NiSO4·6H2O as a new,efficient, and reusable catalyst for the α-aminophosphonates synthesis under mild and eco-friendly conditions

Research on Chemical Intermediates - Nickel (II) sulfate hexahydrate is used for the first time as an efficient catalyst for the one-pot synthesis of α-aminophosphonates by three-component...     

Effects of modified starch and fat on the rheological characteristics of newly formulated processed cheese: Use of experimental design method

This study aims to investigate the impact of the incorporation of starch (modified and non-modified) on the texture of the processed cheese in order to appreciate a new recipe on one hand and to try to reduce fat content (FC) on the other. The modeling of the experimental results has been performed. An experimental design was used (the variable factors are the amount of starch and FC). The dry extract (DE) of cheese and parameters derived from the modeling of rheological results are the selected responses. The cheese with a concentration of modified starch that is greater than 2% has a high viscosity at rest, while the cheese with non-modified starch has a lower viscosity. When the FC exceeds 15%, the viscosity increases as the concentration of the starch exceeds 2%. Below this concentration, the FC effect is negligible except when the starch concentration is 1%, in this case the viscosity decreases.     

Racemization of secondary alcohols catalyzed by ruthenium: application to chemoenzymatic dynamic resolution

In this paper, we have shown that the [RuCl₂(p-cymene)]₂ complex associated with simple hemisalen ligands is able to racemize (S)-1-phenylethanol. The influence on the racemization process of the ligand’s structure as well as the nature of a co-catalyst have been evaluated and optimized. This [RuCl₂(p-cymene)]₂/Ligand/TEMPO racemization system was then associated with the Candida Antarctica B lipase in order to carry out dynamic kinetic resolution experiments on rac-phenylethanol. This led us to identify the best conditions for effective DKR, which was then applied to various secondary benzylic and aliphatic alcohols. It was thus possible to obtain (R)-1-cyclohexylethyl acetate from rac-1-cyclohexylethanol in quantitative conversion and with high enantioselectivity (98%).     

Experimental Determination of the Longitudinal Dispersivity During the Injection of a Micro-Cement Grout in a One-Dimensional Soil Column

In order to describe the basic phenomenon of miscible grout propagation during the injection in a saturated and deformable porous medium, a general mathematical model was proposed, which accounts for the existing coupling between the fluid flow analysis, the miscible grout transport, and the solid skeleton deformation, leading to a realistic prediction of the injected zone. The development of the model was made concurrently with laboratory experiments to determine the model parameters. This paper describes the determination of the longitudinal dispersivity during the transport of a micro-cement grout injected in a one-dimensional soil column, by relying on image processing analysis. The application concerned here is the injection of soils for improving their properties, that is, to reduce permeability, increase mechanical strength or reduce the deformability. The longitudinal dispersion coefficient is an essential parameter governing the mixing process and the evolution of the transition zone, and thus the injection efficiency. Finally, the comparison between simulated results from the developed model and experimental data, essential to validate the model from a phenomenological standpoint, is made.     

New sterically unhindered benzoquinonemonoimines

We accidentally found that the F→OH conversion by direct hydroxylation of electron deficient aryls above 150 °C allows the isolation of the precursors of novel quinonemonoimines 9, previously unknown.     

On minimal non-M_rC-groups

A group $G$ is said to be a minimax group if it has a finite series whose factors satisfy either the minimal or the maximal condition. Let $D(G)$ denotes the subgroup of $G$ generated by all the Chernikov divisible normal subgroups of $G$ . If $G$ is a soluble-by-finite minimax group and if $D(G)=1$ , then $G$ is said to be a reduced minimax group. Also $G$ is said to be an $ M_{r}C$ -group (respectively, $PC$ -group), if $G/C_{G} \left(x^{G}\right)$ is a reduced minimax (respectively, polycyclic-by-finite) group for all $x\in G$ . These are generalisations of the familiar property of being an $FC$ -group. Finally, if $\mathfrak X $ is a class of groups, then $G$ is said to be a minimal non- $\mathfrak X $ -group if it is not an $\mathfrak X $ -group but all of whose proper subgroups are $\mathfrak X $ -groups. Belyaev and Sesekin characterized minimal non- $FC$ -groups when they have a non-trivial finite or abelian factor group. Here we prove that if $G$ is a group that has a proper subgroup of finite index, then $G$ is a minimal non- $M_{r}C$ -group (respectively, non- $PC$ -group) if, and only if, $G$ is a minimal non- $FC$ -group.     

A novel carbon/chitosan paste electrode for electrochemical detection of normetanephrine in the urine

Normetanephrine is a marker for pheochromocytoma, a rare catecholamine-secreting and neuroendocrine tumor, that arises from sympathetic and parasympathetic paraganglia. In this work, a novel carbon/chitosan electrode paste was used for sensitive voltammetric determination of normetanephrine and dopamine in the presence of ascorbic acid and uric acid. The modified electrode has shown an increase in the effective area of up to 68%, well-separated oxidation peaks, and an excellent electrocatalytic activity. The electrochemical response characteristics were investigated by cyclic and differential pulse voltammetry. Interestingly, high sensitivity and selectivity in the linear range of normetanephrine, dopamine, ascorbic acid, and uric acid concentrations were observed. The present method was applied in the urine sample and satisfactory results were obtained showing that this electrode is very suitable in pharmaceutical and clinical preparations.     

Self-assembly reactions between the cis-protected metal corners (N-N)MII (N-N = ethylenediamine, 4,4'-substituted 2,2'-bipyridine; M = Pd, Pt) and the fluorinated edge 1,4-bis(4-pyridyl)tetrafluorobenzene

The self-assembly reactions between the fluorinated ditopic ligand 1,4-bis(4-pyridyl)tetrafluorobenzene (A) and different nitrogen-protected palladium(II) and platinum(II) complexes have been investigated. While dynamic equilibria between molecular triangles and squares were observed when the diimine compounds 4,4'-R2bipy (bipy = 2,2'-bipyridine; R = H, Me, t-Bu) were employed as ancillary ligands, only square species were obtained from ethylenediamine (en) derivatives. Characterization of the obtained metallomacrocycles was accomplished by 1H and 19F NMR spectroscopy in combination with electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI-FT-ICR). Molecular dynamics simulations (UFF) have been performed to interpret the influence of the fluorinated ring on the square/triangle relative stability. Density functional calculations using the GIAO method have been employed for the interpretation of the chemical shift assignments. The study of the ability of these compounds to act as hosts of electron-rich aromatic guests has shown that the palladium ethylenediamine square is capable of establishing this type of intermolecular interaction exclusively in aqueous media. The host-guest stoichiometry and association constants have been determinated by 1H NMR spectroscopy.     

Strong aphicidal activity of GlcNAc(β1→4)Glc disaccharides: synthesis, physiological effects, and chitinase inhibition

The synthesis of four GlcNAc(β1→4)Glc disaccharides containing 2-O-acetyl and/or 6-sulfate groups was performed in high yields with total 1,2-trans stereoselectivity. These disaccharides were evaluated as candidates for insect chitinase inhibition and aphicidal activity. All the compounds prepared displayed physiological effects on M. persicae aphids; however, the inhibition of chitinases of different sources (bacteria, fungus, and aphid) followed different patterns according to subtle structural characteristics.