POLY 17 |
| By manipulating the interaction of charged block copolymer hydrophilic corona blocks with multivalent organic counterions, novel and traditional micelle geometries such as disks and toroids vs. vesicles and cylinders can be controllably self-assembled. Specifically, polyacrylic acid-b-polymethacrylate-b-polystyrene amphiphilic triblock copolymers were studied in water/THF solvent mixtures with organic diamines as counterions. The system has been investigated by means of transmission electron microscopy (TEM), cryo-TEM, and small angle neutron scattering (SANS). By altering the water content of the solvent mixture, the hydrophobic polystyrene chain length, the chemical structure of the diamine counterions, and diamine counterion concentrations, one can predicatively access different structures with the same triblock copolymer and directly characterize the kinetic pathways between different structures. In addition, hierarchical stacking of micelle structures can be induced due to intermicellar interactions and micelles can be formed with internal phase separation with blends of different block copolymers. |
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Multicompartment Micelles: Higher Order Self-assembly of Block Copolymers
8:30 AM-12:00 PM, Sunday, 10 September 2006 San Francisco Marriott -- Salon B2, Oral
Division of Polymer Chemistry |