含ONO供体氨基酸席夫碱的高自旋铁螯合物的氢氧化物离子和DNA攻击动力学研究

L. Abdel‐Rahman, R. El‐Khatib, L. A. E. Nassr, A. Abu‐Dief
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引用次数: 0

摘要

在10 ~ 40℃的温度范围内,研究了由2-羟基萘乙醛与多种氨基酸组成的希夫碱配体的几种新型高自旋Fe(II)配合物在水溶液中的反应性。基于动力学研究,提出并讨论了反应速率规律和可能的反应机理。一般速率方程建议如下:rate = kobs [Complex],其中kobs。= k1 + k2 [OH-]碱催化水解动力学的测量意味着伪一级双阶段速率,由于merand面异构体的存在。观察到的速率常数kobs与取代基R对配体结构的影响有关。从温度对速率的影响;计算了各种热力学参数。计算得到的反应速率常数和活化参数与所研究配合物的稳定性常数吻合较好。关键词:碱催化水解,异构体,反应机理,热力学参数
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kinetic investigation of hydroxide ion and DNA attack on some high spin iron (II) chelates Bearing ONO Donors amino acid Schiff bases
The reactivity of few novel high spin Fe(II) complexes of Schiff base ligands derived from 2-hydroxynaphthaldehyde and some variety of amino acids with OH- ion has been examined in aqueous mixture at temperature in the range 10–40 Co. Based on the kinetic investigations, the rate law and a plausible mechanism were proposed and discussed. The general rate equation was suggested as follows: rate = kobs [Complex], where kobs.= k1 + k2 [OH-]. Base catalyzed hydrolysis kinetics measurements imply pseudo-first-order doubly stage rates due the presence of merand fac-isomers. The observed rate constants kobs are correlated the effect of substituent R in the structure of the ligands.From the effect of temperature on the rate; various thermodynamic parameters have been evaluated. The evaluated rate constants and activation parameters are in a good agreement with the stability constants of the investigated complexes. Keywords: Base catalyzed hydrolysis, Isomer, Reaction mechanism, Thermodynamic parameters
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