Department of Chemistry and Chemical Biology, University of New Mexico, Albuquerque, New Mexico 87131, USA.
J Am Chem Soc. 2013 Jan 23;135(3):982-5. doi: 10.1021/ja311159j. Epub 2013 Jan 14.
The exothermic F + H(2)O → HF + OH reaction has a decidedly "early" or "reactant-like" barrier. According to a naïve interpretation of the Polanyi's rules, translational energy would be more effective than vibrational energy in promoting such reactions. However, we demonstrate here using both quasi-classical trajectory and full-dimensional quantum wave packet methods on an accurate global potential energy surface that excitations in the H(2)O vibrational degrees of freedom have higher efficacy in enhancing the reactivity of the title reaction than the same amount of translational energy, thus providing a counter-example to Polanyi's rules. This enhancement of reactivity is analyzed using a vibrational adiabatic model, which sheds light on the surprising mode selectivity in this reaction.
F + H(2)O → HF + OH 这个放热反应具有明显的“早期”或“反应物样”势垒。根据 Polanyi 规则的直观解释,与振动能相比,平动能更有利于促进此类反应。然而,我们在这里使用准经典轨迹和全维量子波包方法,在一个精确的全局势能表面上进行研究,结果表明 H(2)O 振动自由度的激发比相同数量的平动能更有效地增强了标题反应的反应性,从而为 Polanyi 规则提供了一个反例。使用振动绝热模型分析了这种反应性的增强,该模型揭示了该反应中令人惊讶的模式选择性。