Electrostatic hierarchical co-assembly in aqueous solutions of two oppositely charged double hydrophilic diblock copolymers
Voets, Ilja K.Laboratory of Physical Chemistry and Colloid Science, Wageningen University, The Netherlands - Adolphe Merkle Institute, University of Fribourg, Switzerland
Keizer, Arie deLaboratory of Physical Chemistry and Colloid Science, Wageningen University, The Netherlands
Leermakers, Frans A.M.Laboratory of Physical Chemistry and Colloid Science, Wageningen University, The Netherlands
Debuigne, AntoineCenter for Education and Research on Macromolecules, University of Liège, Belgium
Jérôme, RobertCenter for Education and Research on Macromolecules, University of Liège, Belgium
Detrembleur, ChristopheCenter for Education and Research on Macromolecules, University of Liège, Belgium
Cohen Stuart, Martien A.Laboratory of Physical Chemistry and Colloid Science, Wageningen University, The Netherlands
English
The formation of spherical micelles in aqueous solutions of poly(N-methyl-2-vinyl pyridinium iodide)-block-poly(ethylene oxide), P2MVP-b-PEO and poly(acrylic acid)-block-poly(vinyl alcohol), PAA-b-PVOH has been investigated with light scattering-titrations, dynamic and static light scattering, and ¹H 2D Nuclear Overhauser Effect Spectroscopy. Complex coacervate core micelles, also called PIC micelles, block ionomer complexes, and interpolyelectrolyte complexes, are formed in thermodynamic equilibrium under charge neutral conditions (pH 8, 1 mM NaNO₃, T = 25 °C) through electrostatic interaction between the core-forming P2MVP and PAA blocks. 2D ¹H NOESY NMR experiments show no cross-correlations between PEO and PVOH blocks, indicating their segregation in the micellar corona. Self-consistent field calculations support the conclusion that these C3Ms are likely to resemble a ‘patched micelle’; that is, micelles featuring a ‘spheres-on-sphere’ morphology.