The synthesis, structure, topology and catalytic application of a novel cubane-based copper(II) metal-organic framework derived from a flexible amido tripodal acid

被引:58
作者
Karmakar, Anirban [1 ,2 ]
Oliver, Clive L. [3 ]
Roy, Somnath [2 ]
Ohrstrom, Lars [1 ]
机构
[1] Chalmers Univ Technol, Phys Chem, Chem & Biol Engn, SE-41296 Gothenburg, Sweden
[2] Univ Lisbon, Inst Super Tecn, Ctr Quim Estrutural, P-1049001 Lisbon, Portugal
[3] Univ Cape Town, Dept Chem, Ctr Supramol Chem Res, ZA-7701 Cape Town, South Africa
基金
新加坡国家研究基金会;
关键词
TO-AMORPHOUS TRANSFORMATION; NITROALDOL HENRY REACTION; JAHN-TELLER DISTORTION; COORDINATION POLYMERS; HYDROGEN STORAGE; 3D NETWORKS; LIGAND; COMPLEX; ADSORPTION; CHEMISTRY;
D O I
10.1039/c4dt03087g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A novel chiral metal-organic framework, [Cu-4(HL)(2)(H2O)(4)(MeO)(4)](n) (1), has been successfully synthesized from a tripodal flexible ligand (2S, 2'S, 2 '' S)- 2,2', 2 ''-(benzenetricarbonyltris(azanediyl)) tripropanoic acid (H3L). Compound 1 was characterized by IR and X-ray powder diffraction analysis. The structure was determined by X-ray single crystal diffraction analysis revealing that 1 possesses a 3D network, featuring a tetranuclear cubane-type secondary building block [Cu-4(MeO)(4)](4+), formed via the connection of four metal ions to four methoxide ions. These secondary building blocks are linked by four different HL2- ligands to construct a porous three dimensional framework of the dia topology with one-dimensional channels. Compound 1 also acts as a heterogeneous catalyst for the diastereoselective nitroaldol (Henry) reaction, providing high yields (up to 91%) and good diastereoselectivities under ambient conditions. This catalyst can be recycled without significant loss of activity.
引用
收藏
页码:10156 / 10165
页数:10
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