ISSN:
1089-7690
Source:
AIP Digital Archive
Topics:
Physics
,
Chemistry and Pharmacology
Notes:
Vacuum ultraviolet pulsed field ionization-photoelectron (PFI-PE) spectra for OCS have been obtained in the energy range 15.0–19.0 eV, covering the vibronic bands of OCS+ (A 2Π, B 2Σ+, and C 2Σ+). The ionization energies for the formation of the ground vibrational levels of OCS+ (A 2Π3/2, A 2Π1/2, B 2Σ+, and C 2Σ+) from the ground OCS(X 1Σ+) state have been determined as 15.0759±0.0005 eV, 15.0901±0.0005 eV, 16.0403±0.0005 eV, and 17.9552±0.0005 eV, respectively. We have also generated the theoretical adiabatic three dimensional potential energy functions (PEFs) for OCS+(A 2Π) by employing the complete active space self-consistent field and internally contracted multireference configuration interaction methods. Using these PEFs, the spectroscopic constants and low-lying rovibronic energy levels for OCS+(A 2Π) are calculated variationally. These calculations have made possible the identification of many PFI-PE vibronic bands for OCS+(A 2Π), which are originated from vibronic and Fermi resonance interactions. Owing to the different equilibrium geometries between the OCS+(A 2Π) and OCS(X 1Σ+) states, the PFI-PE spectrum for OCS+(A 2Π) exhibits a long vibronic progression extending well above the OCS+(B 2Σ+) state. On the contrary, the PFI-PE spectra for OCS+ (B 2Σ+ and C 2Σ+) are overwhelmingly dominated by the ground (0,0,0) bands, exhibiting only weak vibrational progressions. © 2002 American Institute of Physics.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1063/1.1455622
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