Argonne National Laboratory, Argonne, Illinois 60439, USA.
J Phys Chem A. 2010 Oct 28;114(42):11238-43. doi: 10.1021/jp102992b.
Photodissociation of acetaldehyde (CH3CHO) at 266 nm produced CH3 and HCO radicals, and single-photon vacuum ultraviolet ionization was used to record velocity map ion images of both CH3+ and HCO+. Comparison of the translational energy distributions from both species indicates that secondary fragmentation of HCO is negligible for 266 nm photodissociation. Thus, the relative photoion signals for CH3+ and HCO+ in the mass spectrometer, combined with the recently measured absolute photoionization cross section of CH3, allowed the determination of the absolute photoionization cross section of HCO (σ(HCO) = 4.8 ± 1.5(2.0), 5.9 ± 1.6(2.2), and 3.7 ± 1.2(1.6) Mb at 10.257, 10.304, and 10.379 eV, respectively). The observed values are quite small but consistent with the similarly small value at threshold for the isoelectronic species NO. This behavior is discussed in terms of the character of the HOMO in both molecules.
在 266nm 时,乙醛(CH3CHO)的光解产生了 CH3 和 HCO 自由基,单光子真空紫外光电离被用来记录 CH3+ 和 HCO+的速度图离子图像。比较两种物质的平移能分布表明,266nm 光解时 HCO 的次级碎裂可以忽略不计。因此,质谱仪中 CH3+和 HCO+的相对光离子信号,结合最近测量的 CH3 的绝对光离子化截面,允许确定 HCO 的绝对光离子化截面(σ(HCO)=4.8±1.5(2.0),5.9±1.6(2.2)和 3.7±1.2(1.6)Mb 在 10.257、10.304 和 10.379eV 处,分别)。观察到的值很小,但与等电子体 NO 的阈下值相当。这种行为是根据两个分子中 HOMO 的特征来讨论的。