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Ganna Gorodyska

Publications and source records attributed to Ganna Gorodyska.

5 recordsLinked to original sources

Adhesion between chemically heterogeneous switchable polymeric brushes and an elastomeric adhesive.

We investigated the adhesive properties of binary heterogeneous polymer brushes made from end-functionalized polystyrene (PS) and poly(2-vinylpyridine) (P2VP) chains. The molecular organization of the mixed brush could be varied reversibly by exposure to selective solvents for PS (toluene) and for P2VP (acidic water). This exposure results in reversible switching of adhesive and wetting properties. The manner in which the adhesion switching occurs can be tuned by the composition of mixed brushes. However, the outer surface composition could be enriched more effectively in PS after the toluene treatment than in P2VP after the acidic water treatment. As a result, the mixed brush compositions that showed the largest difference in properties between an exposure to toluene and an exposure to water were the P2VP-rich compositions. Adhesive properties, tested against a soft hydrophobic pressure-sensitive adhesive (PSA) using a probe test, always showed smaller differences between solvent treatments than wetting properties with water, suggesting a much higher sensitivity of the hydrophobic/hydrophilic brushes to polar molecules than to nonpolar molecules.

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Chemical contrasting in a single polymer molecule AFM experiment.

We developed a simple contrasting procedure to improve the AFM visualization of single positively charged polymer chains deposited on substrates of a relatively high roughness via the decoration of the molecules with hexacyanoferrate anions or negatively charged clusters of cyanide-bridged complexes.

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Cascade of coil-globule conformational transitions of single flexible polyelectrolyte molecules in poor solvent.

We show that hydrophobic flexible polyelectrolyte molecules of poly(2-vinylpyridine) and poly(methacryloyloxyethyl dimethylbenzylammonium chloride) are trapped and frozen due to adsorption on the mica surface, and the observed AFM single molecule structures reflect the molecular conformation in solution. An increase of the ionic strength of the solution induces the cascade of abrupt conformational transitions due to the intrachain segregation from elongated coil to compact globule conformations through intermediate pearl necklace-globule conformations with different amounts of beads per chain. The length of the necklaces and the number of beads decrease, while the diameter of beads increases with the increase of ionic strength. Coexistence at the same time of extended coils, necklaces with different amounts of beads, and compact globules indicates the cascade of the first-order-type phase transitions.

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Mineralization of single flexible polyelectrolyte molecules.

Conformation of a single flexible polyelectrolyte molecule with a hydrophobic backbone in aqueous solution is effected by the interplay of the short-range intramolecular attraction and the long-range Coulomb repulsion. The conformation can be frozen if the molecule is trapped by a solid substrate. With this approach, we prepared the range of single molecule templates from poly(2-vinylpyridine) (P2VP) deposited on the surface of Si-wafer or mica in different conformations from an elongated wormlike coil to compact globule. Pd(+2) was coordinated by P2VP via an ion exchange reaction exposing the samples to palladium acetate acidic aqueous solution. In the next step, Pd(+2) was reduced by dimethylamine borane. This route results in wire-shaped metallic nanoparticle assembles of about 2-5 nm in diameter and 50-700 nm in length. The conformation and size of the underlaying polyelectrolyte molecules determine the dimensions of nanoparticles.

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Single flexible hydrophobic polyelectrolyte molecules adsorbed on solid substrate: transition between a stretched chain, necklace-like conformation and a globule.

Single flexible polyelectrolyte molecules of poly(2-vinylpyridine) undergo conformational transition from a stretched wormlike coil to a necklace-like globule, and to a compact globule depending on pH and ionic strength in aqueous solution in good agreement with recent theoretical reports. AFM investigations allow the visualization of details of the chain conformation on mica and the extraction of quantitative statistics of molecular dimensions.

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