THE ROTATIONAL AND ROTATION VIBRATIONAL SPECTRUM OF $C_{3}OS$ IN HIGHLY EXCITED STATES OF THE LOWEST-LYING BENDING MODE $\nu_{7}$

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1997

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Ohio State University

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The rotational spectrum of tricarbon oxide sulphide C3OS has been recorded in the 2 mm region between 118 GHz and 179 Ghz with a new BWO-based millimeter wave synthesizer. Around 12000 rotational transitions could be observed, including transitions of the isotopomers OCCC33S,OCCC34S,OCC13CS,OC13CCS and O13CCCS in natural abundance. The data was analyzed together with hitherto unassigned rotational transitions from previous measurements between 78 GHz and 118 GHzh. Our analysis led to the characterisation of various new vibrational sates, especially higher excited states of the lowest-lying bending mode ν7 in the main isotopomer; So far, highly excited bending states had been known up to ν7=7 from microwave measurements below 40 GHz. Lately, rotation vibrational TuFIR measurements near 2.4 THz had provided precise term values for the first to the fourth excited state of the bending mode ν7a. Our new rotational data now allowed us to characterize bending states up to ν7=10 and higher. Besides the determination of spectroscopic constants for new states, our data also enabled us to improve spectroscopic constants that had been determined from older measurements. Both together extended our knowledge of the structure and the internal dynamics of the linear heterocumulene C3OS.

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hV. Wagener, M. Winnewisser, and M. Bellini, J. Mol. Spectrosc. \textbf{176}, 425-438 (1996) iM. Winnewisser, E. W. Peau, K. Yamada, and J. J. Christiansen, Z. Naturforsch. \textbf{36a}, 819-830 (1981)


Author Institution: Physikalishch-Chemisches Institut, Justus-Liebig-Universit""at Gie\ss sen 35392; Analytik & Mess technik GmbH, Stollberger Stra\ss e

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