The steady state fluorescence anisotropy of the chromophore dialkylben
zene, which constitutes the crosslinks of polyethylacrylate and polyme
thylmethacrylate networks, has been investigated over a range of tempe
ratures, from -20 to 80 degrees C. In polymethylmethacrylate networks
the limit anisotropy of dialkylbenzene (r(0) = 0.198) and vinylphenyl
side groups of the elastic chains (r(0) = 0.304) have been determined
by applying a correction method (previously reported) to discount arti
facts typical of front face excitation. In polyethylacrylate networks
it was found that the mobility of knots does not change appreciably wi
th temperature even 100 degrees C above the glass transition of the sy
stem (about -10 degrees C). It was concluded that polymer dynamics tha
t affect the mobility of knots is different of that determining the mo
tions of the elastic chains.