15min:
ELECTRONIC TRANSITIONS OF THE HC4S AND HC6S RADICALS STUDIED BY LASER INDUCED FLUORESCENCE SPECTROSCOPY.

MASAKAZU NAKAJIMA, YOSHIHIRO SUMIYOSHI AND YASUKI ENDO, Department of Basic Science, Graduate School of Arts and Sciences, The University of Tokyo, Tokyo 153-8902, Japan .

Laser induced fluorescence spectra of two new vibronic band systems have been observed by discharging a mixture gas, C2H2 0.5%/CS2 0.3% diluted in Ar, in a supersonic jet. All the bands were assigned to 2 Pi3/2-2 Pi3/2 transitions by measuring rotationally resolved spectra. Based on the chemical composition and the ground state combination differences, the spectral carriers were assigned to the HC4S and HC6S radicals. The homogeneous width of the excitation spectra of the HC6S radical is larger than that of HC4S by 0.02 cm-1 (FWHM), which was interpreted as the lifetime broadening of the excited state, corresponding to 270 ps. Vibronic origin of HC4S is located at 500.5 nm, and that of HC6S is at 589.6 nm. Main progressions of both the vibronic systems are assigned to the excitations of the C-S stretching modes, of which frequencies were determined to 505 cm-1 for HC4S, 435 cm-1 for HC6S.