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1.
Abedien Zabardasti Ali Kakanejadifard Motaleb Ghasemian Mohammad Solimannejad 《Structural chemistry》2012,23(4):1155-1161
The molecular interactions between phosphorous ylide (PY) and HX molecules (X?=?F, CN, and N3) were investigated using the MP2 method at 6-311++G(2d,2p) basis set. Three different patterns including non-classical hydrogen bond H···C, X···P interaction and classical hydrogen bond H···X were found for complex formation between PY and HX molecules. From the predicted models, stability of the H···C type complexes are greater than other types. Quantum theories of atoms in molecules and natural bond orbitals methods have been applied to analyze the intermolecular interactions. Good correlations have been found between the interaction energies (SE), the second-order perturbation energy E (2), and the charge transfer qCT in the studied systems. 相似文献
2.
Structural Chemistry - Ab initio calculations were used to analyze the interactions among [B6H6]2? dianion with H2 molecules at the MP2/aug-cc-pVTZ computational level. The vibrational... 相似文献
3.
Abedien Zabaradsti Ali Kakanejadifard Motaleb Ghasemian Mehdi Esmaeilifar 《Structural chemistry》2013,24(5):1607-1614
The molecular interactions between sulfur ylide (SY) and HSX molecules (X = F, Cl and Br) were investigated using the MP2 method with the 6-311++G (2d, 2p) basis set. The SY (CH2=SH2) have two reactive sites: CH2 (denoted as C-interaction) and SH2 (S-interaction) that both could interact with three atoms of HSX molecules. The results show that S···C, X···C, and H···C interactions (C-interactions) is preference over the X···S, H···S, and H···X interactions. Quantum theories of atoms in molecules and natural bond orbitals methods have been applied to analyze the intermolecular interactions. Good correlations have been found between the interaction energies, the second-order perturbation energies E(2), and the charge transfer qCT in the studied systems. 相似文献
4.
Ab initio calculations were used to analyze interactions of BH4 ? with 1?C4 molecules of H2O at the MP2/6-311++G(d,p) and B3LYP/6-311++G(d,p) computational levels. The negative cooperativity for dihydrogen bond clusters containing H2O···H2O hydrogen bonds is more remarkable. The negative cooperativity is increased with increasing the size and also the number of hydrogen bonds in the cluster. The B?CH stretching frequencies show blue shifts with respect to cluster formation. Also greater blue shift of stretching frequencies where predicted for B?CH bonds which did not contribute in dihydrogen bonding with water molecules. The structures obtained have been analyzed with the Atoms in Molecules (AIM) methodology. 相似文献
5.
Ab initio and density functional calculations were used to analyze the interaction between a molecule of cyanic acid (HOCN) and up to 4 molecules of water at the B3LYP/6-311++G(d,p) and MP2/6-311++G(d,p) computational levels. The cooperative effect (CE) is increased with the increasing size of the studied clusters. Red shifts of the H–O stretching frequency for complexes involving HOCN as an H-donor were predicted. The strength of the hydrogen bonds in terms of molecular structures could be deduced from a comparison of HOCN–H2O with HCNO–H2O, HONC–H2O and HNCO–H2O HB clusters. The atom in molecules (AIM) method was used to analyze the cooperative effects on topological parameters. 相似文献
6.
The changes in stabilization energy upon the formation of intermolecular hydrogen, dihydrogen and lithium bond complexes between C2B3H7, LiH and HF have been investigated using MP2 method with aug-cc-pVDZ basis set. The interaction of HF with nido-C2B3H7 could occur through the formation of B–H?δ···+δH–F, C–H+δ···F?δ–H and B–C···H–F classical and non-classical hydrogen bonds. The B–C bonds in backbone of the C2B3H7 as electron donor interact with σ* orbital of HF as electron acceptor. Also interaction of LiH with nido-C2B3H7 resulted in B–C···Li–H and B–H···LiH lithium bonds as well as C–H···H–Li dihydrogen bond complexes. In some of these complexes, LiH interacts with B–C bonds. Results are indicating that more stable complexes belong to interaction of HF and LiH with backbone of the nido-C2B3H7. The AIM and NBO methods were used to analyze the intermolecular interactions; also the electron density at the bond critical point and the charge transfer of obtained complexes were studied. 相似文献
7.
Abedien Zabardasti Ali Kakanejadifard Mozaffar Asadi 《Journal of heterocyclic chemistry》2006,43(5):1157-1160
Some molecular adducts of dimethyltin(IV) dichloride, diphenyltin(IV) dichloride and diphenyltin(IV) dibromide with para‐substituted meso‐tetraphenylporphyrin have been prepared. This adducts with general formula [(Me2SnCl2)2H2T(4‐X)PP], [(Ph2SnCl2)2H2T(4‐X)PP], and [(Ph2SnBr2)2H2T(4‐X)PP]; {X= CH3O, CH3, H, and Cl} have been synthesized and characterized by means of 1H NMR, UV‐Vis, and elemental microanalysis methods. 相似文献
8.
A new supramolecular zinc(II) complex containing 4‐biphenylcarbaldehyde isonicotinoylhydrazone ligand: Nanostructure synthesis,catalytic activities and Hirshfeld surface analysis 下载免费PDF全文
Yunes Abbasi Tyula Abedien Zabardasti Hamid Goudarziafshar Monika Kucerakova Michal Dusek 《应用有机金属化学》2018,32(3)
A new potentially tridentate hydrazone ligand, 4‐biphenylcarbaldehyde isonicotinoylhydrazone (4‐bpinh), was prepared by the condensation of biphenyl‐4‐carboxaldehyde with isonicotinic acid hydrazide. Then, its nano‐sized and single crystal of zinc complex were synthesized using sonochemical and heat gradient methods, respectively. The structure of complex, [Zn(4‐bpinh)2 Br2] (1), was determined by single‐crystal X‐ray diffraction, FT‐IR, and elemental analysis, and the nano‐structure of complex was characterized by FT‐IR, XRD, and SEM. The single crystal X‐ray structure of complex showed that the metal center has a distorted tetrahedral geometry and the hydrazone ligand acts as monodentate trough the pyridyl N atom. Moreover, the analysis of crystal structures indicates the existence of intermolecular interactions such as N/C–H?Br/O, N/C–H?π, and π?π stacking in the stabilization of complex structure which finally led to the formation of the three‐dimensional supramolecular structure. Also, the impact of this interactions was more studied using Hirshfeld surface analysis and corresponding 2D fingerprint plots. Furthermore, the catalytic activity of 1 was studied in the selective oxidation of various sulfides to corresponding sulfoxides using hydrogen peroxide as the oxidative agent. 相似文献
9.
Theoretical investigation of linear and nonlinear optical (NLO) properties in simple complexes consist of alkali metals and π-conjugated systems have been studied at MP2/6-311++G(2d,2p) computational level. Lithium, sodium, and potassium as alkali metals were chosen for interaction with some non-aromatic, aromatic and anti-aromatic systems. For better comparison of results, the π-systems were chosen with the same carbon number: butadiene as a non-aromatic in comparison with cyclobutadiene as an anti-aromatic and hexatriene as a non-aromatic in comparison with benzene as an aromatic system. Results revealed that gap energy of studied π-systems was decreased under the interacting with alkali metals. Furthermore all designed complexes were shown very good results in average polarizability (α) and first hyperpolarizability (β 0) parameters. So these very simple dimer complexes could be introduced as promising innovative nonlinear optical materials. 相似文献
10.
Abedien Zabardasti Saeid Amani Mohammad Solimannejad Maryam Salehnassaj 《Structural chemistry》2009,20(6):1087-1092