Radius of Gyration of Polystyrene Combs and Centipedes in a O Solvent

The molecular weight dependence of the radii of gyration R{sub g} in a {var_theta} solvent (trans-decalin) of one regular branched comb and three regular centipede polystyrenes was studied using a gel permeation chromatography system equipped with a two-angle light scattering detector and a refracti...

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Bibliographic Details
Published inMacromolecules Vol. 38; no. 4
Main Authors Terao, Ken, Farmer, Brandon S, Nakamura, Yo, Iatrou, Hermis, Hong, Kunlun, Mays, Jimmy
Format Journal Article
LanguageEnglish
Published United States 01.01.2005
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Summary:The molecular weight dependence of the radii of gyration R{sub g} in a {var_theta} solvent (trans-decalin) of one regular branched comb and three regular centipede polystyrenes was studied using a gel permeation chromatography system equipped with a two-angle light scattering detector and a refractive index detector. R{sub g} in trans-decalin for each sample of particular molecular weight was about 25% smaller than that in a good solvent (tetrahydrofuran, THF). On the other hand, they are 20--40% larger than the theoretical values from the Gaussian chain model. This difference can be explained with the wormlike comb model developed by Nakamura et al. (Macromolecules 2000, 33, 8323-8328). Persistence lengths thus obtained for each sample were about half of that determined in THF solution. However, they are significantly larger than that for linear polystyrene. These results suggest that a main chain stiffening effect exists in comb polystyrenes even in a {var_theta} solvent.
Bibliography:DE-AC05-00OR22725
USDOE Office of Science (SC)
ISSN:0024-9297
1520-5835
DOI:10.1021/ma049485s