硫腙铜(II)配合物。氧化还原性质与超氧化物歧化酶模拟活性的关系

Zdena Ďuračková , Ma.Antonia Mendiola , Ma.Teresa Sevilla , Aladar Valent
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引用次数: 32

摘要

用循环伏安法研究了铜(II)配合物与开链配体、苄基二硫代氨基脲和大环配体[3,4,10,11-四苯基-1,2,5,8,9,12,13-八氮杂环十四十四-7,14-二硫-2,4,9,11-四烯]的氧化还原行为。铜(II)/铜(I)氧化还原偶的半波电位值和在二甲基亚砜(DMSO)溶液上获得的光谱数据与配合物的超氧化物歧化酶(SOD)模拟活性一致。与开链衍生物相比,大环配合物表现出更强的正还原电位和活性。结果表明,配体的结构和构象对配位化合物中中心原子的氧化还原电位有影响。配位球的变化与以sod模拟活性为代表的化合物生物学功能的变化有关。L1H6衍生物在Cu(II)/Cu(III)过程中呈现准可逆波。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thiohydrazone copper(II) complexes. The relationship between redox properties and superoxide dismutase mimetic activity

The redox behaviour of copper(II) complexes with the open chain ligand, benzilbisthiosemicarbazone, and the macrocyclic one [3,4,10,11-tetraphenyl-1,2,5,8,9,12,13-octaazacyclotetradeca-7,14-dithione-2,4,9,11-tetraene] has been explored by cyclic voltammetry. The half-wave potential values for the copper(II)/copper(I) redox couple and the spectral data obtained on dimethylsulfoxide (DMSO) solution agree with the superoxide dismutase (SOD)-mimetic activity of the complexes. The macrocyclic complexes show more positive reduction potential and more activity than the open chain derivatives. From our results it follows that the structure and conformation of ligand has influence on the redox potential of central atom in coordination compound. The changes in the coordination sphere are connected with the change of biological function of compounds represented by SOD-mimic activity. In addition, the L1H6 derivatives show quasireversible waves associated to Cu(II)/Cu(III) process.

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