In this study, we demonstrate a bottom-up assembly of a monomeric copper complex and a two-dimensional (2-D) heterometallic metal-organic framework (MOF) from a carboxylate-functionalized tridentate Schiff base ligand and metal ions. The obtained 2-D MOF features a unique bimetallic copper center which is different from its monometallic precursor and acts as an efficient heterogeneous catalyst for the Friedel-Crafts reaction and Henry reaction. The MOF catalyst shows a remarkably superior activity compared to its homogeneous counterparts in a wide range of substrates. It is presumably ascribed to the dual activation of the substrates by the active bimetallic copper center confined in the MOF network, which is supported by the significant changes in catalytic activity at low catalyst/substrates ratios when using the 2-D MOF and its precursor as catalysts, respectively. Moreover, the MOF catalyst also shows an excellent stability and recyclability. Our work, therefore, provides a stepwise strategy to design a heterogeneous cooperative catalyst, by taking advantage of the modulated structure of MOF and tunable functionality of the tridentate Schiff base, with high performance in a variety of organic synthesis.
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Zhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R ChinaZhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
Wang, Qian-You
Sun, Zhi-Bing
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Zhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R ChinaZhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
Sun, Zhi-Bing
Zhang, Meng
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Zhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R ChinaZhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
Zhang, Meng
Zhao, Shu-Na
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Zhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R ChinaZhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
Zhao, Shu-Na
Luo, Peng
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Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R ChinaZhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
Luo, Peng
Gong, Chun-Hua
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Zhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R ChinaZhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
Gong, Chun-Hua
Liu, Wen-Xiao
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Zhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R ChinaZhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
Liu, Wen-Xiao
Zang, Shuang-Quan
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Zhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R ChinaZhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
机构:
Max Planck Inst Kohlenforsch, Dept Heterogeneous Catalysis, Kaiser Wilhelm Pl 1, D-45470 Mulheim An Der Ruhr, GermanyMax Planck Inst Kohlenforsch, Dept Heterogeneous Catalysis, Kaiser Wilhelm Pl 1, D-45470 Mulheim An Der Ruhr, Germany
Bengsch, Marco
Neumann, Constanze N.
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Max Planck Inst Kohlenforsch, Dept Heterogeneous Catalysis, Kaiser Wilhelm Pl 1, D-45470 Mulheim An Der Ruhr, GermanyMax Planck Inst Kohlenforsch, Dept Heterogeneous Catalysis, Kaiser Wilhelm Pl 1, D-45470 Mulheim An Der Ruhr, Germany