Zwitterionic Silicone Materials Derived from Aza-Michael Reaction of Amino-Functional PDMS with Acrylic Acid.

Supramolecular zwitterionic silicones are synthesized by aza-Michael reaction between acrylic acid and amine-functional polydimethylsiloxanes. The in-depth characterization of this chemistry, applied for the first time to silicones, is investigated first with model alkylamines (hexylamine, 2-ethylhexylamine and N-propylethylenediamine), a model oligosiloxane (3-aminopropylmethyl bis(trimethylsiloxy)silane), and finally various amino-polysiloxanes. It is shown that after a first acid-base reaction resulting in ionic pairing, aza-Michael addition proceeds smoothly in mild conditions (50 °C, 1-week reaction). Both monoadducts and di-adducts, together with residual amine, are observed by NMR. The supramolecular assembly of the thus-created zwitterionic moieties is highlighted by a concomitant increase in viscosity and phase separation, as observed by transmission electron microscopy, bringing an additional glass transition at -40 °C assigned to highly polar ionic clusters. Below the stoichiometry in acrylic acid, all zwitterionic silicones follow the same classical behavior of nonentangled polymers according to the Rouse model, whereas upon introducing an excess of acrylic acid to amino groups, an enhancement of the elasticity is observed. Finally, silicone elastomers with solid-like behavior and elastomeric mechanical properties are obtained using a high molar mass polymer bearing bifunctional N-(2-aminoethyl)-3-aminopropyl units that favor a high degree of physical crosslinking.

Layer by layer H-bonded assembly of P4VP with various hydroxylated PPFS: impact of the donor strength on growth mechanism and surface features.

Hydrogen bond mediated films made by step by step deposition of poly(4-vinylpyridine) (P4VP) and hydroxylated poly(2,3,4,5,6-pentafluorostyrene) (PPFS) copolymers prepared by thiol para-fluoro coupling, bearing either one (PPFSME) or two (PPFSMPD) hydrogenated hydroxyl groups or a (poly)fluorinated hydroxyl (PPFSOH), respectively, were successfully constructed. The influence of the structural parameters, such as the hydroxyl environment (which dictates the H-bond strength) was in-depth investigated in terms of their impact on (i) growth mechanism, (ii) internal organization, and (iii) surface features. The use of the weaker H-bond donor partner (PPFSME) leads to low quality films composed of irregularly distributed aggregates. While [PPFSMPD/P4VP] multilayer films are comparatively thick and composed of stratified layers with smooth topology, the use of PPFSOH with P4VP yields thin films made of mixed and interpenetrated polymer layers. Playing on the interaction strength appears as a powerful tool to elaborate tailored multilayer films with molecularly tunable properties.

'All-supramolecular' nanocapsules from low-molecular weight ureas through interfacial addition reaction in miniemulsion.

This contribution presents a new strategy for preparing nanocapsules with a shell made of a supramolecular polymer which repeating units are held together by reversible interactions rather than covalent bonds. These nanocapsules were prepared in classical miniemulsion through interfacial addition reaction of a diisocyanate (IPDI) and a monoamine (iBA), forming low-molecular weight bis-ureas moieties which are strong self-complementary interacting molecules through hydrogen-bonding. The nanocapsules present a diameter around 100 nm, and MALDI-TOF MS and (1)H NMR analyses confirm the expected molecular characteristics for the shell. This strategy opens the scope of a new type of nanomaterials exhibiting stimuli-responsiveness due to the reversible interaction linking the repeating units.

Nanomechanical and tribological characterization of the MPC phospholipid polymer photografted onto rough polyethylene implants.

Grafting biomimetic polymers onto biomaterials such as implants is one of the promising approaches to increase their tribological performance and biocompatibility and to reduce wear. In this paper, poly(2-methacryloyloxyethyl phosphorylcholine) (p(MPC)) brushes were obtained by photografting MPC from the rough surface of ultra high molecular weight polyethylene (UHMWPE) joint implants. Such substrates have a high roughness (Ra∼650nm) which often has the same order of magnitude as the brush thickness, so it is very difficult to estimate the vertical density profile of the grafted content. The quality of the p(MPC) grafting was evaluated through a wide range of characterization techniques to reveal the effectiveness of the grafting: atomic force microcopy (AFM) imaging and force spectroscopy, contact angle, SEM/EDX, and confocal microscopy. After testing the methods on smooth glass substrate as reference, AFM nano-indentation proves to be a reliable non destructive method to characterize the thickness and the mechanical properties of the p(MPC) layer in liquid physiological medium. Tribological measurements using a homemade biotribometer confirm that, despite heterogeneity thickness (h=0.5-6µm), the p(MPC) layer covers the roughness of the UHMWPE substrate and acts as an efficient lubricant with low friction coefficient and no wear for 9h of friction.