Polystyrene (PS)/poly(ethylene oxide) (PEO) amphiphilic star-block copolymers and dendrimer-like architectures were prepared using a core-first method. PS stars were first obtained by atom transfer radical polymerization using three and four functional benzyl halides. The chain ends of these star polymers were subsequently modified to generate either the same or twice the number of hydroxyl groups that served to grow the PEO blocks by anionic polymerization of ethylene oxide. Well-defined PS n-b-PEOn (n ) 3 or 4) stars and PS3-b-PEO6 dendrimer-like copolymers exhibiting a monomodal and narrow molar mass distribution were obtained in this way. When spread at the air/water interface, these stars proved to be surface active, forming stable reproducible films. Isotherms yielded A 0 (theoretical surface area occupied by a film at zero pressure) values, allowing for quantitative comparisons between the stars and linear diblock analogues. Both structures demonstrated similar behavior, passing from liquid expanded regions to highly compressed structures at comparable molecular areas.

The synthesis of dendrimer-like polystyrene (PS) of second and third generations by combination of atom transfer radical polymerization (ATRP) and chain end modifications is reported. Calixarene-based cores were used as initiators for ATRP of styrene yielding star polymers containing precisely 4, 6, or 8 arms. The latter were modified in two steps so as to generate PS stars carrying 8, 12, or 16 terminal bromoisobutyrate groups, respectively. These precursors served as multifunctional macroinitiators for the formation of the second generation of dendrimer-like PS. Reiteration of the aforementioned sequence of reactions allowed to derive dendrimer-like polystyrene of third generation that were constituted of 16, 24, or 32 outer arms, respectively. The chain end modification was monitored by 1H NMR spectroscopy. The dendrimer-like PS were also characterized by size exclusion chromatography equipped with a multiangle laser light scattering detector (SEC/MALLS). The actual polymer architecture and the functionality of the stars were confirmed by analysis of the individual arms obtained upon hydrolysis of the ester links present at the core of the stars and at the branching points. The intrinsic viscosities of these dendrimer-like polystyrenes are similar to those reported for regular dendrimers.