Improved cycling performances of binder-free macroporous silicon Li-ion negative electrodes using room temperature ionic liquid electrolyte

Journal of Solid State Electrochemistry - The present article describes the innovative combination of freestanding macroporous silicon layers on copper foil collectors and room temperature ionic,...     

Dimethyl selenide complexes of copper,gallium and indium halides as potential precursors for selenium-containing chalcopyrite semiconducting materials

The coordination chemistry of copper, gallium and indium halides with the simplest possible selenoether i.e. Me₂Se was investigated with the aim to use the resulting complexes as precursors for selenium-containing chalcopyrite semiconducting materials. An optimized general procedure for the high yield synthesis is described and the influence of a halide ion on the structure and solubility of these metal halide dimethyl selenide complexes are discussed. These complexes were characterized by the elemental analysis, FT-IR and ¹H NMR spectroscopy as well as single crystal X-ray structures, the later study showing them to be monomeric for gallium halides, mono- or dimeric for indium halides and either an ion-pairs or 2-D extended structure in the case of copper halides.     

The transfrmation of difluorocarbene into 3,3-diflurocyclopropene

The addition of difluorocarbene to benzobarrelene gives the syn and anti 1,2 mono-adducts. Heating of either of them at 200°C in hexadeuteriobenzene generates naphthalene and 3,3-difluorocyclopropene.     

Diastereoselective route to (2R,5S)- and (2S,5S)-2-methyl-1,6-dioxaspiro[4.5]decane, a pheromone component of the wasp Paravespula vulgaris

A diastereoselective approach to (2R,5S)- and (2S,5S)-2-methyl-1,6-dioxaspiro[4.5]decane 1 and 1a is described. The route starts with an alkylation reaction among the cyclopentanone N,N-dimethylhydrazone 6 and the chiral iodides (R)-3 or (S)-3, derived from the enantiomers of ethyl β-hydroxybutyrate, controlling the estereocenter at C-2 of the molecules. The alkylated products 7 and 7a were easily transformed into the 1,8-O-TBS-1,8-dihydroxy-5-nonanones 9 and 9a in four steps, and a subsequent stereoselective spiroketalization, in acidic media, afforded a Z:E mixture (1:2) of compounds 1 and 1a.     

TT-eigentensors for the Lichnerowicz Laplacian on some asymptotically hyperbolic manifolds with warped products metrics

Let (M =]0, ∞[×N, g) be an asymptotically hyperbolic manifold of dimension n + 1 ≥ 3, equipped with a warped product metric. We show that there exist no TT L ²-eigentensors with eigenvalue in the essential spectrum of the Lichnerowicz Laplacian Δ _L . If (M, g) is the real hyperbolic space, there is no symmetric L ²-eigentensors of Δ _L .     

Coinage Metal Complexes with Di-tertiary-butyl Sulfide as Precursors with Ultra-Low Decomposition Temperature

We report here the synthesis of [Cu₂(TFA)₄(^tBu₂S)₂] ( 1 ), [Ag₄(TFA)₄(^tBu₂S)₄] ( 2 ) and [AuCl(^tBu₂S)] ( 3 ) (TFA=trifluoroacetate), which decompose in solution medium at ultra-low temperature (e. g., in boiling toluene) to afford phase-pure and highly crystalline Cu₉S₅, Ag₂S and metallic Au nanoparticles, respectively. The low decomposition temperature of these precursors is attributed to the facile decomposition mechanism in the di-tertiary-butyl sulfide ligand. These results are a significant step in the direction of establishing a general low-temperature strategy spanning a range of systems including thermodynamically metastable materials and incorporate them in technologies that are sensitive to the harsh conditions.     

An Approach to Transport in Heterogeneous Porous Media Using the Truncated Temporal Moment Equations: Theory and Numerical Validation

In the last decade, the characterization of transport in porous media has benefited largely from numerical advances in applied mathematics and from the increasing power of computers. However, the resolution of a transport problem often remains cumbersome, mostly because of the time-dependence of the equations and the numerical stability constraints imposed by their discretization. To avoid these difficulties, another approach is proposed based on the calculation of the temporal moments of a curve of concentration versus time. The transformation into the Laplace domain of the transport equations makes it possible to develop partial derivative equations for the calculation of complete moments or truncated moments between two finite times, and for any point of a bounded domain. The temporal moment equations are stationary equations, independent of time, and with weaker constraints on their stability and diffusion errors compared to the classical advection–dispersion equation, even with simple discrete numerical schemes. Following the complete theoretical development of these equations, they are compared firstly with analytical solutions for simple cases of transport and secondly with a well-performing transport model for advective–dispersive transport in a heterogeneous medium with rate-limited mass transfer between the free water and an immobile phase. Temporal moment equations have a common parametrization with transport equations in terms of their parameters and their spatial distribution on a grid of discretization. Therefore, they can be used to replace the transport equations and thus accelerate the achievement of studies in which a large number of simulations must be carried out, such as the inverse problem conditioned with transport data or for forecasting pollution hazards.     

Synthesis,characterization and X-ray structures of N-heterocyclic carbene palladium complexes based on calix[4]arenes: highly efficient catalysts towards Suzuki–Miyaura cross-coupling reactions

A new series of calix[4]arene supported N-heterocyclic carbene palladium complexes were developed and fully characterized. A mono-substituted calix[4]arene was prepared through conventional procedures, following with the attachment of imidazolyl derivative groups to compose the precursors of novel NHCs ligands. Undergoing the alkylation with n-butylbromide and corresponding metallation with palladium and pyridine, original complexes were obtained. After a full characterization in solution and solid state, the evaluation of catalytic activity was taken out in Suzuki–Miyaura cross-coupling reactions, which revealed good performances.     

Localized gluing of Riemannian metrics in interpolating their scalar curvature

We show that two smooth nearby Riemannian metrics can be glued interpolating their scalar curvature. The resulting smooth metric is the same as the starting ones outside the gluing region and has scalar curvature interpolating between the original ones. One can then glue metrics while maintaining inequalities satisfied by the scalar curvature. We also glue asymptotically Euclidean metrics to Schwarzschild ones and the same for asymptotically Delaunay metrics, keeping bounds on the scalar curvature, if any. This extends the Corvino gluing near infinity to non-constant scalar curvature metrics.