Search results for " density"

showing 10 items of 2709 documents

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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Unveiling the Reactivity of Cyclic Azomethine Ylides in [3+2] Cycloaddition Reactions within the Molecular Electron Density Theory

2020

Electron density010405 organic chemistryChemistryOrganic ChemistryReactivity (chemistry)Physical and Theoretical Chemistry010402 general chemistryPhotochemistry01 natural sciencesCycloaddition0104 chemical sciencesEuropean Journal of Organic Chemistry
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A molecular electron density theory study of the [3 + 2] cycloaddition reaction of nitrones with ketenes.

2017

The [3 + 2] cycloaddition (32CA) reaction between nitrones and ketenes has been studied within the Molecular Electron Density Theory (MEDT) at the Density Functional Theory (DFT) MPWB1K/6-311G(d,p) computational level. Analysis of the conceptual DFT reactivity indices allows the explanation of the reactivity, and the chemo- and regioselectivity experimentally observed. The particular mechanism of this 32CA reaction involving low electrophilic ketenes has been elucidated by using a bonding evolution theory (BET) study. It is determined that this reaction takes place in one kinetic step only but in a non-concerted manner since two stages are clearly identified. Indeed, the formation of the se…

Electron density010405 organic chemistryChemistryStereochemistryOrganic ChemistryRegioselectivity010402 general chemistryKinetic energy01 natural sciencesBiochemistryCycloaddition0104 chemical sciencesEvolution theoryComputational chemistryElectrophileDensity functional theoryReactivity (chemistry)Physical and Theoretical ChemistryOrganicbiomolecular chemistry
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Understanding the Origin of the Regioselectivity in Non-polar [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory

2020

The regioselectivity in non-polar [3+2] cycloaddition (32CA) reactions has been studied within the Molecular Electron Density Theory (MEDT) at the B3LYP/6-311G(d,p) level. To this end, the 32CA reactions of nine simplest three-atom-components (TACs) with 2-methylpropene were selected. The electronic structure of the reagents has been characterized through the Electron Localisation Function (ELF) and the Conceptual DFT. The energy profiles of the two regioisomeric reaction paths and ELF topology of the transition state structures are studied to understand the origin of the regioselectivity in these 32CA reactions. This MEDT study permits to conclude that the least electronegative X1 end atom…

Electron density010405 organic chemistryChemistrymolecular electron density theoryRegioselectivityElectronic structure010402 general chemistryelectronegativity7. Clean energy01 natural sciencesCycloaddition3. Good health0104 chemical sciencesElectronegativitynon-polar [3+2] cycloaddition reactionsComputational chemistryregioselectivityAtomSingle bondNon polarmolecular mechanismorganic_chemistryTopology (chemistry)Organics
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Understanding the domino reaction between 1-diazopropan-2-one and 1,1-dinitroethylene. A molecular electron density theory study of the [3 + 2] cyclo…

2017

The reaction between 1-diazopropan-2-one and 1,1-dinitroethylene has been studied using the Molecular Electron Density Theory (MEDT) at the B3LYP/6-31G(d,p) computational level. This reaction comprises two domino processes initialised by a common [3 + 2] cycloaddition (32CA) reaction yielding a 1-pyrazoline, which participates in two competitive reaction channels. Along channel I, 1-pyrazoline firstly tautomerises to a 2-pyrazoline, which by a proton abstraction and spontaneous loss of nitrite anion yields the final pyrazole, while along channel II, the thermal extrusion of the nitrogen molecule in 1-pyrazoline gives a very reactive diradical intermediate which quickly yields the final gem-…

Electron density010405 organic chemistryDiradicalGeneral Chemical EngineeringGeneral ChemistryPyrazole010402 general chemistryPhotochemistry01 natural sciencesDominoCycloaddition0104 chemical scienceschemistry.chemical_compoundchemistryCascade reactionElectrophileReactivity (chemistry)RSC Advances
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On the nature of organic electron density transfer complexes within molecular electron density theory.

2019

The structural features of a series of organic molecular complexes formed between the strong electrophilic tetracyanoethylene and twelve benzene derivatives with increased nucleophilic character, herein called Electron Density Transfer Complexes (EDTCs), have been studied using Molecular Electron Density Theory. The favourable nucleophilic/electrophilic interactions, which favour the global electron density transfer (GEDT) towards the electrophile, are responsible for the formation of these species. Molecular complexes presenting a GEDT above 0.05e are classified as EDTCs. Analysis of the Parr functions of the separated reagents and the topological analysis of the electron density of the ED…

Electron density010405 organic chemistryOrganic ChemistryElectronic structureTetracyanoethylene010402 general chemistry01 natural sciencesBiochemistry0104 chemical scienceschemistry.chemical_compoundNucleophilechemistryComputational chemistryReagentElectrophileBenzene derivativesPhysical and Theoretical ChemistryOrganicbiomolecular chemistry
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A molecular electron density theory study of the [3 + 2] cycloaddition reaction between an azomethine imine and electron deficient ethylenes

2018

Electron density010405 organic chemistryOrganic ChemistryImineElectron010402 general chemistryPhotochemistry01 natural sciencesCycloaddition0104 chemical scienceschemistry.chemical_compoundchemistryMolecular mechanismPhysical and Theoretical ChemistrySelectivityJournal of Physical Organic Chemistry
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How does the global electron density transfer diminish activation energies in polar cycloaddition reactions? A Molecular Electron Density Theory study

2017

Abstract The key role of the Global Electron Density Transfer (GEDT) in polar cycloaddition reactions is analysed within the Molecular Electron Density Theory (MEDT) using Density Functional Theory (DFT) calculations at the MPWB1K/6-311G(d) computational level. A comparative MEDT study of the non-polar Diels-Alder reaction between cyclopentadiene (Cp) and ethylene and the polar Diels-Alder reaction between Cp and tetracyanoethylene makes it possible to establish that the GEDT taking place in the direction of the transition state structures favours the bonding changes required for the formation of the new C C single bonds along polar cycloaddition reactions. Analysis of the reactivity indice…

Electron density010405 organic chemistryStereochemistryOrganic ChemistryTetracyanoethylene010402 general chemistry01 natural sciencesBiochemistryCycloaddition0104 chemical scienceschemistry.chemical_compoundchemistryChemical physicsDrug DiscoveryPolarSingle bondReactivity (chemistry)Density functional theoryGround stateTetrahedron
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Investigating the Response of Loop Plasma to Nanoflare Heating Using RADYN Simulations

2018

We present the results of 1D hydrodynamic simulations of coronal loops that are subject to nanoflares, caused by either in situ thermal heating or nonthermal electron (NTE) beams. The synthesized intensity and Doppler shifts can be directly compared with Interface Region Imaging Spectrograph (IRIS) and Atmospheric Imaging Assembly (AIA) observations of rapid variability in the transition region (TR) of coronal loops, associated with transient coronal heating. We find that NTEs with high enough low-energy cutoff (EC) deposit energy in the lower TR and chromosphere, causing blueshifts (up to approximately 20 kilometers per second) in the IRIS Si IV lines, which thermal conduction cannot repro…

Electron density010504 meteorology & atmospheric sciencesFOS: Physical sciencesAstrophysicsElectron01 natural sciencesSun: activity0103 physical sciencesAstrophysics::Solar and Stellar AstrophysicsSun: transition region010303 astronomy & astrophysicsChromosphereSolar and Stellar Astrophysics (astro-ph.SR)0105 earth and related environmental sciencesPhysicsSun: coronaAstronomy and AstrophysicsPlasmaCoronal loopAstronomy and AstrophysicThermal conductionNanoflaresIntensity (physics)Astrophysics - Solar and Stellar Astrophysicsline: profileSpace and Planetary SciencePhysics::Space PhysicsThe Astrophysical Journal
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Carbonyl compounds of Rh, Ir, and Mt: electronic structure, bonding and volatility

2020

With the aim to render assistance to future experiments on the production and investigation of chemical properties of carbonyl compounds of element 109, Mt, calculations of the molecular properties of M(CO)4 and MH(CO)4, where M = Rh, Ir, and Mt, and of the products of their decomposition, M(CO)3 and MH(CO)3, were performed using relativistic Density Functional Theory and Coupled-Cluster methods implemented in the ADF, ReSpect and DIRAC software suites. According to the results, MH(CO)4 should be formed at experimental conditions from the M atom with a mixture of CO and He gases. The calculated first M–CO bond dissociation energies (FBDE) of Mt(CO)4 and MtH(CO)4 turned out to be significant…

Electron densityAdsorptionChemistryGeneral Physics and AstronomyPhysical chemistryDensity functional theoryInteraction modelElectronic structurePhysical and Theoretical ChemistryVolatility (chemistry)QuartzBond-dissociation energyPhysical Chemistry Chemical Physics
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