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STATE SELECTED PHOTODISSOCIATION $(B{^{1}}\Pi_{u} \leftarrow X{^{1}}\Sigma^{+}_{g})$ IN $K_{2}$ BY ALL-OPTICAL TRIPLE RESONANCE SPECTROSCOPY

Please use this identifier to cite or link to this item: http://hdl.handle.net/1811/18602

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Title: STATE SELECTED PHOTODISSOCIATION $(B{^{1}}\Pi_{u} \leftarrow X{^{1}}\Sigma^{+}_{g})$ IN $K_{2}$ BY ALL-OPTICAL TRIPLE RESONANCE SPECTROSCOPY
Creators: Ji, B.; Yiannopoulou, A.; Wang, J. X.; Wang, H.; Kleiber, P. D.; Lyyra, A. M.; Sando, K. M.; Stwalley, W. C.
Issue Date: 1993
Publisher: Ohio State University
Abstract: Final state analysis of the products of molecular photodissociation gives information about the dynamical evolution of the system from short to long range including information about nonadiabatic interaction between potential energy curves and the transition through different angular momentum coupling regions [1]. Applying the all-optical triple resonance (AOTR) technique, specific individual rovibrational levels in $K_{2}$ are selectively photodissociated [2]. Polarization of the resulting atomic fluorescence is measured and analyzed by multichannel quantum defect-half collision theory [3].
URI: http://hdl.handle.net/1811/18602
Other Identifiers: 1993-TB-6
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