Search results for "CALCULATIONS"

showing 10 items of 468 documents

Regularized pseudopotential for mean-field calculations

2019

We present preliminary results obtained with a finite-range two-body pseudopotential complemented with zero-range spin-orbit and density-dependent terms. After discussing the penalty function used to adjust parameters, we discuss predictions for binding energies of spherical nuclei calculated at the mean-field level, and we compare them with those obtained using the standard Gogny D1S finite-range effective interaction.

HistoryNuclear Theory[PHYS.NUCL]Physics [physics]/Nuclear Theory [nucl-th]Binding energyNuclear TheoryFOS: Physical sciencesSpin orbitsMean-field calculationsBinding energy01 natural sciences114 Physical sciencesEducationPseudopotentialNuclear Theory (nucl-th)Effective interactions0103 physical sciencesDensity dependentPenalty method010306 general physicsNuclear theoryPseudopotentialsPhysics010308 nuclear & particles physicsPhysicstiheysfunktionaaliteoriaPenalty functionComputer Science ApplicationsMean field theoryDensity dependentQuantum electrodynamicsydinfysiikkaMean-field level
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Structural and spectroscopic characterisation of 2-(2'-hydroxybenzoyl)pyrrole and its O-methyl derivative

2004

Abstract Density functional theory calculations on the tautomeric and conformational equilibria of 2-(2′-hydroxybenzoyl)pyrrole (HBP) and 2-(2′-methoxybenzoyl)pyrrole (MBP) were performed. Moreover, the experimental IR and UV spectra of the same compounds were recorded and compared with the theoretical data. The presence of an intramolecular hydrogen bond in HBP can be related to the biological activities of some of its derivatives.

Hydrogen bondMethyl derivativeCondensed Matter PhysicsBiochemistryTautomerSettore CHIM/08 - Chimica Farmaceuticachemistry.chemical_compoundUv spectrachemistryComputational chemistryIntramolecular forceDensity functional theoryPhysical and Theoretical ChemistryDFT calculations2-(2′-Hydroxybenzoyl)pyrrole2-(2′-Methoxybenzoyl)pyrrolePyrrole
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Molecular and crystal structure of Ac-(Z)-ΔAbu-NMe2 and Ac-DL-Abu-NMe2 as compared to those of related molecules

2004

Abstract The molecular and crystal structures of two homologous amino acid derivatives: N-acetyl-α,β-dehydro-butyrine N´,N´-dimethylamide (1) and N-acetyl-DL-butyrine N´,N´-dimethylamide (2), have been determined by X-ray crystallography. Similar solid-state association of both compounds is observed; despite different molecular conformation, they form centrosymmetric dimers linked by the intermolecular N–H…O hydrogen bonds. The conformation of two crystallographically independent molecules of 1 [with torsion angles ϕ, ψ, χ 1 ≈ (–47°, 130°, 3°), respectively] is also characteristic of other related diamides – ΔAla, ΔPhe and ΔLeu – previously studied in the solid state. To analyse whether thi…

Hydrogen bondStereochemistryChemistryIntermolecular forceAb initioN′Crystal structureSingle crystal structure analysisCondensed Matter PhysicsN′-dimethylamidesX-ray diffractionInorganic ChemistryCrystallographyButyridine derivativeAb initio quantum chemistry methodsX-ray crystallographyMoleculePeptide designGeneral Materials ScienceAb initio DFT calculationsConformational isomerismZeitschrift Fur Kristallographie
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Molecular dynamics simulations of elementary chemical processes in liquid water using combined density functional and molecular mechanics potentials.…

1997

The first molecular dynamics (MD) simulation of a chemical process in solution with an ab initio description of the reactant species and a classical representation of the solvent is presented. We study the dynamics of proton (deuterium) transfer in strongly hydrogen-bonded systems characterized by an energy surface presenting a double well separated by a low activation barrier. We have chosen the hydroxyl-water complex in liquid water to analyze the coupling between the reactive system and the environment. The proton is transferred from one well to the other with a frequency close to 1 ps−1 which is comparable to the low-frequency band associated to hindered translations, diffusional transl…

Hydrogen bonds ; Molecular dynamics method ; Ab initio calculations Ion exchange ; Solvent effects ; Reaction kinetics theory ; Density functional theory ; Intermolecular mechanicsProtonChemistryGeneral Physics and AstronomyIntermolecular mechanicsMolecular dynamics methodHydrogen bondsUNESCO::FÍSICA::Química físicaMolecular dynamicsAb initio calculations Ion exchangeDeuteriumReaction dynamicsChemical physicsComputational chemistryAb initio quantum chemistry methodsSolvent effectsReaction kinetics theoryDensity functional theoryDensity functional theoryPhysical and Theoretical ChemistrySolvent effectsChemical equilibrium:FÍSICA::Química física [UNESCO]
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Deuterium hyperfine splittings in the rotational spectrum of NH2D as revealed by Lamb-dip spectroscopy

2020

Abstract In the context of radio-astronomical observations, laboratory experiments constitute a cornerstone in the interpretation of rich line surveys due to the concomitant presence of numerous emitting molecules. Here, we report the investigation of three different rotational transitions of mono-deuterated ammonia (NH2D), a species of astrophysical interest, for which the contribution of the deuterium nuclear spin to the rotational spectrum has been resolved for the first time in the millimeter- and submillimeter-wave domain. The effect of hyperfine interactions on the rotational spectrum has been unveiled by a combined theoretical and experimental approach. Quantum-chemical calculations …

HydrogenQuantum-chemical calculationschemistry.chemical_elementContext (language use)010402 general chemistry01 natural sciencesSpectral lineDeuterium fractionationAmmoniaInterstellar medium0103 physical sciencesPhysical and Theoretical ChemistrySpectroscopyHyperfine structureSpectroscopyAstrophysics::Galaxy AstrophysicsLine (formation)Physics010304 chemical physicsSpectrometerAtomic and Molecular Physics and Optics0104 chemical sciencesDeuteriumchemistryHyperfine structureAtomic physicsLamb-dip technique
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Understanding C C bond formation in polar reactions. An ELF analysis of the Friedel Crafts reaction between indoles and nitroolefins

2013

[EN] The Friedel-Crafts (FC) reaction of N-methyl indole 1 with nitroethylene 2 has been studied using DFT methods at the B3LYP/6-31+G** level in order to characterize the bonding changes along the C-C bond-formation process in polar reactions. For this FC reaction a two-step mechanism has been found. The first step is associated with the C-C bond formation between the most electrophilic centre of nitroethylene and the most nucleophilic centre of N-methyl indole, to yield a zwitterionic intermediate IN. The second step corresponds to an intramolecular proton transfer process at IN, regenerating the aromatic system present at the indole. Despite the high electrophilic character shown by nitr…

Indole testNitroolefinsChemistryGeneral Chemical EngineeringGeneral ChemistryPhotochemistryMedicinal chemistrychemistry.chemical_compoundFriedel-CraftsNucleophileNitroethyleneIntramolecular forceElectrophileReactivity (chemistry)CalculationsHOMO/LUMOFriedel–Crafts reaction
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Theoretical study of spiropyran-merocyanine thermal isomerization.

2004

Abstract Quantum mechanical computations at DFT level were carried out on the processes involved in the thermal reaction SP ⇆ ME, where SP is the nitro-substituted spirobenzopyran (1 ′ ,3 ′ -dihydro-1 ′ ,3 ′ ,3 ′ -trimethyl-6-nitro-spiro[2H-1-benzopyran-2,2 ′ - [2H]indole]) in the closed form and ME is the corresponding open form. A detailed theoretical description of the overall reaction is reported along with the thermodynamic parameters for all intermediates and transition states. The obtained activation energy value is in agreement with the available experimental data in solution.

Indole testSpiropyranGeneral Physics and AstronomyActivation energyTransition statechemistry.chemical_compoundphotoreceptor ab initio calculations free energychemistryComputational chemistryThermalMerocyaninePhysical and Theoretical ChemistryQuantumIsomerization
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Microwave, High-Resolution Infrared, and Quantum Chemical Investigations of CHBrF2: Ground and v4 = 1 States

2011

A combined microwave, infrared, and computational investigation of CHBrF(2) is reported. For the vibrational ground state, measurements in the millimeter- and sub-millimeter-wave regions for CH(79)BrF(2) and CH(81)BrF(2) provided rotational and centrifugal-distortion constants up to the sextic terms as well as the hyperfine parameters (quadrupole-coupling and spin-rotation interaction constants) of the bromine nucleus. The determination of the latter was made possible by recording of spectra at sub-Doppler resolution, achieved by means of the Lamb-dip technique, and supporting the spectra analysis by high-level quantum chemical calculations at the coupled-cluster level. In this context, the…

InfraredChemistryAnalytical chemistryCHBrF2Context (language use)rotational spectroscopyhgh-resolution infrared spectroscopyRotational spectroscopyPhysical and Theoretical ChemistryPerturbation theoryAtomic physicsGround stateRelativistic quantum chemistryQUANTUM-CHEMICAL CALCULATIONSHyperfine structureMicrowave
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CO2 and CH2 Adsorption on Copper-Decorated Graphene: Predictions from First Principle Calculations

2022

Calculations were performed using Latvian Super Cluster (LASC), located in Center of Excellence at Institute of Solid State Physics, the University of Latvia, which is supported by European Union Horizon2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under Grant Agreement No. 739508, project CAMART2. The authors would like to express their gratitude for funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 768789 (CO2EXIDE project). In the last stage of investigation and during the preparation of the publication, the authors were assisted by the postdoc D.B. with his own funding from project No. 1.1.1.2/VIAA/l/16/147 (…

Inorganic ChemistryFirst-principles calculationsGeneral Chemical EngineeringCO2 electroreductionGeneral Materials Science:NATURAL SCIENCES::Physics [Research Subject Categories]AdsorptionNanodecorationCondensed Matter Physicsgraphene; nanodecoration; first-principles calculations; adsorption; CO<sub>2</sub> electroreductionGraphen
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Conformational Analysis of beta-Lactam-Containing Ferrocene Peptides

2009

The homochiral 3-amino-1-(4-methoxyphenyl)-4-phenyl-beta-lactam (≡ Alm) was conjugated with Boc-Ala giving Ala-Alm (9) after Boc-deprotection (Boc = tert-butoxycarbonyl, Ala = alanine). Coupling of FcCOOH (1) and Boc-Fca (10) with “ dipeptide” 9 resulted in the formation of FcCO-Ala-Alm (12) and the trisamide Boc-Fca-Ala-Alm (13), respectively (Fc = ferrocenyl, Fca = 1’ -aminoferrocene-1-carboxylic acid). The reactions were accomplished by the HOBt/EDC procedure and the products were obtained in good yields (HOBt = 1-hydroxybenzotriazole, EDC = N-(3-dimethylaminopropyl)-N’ -ethylcarbodiimide hydrochloride). Symmetrically 1, 1’ -disubstituted “ tetrapeptide” Fn(CO-Ala-Alm)2 (14) was prepared…

Inorganic Chemistryconformation analysis ; density functional calculations ; hydrogen bonds ; metallocenes ; molecular modelingchemistry.chemical_compoundDipeptidechemistryMolecular modelTetrapeptideFerroceneHydrogen bondStereochemistryIntramolecular forceLactamConjugated system
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