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   The vibrational predissociation (VP) dynamics of the phenol–water (PhOH–H 2 O) dimer were studied by detecting H 2 O fragments and using velocity map imaging (VMI) to infer the internal energy distributions of PhOH cofragments, pair-correlated with selected rotational levels of the H 2 O fragments. Following infrared (IR) laser excitation of the hydrogen-bonded OH stretch fundamental of PhOH (Pathway 1) or the asymmetric OH stretch localized on H 2 O (Pathway 2), dissociation to H 2 O + PhOH was observed. H 2 O fragments were monitored state-selectively by using 2+1 Resonance-Enhanced Multiphoton Ionization (REMPI) combined with time-of-flight mass spectrometry (TOF-MS). VMI of H 2 O in selected rotational levels was used to derive center-of-mass (c.m.) translational energy ( E T ) distributions. The pair-correlated internal energy distributions of the PhOH cofragments derived via Pathway 1 were well described by a statistical prior distribution. On the other hand, the corresponding distributions obtained via Pathway 2 show a propensity to populate higher-energy rovibrational levels of PhOH than expected from a statistical distribution and agree better with an energy-gap model. The REMPI spectra of the H 2 O fragments from both pathways could be fit by Boltzmann plots truncated at the maximum allowed energy, with a higher temperature for Pathway 2 than that for Pathway 1. We conclude that the VP dynamics depends on the OH stretch level initially excited. 

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