Synthesis and spectroscopic properties of copper(II) complexes derived from thiophene-2-carbaldehyde thiosemicarbazone.: Structure and biological activity of [Cu(C6H6N3S2)2]

被引:105
作者
García-Tojal, J
Garcia-Orad, A
Serra, JL
Pizarro, JL
Lezama, L
Arriortua, MI
Rojo, T
机构
[1] Univ Basque Country, Dept Quim Inorgan, Bilbao 48080, Spain
[2] Univ Burgos, Dept Quim, Burgos 09001, Spain
[3] Univ Basque Country, Dept Biol Anim & Genet, Bilbao 48080, Spain
[4] Univ Basque Country, Dept Bioquim & Biol Mol, Bilbao 48080, Spain
[5] Univ Basque Country, Dept Mineral Petrol, Bilbao 48080, Spain
关键词
copper (II) complexes; spectroscopic properties; thiophene-2-carbaldehyde thiosemicarbazone; biological activity;
D O I
10.1016/S0162-0134(99)00031-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The synthesis, structure and spectroscopic properties on complexes with the formula [Cu(L-III)(2)] (1) and Cu(NO3)(2)(HLIII)(2) (2); where HLIII = thiophene-2-carbaldehyde thiosemicarbazone, have been developed. The molecular structure of compound 1 consists of monomeric entities. The copper(II) ions exhibit distorted square-planar geometry with both bidentate thiosemicarbazone ligands placed in a centrosymmetric way. Metal to ligand pi-backdonation is proposed to explain several structural and spectroscopic features in these complexes. The EPR spectra of compound 1 show an orthorhombic g tensor indicating the presence of weak magnetic exchange interactions. The reaction of compound 1 with,glutathione causes the reduction of the metal ion and the substitution of the thiosemicarbazone ligand by the thiol ligand. This mechanism seems to be related to the cytotoxicity of this complex against Friend Erithroleukemia cells (FLC) and melanome B16F10 cells. (C) 1999 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:45 / 54
页数:10
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