Copper(II) complexes of asymmetrical and symmetrical acyclic pentadentate (N5) mono-Schiff-base ligands.: The X-ray structure of [Cu(ppe-py)](ClO4)2

被引:3
作者
Keypour, H [1 ]
Salehzadeh, S
Pritchard, RG
Parish, RV
机构
[1] Bu Ali Sina Univ, Dept Chem, Hamadan, Iran
[2] UMIST, Dept Chem, Manchester M60 1QD, Lancs, England
关键词
D O I
10.1023/A:1020357327379
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In the presence of copper(II) ion, two asymmetrical tripodal tetraamine ligands N{(CH2)(3)NH2}{(CH2)(2)NH2}(2) (pee), N{(CH2)(3)NH2}(2) {(CH2)(2)NH2} (ppe) an one symmetrical ligand, N{(CH2)(3)NH2}(3) (tpt), were condensed with 2-acetylpyridine. In EtO-H2O solutions the reaction stops after the first condensation stage, and complexes of acyclic pentadentate(N-5) mono-Schiff-base ligands were obtained. With asymmetrical tetraamines there are two possible condensation sites: the primary amine of the propylene, or the ethylene chain. The X-ray structure analysis of one complex, [Cu(ppe-py)] (ClO4)(2), indicates that condensation with 2-acetylpyridine in this case occurs at the propylene chain and the geometry around the copper ion is trigonal-bipyramidal.
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页码:720 / 723
页数:4
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