Issue 2, 1987

High-resolution studies of the electronic spectra of H2S and D2S

Abstract

The complementary techniques of high-resolution vacuum ultraviolet absorption spectroscopy and resonance-enhanced multiphoton ionisation spectroscopy have been employed in a reinvestigation of the vertical electronic spectra of the molecules H2S and D2S. In accord with previous, lower-resolution, absorption studies of H2S the major part of the spectra of both isotopic species may be understood in terms of Rydberg series that arise from promotion of an electron from the highest occupied 2b1 molecular orbital. The electronic symmetries of states involved in six Rydberg series have been established unambiguously through observation of the (partially resolved) rotational structure that accompanies their excitations. A number of additional resonances observed only in the multiphoton ionisation spectra are tentatively attributed to excitations involving Rydberg orbitals comprised predominantly of f and/or g functions. Several of the absorption features (most notably those involving excited sites of B1 symmetry) exhibit anomalous intensity distributions between the various rotational branches. L-uncoupling and/or rovibronic level dependent predissociation are suggested as contributory causes.

Article information

Article type
Paper

J. Chem. Soc., Faraday Trans. 2, 1987,83, 417-434

High-resolution studies of the electronic spectra of H2S and D2S

C. A. Mayhew, J. Connerade, M. A. Baig, M. N. R. Ashfold, J. M. Bayley, R. N. Dixon and J. D. Prince, J. Chem. Soc., Faraday Trans. 2, 1987, 83, 417 DOI: 10.1039/F29878300417

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