Amphiphilic hairy nanoparticles are prepared in a one step, batch, heterogeneous polymerization of styrene or n-butyl acrylate, using a water-soluble poly(sodium acrylate) alkoxyamine macroinitiator based on the SG1 nitroxide.

Most star polymers with controlled molecular weight and low polydispersity are synthesized by living polymerization, in which only initiation and propagation reactions, but not chain transfer reaction, take place. Accordingly, the obtained star polymers are generally not contaminated with linear polymers. Recently, we have developed chain-growth condensation polymerization, a kind of living pol...

Polypyrrole (PPy) nanotubes with highly uniform surface and tunable wall thickness were fabricated by one-step vapor deposition polymerization (VDP) using anodic aluminium oxide (AAO) template membranes, and transformed into carbon nanotubes through a carbonization process.

The aim of this study was to analyse the extent of polymerization of different adhesive films in relation to their permeability. One adhesive of each class was investigated: OptiBond FL; One-Step; Clearfil Protect Bond; and Xeno III. Adhesive films were prepared and cured with XL-2500 (3M ESPE) for 20, 40 or 60 s. Polymerization kinetic curves of the adhesives tested were obtained with differen...

Low polydispersity poly(N-isopropylacrylamide) with a biotin end-group was obtained in one step from a biotinylated initiator for atom transfer radical polymerization and interacted with streptavidin to generate the thermosensitive polymer-protein conjugate.

This study reports a novel super-hydrophobic surface with fluorinated cross-linked poly[cyclotriphosphazene-co-(4,4'-(hexafluoroisopropylidene)diphenol)] microspheres prepared via a single-step precipitation polymerization and simple dip-coating route.

A p-biquinodimethane species formed during the Gilch polymerization of an extremely twisted biphenyl monomer has been identified by in situ(1)H-NMR spectroscopy for the first time. From the identification of chain ends, we conclude that the chain growth during Gilch polymerization of biphenyl type monomers is both radical and anionic in nature.

Lewis acids promote the polymerization of several 2-chloroalkylenedioxythiophenes, providing high-molecular-weight conjugated polymers. The proposed mechanism is a cationic chain-growth polymerization, as confirmed by end-capping reactions and a linear correlation of molecular weight with percent conversion. The "living" character of this process was used to prepare new block copolymers.