INFRARED VIBRATION-ROTATION SPECTRUM OF ARGON-ACETYLENE

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1987

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Ohio State University

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The infrared spectrum of argon-acetylene has been recorded in the three micron wavelength region by observing direct absorption of color center laser radiation by a pulsed molecular beam. Thirty transitions in the PP1,PQ1,RQ0,RR0,RQ1, and RR1 bands of a perpendicular transition have been assigned. The origin of this Ar-HCCH vibrational transition is about 0.3cm−1 lower in energy than the ν3 monomer origin. The rotational structure yields values for A and B-C which are consistent with an earlier radio frequency spectrum of Ar-HCCH. However, (B+C)/2 from the infrared spectrum is much smaller than the earlier prediction. Argon acetylene exhibits an extremely large inertial defect, which explains the poor prediction based on the radio frequency spectrum.

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Author Institution: Department of Chemistry, University of Rochester; Physical Chemistry Laboratory, Oxford University

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