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We use femtosecond two-color mid-infrared spectroscopy to study the dynamics of aqueous solutions of salts in HDO:D2O. We find that the lifetime of the O–H stretch vibration of HDO molecules in the solvation shell of the halogenic anions Cl−, Br−, and I− is much longer than the lifetime of the O–H stretch vibration of the HDO molecule in bulk D2O solution. This difference in lifetime allows for a clear separation of the response of the solvation shell from that of the bulk liquid. A detailed investigation of the spectral dynamics of the solvating HDO molecules reveals that the hydrogen-bond dynamics of these molecules are much slower than the hydrogen-bond dynamics of bulk liquid water.
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Kropman et al. (2001) studied this question.
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