An amphiphilic random copolymer of hydrophilic of poly(ethylene glycol) methyl ether methacrylate with hydrophobic perfluorohexylethyl acrylate, PEGMA77-co-FA23, was synthesized by ATRP and used to investigate self-assembling into nanostructures in water and chloroform solutions, both experimentally and computationally. The dynamic light scattering measurements on water solutions of the copolymer at room temperature evidenced the presence of nanoassemblies with hydrodynamic diameter D h = 4 ± 1 nm. The behavior of fluorescence emission intensity of water solutions with added ethidium bromide suggested confinement of the molecular rotor within a hydrophobic environment of the copolymer. Moreover, these nanoassemblies were thermoresponsive and reversibly collapsed into much larger, multi-chain aggregates with D h = 390 ± 20 nm at a critical temperature of 55 °C (5 mg mL -1 ).Molecular dynamics simulations revealed the formation of single-chain, prolate globular nanoassemblies with a structural variability in water solution at room temperature. The evolutions of the simulated radius of gyration (R g ), asphericity, prolateness and solvent-accessible surface area were analyzed along the folding trajectories. Thus, selffolding appeared to result from the interplay between hydrophobic interactions and structural constraints which leads to rather complex nanostructures (R g = 20-25 Å, 200 ns simulation). By contrast, folding in much more open polymer conformations (R g = 30-40 Å) was predicted for chloroform solutions.

Many synthetic polymers used to form polymerbrush films feature a main backbone with functional, oligomeric side chains. While the structure of such graft polymers mimics biomacromolecules to an extent, it lacks the monodispersity and structural purity present in nature. Here we demonstrate that sidechain heterogeneity within graft polymers significantly influences hydration and the occurrence of hydrophobic interactions in the subsequently formed brushes and consequently impacts fundamental interfacial properties. This is demonstrated for the case of poly(methacrylate)s (PMAs) presenting oligomeric side chains of different length (n) and dispersity. A precise tuning of brush structure was achieved by first synthesizing oligo(2-ethyl-2oxazoline) methacrylates (OEOXMAs) by cationic ring-opening polymerization (CROP), subsequently purifying them into discrete macromonomers with distinct values of n by column chromatography, and finally obtaining poly[oligo(2-ethyl-2-oxazoline) methacrylate]s (POEOXMAs) by reversible addition−fragmentation chain-transfer (RAFT) polymerization. Assembly of POEOXMA on Au surfaces yielded graft polymer brushes with different side-chain dispersities and lengths, whose properties were thoroughly investigated by a combination of variable angle spectroscopic ellipsometry (VASE), quartz crystal microbalance with dissipation (QCMD), and atomic force microscopy (AFM) methods. Side-chain dispersity, or dispersity within brushes, leads to assemblies that are more hydrated, less adhesive, and more lubricious and biopassive compared to analogous films obtained from graft polymers characterized by a homogeneous structure.

Two amphiphilic random copolymers, PEGMAx‐co‐FAy (x = 90 and 70 mol%), are synthesized by ATRP and their solutions are investigated as a function of solvent, concentration, and temperature by DLS and SANS analyses. Both copolymers self‐assemble in nanostructures by single‐chain folding in water solutions over a wide range of temperatures. The values of the DLS hydrodynamic radius and the SANS radius of gyration are found to be ≈4 nm and ≈3.4–3.7 nm, respectively. Moreover, SANS shows the self‐folded nanoassemblies to be prolated spheroids with a ratio of polar/equatorial axes of ≈5:1 for PEGMA90‐co‐FA10 and ≈2:1 for PEGMA70‐co‐FA30. On heating above a critical temperature Tc, multichain microassemblies are formed that revert back to nanoassemblies on cooling below Tc. This temperature‐responsive transition is fully and sharply reversible.

Well-defined amphiphilic pentablock copolymers Siy-(EGx-FAz) 2 composed of polysiloxane (Si), polyethylene glycol (EG), and perfluorohexylethyl polyacrylate (FA) blocks are synthesized by ATRP of FA monomer starting from a difunctional bromo-terminated macroinitiator. Diblock copolymers EGx-FAz are also synthesized as model systems. The block copolymers are used, either alone or blended with a PDMS matrix in varied loadings, to prepare antibiofouling coatings. Angle-resolved XPS and contact angle measurements show that the coating surface is highly enriched in fluorine content but undergoes reconstruction after contact with water.Protein adsorption experiments with human serum albumin and calf serum highlight that diblock copolymers resist protein adhesion better than do pentablock copolymers. Blending of the pentablock copolymer with PDMS results in increased protein adsorption. By contrast, the PDMS-matrix coatings show high removal percentages of sporelings of the green fouling alga Ulva linza. V C 2015 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 000: 000-000, 2015

A novel fluorescent-labeled amphiphilic random terpolymer is synthesized by controlled radical polymerization of a fluorescent molecular rotor monomer, 2-cyano-2-[4-vinyl(1,1’-biphenyl)-4’-yl]vinyljulolidine, a hydrophilic monomer, poly(ethylene glycol) methyl ether methacrylate, and a hydrophobic monomer, perfluorohexylethyl acrylate. Combined dynamic light scattering and fluorescence emission spectroscopy measurements are used to investigate its self-assembly in water solution. Self-assembled nanostructures with a hydrodynamic diameter size Dh of 4 ± 1 nm are detected due to the single-chain folding of the terpolymer in unimer micelles. The fluorescence emission intensity of the terpolymer in water solution is found to be one order of magnitude higher than that in organic solvents, as a result of the preferential encapsulation of the julolidine co-units in hydrophobic compartments of the unimer micelles. The temperature dependence of the self-associative behavior of the amphiphilic terpolymer is also investigated and a critical temperature is identified at which a transition between single-chain unimer micelles and multi-chain aggregates (Dh = 400 ± 40 nm) reversibly takes place on heating-cooling cycles