VIBRATIONAL SPECTROSCOPY OF THE CL-(H2O)(N) ANIONIC CLUSTERS, N=1-5

The hydrogen-bonded and free OH stretch modes of Cl-(H2O)(n) (n = 1-5) have been observed by vibrational predissociation spectroscopy in the 2.6-3.2 mu m region. Besides demonstrating that all clusters form str ong ionic hydrogen bonds, the spectra provide clear evidence of water- water hydrogen-bonding networks in n = 4 and n = 5, with the broad spe ctrum of n = 5 resembling that of large neutral water clusters. No wat er-water hydrogen bonding is seen in n = 2 and n = 3, but these cluste rs appear to be solvated asymmetrically. While the data suggest that C l- ion is solvated on the surface of water clusters, there are discrep ancies between the observed spectra and ab initio predictions. This di sagreement may stem from either zero-point motion or high cluster temp erature, which tend to disrupt hydrogen bonding among the waters.