Fluorescent Azasteroids through Ultrasound Assisted Cycloaddition Reactions

We report here the synthesis and optical spectral properties of several new azasteroid derivatives. The formation of these compounds was explained based on the most probable mechanism. The luminescent heterocycles were synthesized by 1,3-dipolar cycloaddition reactions between benzo[f]quinoline and methylpropiolate or dimethyl acetylenedicarboxylate (DMAD). A selective and efficient way for [3+2]-dipolar cycloaddition of benzo[f]quinolinium ylides under ultrasound (US) irradiation (20 kHz processing frequency) is presented. We report substantially higher yields under US irradiation, whereas the solvent amounts required are at least three-fold less compared to classical heating. The azasteroid derivatives are blue emitters with λ_max of fluorescence around 430–450 nm. A certain influence of the azasteroid substituents concerning absorption and fluorescent properties was observed. Compounds anchored with a bulky pivaloyl group or without a C=O carbonyl group have shown increased fluorescence intensity.     

Displacement immunoassay for the detection of ochratoxin A using ochratoxin B modified glass beads

We report here the development of a new assay for the detection of ochratoxin A (OTA) based on the use of its dechlorinated analogue, ochratoxin B (OTB), in a displacement immunoassay. OTB was immobilised on controlled-pore glass beads followed by the binding of anti-OTA antibody, with anti-IgG antibody peroxidase conjugate used as a label. In this manner, an original bio-sensing material was obtained. Upon incubation of this material with OTA, the toxin competes with OTB for the binding sites of the anti-OTA antibodies and releases the antibody-tagged peroxidase complex into the solution. Compared to classic competitive immunoassays, this newly developed displacement immunoassay presents a similar detection limit and assay time. Moreover, the detection, based on the activity of the horseradish peroxidase, is performed for the first time in situ using wine samples.     

The first example of a recursive function which is not primitive recursive

The first example of a recursive function which is not primitive recursive is usually attributed to W. Ackermann. The authors of the present paper show that such an example can also be found in a paper by G. Sudan, published concomitantly with Ackermann's paper.     

Acetonyl­di­chloro­[(Z)‐2‐chloro‐2‐phenyl­vinyl]­tellurium(IV), helical chains of metal complexes

The primary geometry about the Te^IV atom in the title compound, [TeCl₂(C₈H₆Cl)(C₃H₅O)] or C₁₁H₁₁Cl₃OTe, is a pseudo‐trigonal‐bipyramidal arrangement, with two Cl atoms in apical positions, and the lone pair of electrons and C atoms in the equatorial plane. The Te^IV atom is involved in three secondary interactions, two intramolecular [Te?O = 2.842 (3) Å and Te?Cl3 = 3.209 (1) Å] and one intermolecular [Te?Cl = 3.637 (1) Å], the latter giving rise to a helical chain. These helices are linked by C—H?O interchain interactions.     

Multitime dynamic programming for multiple integral actions

This paper introduces a new type of dynamic programming PDE for optimal control problems with performance criteria involving multiple integrals. The main novel feature of the multitime dynamic programming PDE, relative to the standard Hamilton-Jacobi-Bellman PDE, is that it is connected to the multitime maximum principle and is of divergence type. Introducing a generating vector field for the maximum value function, we present an interesting and useful connection between the multitime maximum principle and the multitime dynamic programming, characterizing the optimal control by means of a multitime Hamilton-Jacobi-Bellman (divergence) PDE that may be viewed as a feedback law. Section 1 recalls the multitime maximum principle. Section 2 shows how a multitime control dynamics determines the multitime Hamilton-Jacobi-Bellman PDE via a generating vector field of the value function. Section 3 gives an example of two-time dynamics with nine velocities proving that our theory works well. Section 4 shows that the Hamilton PDEs are characteristic PDEs of multitime Hamilton-Jacobi PDE and that the costates in the multitime maximum principle are in fact gradients of the components of the generating vector field.     

A robust metal-organic framework constructed from alkoxo-bridged binuclear nodes and hexamethylenetetramine spacers: crystal structure and sorption studies

A neutral 3D metal-organic framework, (3)(∞)[Cu(2)(mand)(2)(hmt)]·H(2)O (1), was constructed from binuclear Cu(2)O(2) alkoxo-bridged nodes, generated by the doubly deprotonated mandelic acid. The nodes are connected by hexamethylenetetramine (hmt) spacers, which act as biconnective bridging ligands, and by carboxylato groups. Channels are observed along the crystallographic c axis. The water molecules from the channels can be easily removed, preserving the architecture of the crystal, which is stable up to 280 °C. The Langmuir surface area was found to be 610 m(2) g(-1). The sorption ability of 1 was investigated using H(2) and CO(2).     

Heat-treatment influence on Ni–Fe–Cu–Mo nanocrystalline alloy obtained by mechanical alloying

The 77Ni14Fe5Cu4Mo (wt%) powders have been obtained by dry mechanical alloying of elemental powders in a planetary mill under argon atmosphere for milling durations ranging from 2 to 28?h. The alloy formation is obtained after 12?C16?h of milling, as shown by the X-ray diffraction and magnetic studies. The crystallite mean size is 13?±?2?nm after 28?h of milling. An optimal heat-treatment temperature was chosen after the analysis of the DSC signals. and the samples were heated at 350?°C for different durations ranging from 0.5 to 4?h. The heat treatment was continued to enhance the alloy formation and to eliminate the internal stresses induced during the milling process. The evolution of the phases amount during the heat treatment was calculated from the X-ray patterns using the Rietveld procedure.     

Comparative rheological study of ionic semi-IPN composite hydrogels based on polyacrylamide and dextran sulphate and of polyacrylamide hydrogels

Ionic semi-interpenetrating polymer networks composite hydrogels were synthesized by free-radical polymerization using dextran sulphate (DxS), acrylamide as monomer and N,N′-methylene(bis)acrylamide as cross-linking agent. The viscoelastic properties of these composite hydrogels were investigated by oscillatory shear measurements under small deformation conditions comparative with those of polyacrylamide gels. Changes of the rheological properties of composite hydrogels have been studied in terms of polymerization temperature, cross-linker ratio, initial monomer concentration and molar mass of DxS. The results showed that the stability of the composite hydrogels obtained at room temperature (22?°C) was relatively low because the storage modulus (G′) was only eight times higher than the loss modulus (G″), while for those obtained by cryopolymerization (?18?°C), the stability was improved, the G′ values being about 30 times higher than those of G″. This behaviour indicated that, by conducting the synthesis of hydrogels below the freezing point of the reaction solutions, an enhancement of the hydrogels elasticity was achieved. The network parameters, i.e. the average molecular weight between two cross-links and the cross-link density of the composite hydrogels prepared at ?18?°C, were estimated from rheological data.