U. Buck et I. Ettischer, STRUCTURE AND STRUCTURAL TRANSITIONS OF SIZE-SELECTED CLUSTERS - (CH3CN)(N) AND (CH3OH)(6), Faraday discussions, (97), 1994, pp. 215-228
Photodissociation spectra of acetonitrile clusters (CH3CN)(n) from n =
4 to n = 13, n = 24 +/- 3, n = 33 +/- 8 have been measured near the m
onomer frequencies of the CC-stretch (920.3 cm(-1)) and the CH3-rock (
1041.8 cm(-1)) mode using a line-tunable CO2 laser. The clusters are s
ize selected by momentum transfer in a scattering experiment with He,
Ne and Ar atoms, respectively. The spectra near the CC-stretch mode ar
e slightly red-shifted and do not depend on the cluster size. Near the
CH3-rock mode there are two series of identical spectra for the even-
sized clusters n = 4, 6, 12 and n = 9 exhibiting three peaks and the o
dd-sized clusters n = 5, 7, 13 and n = 8 showing two peaks, respective
ly. The results are explained by the pairwise antiparallel arrangement
of these molecules with a strong dipole moment. For the methanol hexa
mer a transition between the two energetically lowest-lying isomers ha
s been investigated by measuring their IR spectra.