The
development
of soft anisotropic building blocks is of great interest for various
applications in soft matter. Furthermore, such systems would be important
model systems for ordering phenomena in fundamental soft matter science.
In this work, we address the challenge of creating hollow and anisotropically
shaped thermoresponsive microgels, polymeric networks with a solvent
filled cavity in their center that are swollen in a good solvent.
Sacrificial elliptical hematite silica particles were utilized as
a template for the synthesis of a cross-linked N-isopropylacrylamide
(NIPAm) shell. By varying the amount of NIPAm, two anisotropic microgels
were synthesized with either a thin or thick microgel shell. We characterized
these precursor core–shell and the resulting hollow microgels
using a combination of light, X-ray, and neutron scattering. New form
factor models, accounting for the cavity, the polymer distribution
and the anisotropy, have been developed for fitting the scattering
data. With such models, we demonstrated the existence of the cavity
and simultaneously the anisotropic character of the microgels. Furthermore,
we show that the thickness of the shell has a major influence on the
shape and the cavity dimension of the microgel after etching of the
sacrificial core. Finally, the effect of temperature is investigated,
showing that changes in size, softness, and aspect ratio are triggered
by temperature.