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Updated: Jun 20, 2026

Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by π-π Stacking Interactions
Published on: October 10, 2016
Internal structural characterization of triblock copolymer micelles with looped corona chains
Fernando C Giacomelli1, Izabel C Riegel, Cesar L Petzhold
1Institute of Chemistry, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves 9500, 91501-970 Porto Alegre, Brazil.
Abstract:
We report the characterization through SAXS measurements of micelles produced from a new series of block copolymers: one diblock and four triblock copolymers bearing short poly[5-(N,N-diethylamino)isoprene] and long polystyrene blocks. Micellar aggregates produced in DMF (selective solvent for polystyrene) from the same set of samples were previously successfully characterized through light scattering measurements. The X-ray scattering profiles of starlike (from the diblock copolymer sample) and flowerlike micelles (from the triblock copolymers samples) could be fitted using the spherical copolymer micelle model proposed by Pedersen and Gerstenberg (Macromolecules 1996, 29, 1363.) where in the case of flowerlike micelles, the particles were understood as formed by hypothetical diblock copolymers having half of the true polymeric molar mass. Using the spherical copolymer micelle model, it could be possible to attest the unswollen nature of the micellar cores. The total micellar size suggested thus that the chains forming the corona are extended which is mainly related to a small core surface area per corona chain entering the core (Ac/n), which also induced a small number of aggregation (N(agg)) of all self-assembled particles. The total micellar size fits well with our previous light scattering measurements.
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