Metal Complexes of Cinchonine as Chiral Building Blocks: A Strategy for the Construction of Nanotubular Architectures and Helical Coordination Polymers

被引:88
|
作者
Kaczorowski, Tomasz [2 ]
Justyniak, Iwona [1 ]
Lipinska, Teodozja [3 ]
Lipkowski, Janusz [1 ]
Lewinski, Janusz [1 ,2 ]
机构
[1] Polish Acad Sci, Inst Phys Chem, PL-01224 Warsaw, Poland
[2] Warsaw Univ Technol, Dept Chem, PL-00664 Warsaw, Poland
[3] Univ Podlasie, Inst Chem, PL-08110 Siedlce, Poland
关键词
ENANTIOSELECTIVE PHENYLACETYLENE ADDITION; HETEROGENEOUS ASYMMETRIC CATALYSIS; ALUMINUM COMPLEXES; TRANSITION-METALS; ORGANIC FRAMEWORK; CRYSTAL-STRUCTURE; SEPARATION; MOLECULES; ALKALOIDS; LIGANDS;
D O I
10.1021/ja8098867
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The first chiral bipyridyl-type metalloligands based on aluminum derivatives of cinchonine (CN-H) were synthesized and characterized by single-crystal X-ray diffraction studies. These bischelate complexes, (CN)(2)AlX [X = Cl (1a), Me (1b)] were found to be effective building blocks for the preparation of novel helical nanotubular architectures as well as chiral bimetallic coordination polymers, as demonstrated by the rational synthesis of a helical structure formed by 1 a and ZnCl2. The applied methodology stands as an exemplary strategy for the rational synthesis of chiral metal-organic frameworks through self-organization driven by nonbonding interactions or coordination, which could potentially find applications in enantioselective separations and catalysis.
引用
收藏
页码:5393 / +
页数:5
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