Using nitroxide radicals covalently bonded to the silica surface as spin la
bels, data on the mobility of the interfacial layers for some filled polyme
rs were obtained. The rotational mobility of spin labels was shown to depen
d on the intensity of the molecular motions of adsorbed macromolecules. The
glass transition temperature of the polymer matrix was correlated with the
ratio of the segmental mobility in the boundary layer to that in the bulk
of the polymer. The lower the T-g value for a polymer, the stronger the eff
ect of reduction of segmental mobility of adsorbed chains. In polymer matri
ces with a high glass transition temperature (PS, PVP), the interfacial lay
er and the regions located farther from the surface of filler particles ins
ignificantly differ in their molecular mobility.