首页> 外文期刊>Journal of Solution Chemistry >Spectral and Mechanistic Investigation of the Osmium(VIII) Catalyzed Oxidation of Diclofenac Sodium by the Copper(III) Periodate Complex in Aqueous Alkaline Medium
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Spectral and Mechanistic Investigation of the Osmium(VIII) Catalyzed Oxidation of Diclofenac Sodium by the Copper(III) Periodate Complex in Aqueous Alkaline Medium

机译:Period(Ⅲ)在碱性水溶液中高碘酸铜(Ⅲ)配合物催化双氯芬酸钠氧化的光谱和机理研究

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摘要

The kinetics of the osmium(VIII) (Os(VIII)) catalyzed oxidation of diclofenac sodium (DFS) by diperiodatocuprate(III) (DPC) in aqueous alkaline medium has been studied spectrophotometrically at a constant ionic strength of 1.0 mol⋅dm−3. The reaction showed first order kinetics in [Os(VIII)] and [DPC] and less than unit order with respect to [DFS] and [alkali]. The rate decreased with increase in [periodate]. The reaction between DFS and DPC in alkaline medium exhibits 1:2 [DFS]:[DPC] stoichiometry. However, the order in [DFS] and [OH−] changes from first order to zero order as their concentration increases. Changes in the ionic strength and dielectric constant did not affect the rate of reaction. The oxidation products were identified by LC-ESI-MS, NMR, and IR spectroscopic studies. A possible mechanism is proposed. The reaction constants involved in the different steps of the mechanism were calculated. The catalytic constant (K C) was also calculated for Os(VIII) catalysis at the studied temperatures. From plots of log 10 K C versus 1/T, values of activation parameters have been evaluated with respect to the catalytic reaction. The activation parameters with respect to the slow step of the mechanism were computed and discussed, and thermodynamic quantities were also determined. The active osmium(VIII) and copper(III) periodate species have been identified.
机译:在1.0 mol·dm的恒定离子强度下,通过分光光度法研究了dip(VIII)(Os(VIII))催化二氯丁二酸铜(III)(DPC)氧化双氯芬酸钠(DFS)的动力学。 > −3 。该反应在[Os(VIII)]和[DPC]中显示出一级动力学,并且相对于[DFS]和[碱]而言,小于单元级。随着[periodate]的增加,比率降低。 DFS和DPC在碱性介质中的反应显示出1:2的[DFS]:[DPC]化学计量。但是,[DFS]和[OH -]中的顺序随着浓度增加而从一阶变为零阶。离子强度和介电常数的变化不影响反应速率。通过LC-ESI-MS,NMR和IR光谱学研究鉴定了氧化产物。提出了一种可能的机制。计算了该机理的不同步骤中涉及的反应常数。还计算了在研究温度下Os(VIII)催化的催化常数(K C )。从log 10 K C 与1 / T的关系图中,已评估了催化反应的活化参数值。计算并讨论了与该机构的慢步有关的激活参数,并确定了热力学量。活性active(VIII)和高碘酸铜(III)已被鉴定。

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