期刊
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 12, 期 48, 页码 15644-15652出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c004220j
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资金
- ANR COCOMOUV
- ANR HARMODYN
- L'Universite Paul Sabatier
- CNRS
- US Department of Energy, Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences [DE-AC02-06CH11357]
- European Union [MOLCOTUV-041732]
The predissociation dynamics of the vibrationless level of the 6s (B E-2) Rydberg state of CH3I was studied by femtosecond-resolved velocity map imaging of photoelectrons. By monitoring the decay of the CH3I+ 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 CH3I+ 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 CH3I+. At long delays, the photoelectron spectra are characterized by photoionization of the I(P-2(1/2)) fragment formed by predissociation of the B state.
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