The totally symmetric ring modes of benzene, benzene-d6, pentafluorobe
nzene, hexafluorobenzene, cyclopentane, cycloheptane, cyclopentanone,
cyclohexanone were investigated with customary Raman devices. For the
first time it is shown that a negative or anomalous noncoincidence eff
ect seems to be a general property of aromatic and aliphatic ring vibr
ations. In agreement with the results of isotopic dilution experiments
carried out with benzene and benzene-d6 this new effect is explained
in terms of the pair excitation model as a result of a dominant repuls
ive resonant intermolecular vibrational coupling.