The State Key Laboratory of Molecular Reaction Dynamics, Institute of Chemistry, Chinese Academy of Science, Beijing 100190, China.
J Phys Chem A. 2010 Sep 23;114(37):9999-10004. doi: 10.1021/jp105206q.
The ion-pair dissociation dynamics of SO(2) → SO(+) (X(2)Π,υ) + O(-) ((2)P(J)) in the excitation energy range 14.87-15.15 eV has been studied using the tunable XUV laser and velocity map imaging method. The O(-) yield spectrum, the translational energy distributions, and the angular distributions of the photofragments have been measured. The electronic structures and selected cuts of potential energy surfaces for the ion-pair states have been calculated by employing the quantum chemistry calculation method at the CASSCF/6-311++g** level. The equilibrium structures of the six ion-pair states all have linear geometries. An orbital correlation diagram was drawn to illustrate the ion-pair dissociation mechanism. Combining the experimental and theoretical results, it is concluded that the ion-pair dissociation takes place mainly via the predissociation of Rydberg states (1)A(1) [(C(2)B(1))4db(1)] and (1)A(1) [(D(2)A(1))4sa(1)]. The experimental results confirm the previous theoretical calculation results about the symmetry assignments for the energy sequence of SO(2)(+) as C((2)B(1)) < D((2)A(1)).
SO(2) → SO(+) (X(2)Π,υ) + O(-) ((2)P(J)) 的离子对离解动力学在 14.87-15.15 eV 的激发能量范围内已被研究,方法是使用可调谐 XUV 激光和速度映射成像方法。已经测量了 O(-)产率谱、光碎片的平移能分布和角分布。通过在 CASSCF/6-311++g** 水平上使用量子化学计算方法计算了离子对态的电子结构和选定的势能面切割。六个离子对态的平衡结构均具有线性几何形状。绘制了轨道相关图来说明离子对离解机制。结合实验和理论结果,可以得出结论,离子对离解主要通过 Rydberg 态(1)A(1) [(C(2)B(1))4db(1)] 和 (1)A(1) [(D(2)A(1))4sa(1)] 的预离解发生。实验结果证实了先前关于 SO(2)(+)能量序列的对称性分配的理论计算结果,即 C((2)B(1)) < D((2)A(1))。