Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/4867
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dc.contributor.authorThanh, Truong-
dc.contributor.authorĐặng, Huỳnh Giao-
dc.contributor.authorTruong, Thanh Ngoc-
dc.contributor.authorTran, Vuong Nam-
dc.contributor.authorPhan, Thanh Son Nam-
dc.contributor.authorLe, Thanh Dung-
dc.date.accessioned2018-10-29T02:34:44Z-
dc.date.available2018-10-29T02:34:44Z-
dc.date.issued2015-
dc.identifier.urihttp://dspace.ctu.edu.vn/jspui/handle/123456789/4867-
dc.description.abstractAcrystalline porous metal-organic framework Cu-MOF-74 was synthesized and its properties were examined by a host of techniques, including X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), Fourier transform infrared (FT-IR), atomic absorption spectrophotometry (AAS), and nitrogen physisorption measurements. The Cu-MOF-74 exhibited high activity in oxidative cross-dehydrogenative coupling of amines and α-carbonyl aldehydes to form α-ketoamides using air oxidant. High yields were achieved in the presence of a catalytic amount of the Cu-MOF without any added ligand and base. The activity of Cu-MOF-74 was showed to be higher than that of other frequently reported Cu-MOFs and comparable to common copper salts. Large pore aperture was proposed to strongly contribute to Cu-MOF-74 activity. Furthermore, leaching test indicated no contribution from homogeneous leached species and the catalyst could be recovered and reused several times without a significant degradation in catalytic activity.vi_VN
dc.language.isoenvi_VN
dc.relation.ispartofseriesJournal of Molecular Catalysis A: Chemical;409 .- p.110-116-
dc.subjectMetal-organic frameworkvi_VN
dc.subjectα-Ketoamidesvi_VN
dc.subjectOxidative couplingsvi_VN
dc.subjectHeterogeneous catalystvi_VN
dc.subjectCu-MOF-74vi_VN
dc.titleOxidative cross-dehydrogenative coupling of amines and α-carbonyl aldehydes over heterogeneous Cu-MOF-74 catalyst: A ligand- and base-free approachvi_VN
dc.typeArticlevi_VN
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