School of Chemistry, The University of Manchester, Manchester M13 9PL, England.
J Phys Chem A. 2009 Dec 31;113(52):15298-306. doi: 10.1021/jp906042g.
The angular scattering of a state-to-state chemical reaction contains fundamental information on its dynamics. Often the angular distributions are highly structured and the physical interpretation of this structure is an important and difficult problem. Here, we report a surprising finding for the benchmark F + H(2) --> FH + H reaction, when the product molecule FH is in a vibrational state with quantum number = 3 and a rotational state with quantum number = 3. We demonstrate that the differential cross section (DCS) is an example of (attractive) rainbow scattering, being characterized by an Airy function and its derivative. The rainbow reveals its presence in the DCS by interference with the repulsive (or nearside) scattering producing characteristic diffraction oscillations. The rainbow is broad, which explains why it has not been recognized in the many earlier theoretical and experimental investigations of this reaction. There is an angular region in the DCS where the rainbow dominates, but with the unusual property that the DCS is less intense than in adjoining angular regions. The reaction investigated is F + H(2)(v(i) = 0, j(i) = 0, m(i) = 0) --> FH(v(f) = 3, j(f) = 3, m(f) = 0) + H, where v(i), j(i), m(i) and v(f), j(f), m(f) are initial and final vibrational, rotational and helicity quantum numbers, respectively. The relative translational energy is 0.119 eV. We use rigorous semiclassical (asymptotic) techniques that provide physical insight as well as a mathematically sound and numerically accurate description of the angular scattering. The semiclassical DCS agrees very closely with the exact quantum DCS. The semiclassical scattering amplitude is used to assess the physical effectiveness of the Fuller nearside-farside decomposition for the partial wave series of the F + H(2) reaction, including the effect of one resummation. We also compare the semiclassical and exact quantum nearside, farside, and full local angular momenta and find good agreement. Although our new rainbow has unusual and unexpected properties, similar rainbows are predicted to occur in the DCSs of many state-to-state chemical reactions, since the semiclassical analysis is generic and not specific to the present F + H(2) example.
态到态化学反应的角散射包含其动力学的基本信息。通常,角分布具有高度的结构,而这种结构的物理解释是一个重要且困难的问题。在这里,我们报告了基准 F + H(2) → FH + H 反应的一个令人惊讶的发现,当产物分子 FH 处于振动量子数 = 3 和转动量子数 = 3 的状态时。我们证明了微分截面(DCS)是(吸引力)彩虹散射的一个例子,其特征是艾里函数及其导数。彩虹散射通过与产生特征衍射振荡的排斥(或近侧)散射干涉,在 DCS 中显示其存在。彩虹散射很宽,这解释了为什么在这个反应的许多早期理论和实验研究中都没有发现它。DCS 中有一个角区域,彩虹散射占主导地位,但具有不寻常的特性,即 DCS 的强度低于相邻角区域。所研究的反应是 F + H(2)(v(i) = 0, j(i) = 0, m(i) = 0) → FH(v(f) = 3, j(f) = 3, m(f) = 0) + H,其中 v(i)、j(i)、m(i) 和 v(f)、j(f)、m(f) 分别是初始和最终振动、转动和螺旋量子数。相对平移能为 0.119 eV。我们使用严格的半经典(渐近)技术,这些技术不仅提供了物理洞察力,而且还提供了对角散射的数学上合理且数值准确的描述。半经典 DCS 与精确量子 DCS 非常吻合。半经典散射振幅用于评估富勒近侧-远侧分解对 F + H(2)反应的分波级数的物理有效性,包括一次重排的影响。我们还比较了半经典和精确量子的近侧、远侧和全局部角动量,并发现了很好的一致性。尽管我们的新彩虹具有不寻常和意外的特性,但由于半经典分析是通用的,而不是特定于目前的 F + H(2) 示例,因此预计在许多态到态化学反应的 DCS 中也会出现类似的彩虹。