Spectra of europium-doped yttrium oxide and yttrium vanadate phosphors

The spectral distributions of the visible absorption and fluorescence emission under electron beam excitation of Eu³⁺-doped (Y₂O₃) and (YVO₄) powders have been detected and analyzed. (Y₂O₃: Eu³⁺) has a cubicC crystal structure with a unit cell dimension a=10·61 Å. Its observed transitions from⁷ F ₀ to many upper states have been recognized; the observed number of Stark components is in agreement with that based on theC ₂ site symmetry of the Eu³⁺ ion in Y₂O₃. Eu³⁺-doped yttrium vanadate has a typical zircon tetragonal crystal structure with unit cell dimensions ofc=6·29 Å anda=7·11 Å. The observed transitions in (Eu³⁺: YVO₄) have been identified and assigned in accordance with theD _2d site symmetry of the Eu³⁺ ion in this lattice.The authors would like to express their deep gratitude to Professor G. F. J.Garlick, University of Hull, England, for offering experimental facilities in his Physics Department.     

Role of A-site deficiency in the magneto-transport properties of Pr<Subscript>0.7</Subscript>Sr<Subscript>0.3</Subscript>MnO<Subscript>3</Subscript> relaxed films

The magneto-transport properties of thick relaxed A-site deficient films having the composition Pr Sr_0.3MnO₃ (P_□SMO with the □ symbol for the Pr vacancy) and Pr_0.7Sr MnO₃ (PS_□MO) are studied. A direct comparison with a Pr_0.7Sr_0.3MnO₃ (PSMO)completely relaxed film, deposited under the same growth conditions, shows a reduction of the in-plane parameter a₁₀₀ associated to an enhancement of the out-plane parameter. The strains (bulk strain ε_B and biaxial Jahn-Teller strain ε_J-T) do vary with the nature of the cationic vacancy. For example, an enhancement of ε_B of 9% in the PS_□MO film (Sr deficient) produces a decrease of T_C of 30 K, whereas the Pr deficient P_□SMO film exhibits a large reduction of both ε_B (-16%) and ε_J-T (divided by a factor of 5), which enhances T_C of 12 K, similarly to previous observations on bulk ceramics. With a reduced resistivity (ρ<0.02 Ω cm), the obtained Pr-deficient film, P_□SMO, exhibits the best magneto-transport properties with a decreasing magnetoresistance sensitivity at low field.     

Electrochemical nitric oxide sensor preparation: a comparison of two electrochemical methods of electrode surface modification

Platinum electrodes modified with Mn(II) 5-(N-(8-pyrrole-yl-3,6-dioxa-1-aminooctane)phenylamide-10,15,20-trimethoxyphenylporphyrin (Mn(II)triOMeTCPPyP) using multi-sweep cyclic voltammetry and differential pulse amperometry were evaluated as electrocatalytic surfaces for the oxidation of nitric oxide. The electrodes modified using the pulse amperometric approach were more sensitive towards the detection of nitric oxide. The increased sensitivity led to the attainment of a wider linear dynamic range for the quantification of nitric oxide.     

Synthesis and Antimicrobial Activity of New Pyridothienopyrimidines and Pyridothienotriazines

5‐Acetyl‐3‐amino‐4‐aryl‐6‐methylthieno[2,3‐b]pyridine‐2‐carboxamides ( 5a,b ) were reacted with triethyl orthoformate or nitrous acid to give the corresponding pyrimidinones 6a,b and triazinones 7a,b . The reaction of 5a,b with acetic anhydride was carried out and its products were identified as a mixture of 8‐acetyl‐9‐aryl‐2,7‐dimethylpyrido[3′,2′:4,5]thieno[3,2‐d]pyrimidine‐4(3H)‐one ( 9a,b ) and related 5‐acetyl‐4‐aryl‐3‐biacetylamino‐6‐methylthieno[2,3‐b]pyridine‐2‐carbonitrile ( 10a,b ). Reaction of 7a with some halocompounds afforded the N‐alkylated triazinones 8a‐c . Chlorination of 6a,b and 9a,b with phosphorus oxychloride produced 4‐chloropyrimidines 11a‐d which were used as precursors for the rest of the target heterocycles. Some of the prepared compounds were tested in vitro for their antimicrobial activities.     

A Potentiometric Sensor for Determination of Doxycycline Hydrochloride in Pharmaceutical Preparation and Biological Fluids

This article focused on the construction and characteristics of novelty and sensitivity of modified carbon paste electrodes for determination of doxycycline hydrochloride (DC.HCl) in urine, serum and pharmaceutical preparations. It was based on the incorporation of α-cyclodextrine (α-CD) and multi-walled carbon nanotube (MWCNT) ionophores which improved the characteristics of the electrodes with tricresylphosphate (TCP) (electrode I) and o-nitrophenyloctylether (o-NPOE) (electrode II) as plasticizers, respectively. The constructed electrodes, at optimum paste composition, exhibited good Nernstian response for determination of doxycycline hydrochloride over a linear concentration range from 1.0 × 10^–7 to 1.0 × 10^–2 and 1.22 × 10^–7 to 1.0 × 10^–2 mol L^–1 with detection limit of 1.0 × 10–7 and 1.22 ×10^–7 mol L^–1 and with slope values of (58.7 ± 0.2) mV decade–1 and (58.0 ± 0.6) mV decade–1, for modified carbon paste electrodes (MCPEs; electrodes I and II), respectively. The results showed fast dynamic response time (about 6–7 s) and long lifetime in the range from 4 to 5 months where the response of the electrodes was not affected by pH variation within the range from 2 to 8 and 2 to 7.5 for electrodes I and II, respectively. Electrodes I and II showed high selectivity for doxycycline hydrochloride with respect to a large number of interfering species including foreign inorganic, organic species, excipients and the fillers added to the pharmaceutical preparation. The constructed electrodes were successfully applied for determination of DC.HCl in pure form, its pharmaceutical preparations and biological fluids (urine and serum) using standard addition, calibration curves and potentiometric titration methods. The results obtained using these potentiometric electrodes were comparable with those obtained using official method. The results were satisfactory with excellent percentage recovery comparable or better than those obtained by other routine methods.

     

Spectroscopic and Molecular Docking Studies of Cu(II), Ni(II), Co(II), and Mn(II) Complexes with Anticonvulsant Therapeutic Agent Gabapentin

New Cu(II), Ni(II), Co(II), and Mn(II) complexes of the gabapentin (Gpn) bidentate drug ligand were synthesized and studied using elemental analyses, melting temperatures, molar conductivity, UV–Vis, magnetic measurements, FTIR, and surface morphology (scanning (SEM) and transmission (TEM) electron microscopes).The gabapentin ligand was shown to form monobasic metal:ligand (1:1) stoichiometry complexes with the metal ions Cu(II), Ni(II), Co(II), and Mn(II). Molar conductance measurements in dimethyl-sulfoxide solvent with a concentration of 10⁻³ M correlated to a non-electrolytic character for all of the produced complexes. A deformed octahedral environment was proposed for all metal complexes. Through the nitrogen atom of the –NH₂ group and the oxygen atom of the carboxylate group, the Gpn drug chelated as a bidentate ligand toward the Mn²⁺, Co²⁺, Ni²⁺, and Cu²⁺ metal ions. This coordination behavior was validated by spectroscopic, magnetic, and electronic spectra using the formulas of the [M(Gpn)(H₂O)₃(Cl)]·nH₂O complexes (where n = 2–6).Transmission electron microscopy was used to examine the nanostructure of the produced gabapentin complexes. Molecular docking was utilized to investigate the comparative interaction between the Gpn drug and its four metal [Cu(II), Ni(II), Co(II), and Mn(II)] complexes as ligands using serotonin (6BQH) and dopamine (6CM4) receptors. AutoDock Vina results were further refined through molecular dynamics simulation, and molecular processes for receptor–ligand interactions were also studied. The B3LYP level of theory and LanL2DZ basis set was used for DFT (density functional theory) studies. The optimized geometries, along with the MEP map and HOMO → LUMO of the metal complexes, were studied.     

Comparative Study of Carbon Paste,Screen Printed,and PVC Potentiometric Sensors Based on Copper‐sulphamethazine Schiff Base Complex for Determination of Iodide – Experimental and Theoretical Approaches

New poly vinyl chloride (PVC) membrane, carbon paste (CP), and screen printed (SP) electrodes are constructed for iodide sensing. They are based on copper (II)‐sulphamethazine Schiff base complex as suitable carrier. Mechanism was proved by FT‐IR and UV‐Vis spectroscopy. Computational study involving binding energies calculations at DFT/B3LYP level of theory confirmed the proposed mechanism and agreed the observed selectivity pattern. Responses are near‐Nernstian (?55.0, ?51.0 mV/concentration decade) for PVC, and SP electrodes, and super‐Nernstian (?61.2 mV/concentration decade) for the CP electrode. Lower limit of detection (3.2×10^?6 mol L^?1) and improved selectivity over the highly interfering thiocyanate were obtained in comparison with the previously reported Schiff base complexes‐based iodide sensors.     

SYNTHESIS AND BIOLOGICAL ACTIVITY OF SOME NEW 8-HYDROXYQUINOLINE SULPHONAMIDE DERIVATIVES

Abstract

Some new derivatives containing both 8-hydroxyquinoline and sulphonylamino β-lactams and thiazolidinones have been prepared. These compounds were synthesized from the corresponding 8-hydroxyquinoline sulphonylhydrazide (1) by converting it to hydrazones (2). The latter hydrazones (2) were easily transformed to β-lactams (3) and thiazolidinones (4) by cyclocondensation reaction with chloroacetyl chloride and/or mercaptoacetic acid. Some metal chelates with Fe³⁺. Co²⁺+, Ni²⁺, Cu²⁺ and Cd²⁺ have been prepared for some of the compounds and screened in vitro for their biological activity.     

Aromatic CC Bonds as Dipolarophiles: Facile Reactions of Uncomplexed Electron‐Deficient Benzene Derivatives and Other Aromatic Rings with a Non‐Stabilized Azomethine Ylide

Non‐stabilized azomethine ylide 4 a reacts smoothly at room temperature with a variety of uncomplexed aromatic heterocycles and carbocycles on the condition that the ring contains at least one or two electron‐withdrawing substituents, respectively. Aromatic substrates, including pyridine and benzene derivatives, participate as 2 π components in [3+2] cycloaddition reactions and interact with one, two, or three equivalent(s) of the ylide, depending on their structure and substitution pattern. Thus, this process affords highly functionalized polycyclic structures that contain between one and three pyrrolidinyl ring(s) in useful yields. These results indicate that the site selectivity of the cycloaddition reactions strongly depends on both the nature and the positions of the substituents. In most cases, the second 1,3‐dipolar reaction occurs on the opposite face to the one that contains the first pyrrolidinyl ring. DFT calculations on model compounds indicate that a concerted mechanism features a low activation barrier.