Department of Chemistry, Marquette University, Wehr Chemistry Building, Milwaukee, Wisconsin 53201-1881, USA.
Theoretical Division (T-1, MS B221), Los Alamos National Laboratory, Los Alamos, New Mexico 87545, USA.
J Chem Phys. 2019 Mar 14;150(10):101104. doi: 10.1063/1.5082850.
Accurate calculations of vibrational states in singly and doubly substituted ozone molecules are carried out, up to dissociation threshold. Analysis of these spectra reveals noticeable deviations from the statistical factor of 2 for the ratio between the number of states in asymmetric and symmetric ozone molecules. It is found that, for the lower energy parts of spectra, the ratio is less than 2 in the singly substituted ozone molecules, but it is more than 2 in the doubly substituted ozone molecules. However, the upper parts of spectra, just below dissociation thresholds, exhibit a different behavior. In this energy range, the singly and doubly substituted ozone molecules behave similar, with the ratio of states in asymmetric and symmetric ozone molecules being more than 2 in both cases. This property may contribute to an explanation of the mysterious η-effect in the ozone forming reaction that favors the formation of the asymmetric ozone molecules.
准确计算了单取代和双取代臭氧分子的振动状态,直至离解阈值。对这些光谱的分析表明,不对称和对称臭氧分子中状态数之比的统计因子 2 存在明显偏差。结果发现,对于光谱的较低能部分,单取代臭氧分子中的比值小于 2,但在双取代臭氧分子中大于 2。然而,就在离解阈值以下的光谱的高能部分,表现出不同的行为。在这个能量范围内,单取代和双取代臭氧分子的行为相似,不对称和对称臭氧分子中状态的比值在两种情况下都大于 2。这种性质可能有助于解释臭氧形成反应中的神秘 η 效应,该效应有利于不对称臭氧分子的形成。