Emerging applications for living crystallization-driven self-assembly.

The use of crystallization as a tool to control the self-assembly of polymeric and molecular amphiphiles in solution is attracting growing attention for the creation of non-spherical nanoparticles and more complex, hierarchical assemblies. In particular, the seeded growth method termed living crystallization-driven self-assembly (CDSA) has been established as an ambient temperature and potentially scalable platform for the preparation of low dispersity samples of core-shell fiber-like or platelet micellar nanoparticles. Significantly, this method permits predictable control of size, and access to branched and segmented structures where functionality is spatially-defined.

Formation of disk-like micelles of triblock copolymers in frustrating solvents.

Coil-coil block copolymers rarely self-assemble into flat low-curvature micelles due to the lack of proper interchain association. Here, we report a facile route to prepare disk-like micelles through the self-assembly of amphiphilic polystyrene--polybutadiene--poly(2-vinylpyridine) triblock copolymers in a mixture of acetone and cyclohexane, which shows distinct selectivity towards the PS, PB and P2VP blocks. Subtle solvation/aggregation of these blocks in this frustrating solvent system provides access to low-curvature micellar structures, and thus favors the formation of uniform disk-like micelles.