Polymeric Nanofibers Prepared from Self-Organized Supramolecules

A facile concept to prepare nano-objects based on self-organizing polymeric supramolecules (also called supramolecular block copolymers) is demonstrated using one particular shape, i.e., nanorods or nanofibers. Cylindrical aggregates consisting of a polystyrene (PS) core and a thin corona of poly(4-vinylpyridine) (P4VP) chains are prepared from P4VP(pentadecylphenol)-block-PS comb-coil supramolecules. Diblock copolymers P4VP-block-PS are stoichiometrically (with respect to the number of pyridine groups) hydrogen-bonded with pentadecylphenol (PDP) amphiphiles to yield P4VP(PDP)-block-PS comb-coil supramolecules. By the selection of appropriate relative block lengths for P4VP(PDP) and PS, a micro-phase-separated cylindrical morphology of PS cylinders inside a P4VP(PDP) matrix is obtained. Subsequent removal of the amphiphiles, accounting for ca. 75% of the matrix material, results in cylinders with a core of PS and a corona of easily adjustable thickness of P4VP. The advantages of the present concept compared to the existing procedures are discussed.

Gold-Decorated Block Copolymer Microspheres with Controlled Surface Nanostructures

Gold-decorated block copolymer microspheres (BCP-microspheres) displaying various surface morphologies were prepared by the infiltration of Au precursors into polystyrene-b-poly(4-vinylpyridine) (PS-b-P4VP) microspheres. The microspheres were fabricated by emulsifying the PS-b-P4VP polymers in chloroform into a surfactant solution In water, followed by the evaporation of chloroform. The selective swelling of the P4VP domains in the microspheres by the Au precursor under acidic conditions resulted in the formation of Au-decorated BCP-microspheres with various surface nanostructures. As evidenced by transmission electron microscopy (TEM) and scanning electron microscopy (SEM) measurements, dotted surface patterns were formed when microspheres smaller than 800 nm were synthesized, whereas fingerprint-like surface patterns were observed with microspheres larger than 800 nm. Au nanoparticles (NPs) were located inside P4VP domains near the surfaces of the prepared microspheres, as confirmed by TEM. The optical properties of the BCP-microspheres were characterized using UV-vis absorption spectroscopy and fluorescence lifetime measurements. A maximum absorption peak was observed at approximately 580 nm, indicating that Au NPs are densely packed Into P4VP domains on the microspheres. Our approach for creating Au-NP-hybrid BCP-microspheres can be extended to other NP systems such as Iron-oxide or platinum NPs. These precursors can also be selectively incorporated into P4VP domains and induce the formation of hybrid BCP-microspheres with controlled surface nanostructures