Synthesis and crystal structure of cobalt(II) and copper(II) complexes of 3,3′-biisoxazolidines as chelating ligands

被引:1
|
作者
Raspertova, Ilona V. [1 ]
Ovchynnikov, Vladimir A. [1 ]
Shishkin, Oleg V. [2 ]
Lampeka, Rostislav D. [1 ]
机构
[1] Natl Taras Shevchenko Univ, Dept Chem, UA-01033 Kiev, Ukraine
[2] STC Inst Syngle Crystals, UA-61001 Kharkov, Ukraine
关键词
ENANTIOSELECTIVE 1,3-DIPOLAR CYCLOADDITION; NITRONES;
D O I
10.1007/s11243-012-9626-z
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
New mononuclear Cu(II) and Co(II) complexes [Cu{L-1}(NO3)(2)]center dot H2O (1) and [Co{L-2}(H2O)(3))](NO3)(2) (2), with conformationally flexible isoxazolidine ligands, namely 3,3'-bi{2-methyl-5-phenyl}isoxazolidine (L-1) and 3,3'-bi{2-methyl-5-pyridyl}isoxazolidine (L-2), were synthesized and characterized. X-ray crystallographical analysis reveals that the Cu(II) atoms adopt a distorted octahedral environment. The ligand L-1 forms five-membered chelates via the isoxazolidine nitrogen atoms. The Co(II) atom in 2 is in a distorted octahedral geometry. The ligand L-2 coordinates the metal center with formation of two chelate rings, involving donors of two isoxazolidine and pyridyl groups. In the complex cation, three donor atoms of the ligand occupy the MN3 facial positions.
引用
收藏
页码:607 / 610
页数:4
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