Preparation of highly dispersed gold nanoparticles inside the porous support assisted by amphiphilic vinyl maleate copolymer

An amphiphilic copolymer composed of maleic acid and alkyl (C₁₈) vinyl monomer was encapsulated into the porous support. A series of colloidal gold nanoparticles of known size was substantially immobilized in the composite porous supports based on cross-linked polyacrylate ester and cross-linked polystyrene resin. Maleic acid moiety of the amphiphilic copolymer can act as a stabilizer for gold nanoparticles in analogy to citric acid, whereas alkyl chains play a role for the stable accommodation of the amphiphilic copolymer. Maleic acid stabilizes the gold nanoparticles by flexing the geometrical arrangement of the linear polymer. Presence of C₁₈ alkyl chain in the poly(C₁₈-vinyl maleate) is indispensable to act as spacing group that prevents mutual aggregation of gold nanoparticles. On the other hand, gold nanoparticles with average diameter of less than 8 nm were spontaneously formed by treatment of the composite resin beads with aqueous HAuCl₄ solution, subsequently dispersed inside the pores of resin beads as observed by TEM. We have also elucidated the catalytic activity of the material with the hydrogenation of cinnamaldehyde in supercritical carbon dioxide. Notably, apparent size effect of gold was observed in the selectivity of the reaction.     

Relationship between pacemaker fibrillation thresholds and electrode area.

Energy thresholds for electrical pacing of the heart are lower with small electrodes than with large. Because pacing of the heart during the vulnerable period may produce ventricular fibrillation, it is also pertinent to know if fibrillation threshold is affected by the electrode size. Electrodes of different surface area but of the same material were implanted in 40 dogs and the pacing thresholds were recorded. Ventricular fibrillation was electrically induced by discharging a 2-msec d.c. cathodal pulse of progressively increasing energy into the vulnerable period. It was found that small electrodes required more energy to produce ventricular fibrillation than large electrodes, and the ratio of fibrillation to stimulation threshold was higher for the small-surface-area electrode. The difference between the thresholds and ratios obtained with the various electrodes was statistically significant. A similar experiment was performed in animals with chronically implanted electrodes, producing comparable results. The results indicate that, in regard to pacing and fibrillation thresholds, small electrodes are preferable to large.     

Assessment of groundwater depletion–induced land subsidence and characterisation of damaging cracks on houses: a case study in Mohali-Chandigarh area,India

Bulletin of Engineering Geology and the Environment - The present study identified groundwater depletion–induced land subsidence by spaceborne differential interferometric SAR (DInSAR)...     

Improvement in shape memory in magnesium niobate modified PZST

A modified lead zirconate stannate titanate system (PZST) has been studied for shape memory effect. Addition of magnesium niobate (MN) slows down the dipole relaxation process, leading to increased (∼3-fold improvement) remnant strain in the PZST system (0.99PZST–0.01PMN). Room temperature X-ray diffraction patterns before poling (antiferroelectric (AFE) tetragonal) and after poling (ferroelectric (FE) rhombohedral), clearly demonstrate that the transition to the ferroelectric phase is stable even in the absence of any electric field. A small applied electric field (∼1.7 kV/cm) in the opposite direction was required to bring the sample back to its original shape. Field-induced strain butterfly loops taken at 50 Hz show that the material response time is quite small.     

The effect of modifying an edge-plane pyrolytic graphite electrode with single-wall carbon nanotubes on its use for sensing diclofenac

A simple and highly sensitive sensor based on edge-plane pyrolytic graphite electrode (EPPGE) coated with single-wall carbon nanotubes is proposed for diclofenac determination in nanomolar concentrations. The oxidation of diclofenac occurred in two well-defined peaks having peak potentials ∼439 and ∼854 mV at pH 7.2. The modified electrode showed excellent catalytic activity presenting much higher peak currents than those measured on a bare EPPGE. Under the optimum conditions, the calibration curve was linear in the concentration range 1 × 10⁻⁹-500 × 10⁻⁹ M and 25 × 10⁻⁹-1500 × 10⁻⁹ M for peaks I and II, respectively. The limit of detection for peaks I and II was found as 0.82 × 10⁻⁹ and 22.5 × 10⁻⁹ M, respectively. The developed sensor was applied for the determination of diclofenac in biological and pharmaceutical samples using square-wave voltammetry and the validation of results using high performance liquid chromatography showed excellent agreement.     

A copper–cyclen coordination complex associated with a polyoxometalate anion: Synthesis,crystal structure and electrochemistry of [Cu(cyclen)(MeCN)][W6O19]

The reaction between Cu(NO₃)₂·3H₂O and a tetra-aza macrocycle, more specifically, cyclen in 1:1 MeCN–MeOH solvent mixture forms a Cu²⁺–cyclen coordination complex in situ, that has been reacted with an isopolyanion [W₆O₁₉]^2? in a slow diffusion technique, resulting in the isolation of an ion-pair solid [Cu(cyclen)(MeCN)][W₆O₁₉] (1). Single crystal structural investigation on 1 shows a square pyramidal geometry around the metal centre (copper ion) with an axially bound MeCN solvent molecule. The title compound 1 is the first crystallographically characterized ion-pair compound, in which a transition metal coordination complex of a tetra-aza-crown ether (cyclen) has been associated with a polyoxometalate cluster anion. This communication deals with synthesis, spectroscopic, structural and electrochemical analyses of compound 1.     

Affinity Studies of Hemicyanine Derived Water Soluble Colorimetric Probes with Reactive Oxygen/Nitrogen/Sulfur Species

Peroxynitrite (ONOO^-) is an essential endogenous reactive oxygen species (ROS) generated in mitochondria under various pathological and physiological conditions. An increase in its level in mitochondria is related to numerous diseases. Herein, we report a series of hemicyanine-derived water-soluble colorimetric probes ( 1 – 4 ) and the reactivity of which was studied with various reactive oxygen, nitrogen, and sulfur species. Probes 1 – 4 are formed by conjugating 1,2,3,3-tetramethyl-3H-indolium iodide and 4-hydroxybenzaldehyde or its derivatives through an alkene linkage formed by the Knoevenagel reaction. Oxidative cleavage of the electron-rich double bond of the conjugated hemicyanine dye revealed a discerning affinity of probe 3 towards peroxynitrite among all reactive oxygen species. The rapid change in color of 3 provides a sensitive and selective method for detecting peroxynitrite with a low detection limit of 180 nM. Notably, the water solubility of the probe displays excellent performance for the selective detection of peroxynitrite among ROS and reactive nitrogen (RNS)/sulfur species (RSS). UV-vis, ¹H NMR, and ¹³C NMR spectroscopic data and results from theoretical calculations provide further information on the interaction of peroxynitrite with probe 3 .