Amide functionalized metal-organic frameworks for diastereoselective nitroaldol (Henry) reaction in aqueous medium

被引:44
作者
Paul, Anup [1 ]
Karmakar, Anirban [1 ]
Guedes da Silva, M. Fatima C. [1 ]
Pombeiro, Armando J. L. [1 ]
机构
[1] Univ Lisbon, Inst Super Tecn, Ctr Quim Estrutural, P-1049001 Lisbon, Portugal
关键词
MILD PEROXIDATIVE OXIDATION; SELECTIVE CO2 CAPTURE; LEWIS-ACID CATALYSIS; COORDINATION POLYMER; COPPER(II) COMPLEXES; HYDROGEN-BOND; AQUA COMPLEX; PORE-SIZE; ALDEHYDES; SITES;
D O I
10.1039/c5ra14637b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The two new metal-organic frameworks (MOFs) of zinc(II) and copper(II) [Zn2L2(1,4-BDC)](n)center dot 2n(DMF) (1) and [Cu(L)(2)](n)center dot 4n(DMF)center dot n(H2O) (2) (L = 4-(pyridin-4-ylcarbamoyl)benzoate; BDC = benzenedicarboxylate), respectively, have been synthesized from a pyridyl amide functionalized benzoic acid (HL). They were characterized by elemental, FT-IR, thermogravimetric, powder X-ray and single crystal X-ray diffraction analyses. Single crystal X-ray crystallography reveals that 1 and 2 exhibit 2D and 3D polymeric architectures, respectively. Topological analysis illustrates a 6-connected pcu alpha-Po primitive cubic topology for 1 and an 8-connected body centred cubic (bcu) topology for 2. Both 1 and 2 act as heterogeneous catalysts for the nitroaldol reaction in aqueous medium, with a high yield and moderate to good diastereoselectivities under ambient conditions. They can be recycled and reused without any significant loss of the catalytic efficiency.
引用
收藏
页码:87400 / 87410
页数:11
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