMPLEXES; DIOXYGEN; KINETICS;
D O I
10.1002/chem.201101223
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A Co-based metalorganic framework (MOF) was investigated as a catalytic material in the aerobic epoxidation of olefins in DMF and exhibited, based on catalyst mass, a remarkably high catalytic activity compared with the Co-doped zeolite catalysts that are typically used in this reaction. The structure of STA-12(Co) is similar to that of STA-12(Ni), as shown by XRD Rietveld refinement and is stable up to 270 degrees C. For the epoxidation reaction, significantly different selectivities were obtained depending on the substrate. Although styrene was epoxidized with low selectivity due to oligomerization, (E)-stilbene was converted with high selectivities between 80 and 90%. Leaching of Co was low and the reaction was found to proceed mainly heterogeneously. The catalyst was reusable with only a small loss of activity. The catalytic epoxidation of stilbene with the MOF featured an induction period, which was, interestingly, considerably reduced by styrene/stilbene co-epoxidation. This could be traced back to the formation of benzaldehyde promoting the reaction. Detailed parameter and catalytic studies, including in situ EPR and EXAFS spectroscopy, were performed to obtain an initial insight into the reaction mechanism.
引用
收藏
页码:887 / 898
页数:12
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