Abstract

The vibrational coherence of the H–Cl oscillator in the monomer as well as in small clusters ((HCl) x and (HCl) x (N 2) n ) trapped in argon and nitrogen matrices is explored by means of time-resolved one color degenerate four wave mixing experiments. The time and spectral resolution of the laser source, a picosecond OPO laser, enables the measurement of the vibrational dephasing time of HCl in various well defined (HCl) x (N 2) n structures. The results highlight the environment effect on the dephasing processes.

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