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Selective infrared laser pulses in the femtosecond (fs) time domain may be used to prepare quasi-coherent molecular vibrations in the dissociative continuum of the ground electronic state. These vibrations may be monitored by femtosecond IR+UV pump−probe spectroscopy. The new phenomenon is discovered by means of molecular wave-packet simulations for a two-dimensional model based on ab initio potential-energy surfaces and dipole functions for HONO 2 .
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Manz et al. (1998) studied this question.
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