Palladium Nanoparticles Encapsulated in a Metal-Organic Framework as Efficient Heterogeneous Catalysts for Direct C2 Arylation of Indoles

被引:169
作者
Huang, Yuanbiao [1 ]
Lin, Zujin [1 ]
Cao, Rong [1 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 335002, Fujian, Peoples R China
关键词
C-H activation; heterogeneous catalysis; indoles; metal-organic framework; nanoparticles; palladium; DIRECT C-2 ARYLATION; CHROMIUM TEREPHTHALATE MIL-101; ORGANOMETALLIC CVD-PRECURSORS; ENHANCED HYDROGEN STORAGE; H BOND ARYLATION; GOLD NANOPARTICLES; COORDINATION POLYMER; COUPLING REACTIONS; ROOM-TEMPERATURE; SUZUKI-MIYAURA;
D O I
10.1002/chem.201101705
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Highly dispersed palladium nanoparticles (Pd NPs) encapsulated in the mesoporous cages of the metal-organic framework (MOF) MIL-101(Cr) have been prepared by using the wetness impregnation method. The Pd NPs were characterized by powder X-ray diffraction (PXRD), N-2 adsorption, transmission electron microscopy, inductively coupled plasma atomic emission spectroscopy (ICP-AES), and X-ray photoelectron spectroscopy (XPS). The particles size ((2.6 +/- 0.5) nm) of the obtained Pd NPs was in good agreement with the cage diameters (2.9 and 3.4 nm) of the MOF. The resulting Pd/MIL-101(Cr) catalyst exhibited extremely high catalytic activities in the direct C2 arylation of substituted indoles by using only 0.1 mol% of the Pd catalyst. Moreover, the catalyst is easily recoverable and can be reused several times without leaching into solution and loss of activity. The combination of the highly dispersible Pd NPs within the accessible mesoporous cages and the favorable adsorption of the aryl halides on MIL-101 are suspected to be the main reasons for the observed high activities of the Pd/MIL-101( Cr) catalyst in the direct C2 arylation of indoles.
引用
收藏
页码:12706 / 12712
页数:7
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