Np. Dasilveira et al., DETERMINATION OF THE OPTICAL ANISOTROPY OF ATACTIC POLYSTYRENE USING A GRATING MONOCHROMATOR, Macromolecular chemistry and physics, 197(6), 1996, pp. 1945-1957
To extract the intrinsic molecular scattering from unwanted collision-
induced contributions as much as possible we propose a simple useful m
ethod recording the depolarized Rayleigh spectra using a double gratin
g monochromator and correcting the spectra for the high-frequency wing
s. For this purpose we tested the system polystyrene/CCl4 for which an
asymptotic value of the optical anisotropy (gamma(2))/x congruent to
30 Angstrom(6) with degree of poly merization x > 20 was found. The de
polarized Rayleigh intensity of 2,4-diphenylpentane and anionically po
lymerized atactic polystyrene standards was also measured in dilute so
lutions in the B-solvent bicyclohexyl (theta = 61 degrees C). From the
absolute depolarized Rayleigh ratio we obtained the configurational a
verage optical anisotropy per number of monomer units, (gamma(2))/x. W
e have chosen cumene as a model compound estimating that its optical a
nisotropy is similar to that of a quasi monomer unit. No significant t
emperature dependence of (gamma(2))/x and of the static internal pair
correlation in the temperature range from 25 degrees C up to 80 degree
s C was found.