Department of Chemistry, Wayne State University, Detroit, Michigan 48202, USA.
J Phys Chem A. 2013 Aug 15;117(32):7589-94. doi: 10.1021/jp403030s. Epub 2013 Jun 13.
We present a crossed-beam imaging study of the reaction of chlorine atoms with several butene isomers. A high-intensity pulsed ablation Cl source is used with DC slice imaging and single-photon ionization detection at 157 nm to record the velocity-flux contour maps for these reactions. The target unsaturated hydrocarbons are 1-butene, trans-2-butene, cis-2-butene, and isobutene (2-methylpropene). Data are obtained at collision energies of ~13.0 kcal·mol(-1). Distinct differences in the scattering distributions and in particular the coupling of angular and translational energy release provide insight into the dynamics of this little-studied class of reactions. We find that these distributions reflect the energetics for competition between addition/elimination and direct abstraction in line with ab initio thermochemical data. A possible role for Cl atom roaming mediating the addition/elimination pathway is suggested.
我们呈现了氯原子与几种丁烯异构体反应的交叉束成像研究。使用高强度脉冲烧蚀 Cl 源,结合直流片成像和 157nm 处的单光子电离检测,记录了这些反应的速度-通量等高线图。目标不饱和烃为 1-丁烯、反-2-丁烯、顺-2-丁烯和异丁烯(2-甲基丙烯)。在约 13.0 kcal·mol(-1)的碰撞能下获得数据。散射分布的明显差异,特别是角和平动能量释放的耦合,为这一研究较少的反应动力学提供了深入了解。我们发现,这些分布反映了加成/消除与直接提取之间竞争的能量学,与从头算热化学数据一致。提出了 Cl 原子漫游可能在加成/消除途径中起作用的假设。