Two heterocyclic oximes (E)-N-hydroxy-1-(pyridin-2-yl)methanimine (Hp2ylm) and (E)-N-hydroxy-1-(pyridin-3-yl)methanimine (Hp3ylm) were synthesized from pyridine-2-carbaldehyde and pyridine-3-carbaldehyde, respectively. These oximes were characterized by various spectroscopic tools like UV, IR, MASS and NMR. The inhibition capacity of these oximes against copper corrosion in 0.1 M HNO3 was determined by polarization and impedance spectroscopic studies (EIS). At all concentrations, Hp3ylm exhibited higher inhibition efficiency than Hp2ylm. Attempt was made to illustrate the mechanism of corrosion inhibition by these oximes with the help of adsorption isotherm, scanning electron microscopic (SEM) and quantum chemical studies.

In this review we present recent progress in the cycloaddition reactions of conjugated nitroalkenes with alkenes, conjugated 1,3-dienes or three atoms components (eg. nitrones, azides, diazocompounds, azomethine imines and ylides).

A new series of transition metal complexes of Co(III), Ni(II) and VO(IV) was synthesized with the bidentate Schiff base ligand (HL) derived from the condensation of 2-amino-3-benzyloxypyridine and 5-bromo salicylaldehyde. The synthesized Schiff base ligand and its metal complexes C1-C6 were structurally characterized by satisfactory elemental analysis, spectral studies such as (Mass, IR, ¹H and ¹³C NMR, conductance measurement, UV-vis and magnetic measurements) and thermal studies. The structure of HL was authenticated by X-ray single-crystal analysis. Hirshfeld surface analysis was carried out to understand the nature of intermolecular contacts, the fingerprint plot provides the information about the percentage contribution. Square-pyramidal geometry is proposed for VO(IV) complexes whereas octahedral geometry for Co(III) and Ni(II) complexes. The Schiff base ligand and its metal complexes have been tested in vitro for their antibacterial activities by using well diffusion method against Gram positive bacteria B. subtilis, S. aureus and Gram negative bacteria S. typhi, E. coli and antifungal activities against A. niger, A. flavus, C. albicans and A. Solani. The antimicrobial activity data show that metal complexes are more potent than the parent ligand.

Density functional theory with the basis set of 6-31+G(d) was used to investigate on the carbon nano layers, C(sp2), potential as a drug delivery system for transferring of anti-cancer drug temozolomide to the target tissue. In order to elucidate the possibility of drug transmission by utilizing a carrier, the mechanisms of direct drug degradation, and loaded drug on the carrier are analyzed and examined completely. Two possible and different pathways for direct drug hydrolysis have been considered. According to obtained results activation barriers of these two pathways are 62.17 and 72.10 kcal mol^-1, and 64.30 and 70.10 kcal mol^-1 for two gas mode and also two aqueous solvent conditions respectively. By comparison of outcomes, it can be found out that these activation barriers for both degradation pathways are significantly greater than the activation barriers for drug separation from the surface of carbon carrier (18.59 and 51.92 kcal mol^-1 for gas mode and 11.79 and 44.67 kcal mol-1 for aqueous solvent). Therefore, by studying the achieved outcomes, it can be deduced that separation and releasing of the drug from the carrier occurs faster kinetically than direct degradation of temozolomide, so the drug can reach to the target before direct decomposition.

Pentyl 2-(1H-indole-2-carboxamido)benzoate (5) is obtained in good yield as stable crystals by reaction of pentyl 2-amino benzoate (6) with indole-2-carbonyl chloride acid (7) in the presence of pyridine. The crystal structure of 5 confirms the presence of intramolecular hydrogen bonding (N-H…O) which produces a six-membered ring, and the molecules are linked together by intermolecular hydrogen forces (N-H…O).