Thermal and FTIR spectral studies of various proportions of zinc magnesium ammonium sulfate

Mixed crystals of various proportions of zinc magnesium ammonium sulfate were grown by slow evaporation of aqueous solution at room temperature. The bright and transparent crystals obtained were characterized through thermal (TG–DTA) and FTIR spectral analyses. A fitting decomposition pattern for the compound was formulated on the TG curve which shows two stage mass losses between 133 and 478.75 °C. DTA curve shows exothermic peaks in this temperature range supporting the formulated decomposition pattern. The FTIR spectra show the vibration frequencies due to the formation of zinc magnesium ammonium sulfate mixed crystals. Detailed structural analysis of the compound is under progress.     

Dopant depends on morphological and electrochemical characteristics of LiMn 2– X Mo X O4 cathode nanoparticles

For the first time, solid solutions of LiMn_2–X Mo _X O₄ nanoparticles were synthesized by combustion method at 700 °C in air. The synthesized LiMn_2–X Mo _X O₄ (X?=?0.0–0.2) nanoparticles were characterized by X-ray powder diffraction, Fourier transform infrared spectroscopy (FT-IR), Field emission-scanning electron microscopy, and Particle size analysis. The unit-cell constant is increasing from 8.237 to 8.293 Å with the increase of Mo, the presence of Mo at X?≤?0.05 in LiMn_2–X Mo _X O₄ nanoparticles retained the spinel structure (Fd-3m), whereas on increasing the Mo (X?≥?0.05 %), the ordering of Li⁺ ions in both octahedral and tetrahedral cationic position leads to the lowering of symmetry (P4₁32). On increasing the Mo content, prominent peak splitting and broadening are observed at 600–500 and 830 cm^?1 for Li–Mn–O and Mo–O respectively in the FT-IR spectra. The TG/DTA spectrum reveals that the convenient formation of Li mangano-molybdate is at 700 °C. The voltammograms of all the samples show two redox peaks centered around 4 V except for the sample with higher Mo doping (X?=?0.2). The sample with X?=?0.03 shows higher redox peak current values. A marginal increase of 146 Ω R _ct value was found for the LiMn_1.97Mo_0.03O₄ nanomaterial after 10th cycle which is rather high for the rest of the materials. A discharge capacity retention of 88 % at 50th cycle is observed for X?=?0.03 sample, while the other samples exhibit drastically reduced capacity. The LiMn_1.97Mo_0.03O₄ nanoparticle can able to deliver higher and constant discharge capacity, and it may be a good alternative for the existing cathode materials.     

Reactive iron carbonyl reagents via reaction of metal alkoxides with Fe(CO)5 or Fe2(CO)9: synthesis of cyclobutenediones via double carbonylation of alkynes

Alkoxy bases such as t-BuOK react with Fe(CO)(5) to give reactive iron carbonyl intermediates that in turn react with alkynes at 70 °C in THF to give 1,2-cyclobutenediones in 70-93% yields after CuCl(2)·2H(2)O oxidation. A novel 1,2-diacyloxyferrole derivative was isolated in the reaction of diphenylacetylene with Fe(CO)(5)/t-BuOK in the presence of acetyl chloride in contrast to the formation of a 1,4-diacyloxyferrole complex formed in the reaction using Fe(CO)(5)/Me(3)NO. The Fe(2)(CO)(9)/t-BuOK reagent system also converts the alkynes to corresponding cyclobutenediones in 63-90% yields under similar reaction conditions.     

Exploiting Boron Coordination: B←N Bond Supports a [2+2] Photodimerization in the Solid State and Generation of a Diboron Bis‐Tweezer for Benzene/Thiophene Separation

B←N coordination supports a [2+2] photodimerization in the solid state. The bond is defined by an orthogonal interaction between stilbazole and a phenylboronic ester to enable a stereocontrolled and rapid photoreaction. The cyclobutane photoproduct affords a novel diboron bis‐tweezer adduct that is used to separate a mixture of benzene and thiophene upon crystallization.     

Growth and characterization of tetramethyl ammonium tetrachloro zincate II: A ferroic crystal

Ferroic crystals of tetramethyl ammonium tetrachlorozincate (TMA-ZnCl) were grown by slow evaporation technique and the morphology of the grown crystals varies with different pH values. The compound crystallizes in orthorhombic primitive system at room temperature with non-centro symmetric space group Pmna. The grown crystals were subjected to powder X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, ultraviolet–visible–near-infrared (UV–vis–NIR) spectral studies and thermal studies. Differential scanning calorimetry (DSC) measurement confirms the existence of structural phase transition and the thermogravimetric analysis (TGA) studies reveals that the crystal is thermally stable up to 330 °C. Vicker's microhardness studies expose that the material is mechanically stable up to a load of 60 g. The laser second harmonic generation (SHG) efficiency of the grown crystal was found to be 1.3 times that of potassium dihydrogen orthophosphate (KDP) crystal.     

Cytotoxicity assessment of palbociclib-loaded chitosan-polypropylene glycol nano vehicles for cancer chemotherapy

The delivery of drugs in nanosized carriers arises as a very attractive solution. This study reports the in vitro cytotoxic effect of palbociclib loaded chitosan cross-linked polypropylene glycol nanocarriers. The nanocarriers were prepared by ion gelation using calcium chloride, calcium oxalate, and sodium tripolyphosphate as cross-linking agents. The influence of the cross-linking agent on the size and morphology of the chitosan- polypropylene glycol nanocarriers was studied by Dynamic Light Scattering (DLS), Scanning Electron Microscope (SEM), and Atomic Fluorescence Microscope (AFM). Tripolyphosphate assisted carriers was found higher amount palbociclib encapsulation capacity compared with other two carriers. The drug releasing behavior was studied at pH 6.8 which was based on the bulk erosion principal of the carriers. Palbociclib loaded chitosan-polypropylene glycol carriers were found to show excellent drug releasing kinetics and biocompatibility in in-vitro analysis. The unloaded chitosan-polypropylene glycol carrier was identified to have less inherent cytotoxicity, whereas the loaded carriers are as active as equal to pure palbociclib against the MCF-7 cancer cell line. The palbociclib loaded nanocarriers were studied to determine their potential anticancer activity against the MCF-7 cell line. The IC₅₀ values of three carriers chitosan-polypropylene glycol -I, chitosan-polypropylene glycol -II and chitosan-polypropylene glycol -III was observed 55.4, 51.0 and 38.7 mg/μL respectively. The effect of palbociclib uptake was evaluated by confocal microscopy using acridine orange/ethidium bromide and 4, 6-diamidino-2-phenylindole staining. Palbociclib loaded chitosan-polypropylene glycol nanocarriers show promise as potential candidates for cancer therapeutic applications.     

Determination and dissipation of fipronil and its metabolites in/on sugarcane crop

Fipronil has label claim for managing shoot borer and root borer of sugarcane. The dissipation and metabolism of fipronil in/on sugarcane crop have been studied under tropical field condition by employing a modified quick, easy, cheap, effective, rugged and safe sample preparation method and gas chromatography equipped with electron capture detector. The method could provide 90.27–98.97% recoveries of target analytes from cane leaves and stem with relative standard deviations of less than 5%. The sulphide, desulfinyl and sulfone metabolites of fipronil were detected along with the parent compound even in the 0-day samples of sugarcane leaves and stem collected 2 h post-foliar spraying. The total residues comprising fipronil and its three major metabolites got dissipated to 4.366 µg/g from the initial deposit of 12.977 µg/g within a day after foliar spray. Fipronil sulphide and fipronil desulfinyl were the major metabolites on sugarcane crop. The residues (both parent compound and total residues) reached below the detectable level of 0.005 µg/g on 7 and 15 days after treatment on stem and leaves, respectively. Half-life of fipronil was less than a day on sugarcane crop. The total residues had the half-life of 1.66 and 0.91 days on leaves and stem, respectively.     

Synthesis,growth and properties of a novel organic nonlinear optical material: Benzimidazolium perchlorate

Benzimidazolium perchlorate (BDP) a novel organic nonlinear optical material has been grown by slow evaporation technique. Growth parameters such as metastable zone width and induction period were determined. The relative second harmonic generation (SHG) efficiency of the material was investigated for the first time in the literature and was found to be 1.2 times higher than that of KDP. The grown crystals were subjected to X-ray diffraction, absorption spectrum, Fourier transform infrared (FT-IR) spectroscopy, thermal behavior, CHN analysis, and micro hardness studies.     

Growth and characterization of cinnamic acid–urea single crystal

A single crystal of cinnamic acid–urea was grown by slow evaporation of methanol solution at room temperature. In this research, many analytical methods such as FTIR, second harmonic generation, NMR, and TG–DTA were used. The presence of title compound in the crystal lattice has been qualitatively determined by FTIR analysis. Thermal stability of the grown crystals was evaluated by TG-DTA. Incorporation of urea increases the thermal stability insuring the suitability of material for possible non-linear optical application up to 180 °C.