Eland J H D, Feifel R, Hochlaf M
Physical and Theoretical Chemistry Laboratory, South Parks Road, Oxford OX1 3QZ, United Kingdom.
J Chem Phys. 2008 Jun 21;128(23):234303. doi: 10.1063/1.2937901.
The double photoionization of CF(3)I and the electronic structure and the dissociation dynamics of the CF(3)I(++) dication have been investigated using large ab initio calculations and coincidence techniques. The double photoionization spectrum of CF(3)I consists of a continuous background with a number of narrow bands superimposed. The spectrum is attributed here to the population of groups of close lying electronic states interacting mutually by spin-orbit, spin-spin, and rovibronic couplings. At energies near the vertical double ionization threshold, CF(3) (+)+I(+) ionic fragments are produced. At higher energies, a very specific dissociation with double charge retained on one fragment, CF(3)I(++)-->CF(2)I(++)+F becomes dominant and is attributed to a specific group of dication electronic states.
利用大型从头算计算和符合技术,对CF(3)I的双光电离以及CF(3)I(++)双离子的电子结构和解离动力学进行了研究。CF(3)I的双光电离光谱由一个连续背景和叠加其上的多个窄带组成。在此,该光谱归因于通过自旋轨道、自旋自旋和振转耦合相互作用的近简并电子态组的布居。在接近垂直双电离阈值的能量处,产生CF(3) (+)+I(+)离子碎片。在更高能量下,一种非常特殊的解离,即一个碎片上保留双电荷的CF(3)I(++)-->CF(2)I(++)+F占主导地位,这归因于一组特定的双离子电子态。