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Some tentative explanations for the enthalpy-entropy compensation effect in chemical kinetics: from experimental errors to the Hinshelwood-like model

机译:对化学动力学中焓-熵补偿效应的一些初步解释:从实验误差到类似于欣希尔伍德的模型

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摘要

It has often been proposed that the well-known standard activation enthalpyentropy linear plots usually found in kinetic studies for many series of homologous reactions are mere artefacts generated by the experimental errors committed in the determination of the rate constants. Here it is shown that the experimental errors can explain the existence of a standard activation enthalpy-entropy linear correlation only when the temperature obtained from the slope of that plot (compensation temperature, Tc) is lower than or equal to the mean experimental temperature used in that study (Tm), that is c m T T  . However, when Tc > Tm it is necessary to accept the existence of a real, physicochemically meaningful correlation between the values of o H and o S  for each member of the series of reactions. Four different explanations (thermodynamic interpretation, solvent-cage effect, formation of a binding intermediate and a Hinshelwood-like model) for real enthalpy-entropy compensation effects are analysed in some detail.
机译:经常有人提出,通常在动力学研究中发现的许多系列同源反应的众所周知的标准活化焓-熵线性图仅仅是在确定速率常数时由于实验误差而产生的假象。在这里表明,只有当从该曲线的斜率(补偿温度,Tc)获得的温度低于或等于在实验中使用的平均实验温度时,实验误差才能解释标准激活焓-熵线性相关性的存在。该研究(Tm),即cm TT。但是,当Tc> Tm时,有必要接受一系列反应中每个成员的o HH和oS值之间存在真实的,物理化学上有意义的相关性。对于真实的焓-熵补偿效应,有四种不同的解释(热力学解释,溶剂笼效应,结合中间体的形成和类似于欣希尔伍德的模型)进行了详细分析。

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