Patchy worm-like micelles: solution structure studied by small-angle neutron scattering

Triblock terpolymers exhibit a rich self-organization behavior including the formation of fascinating cylindrical core-shell structures with a phase separated corona. After crystallization-induced self-assembly of polystryrene-(block)-polyethylene-(block)-poly(methyl methacrylate) triblock terpolymers (abbreviated as SEMs = Styrene-Ethylene-Methacrylates) from solution, worm-like core-shell micelles with a patchy corona of polystryrene and poly(methyl methacrylate) were observed by transmission electron microscopy. However, the solution structure is still a matter of debate. Here, we present a method to distinguish in-situ between a Janus-type (two faced) and a patchy (multiple compartments) configuration of the corona. To discriminate between both models the scattering intensity must be determined mainly by one corona compartment. Contrast variation in small-angle neutron scattering enables us to focus on one compartment of the SEMs. The results validate the existence of the patchy structure also in solution.

Structure and interaction of flexible dendrimers in concentrated solution

We study the influence of mutual interaction on the conformation of flexible poly(propyleneamine) dendrimers of fourth generation in concentrated solution. Mixtures of dendrimers with protonated and deuterated end groups are investigated by small-angle neutron scattering up to volume fractions of 0.23. This value is in the range of the overlap concentration of the dendrimers. The contrast between the solute and the solvent was varied by using mixtures of protonated and deuterated solvents. This allows us to investigate the partial structure factors of the deuterated dendrimers in detail. An analysis of the measured scattering intensities reveals that the shape of the flexible dendrimers is practically independent of the concentration in contrast to the pronounced conformational changes of flexible linear polymers.