Colossal magnetoresistance in La0.7Ca0.3−xHgxMnO3 (0⩽x⩽0.2) system over wide temperature range

The divalent substitutions in rare-earth manganites create quenched disorders; those are responsible for the modification of magnetoelectronic properties through competition of two phases. In this regards, the substitution of divalent Hg is rarely studied. Here, we present the results on effect of Hg²⁺ substitution in LCMO manganites. We have synthesized polycrystalline samples with nominal compositions La_0.7Ca_0.3?xHg_xMnO₃ (0?x?0.2) by the standard solid-state reaction method. The X-ray diffraction data revealed monophasic nature without a signature of Hg related or any other impurity phase. The ac susceptibility measurement showed variation in the magnetic transition temperature as well as the transition width. The electrical resistivity measurement showed variation in metal-insulator transition temperature. The magnetoresistance (MR) measurements were carried out at 5 T magnetic field. The samples show varying magnitude of magnetoresistance as high as 74.48%. The distinct feature seen with Hg substitution is the increase in the magnitude of MR and temperature range over which MR value is sustained. It also improves the microstructure of the samples.     

Silver nanocluster redox-couple-promoted nonclassical electron transfer: an efficient electrochemical Wolff rearrangement of alpha-diazoketones

In this work we report the unique electrocatalytic role of benzoic acid protected silver nanoclusters (Ag(n), mean core diameter 2.5 nm) in the Wolff rearrangement (Scheme 1) of alpha-diazoketones. More specifically, the presence of a Ag(n) (0)/Ag(n) (+) redox couple facilitates a nonclassical electron-transfer process, involving chemical reaction(s) interposed between two electron-transfer steps occurring in opposite directions. Consequently, the net electron transfer between the electron mediator (Ag(n)) and alpha-diazoketone is zero. In-situ UV-visible studies using pyridine as a nucleophilic probe indicate the participation of alpha-ketocarbene/ketene as important reaction intermediates. Controlled potential coulometry of alpha-diazoketones using Ag(n) as the anode results in the formation of Wolff rearranged carboxylic acids in excellent yield, without sacrificing the electrocatalyst.     

Spectroscopic studies of interaction of Safranine T with nonionic micelles and mixed micelles

The visible spectra of Safranine T (ST) in micellar solution of Brij 58, Tween 20 and Tween 40 and mixed micellar solution of Brij 58/Tween 20 and Brij 58/Tween 40 indicate formation of 1:1 charge transfer (CT) complex between acceptor ST and donor nonionic micelles and mixed micelles. The experimental CT transition energies are well correlated (through Mulliken's equation) with the vertical ionization potential of the donors. The solvent parameters, i.e. the intramolecular charge transfer energy ET(30) have been determined from the Stokes spectral shift. Variations of ionization potential and micropolarity in the mixed micellar region have been investigated as a function of surfactant composition and the obtained results in mixed micellar medium has been compared to the normal micelles. The critical micelle concentration (CMC) values determined at various surfactant compositions are lower than the ideal values indicating a synergistic interaction. The interaction parameter (beta) and micellar stability has been calculated using regular solution theory.     

Recent developments in bio-molecular electronics techniques for food pathogens

Food borne illnesses contribute to the majority of infections caused by pathogenic microorganisms. Detection of these pathogens originating from different sources has led to increased interest of researchers. New bio-molecular techniques for food pathogen detection are being developed to improve the sensor characteristics such as sensitivity, reusability, simplicity and economic viability. Present article deals with the various methods of food pathogen detection with special emphasis on bio-molecular electronics techniques such as biosensors, microarrays, electronic nose, and nano-materials based methods.     

Proteomic maps-toxicity relationship of halocarbons studied with similarity index and genetic algorithm

In this work we analyzed proteomic maps obtained from hepatocytes, which were treated with 14 halocarbons. A similarity index was introduced as a robust measure of similarity between two maps or between two selections of spots within the maps. A searching algorithm was used to identify the spots that may play an important role in toxicity mechanism. The highest correlation coefficients obtained between the similarity index and biological parameter were larger than 0.9.     

Distribution of cost and profit efficiency: Evidence from Indian banking

This paper uses the nonparametric DEA methodology to estimate cost and profit efficiency of Indian banks during the post-reform period. The results show considerable variation in average levels of profit efficiency across various ownership categories of banks. In general, state owned banks are found to be more efficient than their private counter parts. Further, efficiency tends to be low among the small banks (assets up to Rs. 50 billion), indicating that at the existing scale of operations, these banks are operating far below the efficient frontier. We also examine the distribution of efficiency using nonparametric kernel density estimates. The analysis reveals a rightward-shift of the efficiency distribution over the years. A major part of this shift comes from the state owned banks. Based on the conditional distribution, the study finds strong evidence of ownership explaining the efficiency differential of banks. Additionally, bank size and product-mix are also found to be important, although to a lesser extent.     

A practical formal synthesis of camptothecin

The synthesis of the DE ring of camptothecin using simple and inexpensive starting materials, employing an addition elimination reaction and selective esterification of an aliphatic carboxylic acid as key steps is described.     

Photophysical study of 3-acetyl-4-oxo-6,7-dihydro-12H-indolo[2,3-a]quinolizine in biomimetic reverse micellar nanocavities: a spectroscopic approach

Photophysical properties of 3-acetyl-4-oxo-6,7-dihydro-12H-indolo[2,3-a]quinolizine (AODIQ), a bioactive molecule, has been investigated in well-characterized, monodispersed biomimicking nanocavities formed by sodium bis(2-ethylhexyl)sulfosuccinate (AOT) in heptane using steady-state and picosecond time resolved fluorescence and fluorescence anisotropy. The emission behavior of AODIQ is very much dependent upon the water/surfactant mole ratio (W), i.e., on the water pool size of the reverse micellar core. AODIQ exhibits a sharp decrease in fluorescence anisotropy with increasing W, implying that the overall motional restriction experienced by the molecule is decreased with increased hydration. Some of the depth-dependent relevant fluorescence parameters, namely, fluorescence maxima and fluorescence anisotropy (r), have been monitored for exploiting the distribution and microenvironment around the probe in the reverse micelles. Fluorescence spectral position and fluorescence quenching studies suggest that the probe does not penetrate into the reverse micellar core; rather it binds at the interfacial region. Quantitaive estimates of the micropolarity and microviscosity at the binding sites of the probe molecule have been determined as a function of W.