Positive solutions and pattern formation in a diffusive tritrophic system with Crowley–Martin functional response

Nonlinear Dynamics - In the present work, we have studied a diffusive tritrophic food chain model in which the species at each trophic level interact in accordance with Crowley–Martin...     

Coumarins: antifungal effectiveness and future therapeutic scope

Molecular Diversity - The antifungals that are in current clinical practice have a high occurrence of a side effect and multidrug resistance (MDR). Researchers across the globe are trying to...     

Hydromagnetic instability of streaming fluids in porous medium

The instability of the plane interface between two uniform, superposed, electrically conducting and counter-streaming fluids through a porous medium is considered in the presence of a horizontal magnetic field. In the absence of surface tension, perturbations transverse to the direction of streaming are found to be unaffected by the presence of streaming if perturbations in the direction of streaming are ignored. For perturbations in all other directions there exists instability for a certain wavenumber range. The instability of this system is postponed by the presence of magnetic field. The magnetic field and surface tension are able to suppress this Kelvin-Helmholtz instability for small wavelength perturbations and the medium porosity reduces the stability range given in terms of a difference between the streaming velocities and the Alfvén velocity.This research forms a part of the research project awarded to the first author (R.C.S.) by the University Grants Commission.     

Charge plate technique in recoil study: Evidence for collection of recoil charged species from solid targets on metal electrodes

The occurrence of charge on recoil⁵⁶Mn produced by the (n,γ) reaction in polycrystalline potassium permanganate has been examined using the ‘charge plate technique’. From considerations of capture gamma ray decay schemes and internal conversion it appears that, in a condensed medium, the recoil atom develops charge after losing much of its initial kinetic energy which allows collection on charged electrodes. Preliminary findings were presented at the International Symposium on Radiochemistry and Radiation Chemistry, RC-41 BARC, Bombay, Feb. 4–6 (1991).     

Simultaneous Approximation for Generalized Baskakov-Durrmeyer-Type Operators

The present paper deals with the study of a Durrmeyer-type integral modification of certain modified Baskakov operators. Here we study simultaneous approximation properties for these operators by using the iterative combinations. We obtain an asymptotic formula and an error estimation in terms of higher order modulus of continuity for these operators.      

Sorption and concentration of51Cr(VI) traces on TiO2 and ZrO2 by radioindicator study

The carrier technique has been used to concentrate Cr(VI) radiometrically by studying the carrying efficiency as a function of pH of aqueous medium, added ions, carrying capacity, amount of carrier and subsequent desorption of the activity adsorbed under optimum experimental conditions. The study shows that under optimum experimental conditions, 0.15 g of ZrO₂ and 0.25 g of TiO₂ carry 0.01 mg and 0.001 mg of chromium respectively. Further, the activity carried under the specified conditions can be recovered more or less quantitatively by leaching the carrier.     

Antimicorbial effects of newly synthesized organotin(IV) and organolead(IV) derivatives

Triorganotin(IV) and triorganolead(IV) derivatives of the types Me₃Sn(SCZ) and Ph₃Pb(SCZ) (where SCZ^? is the anion of a semicarbanzone ligand) have been synthesized by substitution reactions of trimethyltin chloride and triphenyl-lead chloride with semicarbazones derived from heterocyclic ketones. The resulting complexes have been characterized by elemental analyses, molecualr weight determinations and conductivity measurements. The mode of bonding has been established on the basis of infrared and ¹H, ¹³C and ¹¹⁹Sn NMR spectroscopic studies. Some respresentative complexes have also been evaluated for their antimicrobial effects on different species of pathogenic fungi and bacteria; the results of these investigations have been reported in the present paper.     

Synthesis of a novel cis-proline-derived cyclic type VI beta-turn mimic via ring-closing metathesis

A cis-proline derived cyclic mimic of a type VI beta-turn is synthesized via a ring-closing metathesis reaction. The solution NMR conformational study indicates that the major conformer of the cyclic peptide adopts a type VIa beta-turn in CDCl(3) and a type VIb beta-turn in DMSO-d(6).     

Reverse turn induced pi-facial selectivity during polyaniline-supported cobalt(II) salen catalyzed aerobic epoxidation of N-cinnamoyl L-proline derived peptides

A novel chemo- and diastereoselective aerobic epoxidation of the N-cinnamoyl peptides catalyzed by polyaniline-supported cobalt(II) salen (PASCOS) is described. The N-cinnamoyl proline derived peptides 1 show a high pi-facial selectivity during these epoxidations. The origin of this diastereoselectivity in 1 has been attributed to (i) the propensity of the N-cinnamoyl proline amide to exist predominantly as trans rotamer in CDCl3, DMSO-d6, and CH3CN medium and (ii) existence of these peptides as organized structures (gamma- and beta-turns) due to the presence of intramolecular hydrogen bonds. An extensive solution NMR and MD simulation study on 1d and 1f indicates that the origin of the high pi-facial selectivity is due to the well-defined gamma- and beta-turns which result in the hindrance of one face of the cinnamoyl double bond in the transition state of the epoxidation reaction.     

Photochemical C–N bond forming reactions for the synthesis of five-membered fused N-heterocycles

Abstract

Few conversions cannot take place with ground-state reactions even with the help of a catalyst, therefore they are made to occur under photochemical conditions. The transfer of electrons took place even with the photochemical excitement of one molecule where redox reaction cannot occur at the ground state. The ground-state reactions resulted in the formation of side products. The substrates did not require any sort of chemical activation for C–N bond construction in the course of photochemical reactions. The source of energy; light has always been the interest of researchers in order to induce chemical reactions ever since the starting of scientific chemistry. The present review encloses the chemistry of photochemical transformations with a focus on their synthetic uses. The organic photochemical reactions prevent the polluting or harmful reagents thus, provides a possibility for sustainable procedures as well as green chemistry. This review article displays the formation of numerous of five-membered fused nitrogen-heterocyclic compounds.