LASER EXCITATION SPECTRUM OF THE SCHUMANN-RUNGE (0,12) BAND OF OXYGEN

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1982

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Ohio State University

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Although the Schumann-Runge system, B3ΣuX3Σg, is the most studied electronic transition of O2, its spectroscopy and predissociation mechanisms are still not very well known, We used a pulsed, tunable dye laser to obtain a high resolution scan of the B-X (0,12) band of vibrationally excited O2 formed by photodissociation of ozone ar 266 nm, the fourth harmonic of a Nd:YAG laser. The triplet splitting due to spin interactions for a number of rotational levels is observed for the first time and rotational levels up to N"" = 47 have been recorded. The broadened rotational lines indicate that the predissociation rate for the ν′=0 level is much higher than previous estimates.

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