金属伴生超氧化物与Trolox抗氧化活性的机理探讨

IF 1.1 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY Canadian Journal of Chemistry Pub Date : 2022-12-09 DOI:10.1139/cjc-2022-0189
Bula Singh, Ranendu Sekhar Das
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引用次数: 0

摘要

Trolox-C (TXC)是α-生育酚的水溶性类似物,可降低水-乙醇介质中金属结合的超氧配合物[(NH3)5Co(µ-O2)Co(NH3)5]5+ (SOC)。在水-酸介质([H+] = 0.02 ~ 0.70 M)中,在TXC、[TXC]浓度至少为[SOC]的10倍以上的伪一级反应条件下,TXC定量地降低了SOC。介质离子强度的变化表明这是两种阳离子之间的反应,正的动力学同位素效应(kH/kD <1)表明TXC的吡喃氧质子化的前平衡步骤。在实验介质酸度范围内,TXC和质子化的TXC即TXCH都是潜在的还原剂。SOC通过单电子转移(SET)降低,动力学分析得出TXC和TXCH在15℃时的二阶速率常数分别为9.7和3.6×103 M-1s-1。
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Mechanistic Approach to the Anti-Oxidant Activities of Metal-Associated Superoxide With Trolox
Trolox-C (TXC) is a water-soluble analogue of α-tocopherol that reduces the metal-bound superoxo complex, [(NH3)5Co(µ-O2)Co(NH3)5]5+ (SOC) in water-ethanol media. In aqueous-acid media ([H+] = 0.02–0.70 M), TXC quantitatively reduces SOC under the pseudo first-order reaction condition where the concentration of TXC, [TXC] was at least ten times or more than that of [SOC]. Variations in media ionic strength suggests for the reaction between two cationic species and a positive kinetic isotope effect (kH/kD <1) indicates for a pre-equilibrium step of protonation of the pyran-oxygen of TXC. Both TXC and the protonated TXC, i.e., TXCH are the potential reductants under the experimental range of media acidity. The reduction of SOC takes place through the single electron transfer (SET) and the kinetic analysis yields the value for second-order rate constants for TXC and TXCH as 9.7 and 3.6×103 M-1s-1 at 15 ºC.
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来源期刊
Canadian Journal of Chemistry
Canadian Journal of Chemistry 化学-化学综合
CiteScore
1.90
自引率
9.10%
发文量
99
审稿时长
1 months
期刊介绍: Published since 1929, the Canadian Journal of Chemistry reports current research findings in all branches of chemistry. It includes the traditional areas of analytical, inorganic, organic, and physical-theoretical chemistry and newer interdisciplinary areas such as materials science, spectroscopy, chemical physics, and biological, medicinal and environmental chemistry. Articles describing original research are welcomed.
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