Phenanthrene-imidazole-based fluorescent sensor for selective detection of Ag+ and F− ions: real sample application and live cell imaging

Research on Chemical Intermediates - 4-Methyl-2,6-bis(1H-phenanthro[9,10-d]imidazol-2-yl)phenol (probe-MPIP) conjugate has been designed as a selective fluorescent probe for silver (Ag+) ions. The...     

Organoruthenium(II) compounds with pyridyl benzoxazole/benzthiazole moiety: studies on DNA/protein binding and enzyme mimetic activities

We report herein synthesis and characterization of four new organoruthenium(II) complexes of the type [RuH(CO)(PPh₃)₂(L_1,2)]Cl (1, 3) and [Ru(CO)(Cl)₂(AsPh₃)(L_1,2)] (2, 4) derived from the reaction of [RuHCl(CO)(EPh₃)₃] (E = P or As) with 2-(pyridine-2yl)benzoxazole (L₁) and 2-(pyridine-2yl)benzthiazole (L₂). Single-crystal X-ray diffraction data of 2 proved octahedral geometry of the complexes with a 1?:?1 ratio between the metal and the coordinated ligands. The binding affinities of 1–4 toward calf-thymus DNA (CT-DNA) and BSA were thoroughly studied by various spectroscopic techniques. Furthermore, the coordination compounds exhibit catecholase-like activities in the aerial oxidation of 3,5-di-tert-butylcatechol to the corresponding o-quinone and phosphatase-like activities in the hydrolysis of 4-nitrophenyl phosphate to 4-nitrophenolate ion. The kinetic parameters have been determined using Michaelis–Menten approach. The highest k_cat values suggested that coordination compounds exhibit higher rates of catalytic efficacy.     

Sensing of Pyrophosphate Anion by a Fluorescent Zn(II) Complex Bearing Acenaphthene Imidazole Moiety

Journal of Analytical Chemistry - Acenaphthene imidazole ligand (AIMP) reacted with zinc acetate for the synthesis of Zn-AIMP complex which was used to detect pyrophosphate (PPi) ions in the...     

Numerical solution of the one-dimensional time-independent Schrödinger’s equation by recursive evaluation of derivatives

We develop a simple numerical method for solving the one-dimensional time-independent Schrödinger’s equation. Our method computes the desired solutions as Taylor series expansions of arbitrarily large orders. Instead of using approximations such as difference quotients for the derivatives needed in the Taylor series expansions, we use recursive formulas obtained using the governing differential equation itself to calculate exact derivatives. Since our approach does not use difference formulas or symbolic manipulation, it requires much less computational effort when compared to the techniques previously reported in the literature. We illustrate the effectiveness of our method by obtaining numerical solutions of the one-dimensional harmonic oscillator, the hydrogen atom, and the one-dimensional double-well anharmonic oscillator.     

Single-Crystalline Optical Microcavities from Luminescent Dendrimers

Microcrystallites are promising minute mirrorless laser sources. A variety of luminescent organic compounds have been exploited along this line, but dendrimers have been inapplicable owing to their fragility and extremely poor crystallinity. Now, a dendrimer family that overcomes these difficulties is presented. First-, second-, and third-generation carbazole (Cz) dendrimers with a carbon-bridged oligo(phenylenevinylene) (COPV2) core (GnCOPV2, n=1–3) assemble to form microcrystals. The COPV2 cores align uni/bidirectionally in the crystals while the Cz units in G2- and G3COPV2 align omnidirectionally. The dendrons work as light-harvesting antennas that absorb non-polarized light and transfer it to the COPV2 core, from which a polarized luminescence radiates. Furthermore, these crystals act as laser resonators, where the lasing thresholds are strongly coupled with the crystal morphology and the orientation of COPV2, which is in contrast with the conventional amorphous dendrimers.     

Double Schiff bases derivatives of chitosan by selective C-6 and C-2 oxidation mediated by 5-fluorosalicylaldehyde aniline by TG-GC-MS and TG-FTIR analysis

Abstract

This enhancement in the activity may be efficient on the basis that ligands mainly possess CH=N bond. The use of a structure-based drug design approach (SBDD) provides a way for investigation as well as to understand the molecular basis of the target protein and ligand molecule interactions at the atomic level. Structure-based drug design is the design and optimization of a chemical structure to identify a compound suitable for clinical testing the drug candidates. Chitosan is a polysaccharide with recognized biological activities for improving the functionality of polysaccharide 5-Fluorosalicylaldehyde aniline system. The used for selectively oxidized chitosan to produce tailored derivatives. C-2-5-Fluorosalicylaldehyde-C-6 aniline double Schiff base derivatives of chitosan were synthesized. The structure and properties of the newly synthesized product were characterized by FT-IR, ¹H-NMR, ¹³C-NMR, GC-Mass spectroscopy, and thermal analysis (DSC/TGA). An exothermic process discusses a DSC and TGA analysis of thermal behavior of this polymer was shown to be a possible thermal polymerization of the double bonds in the polymer chains and thermo-oxidation of the polymer.     

Sonoelectrochemical oxidation for decolorization of Reactive Red 195

The decolorization and degradation of Reactive Red 195 (RR 195) is studied using sonoelectrochemical and electrochemical oxidation. Sonoelectrochemical oxidation was found to be more efficient than electrochemical oxidation. The efficiency of decolorization was found to be 91% and 99% in the case of electrochemical and sonoelectrochemical process, respectively. The effect of different supporting electrolytes and ultrasonic power on decolorization and COD removal has been studied. The decolorization was found to be maximum in the KCl and NaCl as electrolytes. The color removal decreased with increasing ultrasonic power. Response surface methodology was used to assess optimal condition for decolorization and COD removal of RR 195. A Central Composite Design in five most important operating variables; current density, electrolyte concentration, dye concentration, time and sonication power was employed for experimental design and optimization of results. The significance of independent variables and their interactions were tested by means of the analysis of variance with 95% confidence limits. There was good agreement between the experimental and predicated values. Sonoelectrochemical degradation was found to be efficient in decolorizing simulated textile effluent. The results show that ultrasound was significantly enhanced in the electrochemical oxidation.     

Numerical solution of the Burgers’ equation by automatic differentiation

We compute the solution of the one-dimensional Burgers’ equation by marching the solution in time using a Taylor series expansion. Our approach does not require symbolic manipulation and does not involve the solution of a system of linear or non-linear algebraic equations. Instead, we use recursive formulas obtained from the differential equation to calculate exact values of the derivatives needed in the Taylor series. We illustrate the effectiveness of our method by solving four test problems with known exact solutions. The numerical solutions we obtain are in excellent agreement with the exact solutions, while being superior to other previously reported numerical solutions.