OPTICAL-OPTICAL DOUBLE RESONANCE SPECTROSCOPY OF THE A-X AND B-X SYSTEMS OF $Na_{3}$

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1996

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Ohio State University

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In the B state of Na3, the three sodium nuclei can perform an almost free pseudorotational motion in the molecular plane. This purely vibrational movement is characterized by quantum numbers u (denoting the radial displacement amplitude) and j (the vibronic angular momentum). Recent work from this lab has shown that for j>0. each rotational level in the B state splits into two Coriolis components. Furthermore, this study indicates that the vibronic angular momentum is integer quantized1. The corresponding rotational analysis was based on a simple model assuming well separated vibronic bands--as is the case for u1--and rotational quantum numbers J13. This talk reports new optical-optical double resonance experiments in which the frequency of the labeling laser was truned to a transition in the A-X system--previously investigated by the groups of Demtrouder3 and Tiemann4. A second laser was scanned across the u=0 and 1, j=0,1, 2, and 3 vibronic bands in the B-X system. Such a technique gives a greatly improved signal to noise ratio in comparison with our earlier studies in which labeling was done in the B state. The previously unrecorded u=0 spectrum is of particular theoretical interest because the j=0 and 1 sublevels lie somewhat closer together than the corresponding pairs in u1 states suggesting that these levels lie near (or even below) the pseudorotational barrier. Efforts are underway to determine the height of the barrier from an analysis of the u=0 spectrum.

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1 W.E. Ernst and S. Rakowsky, Phys. Rev. Lett. 74, 58 (1995). 2 W.E. Ernst and S. Rakowsky, Ber. Bunsenges. Phys. Chem. 99, 441 (1995). 3 H.-A. Eckel, J.M. Gress, J. Biele, and W. Demtr""{o}der, J. Chem, Phys. 98, 135 (1993). 4 M. Meyer zur Heide, E. Tiemann, and D. Wendlandt, Chem. Phys. Lett. 199, 590 (1992).


Author Institution: Department of Physics, The Pennsylvania State University

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