Velarde Luis, Habteyes Terefe, Grumbling Emily R, Pichugin Kostyantyn, Sanov Andrei
Department of Chemistry, University of Arizona, Tucson, Arizona 85721-0041, USA.
J Chem Phys. 2007 Aug 28;127(8):084302. doi: 10.1063/1.2766948.
Photodetachment from NO(-)(N(2)O)(n) cluster anions (n< or =7) is investigated using photoelectron imaging at 786, 532, and 355 nm. Compared to unsolvated NO(-), the photoelectron anisotropy with respect to the laser polarization direction diminishes drastically in the presence of the N(2)O solvent, especially in the 355 nm data. In contrast, a less significant anisotropy loss is observed for NO(-)(H(2)O)(n). The effect is attributed to photoelectron scattering on the solvent, which in the N(2)O case is mediated by the (2)Pi anionic resonance. No anionic resonances exist for H(2)O in the applicable photoelectron energy range, in line with the observed difference between the photoelectron images obtained with the two solvents. The momentum-transfer cross section, rather than the total scattering cross section, is argued to be an appropriate physical parameter predicting the solvent effects on the photoelectron angular distributions in these cluster anions.
利用光电子成像技术,在786、532和355纳米波长下研究了从NO(-)(N(2)O)(n)团簇阴离子(n≤7)的光剥离过程。与未溶剂化的NO(-)相比,在存在N(2)O溶剂的情况下,相对于激光偏振方向的光电子各向异性急剧减小,特别是在355纳米的数据中。相比之下,对于NO(-)(H(2)O)(n),观察到的各向异性损失较小。这种效应归因于光电子在溶剂上的散射,在N(2)O的情况下,这是由(2)Pi阴离子共振介导的。在适用的光电子能量范围内,H(2)O不存在阴离子共振,这与用两种溶剂获得的光电子图像之间观察到的差异一致。动量转移截面,而不是总散射截面,被认为是预测溶剂对这些团簇阴离子中光电子角分布影响的合适物理参数。