Rotationally resolved spectroscopy of the A≈ 2A1←X≈ 2B1 transition of H2S+ above the barrier to linearity using the mass-analyzed threshold ionization photofragment excitation technique

The A approximate to (2)A(1)<- X approximate to B-2(1) transitions of H2S+ above the barrier to linearity have been investigated with the energy resolution high enough to identify individual rotational transition lines for the first time. The rotational cooling of the cation is achieved either by the direct ionization or mass-analyzed threshold ionization (MATI) technique employed in the vacuum-ultraviolet laser excitation of the jet-cooled H2S. Subsequent photoexcitation leads to the H2S+-> H-2+S+ dissociation and the S+ product yield taken as a function of the excitation energy gives the photofragment excitation (PHOFEX) spectra. The combined use of MATI and PHOFEX techniques greatly simplifies the spectrum allowing the accurate identification of the rotationally resolved bands which is otherwise a formidable task due to the intrinsic complexity of the A approximate to (2)A(1)<- X approximate to B-2(1) transition. Highly excited states of A approximate to(0,7,0), A approximate to(0,8,0), and A approximate to(0,9,0) vibronic levels with different K quantum numbers which are located above the barrier to linearity are thoroughly investigated. The bent-to-quasilinear transition of H2S+ above the barrier to linearity shows the characteristics of the Renner-Teller effect, showing the large A rotational constant and strong intensity borrowing of the highly vibrationally excited ground levels such as X approximate to(0,23,0) or X approximate to(0,24,0) in the dipole-allowed excitation. Spectroscopic parameters of term values, rotational, and spin-orbit coupling constants are precisely determined in this work, providing the most quantitative spectroscopic structure of the H2S+ to date. Quantum-state dependent photodissociation dynamics are also discussed from spectral features of PHOFEX.