The presence of poly(1,2-butadiene) in the solvent Aroclor enhances th
e mean solvent rotational mobility relative to the neat solvent case e
ven though the polymer has a higher glass transition temperature than
that of the solvent. This interesting behavior found earlier by photon
correlation spectroscopy is confirmed by dielectric relaxation and Fa
bry-Perot interferometry. The new data extend significantly the freque
ncy and temperature ranges of observation of the modification of the A
roclor dynamics in solutions of poly(1,2-butadiene) and quantify the r
ate at which the addition of the polymer alters the mean solvent reori
entation time as a function of temperature.