Ion-Temperature-Gradient-Driven Modes with Nonthermal Electron Distributions in Bi-ion Dusty Magnetoplasma

The effect of nonthermal distributions of electrons on ion-temperature-gradient (ITG)-driven drift modes in the presence of tiny dust particles for bi-ion magneto plasmas is investigated. The dynamics of bi-ions and dust particles is considered for the study of low-frequency (less than the gyrofrequencies of dust and ions) ITG mode. A new dispersion relation is derived and analyzed numerically as well as analytically. Three different distributions for nonthermal electrons (Kappa, q, and Cairns distribution) are used. It is found that the presence of nonthermal electrons in bi-ion dusty magnetoplasma reduces the growth rate of the ITG instability. These results should be useful for laboratory and space plasmas where nonthermal electrons and dust is always present.     

A Comprehensive Review on <Emphasis Type="SmallCaps">l</Emphasis>-Asparaginase and Its Applications

l-asparaginase (LA) catalyzes the degradation of asparagine, an essential amino acid for leukemic cells, into ammonia and aspartate. Owing to its ability to inhibit protein biosynthesis in lymphoblasts, LA is used to treat acute lymphoblastic leukemia (ALL). Different isozymes of this enzyme have been isolated from a wide range of organisms, including plants and terrestrial and marine microorganisms. Pieces of information about the three-dimensional structure of l-asparaginase from Escherichia coli and Erwinia sp. have identified residues that are essential for catalytic activity. This review catalogues the major sources of l-asparaginase, the methods of its production through the solid state (SSF) and submerged (SmF) fermentation, purification, and characterization as well as its biological roles. In the same breath, this article explores both the past and present applications of this important enzyme and discusses its future prospects.     

Structural characterization of a mixed-ligand complex of copper(II) with 1,10-phenanthroline and the <Emphasis Type="Italic">m</Emphasis>-aminobenzoate ion

A new copper(II) complex of 1,10-phenanthroline (C1₂H₈N₂) and the meta-aminobenzoate ion (m-amb; C₇H₆NO ₂ ^? ), having the formula Cu(C₁₂H₈N₂)(C₇H₆NO₂)Cl?0.5H₂O, is prepared and characterized by elemental analysis, IR spectroscopy, and single crystal X-ray diffraction. The structure is built up from monomeric units in which the coordination environment around the metal ion is a square plane arising from a bidentate 1,10-phenanthroline molecule, a monodentate m-amb anion, and a chloride ion. A very long (Cu–N = 2.856(5) Å) bond to the nitrogen atom of an adjacent m-amb ion generates [101] polymeric chains in the crystal. The crystal structure is consolidated by N–H???O and O–H???O hydrogen bonds and C–H???O, C–H???Cl, and aromatic π–π stacking interactions. Crystal data: C₁₉H₁₅ClCuN₃O_2.5, M _r = 424.33, monoclinic, P2₁/n (No. 14), a = 9.8200(5) Å, b = 10.9291(7) Å, c = 16.3803(9) Å, β = 105.293(3)°, V = 1695.74(17) ų, Z = 4, R(F) = 0.043, wR(F ²) = 0.122.     

Peristaltic motion of Sisko fluid in an inclined asymmetric tapered channel with nonlinear radiation

Peristaltic pumping of Sisko fluid through the non-uniform asymmetric channel is addressed. Main motivations are given to nonlinear radiation and inclined magnetic field. The perturbation technique and lubrication approach are utilized for development of governing problems and solutions. Resulting equations are solved for velocity, temperature, pressure and stream function. Trapping phenomenon is also observed. Variation of pertinent parameters is plotted and illustrated physically. The larger inclination of the magnetic field leads to a rise in velocity. Moreover, the size of trapping bolus tends to reduce and finally disappears for the larger fluid parameter. To our knowledge, such attempt for linear radiation and without inclined magnetic field does not exist even for both symmetric and asymmetric channels. Further it should be noted that problem remains nonlinear even after utilizing long wavelength and low Reynolds number assumptions.

     

Aurones and Analogues: Promising Heterocyclic Scaffolds for Development of Antioxidant and Antimicrobial Agents

Russian Journal of General Chemistry - Synthesis of some new multi-functional analogues of 2′-hydroxy chalcone containing isoxazole and pyrazole functions were synthesized, and their...     

First-principles study of vibrational properties of TiSiO4 clusters

First-principles calculations were performed to investigate the vibrational properties of monomers and dimers of titania, silica, and titania-silica hybrid clusters. Density functional theory-based formulism was employed to optimize the geometry at the B3LYP level and calculate the infrared and Raman spectra of the clusters by using the GGA-PBE exchange-correlation functional. It was found that the vibrational spectra of Ti₂O₄, Si₂O₄, and TiSiO₄ hybrid clusters provide fingerprint information about structures and structural transitions during the formation of cluster structures. In the case of Si₂O₄ the mode at 410 cm⁻¹ exhibited the largest vibration of Si atoms, whereas in the case of Ti₂O₄ the mode at 442 cm⁻¹ exhibited the largest vibration of Ti atoms. The hybrid cluster TiSiO₄ was structured using two different methods to explore the effects of starting geometry on the structures and vibrational modes of the clusters. The structural properties of the clusters remained unchanged but vibrational modes were found to be different. It is found that Si shows notable vibrations, but the metal atom Ti merely shows any vibration in the case of TiSiO₄ hybrid clusters. The low and intermediate frequency modes were stiffened, whereas the three highest frequency modes were softened when the starting geometry of the hybrid clusters was changed from Si₂O₄ to Ti₂O₄.     

Microbial transformation of oleanolic acid by Fusarium lini and alpha-glucosidase inhibitory activity of its transformed products

The biotransformation of a pentacyclic triterpene, oleanolic acid (1), with Fusarium lini afforded two oxidative metabolites, 2alpha,3beta-dihydroxyolean-12-en-28-oic acid (2), and 2alpha,3beta,11beta-trihydroxyolean-12-en-28-oic acid (3). Metabolite 3 was found to be a new compound. The structures were characterized on the basis of spectroscopic studies. These metabolites exhibited a potent inhibition of alpha-glucosidase enzyme.     

Synthesis and characterization of new soluble and thermally stable poly(ester-imide)s derived from N-[3,5-bis(N-trimellitoyl)phenyl]phthalimide and various bisphenols

A new dicarboxylic acid chloride (2) bearing three preformed imide rings was synthesized by treating N-(3,5-diaminophenyl)phthalimide with trimellitic anhydride followed by refluxing with thionyl chloride. A novel family of aromatic poly(ester-imide)s with inherent viscosities of 0.27-0.35 dl g⁻¹ were prepared from 2 with various bisphenols such as resorcinol (3a), hydroquinone (3b), 2,2′-dihydroxybiphenyl (3c), 4,4′-dihydroxybiphenyl (3d), bisphenol-A (3e), 2,2′-dimethyl-4,4′-dihydroxybiphenyl (3f), 1,5-dihydroxynaphthalene (3g), 2,7-dihydroxynaphthalene (3h), and 2,2′-dihydroxy-1,1′-binaphthyl (3i) by high-temperature solution polycondensation in nitrobenzene using pyridine as hydrogen chloride quencher. All of the resulted polymers were fully characterized by FT-IR and NMR spectroscopy and elemental analyses. The poly(ester-imide)s exhibited excellent solubility in some polar organic solvents. From differential scanning calorimetry, the polymers showed glass-transition temperatures between 259 and 353 °C. Thermal behaviors of the obtained polymers were characterized by thermogravimetric analysis and the 10% weight loss temperatures of the poly(ester-imide)s were found to be in the range between 451 and 482 °C in nitrogen. Furthermore, crystallinity of the polymers was estimated by means of wide-angle X-ray diffraction.     

Voltammetry and Spectroscopy Study of In Vitro Interaction of Fenitrothion with DNA

The interaction of Fenitrothion with DNA has been studied using the voltammetric and spectroscopic methods. An irreversible reduction was concluded from the CV data of Fenitrothion. The values of (αn)_f=1.91 and (αn)_b=2.06 were measured and the reduction process of Fenitrothion was performed with 4 electrons. By using non‐linear regression analysis of CV data, the binding constant, binding site size, and diffusion coefficient for free Fenitrothion (D_f) and DNA‐Fenitrothion (D_b) were calculated as: 1.03×10⁴, 1.204, 5.2×10^?4 and 1.72×10^?5, respectively. Also the voltammetric, spectroscopic, thermodynamic and activation energy of DNA‐Fenitrothion complex revealed that the mode of interaction might be partial‐intercalative and complex formation is entropy favored.