Small-angle neutron scattering was used to characterize the structure of arborescent polystyrene-graft-poly(2-vinylpyridine) copolymers dissolved in methanol-d4 (CD3OD). A radial density profile based on a power law functional form provided a good fit to the scattering data. While a model with homogeneous density profiles in the core and shell, respectively, and with a size distribution (a polydisperse core-shell model) also fits the data comparably well, the extra parameters required for this fit are difficult to justify on the basis of the data. In addition, unconstrained fits using the core-shell model failed to converge to values of the overall molecular size and molecular weight which agreed with values determined from independent light scattering measurements which leads to the conclusion that the power law model is a more appropriate function for describing the radial density function of these molecules. The density profile from either model showed that the polystyrene core of the molecules is not collapsed. Values of the second virial coefficient, A(2), have been calculated from Zimm plots and it was found that A(2) decreased as a function of generation to close to zero for the highest generation (i.e. highest molecular weight) polymers. Finally, it was found that the radius of gyration of the polymers increases with the molecular weight according to the scaling relationship, R-g similar to M-w(v) with v = 0.24 +/- 0.04. (C) 2003 Published by Elsevier Ltd.