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CV and NMR study on the reaction of Mo(VI) with 3,4-dihydroxybenzoic acid and ascorbic acid in aqueous solution

机译:Mo(VI)与3,4-二羟基苯甲酸和抗坏血酸在水溶液中反应的CV和NMR研究

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The gradual release of the ligand 3,4-dihydroxybenzoic acid (3,4-DHBA) from its molybdenum complex in the presence of ascorbic acid (AscA) in a weakly acidic aqueous solution (pH similar to 3.5) is described. We observed that the formation of the 3,4-DHBA-semiquinone oxidation state and the semidehydroascorbate is a pre-requisite for the release of the 3,4-DHBA ligand. The interaction of these radicals leads at the same time to the further degradation of AscA resulting in, among other compounds, threonic acid which participates in the reaction with molybdenum. The comparison of the complexing ability indicated that threonic acid competes with protocatechuate, while ascorbic acid is a less good ligand for the Mo(VI). Solution studies on the reaction mechanism were performed by cyclic voltammetry, NMR spectroscopy and UV-Vis spectroscopy. Isolated precipitates were investigated by NMR spectroscopy. The antioxidant properties of 3,4-DHBA and AscA were also compared using the stable radical 2,2-diphenyl-1-picrylhydrazyl (DPPH). (C) 2006 Elsevier B.V. All rights reserved.
机译:描述了在弱酸性水溶液(pH值类似于3.5)中,在抗坏血酸(AscA)存在下,配体3,4-二羟基苯甲酸(3,4-DHBA)从其钼配合物中逐渐释放的现象。我们观察到3,4-DHBA-半醌氧化态和半脱氢抗坏血酸的形成是释放3,4-DHBA配体的先决条件。这些自由基的相互作用同时导致AscA的进一步降解,从而导致苏糖酸与其他钼反应参与其中。络合能力的比较表明,苏糖酸与原儿茶酸竞争,而抗坏血酸是Mo(VI)的较差配体。通过循环伏安法,NMR光谱和UV-Vis光谱对反应机理进行溶液研究。通过NMR光谱研究分离的沉淀物。还使用稳定的自由基2,2-二苯基-1-吡啶并肼基(DPPH)比较了3,4-DHBA和AscA的抗氧化性能。 (C)2006 Elsevier B.V.保留所有权利。

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