5-硝基抑菌素与Morpholine在水-甲醇和水-乙腈混合溶剂中的反应动力学及机理

IF 1.4 4区 化学 Q4 CHEMISTRY, PHYSICAL
Alaa Z. Omar, Farah A. Rabah, Shawky El-Shazly, Magda F. Fathalla, Ezzat A. Hamed, Mohamed A. El-Atawy
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引用次数: 0

摘要

在25 ~ 45℃的温度范围内,在溶剂组成(10 ~ 90% v/v)范围内,用分光光度法测定了5-硝基硝素与啉在水-乙腈和水-甲醇溶剂中的反应动力学。在拟一级条件下测定了5-硝基化素的反应速率,整个反应速率为二级。在两种混合溶剂中,反应速率常数随有机溶剂比的增加而降低,随水比的增加而显著增加。计算并解释了热力学活化参数。两种溶剂的对数kN和介电常数的倒数之间均存在线性和非线性关系,这表明5-硝基化素与啉的反应取决于介质的特异性和非特异性溶剂化。利用Kamlet-Taft溶剂化参数对反应性进行了单、对偶和多元回归分析,并成功地应用于水-乙腈和水-甲醇混合物。最后,提出了反应机理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Kinetics and Mechanism for the Reaction of 5-Nitroisatin with Morpholine in Water–Methanol and Water–Acetonitrile Mixed Solvents

Kinetics and Mechanism for the Reaction of 5-Nitroisatin with Morpholine in Water–Methanol and Water–Acetonitrile Mixed Solvents

The kinetics of the reaction of 5-nitroisatin with morpholine in water–acetonitrile and water–methanol solvents was followed spectrophotometrically in the ranges of solvent composition (10–90% v/v) over the temperature range from 25 to 45 °C. The reaction was measured under pseudo-first-order condition respect to 5-nitroisatin and the overall reaction is second-order rate. The rate constant of reaction decreased with increasing organic solvent ratios and strongly increased with increasing water ratios in both mixed solvents. The thermodynamic activation parameters were calculated and explained. Both linearity and non-linearity were observed between log kN and reciprocal dielectric constant for both solvents suggesting that the reaction of 5-nitroisatin with morpholine depends on specific as well as non-specific solvation of the medium. The reactivity was analyzed in the light of various single, dual, and multiple-regression equations using Kamlet–Taft solvatochromic parameters which were applied successfully to the mixed aqueous–acetonitrile and aqueous–methanol mixtures. Finally, a mechanism for the reaction is proposed.

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来源期刊
Journal of Solution Chemistry
Journal of Solution Chemistry 化学-物理化学
CiteScore
2.30
自引率
0.00%
发文量
87
审稿时长
3-8 weeks
期刊介绍: Journal of Solution Chemistry offers a forum for research on the physical chemistry of liquid solutions in such fields as physical chemistry, chemical physics, molecular biology, statistical mechanics, biochemistry, and biophysics. The emphasis is on papers in which the solvent plays a dominant rather than incidental role. Featured topics include experimental investigations of the dielectric, spectroscopic, thermodynamic, transport, or relaxation properties of both electrolytes and nonelectrolytes in liquid solutions.
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