Interplay of Magnetic Exchange Interactions and Ni?S?Ni Bond Angles in Polynuclear Nickel(II) Complexes

The ability of bridging thiophenolate groups (RS^?) to transmit magnetic exchange interactions between paramagnetic Ni^II ions is examined. Specific attention is paid to complexes with large Ni? SR? Ni angles. For this purpose, dinuclear [Ni₂L¹(μ‐OAc)?I₂][I₅] ( 2 ) and trinuclear [Ni₃L²(OAc)₂][BPh₄]₂ ( 3 ), where H₂L¹ and H₂L² represent 24‐membered macrocyclic amino‐thiophenol ligands, are prepared and fully characterized by IR‐ and UV/Vis spectroscopy, X‐ray crystallography, static magnetization M measurements and high‐field electron spin resonance (HF‐ESR). The dinuclear complex 2 has a central N₃Ni₂(μ‐S)₂(μ‐OAc)Ni₂N₃ core with a mean Ni? S? Ni angle of 92°. The macrocycle L² supports a trinuclear complex 3 , with distorted octahedral N₂O₂S₂ and N₂O₃S coordination environments for one central and two terminal Ni^II ions, respectively. The Ni? S? Ni angles are at 132.8° and 133.5°. We find that the variation of the bond angles has a very strong impact on the magnetic properties of the Ni complexes. In the case of the Ni₂‐complex, temperature T and magnetic field B dependencies of M reveal a ferromagnetic coupling J=?29 cm^?1 between two Ni^II ions (H=JS₁S₂). HF‐ESR measurements yield a negative axial magnetic anisotropy (D<0) which implies a bistable (easy axis) magnetic ground state. In contrast, for the Ni₃‐complex we find an appreciable antiferromagnetic coupling J′=97 cm^?1 between the Ni^II ions and a positive axial magnetic anisotropy (D>0) which implies an easy plane situation.     

Microwave-induced bismuth nitrate-catalyzed synthesis of dihydropyrimidones via Biginelli condensation under solventless conditions

Microwave-induced bismuth nitrate-catalyzed efficient and extremely rapid synthesis of 4-aryl-3,4-dihydropyrimidones via Biginelli condensation reaction has been developed in excellent yield.     

Degradation of Triclosan under Aerobic, Anoxic, and Anaerobic Conditions

Triclosan (2, 4, 4??-trichloro-2??-hydroxyl diphenyl ether) is a broad-spectrum antimicrobial agent present in a number of house hold consumables. Aerobic and anaerobic enrichment cultures tolerating triclosan were developed and 77 bacterial strains tolerating triclosan at different levels were isolated from different inoculum sources. Biodegradation of triclosan under aerobic, anoxic (denitrifying and sulphate reducing conditions), and anaerobic conditions was studied in batch cultures with isolated pure strains and enrichment consortium developed. Under aerobic conditions, the isolated strains tolerated triclosan up to 1?g/L and degraded the compound in inorganic-mineral-broth and agar media. At 10?mg/L level triclosan, 95?±?1.2% was degraded in 5?days, producing phenol, catechol and 2, 4-dichlorophenol as the degradation products. The strains were able to metabolize triclosan and its degradation products in the presence of monooxygenase inhibitor 1-pentyne. Under anoxic/anaerobic conditions highest degradation (87%) was observed in methanogenic system with acetate as co-substrate and phenol, catechol, and 2, 4-dichlorophenol were among the products. Three of the isolated strains tolerating 1?g/L triclosan were identified as Pseudomonas sp. (BDC 1, 2, and 3).     

Fabrication of surfactant-free quercetin-loaded PLGA nanoparticles: evaluation of hepatoprotective efficacy by nuclear scintigraphy

Journal of Nanoparticle Research - This paper investigates the global nanotechnology and nanoscience (NN) indicators in a developmental context, during three 5-year periods from 2000 to 2014....     

Optical and electron beam studies of gamma-irradiated AlGaN/GaN high-electron-mobility transistors

The impact of ⁶⁰Co gamma-irradiation on n-channel AlGaN/GaN high-electron-mobility transistors was studied by means of temperature-dependent electron beam-induced current (EBIC) and cathodoluminescence (CL) techniques. For the doses up to ～250?Gy, an enhancement of minority carrier transport was observed as evident from the EBIC measurements. This enhancement is associated with internal electron irradiation induced by the primary gamma photons. For the doses above ～250?Gy, deterioration in minority carrier transport was explained by carrier scattering on radiation-induced defects. It is shown that calculated activation energy from the EBIC and CL measurements follows exactly the same trend, which implies that the same underlying phenomenon is responsible for observed findings.     

Iron (III) Perchlorate Adsorbed on Silica Gel: A Reagent for Organic Functional Group Transformations

Adsorption of Fe(ClO₄)₃(H₂O)₆ onto chromatographic‐grade silica gel in the presence of organic solvents (S=water, acetonitrile, or lower fatty acids) produces a supported reagent, Fe(ClO₄)₃(S)₆/SiO₂. This reagent has been found to be effective for the rapid organic functional group transformations such as dimerization of alkynes, aromatic hydrocarbons, selective oxidation of thiols to disulfides, and transannular reactions in 1,5‐cyclooctadienes on grinding using pestle and mortar in the solid state.     

A new synthesis of aryl hetaryl ketones via SRN1 reactions of halogenated heterocycles with potassiophenylacetonitrile followed by phase-transfer catalyzed decyanation

Reaction of halogenated pyridines, quinolines, pyrimidines, and pyrazines with potassiophenylacetonitrile ( 5 ) in liquid ammonia under near-uv irradiation affords secondary nitriles, which then undergo oxidative decyanation under phase-transfer catalytic conditions to afford aryl hetaryl ketones in excellent yields.     

Electrolysis of sodium chloride using composite poly(styrene-co-divinylbenzene) cation exchange membranes

Composite cation exchange membranes are prepared from cross-linked styrene-divinylbenzene copolymers for the electrolysis of sodium chloride to produce sodium hydroxide and chlorine by selective removal of sodium ions. It is prepared from a syrup of the polymer using dual initiating system and is modified with chloroacetic acid to introduce acid functional groups (COO⁻) on its surface. The effect of the modification is confirmed by FTIR, SEM, contact angle, water content, and ion exchange capacity measurements. The performance of the membrane has been evaluated in terms of current efficiency and power consumption and the effect of current density, salt concentration and flow rate on efficiency has been studied. Our membrane has an ion exchange capacity of 0.833 meq./g which is close to that of the commercially available Nafion-117 membrane having an ion exchange capacity 0.9 meq./g. The Nafion-117 used for electrodialysis of sodium sulfate has a current efficiency of around 90% and specific energy consumption of 0.1 kW/mol at 2N concentration of the salt at 1000 A/m². Our membrane used for electrodialysis of sodium chloride has a current efficiency of 93% and a power consumption of around 0.3122 kW/mol at the same concentration of salt and at a current density of 254 A/m². The two-dimensional space-charge model in cylindrical coordinates has been solved semi-analytically to obtain the effective wall potential and pore size of the membrane which are difficult to measure directly. The experimentally obtained solute flux and current density have been fitted to the model and optimum values of effective wall potential and pore diameter have been determined to be 98.5 mV and 0.8 nm, respectively.