首页> 外文期刊>Oxidation Communications >MECHANISTIC INVESTIGATION OF OXIDATION OF CIPROFLOXACIN BY SODIUM N-CHLOROBENZENESULPHONAMIDE IN ACDD MEDIUM. A KINETIC STUDY
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MECHANISTIC INVESTIGATION OF OXIDATION OF CIPROFLOXACIN BY SODIUM N-CHLOROBENZENESULPHONAMIDE IN ACDD MEDIUM. A KINETIC STUDY

机译:N-氯苯甲磺酸钠在ACDD培养基中氧化环丙沙星的机理研究。运动学

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摘要

The kinetics of oxidation of ciprofloxacin (CPF) by sodium N-chlorobenzenesulphona-mide or chloramine-B (CAB) in HC1 medium at 30°C shows first order dependence each on oxidant, substrate and H~+ ion concentrations, but is independent of [Cl~-]. The reaction is subjected to changes in: (a) ionic strength; (b) dielectric constant, and (c) added reaction product, and the subsequent effects on the reaction rate are studied. The reaction was studied at different temperatures, and activation parameters have been computed for the overall reaction from the Arrhenius plot. Oxidation products were identified by TLC and spectral (IR and NMR) analysis. A mechanism involving interaction of conjugate acid (PhS02NHCl) and substrate giving an intermediate complex in a slow step has been suggested. The proposed mechanism and the derived rate law are consistent with the observed kinetics.
机译:在30°C的HC1介质中,N-氯苯磺酰亚胺钠或氯胺B(CAB)对环丙沙星(CPF)的氧化动力学显示出一级依赖于氧化剂,底物和H〜+离子的浓度,但与[Cl〜-]。反应发生以下变化:(a)离子强度;研究了(b)介电常数和(c)添加的反应产物,以及其对反应速率的后续影响。在不同温度下对反应进行了研究,并根据Arrhenius图计算了整个反应的活化参数。通过TLC和光谱(IR和NMR)分析鉴定氧化产物。已经提出了在缓慢的步骤中涉及共轭酸(PhSO 2 NHCl)和底物的相互作用的机理,从而给出中间体配合物。所提出的机理和导出的速率定律与观察到的动力学一致。

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