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Time-resolved photoelectron spectroscopy of the CH{sub 3}I B{sup I}E 6s [2] state.

Journal Article · · Physical Chemistry Chemical Physics
DOI:https://doi.org/10.1039/C004220J· OSTI ID:1039503
; ; ;  [1]
  1. Chemical Sciences and Engineering Division
The predissociation dynamics of the vibrationless level of the 6s (B {sup 2}E) Rydberg state of CH{sub 3}I was studied by femtosecond-resolved velocity map imaging of photoelectrons. By monitoring the decay of the CH{sub 3}I{sup +} produced by photoionizing the B state, the predissociation lifetime was measured to be 1310 {+-} 70 fs. Photoelectron spectra were recorded as a function of the excitation scheme (one or two photons to the B state), and as a function of the ionizing wavelength. All of these photoelectron spectra show a simple time dependence that is consistent with the decay time of the CH{sub 3}I{sup +} ion signal. The photoelectron angular distributions for the ionization of the B state depend on the excitation scheme and the ionizing wavelength, and show a strong dependence on the vibrational modes excited in the resulting CH{sub 3}I{sup +}. At long delays, the photoelectron spectra are characterized by photoionization of the I({sup 2}P{sub 1/2}) fragment formed by predissociation of the B state.
Research Organization:
Argonne National Laboratory (ANL)
Sponsoring Organization:
SC; ANR COCOMOUV; ANR HARMODYN
DOE Contract Number:
AC02-06CH11357
OSTI ID:
1039503
Report Number(s):
ANL/CSE/JA-66481
Journal Information:
Physical Chemistry Chemical Physics, Journal Name: Physical Chemistry Chemical Physics Journal Issue: 48 Vol. 12; ISSN 1463-9076
Country of Publication:
United States
Language:
ENGLISH

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