Crystal structures and magnetic properties of nitroxide radical-coordinated copper(II) and cobalt(II) complexes

被引:4
|
作者
Gao, Yan-Li [1 ,2 ]
Inoue, Katsuya [2 ,3 ]
机构
[1] Yulin Univ, Sch Chem & Chem Engn, Yulin 719000, Peoples R China
[2] Hiroshima Univ, Dept Chem, 1-3-1 Kagamiyama, Higashihiroshima, Hiroshima 7398526, Japan
[3] Hiroshima Univ, Ctr Chiral Sci, 1-3-1 Kagamiyama, Higashihiroshima, Hiroshima 7398526, Japan
关键词
M(HFAC)(2) M; ORGANIC RADICALS; CU-II; TEMPO; OXIDATION; ALCOHOLS; EXCHANGE; ADDUCTS;
D O I
10.1007/s11243-018-00297-w
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The crystal structures and magnetic properties of three coordination compounds constructed from various nitroxide radicals L and M-II(hfac)(2)(H2O)(2) building blocks (M=Cu or Co and hfac=hexafluoroacetylacetonato) are described. In [(1)Cu(hfac)(2)](n), 4, the radical ligand L is coordinated to the metal through the oxygen atom of the nitroxide group and oxygen atom of its hydroxyl group, leading to a one-dimensional chain system. In [(2)(2)Cu(hfac)(2)](n), 5, two hydroxyl oxygen atoms of the radical ligand are coordinated to the metal, and the Co-II centers adopt distorted octahedral geometry to give a mononuclear compound. For [(L)Cu(hfac)(2)](n), 6, the oxygen atom of the nitroxide group and nitrogen atom of the amino group of L are coordinated to the metal, leading to a one-dimensional chain system. The magnetic susceptibility study of the copper coordination compound 4 revealed weak ferromagnetic interactions between the metal center and the organic radical. The cobalt coordination compounds 5 and 6 both show antiferromagnetic interactions.
引用
收藏
页码:283 / 292
页数:10
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