Shallow water analogue of the standing accretion shock instability: experimental demonstration and a two-dimensional model

Despite the sphericity of the collapsing stellar core, the birth conditions of neutron stars can be highly nonspherical due to a hydrodynamical instability of the shocked accretion flow. Here we report the first laboratory experiment of a shallow water analogue, based on the physics of hydraulic jumps. Both the experiment and its shallow water modeling demonstrate a robust linear instability and nonlinear properties of symmetry breaking, in a system which is one million times smaller and about one hundred times slower than its astrophysical analogue.     

Finite Size Scaling of the Dynamical Free-Energy in a Kinetically Constrained Model

We determine the finite size corrections to the large deviation function of the activity in a kinetically constrained model (the Fredrickson-Andersen model in one dimension), in the regime of dynamical phase coexistence. Numerical results agree with an effective model where the boundary between active and inactive regions is described by a Brownian interface.     

Management of the risk of backorders in a MTO–ATO/MTS context under imperfect requirements

Production systems are often classified according to the way production is released, e.g. make-to-stock (MTS), make-to-order (MTO), assembly-to-order (ATO) or engineer-to-order (ETO). The choice of a type of production depends on the decoupling point between customer and supplier. In some supply chains, like in the aeronautical sector, a customer may work according to a MTO process (since his product is highly specific) while his supplier works with a MTS process (since he delivers variants of standards components). This situation sets specific problems that are seldom considered in the literature, especially when collaboration between actors is required for an efficient management of the supply chain, which is the case when uncertainties are present. In this paper, we propose a method based on fuzzy modelling allowing a customer to choose a plan taking into account the uncertainty on his requirements when he works in MTO–ATO while his supplier is in MTS.     

Evolution of glass properties during a substitution of S by Se in Ge28Sb12S60 −xSex glass network

In this paper, a detailed study to examine the influence of chalcogen S/Se mole % in the Ge₂₈Sb₁₂S_60 ?xSe_x glass system, with x = 0, 15, 30, 45 and 60, is presented that provides insight into the effect of chalcogen content on the glass network and properties. Specifically, we report results of a systematic study to evaluate the relationship between compositional variation, glass properties and dominant bonding configurations. These materials are important to applications in optics manufacturing where correlation of physical and optical properties is required to predict fabrication behavior and ultimate material performance. It has been found that the dominant bonds in the glass system change upon reaching a specific molar ratio (percentage, %) of chalcogen substitution, between 30 < x < 45 mol%, changing from Ge―Se to Sb―Se bonds as the dominant bond type. This singularity has been observed using micro-Raman spectroscopy and X-ray photoelectron spectroscopy. This effect of the dominant bond configurational change was also shown to impart changes in important physical properties including micro-hardness, thermal properties, and the glass' viscometric behavior. Results indicate that the observed dominant bond change was responsible for a constant value in the evolution of both the micro-hardness and calorimetric glass transition temperature. The viscosity was also affected by the change in dominant bond type, breaking the monotony of the viscosity evolution during the S substitution, due to the total strength of the vitreous system which does not linearly increase.     

Boron-mediated polymerization of ylides derived from allylic arsonium salts: influence of the double bond substitution on the outcome

New oligomers or polymers are prepared by polymerization of arsonium ylides in the presence of boron compounds.     

Single lanthanide-doped oxide nanoparticles as donors in fluorescence resonance energy transfer experiments

We used lanthanide-ion doped oxide nanoparticles, Y(0.6)Eu(0.4)VO(4), as donors in fluorescent resonance energy transfer (FRET) experiments. The choice of these nanoparticles allows us to combine the advantages of the lanthanide-ion emission, in particular the long lifetime and the large Stokes shift between absorption and emission, with the detectability of the nanoparticles at the single-particle level. Using cyanine 5 (Cy5) organic molecules as acceptors, we demonstrated FRET down to the single-nanoparticle level. We showed that, due to the long donor lifetime, unambiguous and precise FRET measurements can be performed in solution even in the presence of large free acceptor concentrations. Highly efficient energy transfer was obtained for a large number of acceptor molecules per donor nanoparticle. We determined FRET efficiencies as a function of Cy5 concentration which are in good agreement with a multiple acceptor-multiple donor calculation. On the basis of the donor emission recovery due to acceptor photobleaching, we demonstrated energy transfer from single-nanoparticle donors in fluorescence microscopy experiments.     

Convenient asymmetric synthesis of beta-trifluoromethyl-beta-amino acid, beta-amino ketones, and gamma-amino alcohols via Reformatsky and Mannich-type reactions from 2-trifluoromethyl-1,3-oxazolidines

The stereoselective syntheses of beta-trifluoromethyl-beta-amino ester, beta lactams, and beta-amino ketones starting from an oxazolidine derived from trifluoroacetaldehyde hemiacetal and (R)-phenylglycinol are reported. The Mannich-type reaction involving a chiral fluorinated iminium ion occurred in a good yield and with a higher stereoselectivity (dr up to 96:4) than that of the Reformatsky-type reaction. This straightforward strategy was applied to the short syntheses of (R)-3-amino-4,4,4-trifluorobutanoic acid, a series of novel enantiopure unprotected fluorinated beta-amino ketones, and their corresponding gamma-amino alcohols.     

The first catalytic Sakurai reaction of N-alkoxycarbonylamino sulfones with allyltrimethylsilane

We report the first catalytic Sakurai reaction of N-alkoxycarbonylamino sulfones with allylsilanes. The allylation reaction of N-alkoxycarbonylamino phenylsulfones with allyltrimethylsilane proceeded smoothly with low catalyst loading of bismuth triflate (2.0 mol%) to afford the corresponding protected homoallylic amines in moderate to very good yields (up to 96%).