photoelectron-imaging-of-anions-illustrated-by-310-nm-detachment-of-f

Photoelectron Imaging of Anions Illustrated by 310 Nm Detachment of F<sup>&#8722;</sup>

Anion photoelectron imaging is a very efficient method for the study of energy states of bound negative ions, neutral species and interactions of unbound ...

Washington University in St. Louis

We report photoelectron spectra of CHCN, recorded at photon energies between 13 460 and 15 384 cm, which show rapid intensity variations in particular detachment channels. The branching ratios for various spectral features reveal rotational structure associated with autodetachment from an intermediate anion state. Calculations using equation-of-motion coupled-cluster method with single and double excitations reveal the presence of two dipole-bound excited anion states (a singlet and a triplet). The computed oscillator strength for the transition to the singlet dipole-bound state provides an estimate of the autodetachment channel contribution to the total photoelectron yield. Analysis of the different spectral features allows identification of the dipole-bound and neutral vibrational levels involved in the autodetachment processes. For the most part, the autodetachment channels are consistent with the vibrational propensity rule and normal mode expectation. However, examination of the rotational structure shows that autodetachment from the ν (v = 1 and v = 2) levels of the dipole-bound state displays behavior counter to the normal mode expectation with the final state vibrational level belonging to a different mode.

Justin Lyle

Department of Chemistry

Washington University in St. Louis

Photoelectron Imaging of Anions Illustrated by 310 Nm Detachment of F⁻

Justin Lyle

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Department of Chemistry

Washington University in St. Louis

Photoelectron Imaging of Anions Illustrated by 310 Nm Detachment of F−

Department of Chemistry

Photoelectron Imaging of Anions Illustrated by 310 Nm Detachment of F⁻