AC/DC conductivity and dielectric relaxation behavior of aqueous solutions of 1-butyl-3-methylimidazolium chloride

The complex relative dielectric function ɛ*(f) = ɛ' - jɛ" of aqueous solutions of 1-butyl-3-methylimidazolium chloride [BMiM][Cl] of varying concentrations, has been measured using precision LCR meter in the frequency range 20 Hz to 2 MHz at four different temperatures 293.15, 303.15, 313.15 and 323.15 K. Complex ac conductivity σ*(f) of the liquid samples have been determined from the measured ɛ*(f). DC conductivity σdc of the samples have also been determined. Values of σdc at different concentrations have been fitted to the empirical Casteel-Amis (CA) equation. The influence of concentration and temperature variation on the complex permittivity and electrical conductivity of the solutions of [BMiM][Cl] in distilled water has been discussed. The molar conductivities and the infinite dilution conductance of these ionic liquids have also been determined. Orientational relaxation behavior of the aqueous solutions of [BMiM][Cl] has also been studied by measuring complex permittivity in the frequency range 1 GHz to 20 GHz using vector network analyzer. Various processes contributed to the electrical/dielectric properties of the solutions of [BMiM][Cl] in distilled water have been explored

Ytterbium triflate (and trimethylsilyl triflate) catalyzed isomerization of glycidic esters to α-hydroxy-β,γ-unsaturated esters and their conversion into cyclopentanoids using Johnson-Claisen rearrangement

A variety of glycidic esters undergo smooth isomerization to the corresponding α-hydroxy-β, γ-unsaturated esters upon reaction with Yb(OTf)3 or TMSOTf. These α-hydroxy-β, γ-unsaturated esters undergo Johnson-Claisen rearrangement to appropriately substituted diesters, some of which are converted into cyclopentanoids

Microwave Dielectric Relaxation Spectroscopy of Nano Filler Loaded Epoxy Composite

643-650Present work reports the result of spectroscopic dielectric relaxation study of (Bisphenol A-(epichlorhydrin): epoxy) and hardener (N(3-dimethylaminopropyl)-1,3-propylenediamine: hardener) doped with a range of concentrations of inorganic nano-fillers (SiO2, Al2O3, TiO2 and ZnO) and their mixtures. Measurements of complex permittivity of neat epoxy (epoxy + hardener), nano-epoxy composite (nano filler + neat epoxy) and mixed-nano epoxy composites (mixed nano filler + neat epoxy) are carried out using vector network analyzer along with SPEAG dielectric assessment kit over the frequency range of 200 MHz to 20 GHz at a constant temperature of 300.15 K. Obtained results are analyzed in order to attain the structural information and polarization mechanisms exhibited in these composites. Influence of varying concentrations of inorganic nano-fillers on the dielectric behavior of neat epoxy is explicitly conferred. From the obtained dielectric properties; other microwave energy parameters like power reflected (Pr), power transmitted (Pt) and penetration depth (dp) are also determined at a spot frequency of 2.45 GHz and examined to gain additive information in view of their specific industrial and medical applications

Microwave Dielectric Relaxation Spectroscopy of Nano Filler Loaded Epoxy Composite

Present work reports the result of spectroscopic dielectric relaxation study of (Bisphenol A-(epichlorhydrin): epoxy) and hardener (N(3-dimethylaminopropyl)-1,3-propylenediamine: hardener) doped with a range of concentrations of inorganic nano-fillers (SiO2, Al2O3, TiO2 and ZnO) and their mixtures. Measurements of complex permittivity of neat epoxy (epoxy + hardener), nano-epoxy composite (nano filler + neat epoxy) and mixed-nano epoxy composites (mixed nano filler + neat epoxy) are carried out using vector network analyzer along with SPEAG dielectric assessment kit over the frequency range of 200 MHz to 20 GHz at a constant temperature of 300.15 K. Obtained results are analyzed in order to attain the structural information and polarization mechanisms exhibited in these composites. Influence of varying concentrations of inorganic nano-fillers on the dielectric behavior of neat epoxy is explicitly conferred. From the obtained dielectric properties; other microwave energy parameters like power reflected (Pr), power transmitted (Pt) and penetration depth (dp) are also determined at a spot frequency of 2.45 GHz and examined to gain additive information in view of their specific industrial and medical applications

Withanolides and related steroids

Since the isolation of the first withanolides in the mid-1960s, over 600 new members of this group of compounds have been described, with most from genera of the plant family Solanaceae. The basic structure of withaferin A, a C28 ergostane with a modified side chain forming a δ-lactone between carbons 22 and 26, was considered for many years the basic template for the withanolides. Nowadays, a considerable number of related structures are also considered part of the withanolide class; among them are those containing γ-lactones in the side chain that have come to be at least as common as the δ-lactones. The reduced versions (γ and δ-lactols) are also known. Further structural variations include modified skeletons (including C27 compounds), aromatic rings and additional rings, which may coexist in a single plant species. Seasonal and geographical variations have also been described in the concentration levels and types of withanolides that may occur, especially in the Jaborosa and Salpichroa genera, and biogenetic relationships among those withanolides may be inferred from the structural variations detected. Withania is the parent genus of the withanolides and a special section is devoted to the new structures isolated from species in this genus. Following this, all other new structures are grouped by structural types. Many withanolides have shown a variety of interesting biological activities ranging from antitumor, cytotoxic and potential cancer chemopreventive effects, to feeding deterrence for several insects as well as selective phytotoxicity towards monocotyledoneous and dicotyledoneous species. Trypanocidal, leishmanicidal, antibacterial, and antifungal activities have also been reported. A comprehensive description of the different activities and their significance has been included in this chapter. The final section is devoted to chemotaxonomic implications of withanolide distribution within the Solanaceae. Overall, this chapter covers the advances in the chemistry and biology of withanolides over the last 16 years.Fil: Misico, Rosana Isabel. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Orgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Unidad de Microanálisis y Métodos Físicos Aplicados a la Química Orgánica (i); ArgentinaFil: Nicotra, V.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Instituto Multidisciplinario de Biología Vegetal (p); Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Química Orgánica; ArgentinaFil: Oberti, Juan Carlos María. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Instituto Multidisciplinario de Biología Vegetal (p); Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Química Orgánica; ArgentinaFil: Barboza, Gloria Estela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Instituto Multidisciplinario de Biología Vegetal (p); Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Departamento de Farmacia; ArgentinaFil: Gil, Roberto Ricardo. University Of Carnegie Mellon; Estados UnidosFil: Burton, Gerardo. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Química Orgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Unidad de Microanálisis y Métodos Físicos Aplicados a la Química Orgánica (i); Argentin

Structural Modification in Carbon Nanotubes by Boron Incorporation

We have synthesized boron-incorporated carbon nanotubes (CNTs) by decomposition of ferrocene and xylene in a thermal chemical vapor deposition set up using boric acid as the boron source. Scanning and transmission electron microscopy studies of the synthesized CNT samples showed that there was deterioration in crystallinity and improvement in alignment of the CNTs as the boron content in precursor solution increased from 0% to 15%. Raman analysis of these samples showed a shift of ~7 cm−1in wave number to higher side and broadening of the G band with increasing boron concentration along with an increase in intensity of the G band. Furthermore, there was an increase in the intensity of the D band along with a decrease in its wave number position with increase in boron content. We speculate that these structural modifications in the morphology and microstructure of CNTs might be due to the charge transfer from boron to the graphite matrix, resulting in shortening of the carbon–carbon bonds

Optimizing enzymatic dyeing of wool and leather

This work reports on the environmental friendly enzymatic dyeing of wool and leather performed at low temperature and mild pH conditions without any dyeing auxiliaries. The substrates have been dyed with “in situ” generated pigment by means of laccase-catalyzed oxidative coupling of dye modifier 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) and dye precursor 1,3-benzenediol in a batchwise process. The process reaction variables (laccase, precursor and modifier concentrations, temperature and dyeing time) were optimized by response surface methodology using an appropriate experimental design. The temperature, precursor concentration, interaction between precursor and modifier and time are the most important factors in the dyeing process. The best-optimized wool dyeing conditions (2 h reaction time, 50 μl laccase (0.1 U), 500 mM precursor, 10 mM modifier at 40 °C) were then successfully applied onto leather material. The enzymatic-dyeing optimized process can be successfully performed on wool and leather at low temperature and mild pH obtaining different hues and depths of shades by varying the modifier concentration and time. The colouring enzymatic system has a good reusability (which has a huge advantage in terms of cost reduction) and washing durability and is comparable in terms of fastness properties to the traditional dyeing process for both wool and leather.The authors acknowledge the Portuguese Foundation for Science and Technology (FCT) for funding the project UID/CTM/00264/2019 and A. Zille contract IF/00071/2015