Raman, IR, UV-vis and EPR characterization of two copper dioxolene complexes derived from L-dopa and dopamine

被引:44
作者
Barreto, Wagner J. [1 ]
Barreto, Sonia R. G. [1 ]
Ando, Romulo A. [2 ]
Santos, Paulo S. [2 ]
DiMauro, Eduardo [3 ]
Jorge, Thiago [1 ]
机构
[1] Univ Estadual Londrina, Dept Chem, CCE, Lab Environm Phys Chem, BR-86051990 Londrina, PR, Brazil
[2] Univ Sao Paulo, Inst Chem, Lab Mol Spect, BR-05508000 Sao Paulo, Brazil
[3] Univ Estadual Londrina, Dept Phys, BR-86051990 Londrina, PR, Brazil
基金
巴西圣保罗研究基金会;
关键词
Resonance Raman; Dioxolene; Metal complex; Catecholate; Semiquinone; Wilson disease;
D O I
10.1016/j.saa.2008.04.014
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
The anionic complexes [Cu(L(1-))(3)](1-), L(-) = dopasemiquinone or L-dopasemiqui none, were prepared and characterized. The complexes are stable in aqueous solution showing intense absorption bands at ca. 605 nm for Cu(II)-L-dopasemiquinone and at ca. 595 nm for Cu(II)-dopasemiquinone in the UV-vis spectra, that can be assigned to intraligand transitions. Noradrenaline and adrenaline, under the same reaction conditions, did not yield Cu-complexes, despite the bands in the UV region showing that noradrenaline and adrenaline were oxidized during the process. The complexes display a resonance Raman effect, and the most enhanced bands involve ring modes and particularly the vCC + vCO stretching mode at ca. 1384 cm(-1). The free radical nature of the ligands and the oxidation state of the Cu(II) were confirmed by the EPR spectra that display absorptions assigned to organic radicals with g= 2.0005 and g = 2.0923, and for Cu(II) with g = 2.008 and g = 2.0897 for L-dopasemiquinone and dopasemiquinone, respectively. The possibility that dopamine and L-dopa can form stable and aqueous-soluble copper complexes at neutral pH, whereas noradrenaline and adrenaline cannot, may be important in understanding how Cu(II)-dopamine crosses the cellular membrane as proposed in the literature to explain the role of copper in Wilson disease. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1419 / 1424
页数:6
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