Vibrational dynamics of SCCl2 from the zero point to the first dissociation limit

Brent Strickler, Martin Gruebele

Research output: Contribution to journalArticlepeer-review

Abstract

Over one thousand X̃ ← B̃ vibronic transitions of the SC35Cl2 and SC35Cl37Cl isotopomers, originating from eight B state vibrational levels, have been measured by dispersed fluorescence spectroscopy and stimulated emission pumping. The observed ground state vibrational energy levels involve all six vibrational modes, and have up to 28 quanta of combined excitation. The energy window extends from the fundamental vibrations to beyond the molecular dissociation limit near E/h = 600 THz. 375 ground state vibrational levels of SC 35Cl2 have been assigned and fitted to an effective Hamiltonian. 35-37 chlorine isotopomer splittings are regular except for a few resonances when ν1 ≥ 7 and ν4 ≥ 6. Regular progressions up to 600 THz indicate the conservation of at least two good vibrational quantum numbers at the SCCl-Cl and SC-Cl2 dissociation limits. A subset of over 100 transitions up to E/h = 240 THz was used to refine a 6-D ab initio potential surface represented in bond distance coordinates. This surface, together with a previously computed B state potential surface and transition dipole surface, also reproduces the spectral intensities of the ν14 polyads up to E/h = 240 THz. SCCl2 is an excellent model system for intramolecular vibrational redistribution (IVR) among skeletal vibrations ranging from isolated resonances to extensively mixed quantum states. The newly extended spectra show that half of the 6-D quantum state space remains highly structured up to the first dissociation limit near 600 THz, resulting in sub-exponential IVR dynamics except at short times.

Original languageEnglish (US)
Pages (from-to)3786-3800
Number of pages15
JournalPhysical Chemistry Chemical Physics
Volume6
Issue number14
DOIs
StatePublished - Jul 21 2004

ASJC Scopus subject areas

  • Physics and Astronomy(all)
  • Physical and Theoretical Chemistry

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