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The benzimidazole moiety in the title molecule, C19H25N5O, is almost planar and oriented nearly perpendicular to the triazole ring. In the crystal, C—H...O hydrogen bonds link the molecules into a network structure. There are noμ-μinteractions present but two weak C—H...π(ring) interactions are observed. A Hirshfield surface analysis of the crystal structure indicates that the most important contributions for the crystal packing are from H...H (62.0%), H...C/ C...H (16.1%), H...N/N...H (13.7%) and H...O/O...H (7.5%) interactions. Evaluation of the electrostatic, dispersion and total energy frameworks indicate that the stabilization is dominated via the dispersion energy contributions in the title compound. [ABSTRACT FROM AUTHOR]

This work reports on an inhibition and adsorption performance study of two quinazoline derivatives ((2-(2-chlorophenyl)-2,3-dihydroquinazolin-4(1H)-one) and (2-(2,4- dichlorophenyl)-2,3-dihydroquinazolin-4(1H)-one)) named ZB3 and ZB4, which were synthesized and examined using carbon nuclear magnetic resonance (13C NMR) and proton nuclear magnetic resonance (1H NMR) spectroscopy. The assessment of the corrosion prevention of these two compounds for MS in 1.0 M HCl was performed employing potentiodynamic polarization (PDP) and (EIS) electronic impedance spectroscopy. The experiments performed showed that both derivatives operate well to prevent corrosion and their efficiencies exceed 85% at a concentration of 10-3. Moreover, it is discovered that the three chemicals' adsorption on the m-steel surface complies with Langmuir adsorption isotherm equation. The m-steel surface submerged in the corrosive solution was characterized by scanning electron spectroscopy (SEM) in conjunction with energy dispersive spectroscopy (EDS), spectroscopy using atomic force microscopy (AFM), X-Ray diffraction, and FTIR analysis. The findings showed that the examined inhibitors are well adsorbed, generating a barrier layer for the msteel's surface. DFT calculations and Monte Carlo (MC) simulation were used to directly correlate the electronic and adsorption properties, respectively, with the experimental corrosion inhibition efficiencies obtained for quinazoline and its 2 investigated derivatives. [ABSTRACT FROM AUTHOR]

In the present study, a simplest and most effective method was applied to removal of Cu2+ ions from an aqueous solution using Montmorillonite clay, nontoxic and abundantly available as an adsorbent. The used adsorbent was characterized using X-ray diffraction (XRD), the X-ray fluorescence spectrometry, Fourier Transform Infrared Spectroscopy (FT-IR) and scanning electron microscope (SEM) coupled with EDX analysis. Adsorption experiments were conducted under various conditions, i.e., contact time, initial concentration, pH of Cu(II) ions solution, adsorbent mass, and particle size. The results proved that the adsorption of Cu(II) ions by Montmorillonite clay was favorable at pH=5.5 with an extraction yield of 85% after 30 min contact. The equilibrium isotherm data were analyzed using the Langmuir and Freundlich equations. In all cases, the adsorption process fitted the second-order kinetics well, and the isotherm equation due to Freundlich showed good fits with the experimental data. In order to value our Cu-Montmorillonite clay (Cu-MC) support, we thought of applying it as recyclable heterogeneous catalyst for the condensation of Knoevenagel. The model reaction was carried out at room temperature, using a quantity of 0.5 mg of catalyst and a volume of 2ml of ethanol, the reaction yield was excellent (87%). The recyclable solid catalyst was effective for five successive cycles, indicating that this clay is a potentially eco-friendly heterogeneous catalyst. [ABSTRACT FROM AUTHOR]