Journal of Chemical Physics, Vol.105, No.6, 2141-2152, 1996
Resonance-Enhanced Multiphoton Ionization Spectroscopy of Carbonyl Sulfide
Rydberg excited states of the OCS molecule in the energy range 70500-86000 cm(-1) have been investigated via the two and three photon resonance enhancements they provide in the mass resolved multiphoton ionization (MPI) spectrum of a jet-cooled sample of the parent molecule. Spectral interpretation has been assisted by companion measurements of the kinetic energies of the photoelectrons that accompany the various MPI resonances. The present study supports the earlier conclusions of Weinkauf and Boesl [J. Chem. Phys. 98, 4459 (1993)] regarding five Rydberg origins in the 70500-73000 cm(-1) energy range, attributable to, respectively, states of (II)-I-3, (II)-I-1, (3) Delta, (1) Delta and (1) Sigma(+) symmetry arising from the 4p lambda <-- 3 pi orbital promotion. We also identify a further 21 Rydberg origins at higher energies. These partition into clumps with quantum defects ca. 3.5 and 4.5, which we associate with the orbital promotions np lambda <-- 3 pi (n = 5,6), and others with near integer quantum defect which are interpretable in terms of excitation to s,d and (possibly) f Rydberg orbitals. We also identify MPI resonances attributable to CO(X (1) Sigma(+)) fragments and to S atoms in both their ground ((3)p) and excited (D-1) electronic states. Analysis of the former resonances confirms that the CO(X) fragments resulting from one photon dissociation of OCS at excitation wavelengths ca. 230 nm are formed with a highly inverted, bimodal rotational state population distribution, whilst the latter are consistent with previous reports of the wavelength dependence for forming ground and excited state S atoms in the near uv photolysis of OCS.
Keywords:PHOTOELECTRON-SPECTROSCOPY;VACUUM-ULTRAVIOLET;PHOTO-IONIZATION;QUANTUM YIELDS;OCS MONOMERS;STATE;SPECTRA;PHOTODISSOCIATION;MOLECULES;ENERGY