We report degenerate subpicosecond excite-probe experiments at a wavel
ength close to the absorption peak of an excited vibrational state of
two different metalphthalocyanine solutions. By using this technique,
we were able to resolve in time the vibrational relaxation within the
first electronic excited state of the molecule. A four-level model is
used to explain the observed nonlinear response. Theoretical modeling
allows us to obtain both the vibrational relaxation time, and two diff
erent excited-state absorption cross-sections for each of the samples
studied.