SPECTROSCOPY OF HIGHLY ROTATIONALLY EXCITED Bal $C^{2}\Pi - X^{2}\Sigma^{+}$

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1989

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Ohio State University

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A supersonic beam of HI crosses an effusive beam of Ba and the resulting Bal X2Σ+ product is probed using a single-mode CW ring dye laser at ∼550nm via laser induced fluorescence of the Bal C2ΠX2Σ+ band system. Under these experimental conditions. Bal v=0 product is formed with rotational quantum numbers in excess of 500. For the isolated P2 and P12 branches of the C - X (0,0) band, single rovibronic transitions with J ranging from ∼350 to ∼500 are readily resolved. Previous studies1 employing a thermal oven source provided definitive assignments of the Bal C - X (0,0) band for low J values (J<200). These data were combined with the line positions obtained in the present study to perform a nonlinear least squares fit to the energy differences calculated from the upper and lower state model Hamiltonians. This permits rotational assignment of the high J transitions. The resulting spectroscopic constants enable a detailed explanation of the observed high-J bandhead features in the Bal CXΔv=0 sequence that characterize the Bal product.

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1 M. A. Johnson, C. Noda, J. S. McKillop, and R. N. Zare, Can, J. Phys 62, 1467 (1984).


Author Institution: Department of Chemistry, Stanford University

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