Search results for "Single bond"

showing 10 items of 66 documents

A Molecular Electron Density Theory Study of the Role of the Copper Metalation of Azomethine Ylides in [3 + 2] Cycloaddition Reactions.

2018

The copper metalation of azomethine ylides (AYs) in [3 + 2] cycloaddition (32CA) reactions with electron-deficient ethylenes has been studied within the Molecular Electron Density Theory (MEDT) at the MPWB1K/6-311G(d,p) level, in order to shed light on the electronic effect of the metalation in the course of the reaction. Analysis of the Conceptual Density Functional Theory reactivity indices indicates that the metalation of AYs markedly enhances the nucleophilicity of these species given the anionic character of the AY framework. These 32CA reactions take place through stepwise mechanisms characterized by the formation of a molecular complex. Both nonmetalated and metalated 32CA reactions …

010405 organic chemistryChemistryMetalationOrganic ChemistryRegioselectivity010402 general chemistry01 natural sciencesMedicinal chemistryCycloaddition0104 chemical sciencesNucleophileElectronic effectSingle bondDensity functional theoryReactivity (chemistry)The Journal of organic chemistry
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Unveiling the high reactivity of cyclohexynes in [3 + 2] cycloaddition reactions through the molecular electron density theory

2018

[3 + 2] cycloaddition (32CA) reactions of cyclohexyne, a cyclic strained acetylene, with methyl azide and methoxycarbonyl diazomethane have been studied within the Molecular Electron Density Theory (MEDT) at the MPWB1K/6-311G(d) computational level. These 32CA reactions, which take place through a one-step mechanism involving highly asynchronous transition state structures, proceed with relatively low activation enthalpies of 6.0 and 4.3 kcal mol-1, respectively, both reactions being strongly exothermic. The reactions are initiated by the creation of a pseudoradical center at one of the two acetylenic carbons of cyclohexyne with a very low energy cost, 1.0 kcal mol-1, which promotes the eas…

010405 organic chemistryOrganic ChemistryRegioselectivityElectronic structure010402 general chemistry01 natural sciencesBiochemistryCycloaddition0104 chemical scienceschemistry.chemical_compoundchemistryAcetyleneComputational chemistrySingle bondReactivity (chemistry)Physical and Theoretical ChemistryGround stateMethyl azideOrganic & Biomolecular Chemistry
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Comparative evaluation of shear bond strength of universal dental adhesives : an in vitro study

2017

Background Patient demand for tooth colored restorations and desire for minimally invasive restorations have made composites an indispensable part of the restorative process. An important factor affecting the intra-oral performance of composite restorations is bonding. Material and methods Ninty six freshly extracted molar teeth were collected and occlusal 3mm is removed using a diamond disc to expose dentine. Following with samples were divided in to two main groups (self-etch & total etch). Each main group is again sub divided in to three groups each according to bonding agent used (Tetric N- Bond Universal, Single Bond Universal, Tetric N Bond Total etch in total etch group and Clear Fil…

0301 basic medicineMolar030103 biophysicsUniversal testing machineMaterials sciencebusiness.industryBond strengthComposite numberDentistry030206 dentistryDentine bonding agents:CIENCIAS MÉDICAS [UNESCO]Shear bond03 medical and health sciences0302 clinical medicinestomatognathic systemUNESCO::CIENCIAS MÉDICASSingle bondAdhesiveComposite materialbusinessGeneral Dentistry
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Investigation of molecular dimers by ensemble and single molecule spectroscopy

2002

International audience; We have investigated molecular dimers with different electronic coupling strengths by bulk and single molecule spectroscopy. In one of the dimers the two monomers (perylene-monoimide) are directly connected via a single bond while in the other one they are separated by the benzil motif. The close proximity of the monomers in the first case gives rise to excitonic band splitting which is clearly observable in the bulk absorption spectra. For the benzil structure the electronic interactions are governed by Förster-type energy hopping between the monomers. Fluorescence intensity trajectories at the single molecule level show one-step and two-step bleaching behaviour whi…

Absorption spectroscopyExcitonBiophysics010402 general chemistryPhotochemistry01 natural sciencesBiochemistrychemistry.chemical_compoundElectronic interactionsSingle bondMolecule[CHIM]Chemical SciencesEmission spectrum010405 organic chemistryGeneral ChemistryCondensed Matter PhysicsMolecular aggregatesAtomic and Molecular Physics and Optics0104 chemical sciences3. Good healthCoupling (physics)MonomerchemistryChemical physicsExcitonsBenzilSingle molecule spectroscopy
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Hydroxo Hydrido Complexes of Iron and Cobalt (Sn−Fe−Sn, Sn−Co−Sn): Probing Agostic Sn⋅⋅⋅H−M Interactions in Solution and in the Solid State

2000

Bis(toluene)iron 9 reacts with Lappert's stannylene [Sn[CH(SiMe3)2]2] (4) to form the paramagnetic bis-stannylene complex [[(eta6-toluene)Fe-Sn-[CH(SiMe3)2]2]2] (10). Compound 10 reacts with H2O to form the hydroxo hydrido complex [(eta6-C7H8)(mu-OH)(H)-Fe-[Sn[CH(SiMe3)2]2]2] (12) in high yield; its solid-state structure has been elucidated by X-ray and neutron diffraction analysis. In agreement with the 1H NMR results, 12 contains a hydridic ligand whose exact coordination geometry could be determined by neutron diffraction. The 1H and 119Sn NMR analysis of 12 suggested a multicenter Sn/Sn/H/Fe bonding interaction in solution, based on significantly large values of J(Sn,H,Fe) = 640+/-30 Hz…

Agostic interactionChemistryLigandHydrideOrganic ChemistryInorganic chemistryNeutron diffractionIsolobal principleGeneral ChemistryCatalysisCrystallographySingle bondIsostructuralCoordination geometryChemistry - A European Journal
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Analysis of the CIPSI/DCCI approach to characterize the HF AND F2 single bond

1990

Abstract The aim of the present work is to account for the main differential correlation contributions occurring during the bond breaking process of HF and F2 molecules in an accurate and inexpensive way. Starting from the dissociation-consistent configuration interaction (DCCI) scheme by Goddard and co-workers the corresponding contributions are evaluated within the framework reported by Malrieu and co-workers, namely configuration interaction by perturbation with multiconfigurational zeroth-order wavefunction selected by iterative process (CIPSI). In addition, the DCCI scheme has been improved by introducing the dispersion effects associated with the valence MOs adjacent to the bond. The …

Bond lengthValence (chemistry)Electronic correlationComputational chemistryChemistryGeneral Physics and AstronomySingle bondElectronic structurePhysical and Theoretical ChemistryConfiguration interactionWave functionMolecular physicsDiatomic moleculeChemical Physics
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Ab initio calculations on the molecular structure of fluorocyanopolyynes

1998

Abstract The molecular structure of the first three members of the fluorocyanopolyynes was studied by ab initio Hartree-Fock calculations with a polarized double zeta basis set and at MP2 level with the same basis set. Alternating triple and single bonds were found; a theoretical estimate of rotational constants and dipole moments was performed and a comparison with the available experimental data was made. An analysis of the theoretical vibrational frequencies of the title compounds was carried out.

ChemistryAb initioCondensed Matter PhysicsBiochemistryMolecular physicsDipoleAb initio quantum chemistry methodsPhysics::Atomic and Molecular ClustersSingle bondMoleculeRotational spectroscopyPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsSIESTA (computer program)Basis setJournal of Molecular Structure: THEOCHEM
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Unravelling the mechanism of the ketene-imine Staudinger reaction. An ELF quantum topological analysis

2015

The mechanism of the ketene-imine Staudinger (KI-S) reaction between t-butyl-cyano ketene and N-phenyl phenylimine has been studied using DFT methods at the MPWB1K/6-311G(d) computational level. The reaction takes place through a two-step mechanism: (i) the first step is the nucleophilic attack of the imine nitrogen lone pair on the central carbon of the ketene yielding a zwitterionic (ZW) intermediate; (ii) the second step, which is the rate- and stereoselectivity-determining step, is a ring-closure process achieved by a nucleophilic attack of the terminal carbon atom of the ketene on the imine carbon atom. Due to the unfeasibility of a cis/trans and an E/Z stereoisomerisation at the ZW in…

ChemistryStereochemistryGeneral Chemical EngineeringImineKeteneGeneral ChemistryTopologychemistry.chemical_compoundNucleophileSingle bondStaudinger reactionConrotatory and disrotatoryHOMO/LUMOLone pairRSC Advances
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Impurity levels and nonlinear optical properties of doped BaTiO3 from extended cluster LDA calculations

1997

The electronic structures of some transition-metal ions doping the ferroelectric oxide BaTiO3 are calculated through the density functional theory framework (LCAO-LSD ADF method) on extended clusters [XO6Ba8Ti6] embedded in a punctual charge set depicting the crystalline environment. The transition ions X are Fen+(n = 2, 3, 4, 5), Ti3+, Nb4+, and Nb5+. Some related defects like Fe(SINGLE BOND)Vo, where Vo stands for a lacunar oxygen site, are also investigated through a similar process. The positions of impurity levels insides the O2p(SINGLE BOND)Ti3d band gap are obtained from eigenvalues and related optical transition or ionization energies are calculated using excited states. This allows…

CrystalTetragonal crystal systemChemistryBand gapExcited stateSingle bondMolecular orbitalDensity functional theoryPhysical and Theoretical ChemistryIonization energyAtomic physicsCondensed Matter PhysicsAtomic and Molecular Physics and OpticsInternational Journal of Quantum Chemistry
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Are one-step aromatic nucleophilic substitutions of non-activated benzenes concerted processes?

2019

Aromatic nucleophilic substitution (SNAr) reactions of non-electrophilically activated benzenes have been studied within the Molecular Electron Density Theory (MEDT) at the B3LYP/6-311+G(d) computational level. These reactions, taking place through a one-step mechanism, present a high activation Gibbs free energy, ΔG≠ = 31.0 kcal mol-1, which decreases to 22.1 kcal mol-1 in the intramolecular process. A topological analysis of the electron localisation function along the reaction paths permits establishing the non-concerted nature of these SNAr reactions. A series of unstable structures, with similar electronic structures to those of Meisenheimer intermediates, are characterised. The presen…

Electron density010405 organic chemistryChemistryOrganic ChemistryOne-Step010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesGibbs free energysymbols.namesakeNucleophileNucleophilic aromatic substitutionComputational chemistryIntramolecular forcesymbolsNucleophilic substitutionSingle bondPhysical and Theoretical ChemistryOrganicbiomolecular chemistry
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