We have measured the time-integrated fluorescence of coumarin 153 in a glas
s-forming solvent in order to assess the inhomogeneous linewidth as a funct
ion of temperature. A maximum of this width is observed at a temperature wh
ere the structural relaxation time of the solvent matches the excited state
lifetime of the dye of a few nanoseconds. This feature can be explained on
ly on the basis of a relaxation time dispersion which originates from a spa
tial distribution of solvent response times. Therefore, liquid dynamics in
the regime of nanosecond time scales are heterogeneous with respect to the
structural relaxation time. (C) 2001 American Institute of Physics.