物理化学力学取代过渡态理论

IF 2.8 2区 化学 Q3 CHEMISTRY, PHYSICAL
Nikolai M. Kocherginsky*, 
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引用次数: 0

摘要

本文首先回顾了过渡态理论(TST)的基本原理,并举了一个教科书上的例子,说明基于过渡态理论描述可逆反应时经常被遗忘的问题。然后,我们简要介绍我们建议的一种方法,即物理化学力学。这种方法最初是用来描述化学质量迁移的速率和平衡的。在此,我们证明,基于经典力学的方法同样适用于基本单分子、双分子和电化学反应的动力学。传统的过渡态形成假平衡假设已不再必要。对补偿效应和隧道效应给出了简单的解释。此外,还解释了强放热氧化还原反应速率常数的反转区。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Physicochemical Mechanics Instead of Transition State Theory

Physicochemical Mechanics Instead of Transition State Theory

This article initially reminds the basics of transition state theory (TST) and gives a textbook example illustrating the often-forgotten problems with TST-based description of reversible reactions. Then, we briefly describe a suggested by us approach called physicochemical mechanics. It was initially developed to describe both the rates and equilibria of chemical mass transport. Here, we show that the same classical mechanics-based approach is working for the kinetics of elementary mono-, bimolecular, and electrochemical reactions. Traditional assumptions regarding pseudoequilibrium for transition state formation are not necessary anymore. A simple interpretation of compensation and tunneling effects is given. The inversion zone for rate constants of strongly exothermic redox reactions is also explained.

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来源期刊
The Journal of Physical Chemistry A
The Journal of Physical Chemistry A 化学-物理:原子、分子和化学物理
CiteScore
5.20
自引率
10.30%
发文量
922
审稿时长
1.3 months
期刊介绍: The Journal of Physical Chemistry A is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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