Eberhardt M K, Santos C, Soto M A
University of Puerto Rico, Department of Pathology, San Juan 00936-5067.
Biochim Biophys Acta. 1993 May 7;1157(1):102-6. doi: 10.1016/0304-4165(93)90084-l.
Co2+ ions (Co(NO3)2.6H2O) react with H2O2 only in presence of EDTA to yield OH radicals and Co3+. This reaction was carried out in unbuffered aqueous solutions (pH = 2.6). The formation of Co3+ was confirmed by spectroscopy. The Co(3+)-EDTA complex shows two typical absorptions at 382 nm and 532 nm. The Co(3+)-EDTA complex can be prepared by a number of oxidizing agents, like Fe3+, Fe(3+)-EDTA, Ag+, Ag2+, Ce4+, and hydroxyl radicals. Since Fe3+ oxidizes Co(2+)-EDTA to Co(3+)-EDTA and Fe2+ we initiate a chain reaction for .OH formation. Our results show that there are two modes for H2O2 decomposition: (1) One electron transfer to give OH radicals and (2) Decomposition of H2O2 to H2O and O2 without intermediate .OH formation. This reaction depends strongly on the pH of the buffer. The H2O2 decomposition increases with increasing pH and increasing Co2+ concentration.
钴离子(硝酸钴六水合物)仅在乙二胺四乙酸(EDTA)存在的情况下与过氧化氢反应,生成羟基自由基和三价钴离子。该反应在未缓冲的水溶液(pH = 2.6)中进行。通过光谱法证实了三价钴离子的形成。三价钴 - 乙二胺四乙酸络合物在382纳米和532纳米处显示出两个典型吸收峰。三价钴 - 乙二胺四乙酸络合物可以通过多种氧化剂制备,如铁离子、铁(Ⅲ)-乙二胺四乙酸、银离子、银离子、铈离子和羟基自由基。由于铁离子将二价钴 - 乙二胺四乙酸氧化为三价钴 - 乙二胺四乙酸和亚铁离子,我们引发了羟基自由基形成的链式反应。我们的结果表明,过氧化氢分解有两种模式:(1)单电子转移生成羟基自由基;(2)过氧化氢分解为水和氧气,不形成中间产物羟基自由基。该反应强烈依赖于缓冲液的pH值。过氧化氢分解随着pH值升高和钴离子浓度增加而增加。