Optoelectronic and biological quantification of semi-conducting,crimson europium chelates with fluorinated β-keto acid and N-donor ancillary ligands

Research on Chemical Intermediates - Five luminescent ternary and one binary Europium(III) complexes were synthesised with β-keto acid as primary ligand and neocuproine(neo),...     

Identification and quantification of anthocyanins,flavonoids, and phenolic acids in flowers of Rhododendron arboreum and evaluation of their antioxidant potential

The current study aimed to investigate the anthocyanins, non-anthocyanins (flavonoids and phenolic acids), and free radicals scavenging potential in the flowers of Rhododendron arboreum using ultra high performance liquid chromatography with ion mobility quadrupole time of flight tandem mass spectrometry. A total of 25 constituents including nine anthocyanins, six phenolic acids, and ten flavonoids were identified in the flower extract. The major anthocyanins identified were cyanidin-3-O-β-galactoside ( 1 ), cyanidin-3-O-α-arabinoside ( 4 ), and cyanidin-3-O-rhamnoside ( 8 ), while quercetin glycosides were the main identified flavonoids in R. arboreum flowers. Additionally, ultra high performance liquid chromatography methods were developed and validated for the quantification of nine compounds (anthocyanins, flavonoid glycosides, and phenolic acids); five of them were quantified using internal standards. The extracts were analyzed for total phenolics (123.6 mg GAE/g), anthocyanin content (1.76% w/w), and evaluated for antioxidant properties against 2,2-diphenyl-1-picrylhydrazyl radical (IC₅₀: 102.06 and 96.92 μg/mL) and 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) radical cation (112.25 and 45.59 μM TE/g) assays. The profiling of R. arboreum for anthocyanins is reported for the first time. The findings suggest that the flowers are a promising source of bioactive constituents and could be used as functional food, antioxidants, and nutraceuticals.     

Stereoselective synthesis of trans-3-functionalized-4-pyrazolo[5,1-b]thiazole-3-carboxylate substituted β-lactams: Potential synthons for diverse biologically active agents

Abstract

An efficient protocol for the stereoselective synthesis of pyrazolo[5,1-b]thiazole-3-carboxylate tethered β-lactam conjugates 8a–j from novel pyrazolo [5,1-b]thiazole-3-carboxylate substituted Schiff’s bases 6a–f is reported here. The reaction between various ketene precursors and novel Schiff’s bases 6a–f afforded exclusive formation of trans-β-lactams 8a–j. The substrate scope of this approach was investigated extensively by varying different groups (R, Z). All the novel compounds were characterized using various spectroscopic techniques, such as FT-IR, ¹H NMR, ¹³C NMR, elemental analysis, ¹³C NMR (DEPT-135), and mass spectrometry in representative cases. Single crystal X-ray crystallographic study of trans-ethyl 7-(1-(4-methoxyphenyl)-4-oxo-3-phenoxyazetidin-2-yl)-6-methyl-2-(methylthio)pyrazolo[5,1-b]thiazole-3-carboxylate 8a has confirmed the molecular structure and the stereochemical outcome. To the best of our knowledge, the synthesis of such types of Schiff’s bases and β-lactam conjugates has not been reported so far.     

Electrooptic properties of polycrystalline SnSe thin films

It is observed from the studies of electrical resistivity of films of SnSe of different thicknesses and substrate temperatures that resistivity decreases with increase in thickness and substrate temperature. The study of variation in band gap with thickness shows a linear relationship between band gap and 1/t². Finally, band gap – substrate temperature studies show that the band gap increases with substrate temperature.     

Growth of hollow Se–Te whisker crystals

On the basis of micro- and macro-morphological studies the mechanism responsible for the growth of Se–Te whiskers has been suggested. It has been shown that Sc–Te whiskers grow by layer growth mechanism in which screw dislocation is not the source of step but the growth proceeds by two-dimensional nucleation. This has been supported by the supersaturation data. The plausible mechanism for the growth of hollow whiskers has also been suggested.     

Electrical conduction mechanism of polyvinylidenefluoride (PVDF) – polysulfone (PSF) blend film

The electrical conductivity of polyvinylidenefluoride (PVDF) – polysulfone (PSF) blend films have been measured by studying the I–V characteristics in the temperature range of 298–398 K. The results are shown by measuring the dependence of current on field, temperature, and blending compositions in the form of I–V characteristics and analysis has been made by interpretation of Poole–Frenkel, Schottky ln (J) vs. T plots, Richardson and Arrhenius plots. For individual polymers, the conduction mechanism observed to be a Poole–Frenkel type. On blending, the charge conduction appears to be the Schottky emission at lower temperature while Poole–Frenkel mechanism at higher temperature. The analysis of these results suggests that Pool–Frenkel mechanism is mainly responsible for the observed conduction. The conductivity was found to increase with an increase in the polysulfone concentration in the blend; it could be justified in terms of mobility of charge carriers. It is found that mobility of charge carriers increases with the increase in polysulfone concentration in the blend.     

Observation of a donor exciton band in silicon

Far-infrared transmission measurements on P-doped Si at donor concentrations below the metal-insulator transition show absorption bands from donor pairs. We identify the lowest energy band as charge transfer excitations from a donor to its neigbhor, forming excitons (D⁺D^-) in the Mott-Hubbard gap. The results suggest that charge transfer states in complexes dominate the low-energy optical excitations as the insulator approaches the Mott density.