HETEROCYCLIZATION OF AMINOTHIAZOLES

Several new 2-arylidinoamino-4-(3-coumaryl)thiazole derivatives were synthesized via the reaction of 2-amino-4-(coumaryl)thiazole with aromatic aldehydes and other reagents. Structural elucidations were based on elementary analysis and spectral data studies.     

Characterization and Valorization of the Agricultural Waste Obtained from Lavandula Steam Distillation for Its Reuse in the Food and Pharmaceutical Fields

The main focus of the current research was the characterization of the by-products from the steam distillation of Lavandula angustifolia Mill. (LA) and Lavandula x intermedia Emeric ex Loisel (LI) aerial parts, as they are important sources of bioactive compounds suitable for several applications in the food, cosmetic, and pharmaceutical industries. The oil-exhausted biomasses were extracted and the total polyphenol and flavonoid contents were, respectively, 19.22 ± 4.16 and 1.56 ± 0.21 mg/g for LA extract and 17.06 ± 3.31 and 1.41 ± 0.10 mg/g for LI extract. The qualitative analysis by liquid chromatography-electrospray tandem mass spectrometry (HPLC-ESI-MS) revealed that both the extracts were rich in phenolic acids and glycosylated flavonoids. The extracts exhibited radical scavenging, chelating, reducing activities, and inhibitory capacities on acetylcholinesterase and tyrosinase. The IC50 values against acetylcholinesterase and tyrosinase were, respectively, 5.35 ± 0.47 and 5.26 ± 0.02 mg/mL for LA, and 6.67 ± 0.12 and 6.56 ± 0.16 mg/mL for LI extracts. In conclusion, the oil-exhausted biomasses demonstrated to represent important sources of bioactive compounds, suitable for several applications in the food, cosmetic, and pharmaceutical industries.     

Efficient and green syntheses of novel γ-aminophosphonate and phosphine oxide derivatives

Two synthetic protocols leading to novel γ-aminophosphonate and phosphine oxide derivatives, by reductive amination of γ-phosphonylketones, are reported. The first method involved a two-step procedure. Imine intermediates were first isolated from the p-toluenesulfonic acid-catalyzed reaction of primary amines with γ-ketophosphonates and phosphine oxides, then reduced with NaBH₄ in refluxing ethanol. The second method consists of a one-pot procedure which includes the condensation of γ-ketophosphonates and phosphine oxides with primary amines, in the presence of molecular sieves, followed by reduction with NaBH₄. These methods offer significant advantages over prior reports, such as efficiency, generality, and good yields. Furthermore, they are green protocols avoiding hazardous hydrides and solvents.     

Polymorphism in PbBiOXO4 compounds (X=V, P, As): Part II—PbBiOPO4 and PbBiOAsO4 structures and characterization of related solid solutions

Reinvestigation of PbBiOXO₄ (X=V, P, As) thermal behaviour revealed a phase transition for V- and P-compounds, but no transition for the As-compound. As shown by single-crystal X-ray diffraction and high-resolution neutron powder diffraction, α-PbBiOVO₄ transforms to β-PbBiOVO₄ at 550 °C. The two PbBiOPO₄ varieties are isomorph to the vanadate forms, while PbBiOAsO₄ adopts the β-type structure whatever the temperature. PbBiP_1−xOAs_xO₄ and PbBiV_1−xOM_xO₄ (M=As, P, Cr, Mn) solid solutions display both triclinic and monoclinic domains, and the α→β transition temperature is a function of the substitution rate. The ionic conductivity of these compounds was investigated by impedance spectroscopy. The analysis of free space in the β-PbBiOVO₄ structure allows to propose a one-dimensional oxygen diffusion pathway along [010] when the temperature increases.     

Measures of noncompactness and essential pseudospectra on Banach space

In this research article, we work with the notion of the measures of noncompactness in order to establish some results concerning the essential pseudospectra of closed, densely defined linear operators in the Banach space. We start by giving a refinement of the definition of the essential pseudospectra by means of the measure of noncompactness, and we give sufficient conditions on the perturbed operator to have its invariance. Copyright © 2013 John Wiley & Sons, Ltd.     

Dual topology of the Heisenberg motion groups

Let ? _n be the (2n + 1)-dimensional Heisenberg group, and let T ⁿ be the n-dimensional torus acting on ? _n by automorphisms. In this paper, we describe the space of admissible coadjoint orbits of the Heisenberg motion group G _n = T ⁿ ? ? _n and we determine the topology of this space. We show that the bijection between the unitary dual ? _n of G _n and its admissible coadjoint orbit space is a homeomorphism.     

On the existence of semifields of prime power order admitting free automorphism groups

The purpose of this paper is to prove the existence of semifields of order q ⁴ for any odd prime power q = p^r, q > 3, admitting a free automorphism group isomorphic to Z ₂ × Z ₂.     

Polymorphism in PbBiOXO4 compounds (X=V, P, As). Part I: Crystal structures of α- and β-PbBiOVO4

Reinvestigation of PbBiOVO₄ thermal behaviour revealed a phase transition. As shown by single-crystal X-ray diffraction and high-resolution neutron powder diffraction, α-PbBiOVO₄ transforms to β-PbBiOVO₄ at 550 °C. At 25 °C, α-PbBiOVO₄ is triclinic, S.G. P-1, Z=2, with a=5.6088(3), b=7.1109(3), c=7.2978(3) Å, α=108.957(2), β=111.889(2), and γ=94.833(2)°. Above 550 °C, β-PbBiOVO₄ is monoclinic, S.G. C2/m, Z=4, with a=13.61(1), b=5.64(1), c=7.18(1) Å, and β=113.75(1)°. Both structures are built upon (O₂Bi₂Pb₂)_∞ chains parallel to the [100] direction in the α polymorph and [001] in the β-polymorph. These chains are undulated in α and linear in β. In both structures, VO₄ tetrahedra are organized in two sets of rows parallel to (O₂Bi₂Pb₂)_∞ chains, thus building layers of (OBiPb) sandwiched by two layers of VO₄ oriented head to tail; VO₄ displays different orientations in α- and β-PbBiOVO₄.