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反作用力与反应的过渡区域。

The reaction force and the transition region of a reaction.

作者信息

Toro-Labbé Alejandro, Gutiérrez-Oliva Soledad, Murray Jane S, Politzer Peter

机构信息

Laboratorio de Química Teórica Computacional (QTC), Facultad de Química, Pontificia Universidad Católica de Chile, Vicuña Mackenna 4860, Casilla 306, Correo 22, Santiago, Chile.

出版信息

J Mol Model. 2009 Jun;15(6):707-10. doi: 10.1007/s00894-008-0431-8. Epub 2008 Dec 16.

Abstract

The reaction force F(R) and the position-dependent reaction force constant kappaF(R) are defined by F(R)=-deltaV(R)/deltaR and kappa(R)=delta2V(R)/deltaR2, where V(R) is the potential energy of a reacting system along a coordinate R. The minima and maxima of F(R) provide a natural division of the process into several regions. Those in which F(R) is increasing are where the most dramatic changes in electronic properties take place, and where the system goes from activated reactants (at the force minimum) to activated products (at the force maximum). Kappa(R) is negative throughout such a region. We summarize evidence supporting the idea that a reaction should be viewed as going through a transition region rather than through a single point transition state. A similar conclusion has come out of transition state spectroscopy. We describe this region as a chemically-active, or electronically-intensive, stage of the reaction, while the ones that precede and follow it are structurally-intensive. Finally, we briefly address the time dependence of the reaction force and the reaction force constant.

摘要

反作用力F(R)和位置相关的反作用力常数κF(R)由F(R)=-δV(R)/δR和κ(R)=δ²V(R)/δR²定义,其中V(R)是反应体系沿坐标R的势能。F(R)的最小值和最大值将反应过程自然地划分为几个区域。在F(R)增加的区域,电子性质发生最显著的变化,体系从活化反应物(在力的最小值处)转变为活化产物(在力的最大值处)。在这样一个区域中,κ(R)始终为负。我们总结了支持如下观点的证据:反应应被视为经历一个过渡区域,而非通过单一的点过渡态。类似的结论也来自过渡态光谱学。我们将这个区域描述为反应的化学活性或电子密集阶段,而在其之前和之后的阶段是结构密集阶段。最后,我们简要讨论了反作用力和反作用力常数的时间依赖性。

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