Unravelling the thermo-responsive evolution from single-chain to multiple-chain nanoparticles by thermal field-flow fractionation

The amphiphilic block copolymer polystyrene-polyethylene oxide (PS-PEO) is shown for the first time to exhibit unique thermo-responsive transformation into single-chain nanoparticles (SCNPs), as characterized by thermal field-flow fractionation (ThFFF) with multiple detectors. In toluene, the PEO blocks are shown to fold and collapse into spheres that are stabilized by PS shells (SCNP-shells), and solvophobic interactions are prescribed as the critical determinant of the overall dynamics of formation as a function of temperature. Contrary to the typically expected random coil conformation, PS-PEO is shown to formulate SCNP-shell nanostructures. Below a critical temperature threshold of 20 & DEG;C, the SCNP-shell nanostructures are shown to collate into much larger, multiple-chain nanoparticles (MCNPs) with multiple morphologies. The associated conformational evolutions in microstructure from SCNP-shell nanostructures to MCNPs are characterized in-depth with respect to their size, shape, morphology, molar mass, and their respective distributions.

Automated summary

For the first time, the amphiphilic block copolymer polystyrene-polyethylene oxide (PS-PEO) has been shown to transform into thermo-responsive single-chain nanoparticles (SCNPs). The formation of SCNP-shells, stabilized by PS shells, is influenced by solvophobic interactions at different temperatures. Below a critical temperature threshold of 20°C, the SCNP-shell nanostructures collate into larger multiple-chain nanoparticles (MCNPs) with various morphologies. In-depth characterization of the conformational evolutions from SCNP-shell nanostructures to MCNPs is conducted regarding size, shape, morphology, molar mass, and their respective distributions.