Departamento de Química Física I, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, 28040 Madrid, Spain.
J Chem Phys. 2012 Feb 21;136(7):074303. doi: 10.1063/1.3683252.
Femtosecond time-resolved velocity map imaging experiments are reported on several vibronic levels of the second absorption band (B-band) of CH(3)I, including vibrational excitation in the ν(2) and ν(3) modes of the bound (3)R(1)(E) Rydberg state. Specific predissociation lifetimes have been determined for the 2(0)(1) and 3(0)(1) vibronic levels from measurements of time-resolved I*((2)P(1/2)) and CH(3) fragment images, parent decay, and photoelectron images obtained through both resonant and non-resonant multiphoton ionization. The results are compared with our previously reported predissociation lifetime measurements for the band origin 0(0) (0) [Gitzinger et al., J. Chem. Phys. 132, 234313 (2010)]. The result, previously reported in the literature, where vibrational excitation to the C-I stretching mode (ν(3)) of the CH(3)I (3)R(1)(E) Rydberg state yields a predissociation lifetime about four times slower than that corresponding to the vibrationless state, whereas predissociation is twice faster if the vibrational excitation is to the umbrella mode (ν(2)), is confirmed in the present experiments. In addition to the specific vibrational state lifetimes, which were found to be 0.85 ± 0.04 ps and 4.34 ± 0.13 ps for the 2(0)(1) and 3(0)(1) vibronic levels, respectively, the time evolution of the fragment anisotropy and the vibrational activity of the CH(3) fragment are presented. Additional striking results found in the present work are the evidence of ground state I((2)P(3/2)) fragment production when excitation is produced specifically to the 3(0)(1) vibronic level, which is attributed to predissociation via the A-band (1)Q(1) potential energy surface, and the indication of a fast adiabatic photodissociation process through the repulsive A-band (3)A(1)(4E) state, after direct absorption to this state, competing with absorption to the 3(0)(1) vibronic level of the (3)R(1)(E) Rydberg state of the B-band.
飞秒时间分辨速度映射成像实验报告了 CH(3)I 第二吸收带(B 带)的几个振动态的情况,包括束缚(3)R(1)(E)里德伯态中 ν(2)和 ν(3)模式的振动激发。通过测量时间分辨的 I*((2)P(1/2))和 CH(3)碎片图像、母体衰减以及通过共振和非共振多光子电离获得的光电子图像,确定了 2(0)(1)和 3(0)(1)振动态的特定预解离寿命。结果与我们之前报道的带起源 0(0)(0)[Gitzinger 等人,J. Chem. Phys. 132,234313(2010)]的预解离寿命测量结果进行了比较。先前在文献中报道的结果是,CH(3)I(3)R(1)(E)里德伯态中 C-I 伸缩模式(ν(3))的振动激发导致预解离寿命比相应的无振动状态慢四倍,而如果振动激发到伞状模式(ν(2)),则预解离速度快两倍,在本实验中得到了证实。除了特定振动状态的寿命外,2(0)(1)和 3(0)(1)振动态的寿命分别为 0.85±0.04 ps 和 4.34±0.13 ps,还呈现了碎片各向异性和 CH(3)碎片振动活性的时间演化。本工作中发现的其他显著结果是,当激发专门产生到 3(0)(1)振动态时,存在基态 I((2)P(3/2))碎片产生的证据,这归因于通过 A 带(1)Q(1)势能面的预解离,以及直接吸收到该状态后,通过排斥的 A 带(3)A(1)(4E)态的快速绝热光解离过程的指示,与吸收到 B 带的(3)R(1)(E)里德伯态的 3(0)(1)振动态竞争。