posted on 2015-11-24, 00:00authored bySibel Ciftci, Alexander J. C. Kuehne
Palladium-catalyzed
cross-coupling dispersion polymerizations follow
a step-growth mechanism and deliver highly monodisperse particles.
This is surprising, considering the high polydispersity usually inherent
to classical polycondensations at high conversion. Here we present
a novel Heck-type dispersion polymerization yielding fluorescent submicrometer
particles with an extremely narrow size distribution. We investigate
the kinetics of the dispersion polymerization to unravel the mechanism
behind the formation of monodisperse particles. We find that, at medium
conversion, only one type of oligomer forms nuclei for the particles.
These seed particles phase separate from solution at a critical molecular
weight. Oligomers, reaching the critical molecular weight for dissolution
after this initial nucleation event, condensate onto the existing
nuclei, leading to uniform growth of the particles. Higher molecular
weight material is obtained toward high conversion by coupling reactions
inside of the particles. The comprehension of the mechanism behind
particle formation will enable adaptation of other reactions to the
dispersion polymerization protocol. The monodisperse polymer particles
produced here are ideal materials for self-assembled organic photonics,
optoelectronics, or fluorescent biomedical probes and markers.