| Abstract: | We describe a new method for the synthesis of core–shell photolabile nanoparticles. The synthesis begins with the batch emulsion copolymerization of n‐butyl methacrylate (BMA) and ethylene glycol dimethacrylate to form small (20‐nm‐diameter) crosslinked particles with a narrow size distribution. These seeds are then used for a second‐stage emulsion copolymerizations in which BMA and various polar monomers, including methacrylic acid, are added under monomer‐starved conditions. After characterization of the particles, they are transferred to an N,N‐dimethylformamide solution. The cesium salt of the carboxylic acid groups is reacted with 2‐bromo‐1‐phenyl‐octadecan‐1‐one to convert various fractions of the ? COOH groups to the corresponding 2‐benzoylheptadecyl ester groups. These aliphatic ester groups render the surface sufficiently hydrophobic that the particles can be dispersed in common aliphatic hydrocarbons solvents to yield colloidal dispersions, sterically stabilized by the dangling aliphatic chains. Ester groups with a phenyl ketone attached to the β‐carbon are photolabile. Irradiation of the particles with UV light detaches the sterically stabilizing chains from the particle and transforms the surface groups back to COOH groups. This leads to flocculation of the particles. The emphasis in this article is on the optimization of the particle synthesis and the characterization of the particles obtained. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 2642–2657, 2001 |
