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Öğe Azo-methoxy-calix[4]arene complexes with metal cations for chemical sensor applications: Characterization, QTAIM analyses and dispersion-corrected DFT- computations(Pergamon-Elsevier Science Ltd, 2022) Gassoumi, B.; Echabaane, M.; Ben Mohamed, F. E.; Nouar, L.; Madi, F.; Karayel, Arzu; Ben Chaabane, R.In this work, the structures, quantum chemical descriptors, morphologic characterization of the azomethoxy-calix[4]arene were investigated. The analyses and interpretation of the theoretical and the experimental IR spectroscopy results for the corresponding compounds was performed. The complexation of the azo-methoxy-calix[4]arene with Zn2+, Hg2+, Cu2+, Co2+, Ni2+, Pb2+ and Cd2+ metal cations has been calculated by the dispersion corrected density functional theory (DFT-D3). The values of the interaction energies show that the specific molecule is more selective to the Cu2+ cation. The study of the reactivity parameters confirms that the azo-methoxy-calix[4]arene molecule is more reactive and sensitive to the Cu2+ cation than that Co2+ and Cd2+. In addition, the investigation of the electrophilic and nucleophilic sites has been studied by the molecular electrostatic potential (MEP) analysis. The Hirshfeld surface (HS) analysis of the azo-methoxy-calix[4]arene-Cu2+ interaction have been used to understand the Cu...hydrogen-bond donors formed between the cation and the specific compound. The Quantum Theory of Atoms in Molecules (QTAIM) via Non covalent Interaction (NCI) analysis was carried out to demonstrate the nature, the type and the strength of the interaction formed between the Cu2+ cation and the two symmetrical ligands and the cavity. Finally, the chemical sensor properties based on the Si/SiO2/Si3N4/Azo-methoxy-calix[4]arene for detection of Cu2+ cation were studied. Sensing performances are determined with a linear range from 10(-5.2) to 10(-2.2) M. The Si/SiO2/Si3N4/azo-methoxy-calix[4]arene structure is a promoter to have a good performance sensor. (C) 2021 Elsevier B.V. All rights reserved.Öğe In silico exploration of O-H center dot center dot center dot X2+ (X = Cu, Ag, Hg) interaction, targeted adsorption zone, charge density iso-surface, O-H proton analysis and topographic parameters theory for calix[6]arene and calix[8]arene as model(Elsevier, 2021) Gassoumi, B.; Ben Mohamed, F. E.; Castro, M. E.; Melendez, F. J.; Karayel, Arzu; Nouar, L.; Ben Ouada, H.In this work, the best adsorption targeted zones of the metal cations Ag2+, Cu2+ and Hg2+ at the surfaces or inside, outside the cavity of the calix[6] (CX[6]), calix[8]arene (CX[8]), NUBMOM (NUB-.) and LAYKUR (LAY-.) have been discussed. For X2+=Ag, Cu and Hg adsorbed onto the surface of CX[6,8], NUB-., and LAY-. and the morphologies of these complexes have been explained, the specific chosen surface structure has interfacial chemical properties to facilitate the stabilization of the cation in each targeted zone. The stability mechanisms have been investigated for the specific systems to understand the role of the cooperativity of the O center dot center dot center dot H (forming a donor-acceptor couple) bonding interactions for good selectivity to the cation in each host-guest in the acetonitrile solvent medium and the gas phase. For this purpose, all the host-guests chemical structures were investigated by the IR spectroscopy and O-H proton approach. The UV-visible absorption spectroscopy and the total DOS Orbital showed that all molecules possess a maximum absorption band in the range between 0.5 and 3.5 eV assigned to pi-pi* or n-pi* transitions, the minimum band is characterized for the CX[6,8]-Cu2+, NUB-.Cu2+ and LAY-.Cu2+, while the highest band is specified for the complexation with the cation Ag2+. The Hirshfeld surface and the molecular electrostatic potential topography have demonstrated the selected targeted zone for the most stable configurations. The nature and the type of interaction formed between the chosen cation and the targeted area of the CX[6,8], NUB-. and LAY-. were typically studied by the Atom in Molecules (AIM) approach via non-covalent interaction (NCI) analyses. According to theoretical calculations, Cu2+, Ag2+ and Hg2+ cations were complexed with CX[6] and CX [8]-arenes in endo and exo-type form. In the endo complexes, it has been observed that Cu2+ and Ag2+ cations enter the lower rim space where calixarene hydroxyl groups are located and form a complex in square planer geometry, as expected. This situation shows that the copper cation is planarly located in the calixarene core. These results show that the theoretical results are in good agreement with the experimental ones. In addition, our simulations point out the calix[6] arene and calix[8]arene were complexed with cations by pinched conformation, corresponding to best stable state. (C) 2021 Elsevier B.V. All rights reserved.Öğe Revealing the effect of Co/Cu (d7/d9) cationic doping on an electronic acceptor ZnO nanocage surface for the adsorption of citric acid, vinyl alcohol, and sulfamethoxazole ligands: DFT-D3, QTAIM, IGM-NCI, and MD analysis(ELSEVIER SCIENCE SA, 2023) Gassoumi, B.; Mahmoud, A.M. Ahmed; Nasr, S.; Karayel, Arzu; Özkınalı, SevilThe electron-spin duality and propagation of the active sites of free electrons are of interest for adsorbing the guests and fixing them with strong hydrogen bonds (HB). The coherence of the systems with the guests is one of the main parameters that favor the experimentation of new systems on primary column adsorption phenomena. The stability and the adaptable symmetries in all directions justify the use of a “nanocage” (ZnO) for studying adsorption phenomena. The formation of stable electronic charge transfer paths between sites occupied by very stable atomic orbitals ensures the success of the adsorption of the ligands. Electronic characterization (MES, FMO, DOS, and cationic doping) is used to describe the movement of the intra-Cu-Co/Zn19O20 electrons. The phenomena of charge transfer, stability, types of orbital occupations, adsorption sites, electron migration direction, conductivity, and reactivity of such systems are thoroughly explored. Based on these findings, the efficiency of a Cu–Co/Zn19O20 nanocage to adsorb three different ligands (medical ligands, prostate biomarkers, and antibiotics) is studied. From the reactivity parameter discussions, it is found that the copper or cobalt-doped nanocage-Citric Acid has a strongly electronegative index (4.40 eV and 4.91 eV) and hardness (1.99 eV and 1.82 eV) properties. The Fourier transform infrared analyses and orbital localizations (? and ?) clearly demonstrate that the charge transfer occurs inter-surface, from nanocages to adsorbed ligands. Bader’s theory analysis for the adsorption ligands VA (Vinyl Alcohol), CA (Citric Acid), and SMX (Sulfamethoxazole) by the doped copper and cobalt nanocages demonstrates that these systems are much more adequate for adsorbing the ligand antibiotics than the other hosts. The highly adsorbent energy of sulfamethoxazole by Cu–Zn19O20 is equal to ? 582.86 kJ. mol-1. The IGM-NCI/ELF analyses support these findings, revealing that the Cu/Co–Zn19O20 nanocages adsorb SMX via hydrogen bonding and van der Waals interactions, as they also did in DFT-D3 and FT-IR analyses. LOL analyses support this claim by visualizing single-pair spins in excess surrounding acceptor atoms (O) in the two systems. Molecular dynamics simulations show that SMX is quickly adsorbed by nanocages of Zn19O20 doped with copper (d9) or cobalt (d7).Öğe Theoretical assessment of calix[4]arene-N-beta-ketoimine (n=1-4) derivatives: Conformational studies, optoelectronic, and sensing of Cu(2+)cation(Springer, 2021) Gassoumi, B.; Ben Mohamed, F. E.; Khedmi, N.; Karayel, Arzu; Echabaane, M.; Ghalla, H.; Ben Chaabane, R.Herein, we have investigated the key functions of the calix[4]arene, abbreviated as CX [1], and designed its several derivatives by substitution of the functional groups. Molecular geometry provides an intuitive understanding of the effect of functional groups on various physical properties. The addition of the N-beta -ketoimine (n=1-4) ligands has a direct effect on the stretching vibration of the H-bonding interaction. The results showed that all molecules possess absorption bands at 190 nm and in the range between 200 and 300 nm assigned to pi-pi* and n-pi* transitions. HOMO-LUMO energy gap of the CX[4]-N-beta -ketoimine, one with chemical hardness of 1.62 eV, has been found to be 3.24 eV calculated at B3LYP/6-31+G(d) level of theory. This finding explains the good kinetic stability of this compound. The large values of electrophilicity make the current molecules as a good electrophilic species. The atom in molecule (AIM) and the reduced density gradient (RDG) analyses showed the type and the strength of the interactions taking place between Cu2+ and the beta -ketoimine ligands.
