Gold and Silver Nanoparticles Supported on Metal-organic Frameworks: a Highly Active Catalyst for Three-component Coupling Reaction
Engineering metal-organic frameworks(MOF) for heterogeneous catalysts have been of extreme interest since they have large pore size within the crystalline framework and well defined pore architecture. Ni-containing MOF Ni2(3,5-Pydc)2(H2O)8·2H2O(1·H2O) was prepared by solvothermal method from 3,5-pyr...
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Veröffentlicht in: | Chemical research in Chinese universities 2016-06, Vol.32 (3), p.443-450 |
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Sprache: | eng |
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Zusammenfassung: | Engineering metal-organic frameworks(MOF) for heterogeneous catalysts have been of extreme interest since they have large pore size within the crystalline framework and well defined pore architecture. Ni-containing MOF Ni2(3,5-Pydc)2(H2O)8·2H2O(1·H2O) was prepared by solvothermal method from 3,5-pyridinedicarboxylic acid, D-camphoric acid and Ni(NO3)2·6H2O in dimethylformamide(DMF)/water(volume ratio 2:1). And two gold and silver functionalized 1·H2O catalysts were prepared by impregnation method. Catalysts 2.53%Au/MOF and 4.23%Ag/MOF were in-depth characterized by single crystal X-ray diffraction, powder X-ray diffraction(PXRD), thermogravimetric analysis(TGA), transmission electron microscopy(TEM), and inductively coupled plasma-atomic emission spectroscopy(ICP-AES). Their catalytic performance was examined in one-pot synthesis of structurally divergent propargylamines via three component coupling of aldehyde, alkyne, and amine(A3) in 1,4-dioxane. The resuits show that the catalysts all displayed high reactivities, and a selectivity of 100% for propargylamines. Catalysts 2.53%Au/MOF and 4.23%Ag/MOF have proved to be applicable to a wide range of substrates. Catalysts 2.53%Au/MOF and 4.23%Ag/MOF can be easily recycled and used repetitively at least 3 times with a slight drop in activity. These features render the catalysts particularly attractive in the practice of propargylamines synthesis in an environmentally friendly manner. |
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ISSN: | 1005-9040 2210-3171 |
DOI: | 10.1007/s40242-016-5435-9 |