Abstract
The mass-resolved excitation spectrum of the B 3II1-X 1Σ+ transition of HgAr was measured by the two-color resonantly enhanced two-photon ionization method using a high-resolution reflectron time-of-flight mass spectrometer. The rotational structures were recorded with high spectral resolution (∼0.05 cm-1) for the (υB,0) bands (υB = 0-9) of a single isotopomer 200HgAr. From the rotational analysis, the presence of an Ω-type doubling was identified for the first time, which is caused by the rotational perturbation from the nearby highly excited vibrational levels of the A 3Π0+ state. The spacing between the Ω-type doublets was found to exhibit a characteristic reversal as a function of υB. From the deperturbation of the Ω-type doubling, the vibrational level energies of the A state in the vibrationally highly excited region were derived, from which its long-range interaction potential was determined. © 1998 American Institute of Physics.
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CITATION STYLE
Hishikawa, A., Sato, H., & Yamanouchi, K. (1998). Ω-type doubling reversal in the B 3II1 state of 200HgAr as a probe of the long-range potential of the A 3II0+ state. Journal of Chemical Physics, 108(22), 9202–9205. https://doi.org/10.1063/1.476415
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