Suppr超能文献

F(2P)+CH4氢提取反应的新分析势能面:动力学与动力学

New analytical potential energy surface for the F(2P)+CH4 hydrogen abstraction reaction: kinetics and dynamics.

作者信息

Espinosa-García J, Bravo J L, Rangel C

机构信息

Departamento de Química Física, Universidad de Extremadura, 06071 Badajoz, Spain.

出版信息

J Phys Chem A. 2007 Apr 12;111(14):2761-71. doi: 10.1021/jp0688759. Epub 2007 Mar 9.

Abstract

A new potential energy surface for the gas-phase F(2P)+CH4 reaction and its deuterated analogues is reported, and its kinetics and dynamics are studied exhaustively. This semiempirical surface is completely symmetric with respect to the permutation of the four methane hydrogen atoms, and it is calibrated to reproduce the topology of the reaction and the experimental thermal rate constants. For the kinetics, the thermal rate constants were calculated using variational transition-state theory with semiclassical transmission coefficients over a wide temperature range, 180-500 K. The theoretical results reproduce the experimental variation with temperature. The influence of the tunneling factor is negligible, due to the flattening of the surface in the entrance valley, and we found a direct dependence on temperature, and therefore positive and small activation energies, in agreement with experiment. Two sets of kinetic isotope effects were calculated, and they show good agreement with the sparse experimental data. The coupling between the reaction coordinate and the vibrational modes shows qualitatively that the FH stretching and the CH3 umbrella bending modes in the products appear vibrationally excited. The dynamics study was performed using quasi-classical trajectory calculations, including corrections to avoid zero-point energy leakage along the trajectories. First, we found that the FH(nu',j') rovibrational distributions agree with experiment. Second, the excitation function presents an oscillatory pattern, reminiscent of a reactive resonance. Third, the state specific scattering distributions present reasonable agreement with experiment, and as the FH(nu') vibrational state increases the scattering angle becomes more forward. These kinetics and dynamics results seem to indicate that a single, adiabatic potential energy surface is adequate to describe this reaction, and the reasonable agreement with experiment (always qualitative and sometimes quantitative) lends confidence to the new surface.

摘要

报道了气相F(2P)+CH4反应及其氘代类似物的一个新的势能面,并对其动力学和动力学进行了详尽研究。这个半经验势能面对于四个甲烷氢原子的排列是完全对称的,并且经过校准以重现反应的拓扑结构和实验热速率常数。对于动力学,使用变分过渡态理论和半经典透射系数在180 - 500 K的宽温度范围内计算热速率常数。理论结果重现了实验随温度的变化。由于入口谷中势能面的平坦化,隧穿因子的影响可以忽略不计,并且我们发现与温度直接相关,因此活化能为正且较小,这与实验结果一致。计算了两组动力学同位素效应,它们与稀疏的实验数据显示出良好的一致性。反应坐标与振动模式之间的耦合定性地表明,产物中的FH伸缩振动和CH3伞形弯曲振动模式出现了振动激发。动力学研究使用准经典轨迹计算进行,包括修正以避免沿轨迹的零点能量泄漏。首先,我们发现FH(nu',j')振转分布与实验结果一致。其次,激发函数呈现出振荡模式,让人联想到反应共振。第三,态分辨散射分布与实验结果呈现出合理的一致性,并且随着FH(nu')振动态的增加,散射角变得更向前。这些动力学和动力学结果似乎表明,一个单一的绝热势能面足以描述该反应,并且与实验结果的合理一致性(总是定性的,有时是定量的)为新势能面提供了可信度。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验