Organic-Inorganic Hybrid Ladder-like Polysilsesquioxanes as Compatibilized Nanofiller for Nanocomposite Materials.

Nanocomposite materials composed of an organic matrix and an inorganic nanofiller have been the subject of intense research in recent years. Indeed, the synergy between these two phases confers improved properties thanks to an increased surface-volume ratio, which reinforces the interactions between the particles and the polymer matrix. These interactions depend on many factors such as the shape, size and dispersion of the nanoobjects.

Characterization of Poly(methyl methacrylate)- and Polystyrene-Based Block Copolymers by Liquid Chromatography under Limiting Conditions of Desorption Gradient.

Size exclusion chromatography-gradient (SEC-Gradient) is a powerful technique to separate polymers by their chemical composition. The stationary phase is first conditioned with a gradient from adsorli to desorli, and polymer samples are injected after the gradient in SEC conditions. Since its first description in 2011 by Schollenberger and Radke, it has never been applied to block copolymers.

Association between selective serotonin reuptake inhibitors use and blood transfusion risk in older adults after hip fracture: a cohort study.

Background: Hip fracture is common and associated with high morbidity and mortality rates. Selective serotonin reuptake inhibitors (SSRIs) influence platelet hemostasis and might result in abnormal bleeding. This study aims to determine whether the use of SSRIs in older patients undergoing hip fracture surgery is associated with the risk of perioperative red blood cell (RBC) transfusion.

Through Space π-Electrons Communication in [2,2]-Paracyclophanes: Unprecendented Stabilization of Radicals.

Efforts to understand radical stability have led to considerable progress in radical chemistry. In this article, we investigated a novel approach to enhancing the radical stability of carbon-centered radicals through space electron delocalization within [2,2]-paracyclophanes. Alkoxyamines possessing a paracyclophane scaffold exploit face-to-face π-π-interactions between the aromatic rings to effectively lower bond dissociation energy (BDE) for NO-C bond homolysis.

α-Trifluoromethylated Quinolines as Safe and Storable PET-Donor for Radical Polymerizations.

In the quest for powerful, safe, and storable photoinduced-electron transfer (PET) donors, the attention is turned to the α-trihalomethylated amine moiety that is not studied in the context of PET-reductants. The thermal and photophysical properties of α-trifluoromethylated quinolines are thus studied and their reducing abilities evaluated as initiators of polymerization reactions. Polymers of high molecular weights are obtained through a radical polymerization process and the PET-donor can be stored within the monomer for several months without losing its efficiency.