IR signature of the photoionization-induced hydrophobic→hydrophilic site switching in phenol-Arn clusters

IR spectra of phenol-Ar-n (PhOH-Ar-n) clusters with n=1 and 2 were measured in the neutral and cationic electronic ground states in order to determine the preferential intermolecular ligand binding motifs, hydrogen bonding (hydrophilic interaction) versus pi bonding (hydrophobic interaction). Analysis of the vibrational frequencies of the OH stretching motion, nu(OH), observed in nanosecond IR spectra demonstrates that neutral PhOH-Ar and PhOH-Ar-2 as well as cationic PhOH+-Ar have a pi-bound structure, in which the Ar atoms bind to the aromatic ring. In contrast, the PhOH+-Ar-2 cluster cation is concluded to have a H-bound structure, in which one Ar atom is hydrogen-bonded to the OH group. This pi -> H binding site switching induced by ionization was directly monitored in real time by picosecond time-resolved IR spectroscopy. The pi-bound nu(OH) band is observed just after the ionization and disappears simultaneously with the appearance of the H-bound nu(OH) band. The analysis of the picosecond IR spectra demonstrates that (i) the pi -> H site switching is an elementary reaction with a time constant of similar to 7 ps, which is roughly independent of the available internal vibrational energy, (ii) the barrier for the isomerization reaction is rather low(< 100 cm(-1)), (iii) both the position and the width of the H-bound nu(OH) band change with the delay time, and the time evolution of these spectral changes can be rationalized by intracluster vibrational energy redistribution occurring after the site switching. The observation of the ionization-induced switch from pi bonding to H bonding in the PhOH+-Ar-2 cation corresponds to the first manifestation of an intermolecular isomerization reaction in a charged aggregate. (c) 2007 American Institute of Physics.