Search results for " DFT."

showing 10 items of 87 documents

DFT/TD-DFT Framework of Mixed-Metal Complexes with Symmetrical and Unsymmetrical Bridging Ligands—Step-By-Step Investigations: Mononuclear, Dinuclear…

2021

Recently, mono- and dinuclear complexes have been in the interest of scientists due to their potential application in optoelectronics. Herein, progressive theoretical investigations starting from mononuclear followed by homo- and heterometallic dinuclear osmium and/or ruthenium complexes with NCN-cyclometalating bridging ligands substituted by one or two kinds of heteroaryl groups (pyrazol-1-yl and 4-(2,2-dimethylpropyloxy)pyrid-2-yl) providing the short/long axial symmetry or asymmetry are presented. Step-by-step information about the particular part that built the mixed-metal complexes is crucial to understanding their behavior and checking the necessity of their eventual studies. Evaluat…

TechnologyMicroscopyQC120-168.85complexesTQH201-278.5pyrene bridging ligands; complexes; osmium; ruthenium; DFT; TD-DFTosmiumEngineering (General). Civil engineering (General)DFTArticleTK1-9971pyrene bridging ligandsDescriptive and experimental mechanicsGeneral Materials ScienceElectrical engineering. Electronics. Nuclear engineeringTA1-2040rutheniumTD-DFTMaterials
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Oxadiazolyl-pyridines and perfluoroalkyl-carboxylic acids as building blocks for protic ionic liquids: crossing the thin line between ionic and hydro…

2012

A series of 18 samples has been prepared in order to obtain fluorinated materials as Protic Ionic Liquids (PILs). These were synthesized by appropriately mixing 1,2,4-oxadiazoles derivatised with two pyridines, or one pyridine and a fluorinated chain, and perfluoroalkyl-carboxylic acids, either mono- or dicarboxylic, leading to symmetric and non-symmetric materials. Many of them showed low melting points. However, the possibility of classifying the synthesized materials as PILs is discussed in terms of effective ionicity of the systems by the combination of Density Functional Theory (DFT) calculation and IR spectroscopy. The important outcome of our investigation is that the complete proton…

Thermogravimetric analysisInorganic chemistryionic liquids; sold state nmr; Differential scanning calorimetry; DFT calculationsGeneral Physics and AstronomyIonic bondingInfrared spectroscopysold state nmrDFT calculationsionic liquidschemistry.chemical_compoundDifferential scanning calorimetrychemistryDifferential scanning calorimetryIonic liquidPyridinePolymer chemistryMelting pointDensity functional theoryProtic Ionic Liquids Fluorinated compoundsPhysical and Theoretical ChemistryPhysical chemistry chemical physics : PCCP
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Through-space spin-spin coupling in acetylenic systems. Ab initio and DFT calculations

2003

Abstract: We have investigated, by means of ab initio and DFT calculations, the magnitude of through-space spin-spin couplings ( J CH and J HH ) in CH/π bonded van der Waals dimers involving acetylene, and in a structurally related covalent compound (4-ethynylphenanthrene). Within regions where the interaction is stabilizing J HH couplings are very small (< 0.1 Hz) for all complexes. In the acetylene-methane complex J CH is also very small, whereas in the acetylene-benzene complex and the acetylene dimer it shows a relatively large dependence on the tilt angle from the T-shaped arrangement, for which the smallest values are calculated, to a parallel slipped arrangement where J CH is ca. 0.5…

Through-space couplingDimerAb initioDFTCatalysisspin-spin couplinglcsh:ChemistryInorganic Chemistrychemistry.chemical_compoundsymbols.namesakeNMR spectroscopyComputational chemistryThrough-space coupling / NMR / ab initio / DFTPhysics::Atomic and Molecular ClustersPhysics::Chemical PhysicsPhysical and Theoretical ChemistryNMR spectroscopy; computational chemistry; spin-spin couplingSpin (physics)lcsh:QH301-705.5Molecular BiologySpectroscopyCouplingab initioChemistryOrganic ChemistryGeneral MedicineNuclear magnetic resonance spectroscopycomputational chemistryNMRComputer Science ApplicationsCrystallographylcsh:Biology (General)lcsh:QD1-999AcetyleneCovalent bondsymbolsCondensed Matter::Strongly Correlated ElectronsComputingMethodologies_GENERALvan der Waals force
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Theoretical study of the interaction between sodium ion and a cyclopeptidic tubular structure.

2007

DFT calculations have been carried out to describe the pathway of a sodium ion along the stacking direction of a tubular structure set up by five cyclopeptidic units, which can be considered a suitable model of a hollow tubular structure of indefinite length. A lattice of points inside the tubular structure is defined and the DFT interaction energy values with a sodium ion are obtained. The data allow predicting a zigzag path of the ion inside the hosting structure. © 2007 Wiley Periodicals, Inc. J Comput Chem, 2007

Tubular aggregates alkaline ions DFTModels MolecularNanotubes PeptideNanotubeChemistrySodiumSodiumStackingGlycineMolecular Conformationchemistry.chemical_elementGeneral ChemistryInteraction energyMolecular physicsPeptides CyclicIonComputational MathematicsZigzagComputational chemistryLattice (order)ThermodynamicsComputer SimulationOligopeptidesJournal of computational chemistry
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Structural, energetic and kinetic database of catalytic reactions: Benzyl alcohol to benzaldehyde oxidation on MnOx clusters

2021

Abstract Data here reported are connected with the research article “Benzyl Alcohol to Benzaldehyde Oxidation on MnO x Clusters: Unraveling Atomistic Features” Gueci et al. [1] . This work described and discussed structural and energetic results, calculated by Density Functional Theory (DFT). In order to get kinetic information, DFT results were refined by an original approach, which will be shortly described in the following article. The crossed analysis of experimental and computational energetic and kinetic data allowed to (i) reconstruct the complicated lattice that connects the primary and secondary mechanisms of the reaction and (ii) identify alternative process pathways capable of by…

Work (thermodynamics)Science (General)MultidisciplinaryMaterials scienceMnOx Oxidative–dehydrogenation Deactivation Remediation DFT Reaction kineticMnOxComputer applications to medicine. Medical informaticsKineticsDeactivationReaction kineticR858-859.7RemediationAlternative processHeterogeneous catalysisDFTCatalysisBenzaldehydeQ1-390chemistry.chemical_compoundchemistryBenzyl alcoholComputational chemistryDensity functional theoryOxidative–dehydrogenationSettore CHIM/02 - Chimica FisicaData in Brief
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Comparative Experimental and Theoretical Study of the Fe L-2,L-3-Edges X-ray Absorption Spectroscopy in Three Highly Popular, Low-Spin Organoiron Com…

2019

The occupied and unoccupied electronic structures of three highly popular, closed shell organoiron complexes ([Fe(CO)(5)], [(eta(5)-C5H5 )Fe(CO)(mu-CO)](2), and [(eta(5)-C5H5)(2)Fe]) have been theoretically investigated by taking advantage of density functional theory (DFT) calculations coupled to the isolobal analogy (Elian et al. Inorg. Chem. 1976, 15, 1148). The adopted approach allowed us to look into the relative role played by the ligand -&gt; Fe donation and the Fe -&gt; ligand back-donation in title molecules, as well as to investigate how CO- (terminal or bridging) and [(eta(5)-C5H5)](-)-based pi* orbitals compete when these two ligands are simultaneously present as in [(eta(5)-C5H…

XASXAS spectroscopy Organoiron complexes DFT.High Resolution X-Ray Absorption SpectroscopyFe L23 edgegas phasedensity functional theory
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Unveiling the Unexpected Reactivity of Electrophilic Diazoalkanes in [3+2] Cycloaddition Reactions within Molecular Electron Density Theory

2021

The [3+2] cycloaddition (32CA) reactions of strongly nucleophilic norbornadiene (NBD), with simplest diazoalkane (DAA) and three DAAs of increased electrophilicity, have been studied within the Molecular Electron Density Theory (MEDT) at the MPWB1K/6-311G (d,p) computational level. These pmr-type 32CA reactions follow an asynchronous one-step mechanism with activation enthalpies ranging from 17.7 to 27.9 kcal&middot

analytical_chemistryExergonic reactiondiazoalkanes010405 organic chemistryNorbornadienemolecular electron density theoryGeneral Medicine010402 general chemistry01 natural sciencesCycloadditionElectron localization function3. Good health0104 chemical scienceslcsh:Chemistrychemistry.chemical_compoundlcsh:QD1-999conceptual DFTchemistryNucleophileComputational chemistryelectron localization functionElectrophilenorbornadieneReactivity (chemistry)Acetonitrile
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Effects of the net charge on abundance and stability of supramolecular surfactant aggregates in gas phase

2011

Self-assembling of amphiphilic molecules under electrospray ionization (ESI) conditions is characterized by quite unexpected phenomenology. The noticeable differences with respect to the condensed phase are attributable to the absence of the surfactant-solvent interactions, the presence of net charge in the aggregates, and the strong deviation from equilibrium conditions. Aiming to investigate the effects of the net charge on abundance and stability of supramolecular surfactant aggregates, positively and negatively charged aggregates of sodium bis(2-ethylhexyl)sulfosuccinate (AOT) and sodium methane sulfonate (MetS), butane sulfonate (ButS) and octane sulfonate (OctS) have been studied by E…

anhydrous reverse micellechemistry.chemical_classificationself-assembling; anhydrous reverse micelles; electrospray ionization; energy-resolved mass spectrometry; DFT calculationsChemistryElectrospray ionizationenergy-resolved mass spectrometryelectrospray ionizationSupramolecular chemistryAnalytical chemistryMethane sulfonateDFT calculationsPhotochemistryMass spectrometryself-assemblingchemistry.chemical_compoundSulfonatePhase (matter)SpectroscopyAlkylOctane
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Alkane dehydrogenation on defective BN quasi-molecular nanoflakes: DFT studies

2020

Lower alkanes are feedstocks readily available but relatively inert. The con- version of low cost alkanes to industrially relevant alkenes is usually carried out on metal-based heterogeneous catalysts. Considering both the cost and the potential harmfulness of the metal involved in the dehydrogenation cat- alysts (typically, platinum or chromium), the study of metal-free processes represents an important challenge for the industrial chemistry in order to address more sustainable protocols and different routes either to activate or transform alkanes. Framed in this context, it was investigated, using a den- sity functional theory approach, the potential dehydrogenation activity of de- fectiv…

chemistry.chemical_classificationAlkaneMaterials science010405 organic chemistryProcess Chemistry and Technologychemistry.chemical_elementContext (language use)010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundHydrocarbonchemistryChemical engineeringBoron nitrideSettore CHIM/03 - Chimica Generale E InorganicaDehydrogenationPhysical and Theoretical ChemistryPlatinumBoronMetal-free processes Low cost alkanes conversion Quasi-molecular BN nanoflakes DFT modeling
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Counterion influence on the N–I–N halogen bond

2015

A detailed investigation of the influence of counterions on the [N–I–N]+ halogen bond in solution, in the solid state and in silico is presented. Translational diffusion coefficients indicate close attachment of counterions to the cationic, three-center halogen bond in dichloromethane solution. Isotopic perturbation of equilibrium NMR studies performed on isotopologue mixtures of regioselectively deuterated and nondeuterated analogues of the model system showed that the counterion is incapable of altering the symmetry of the [N–I–N]+ halogen bond. This symmetry remains even in the presence of an unfavorable geometric restraint. A high preference for the symmetric geometry was found also in …

chemistry.chemical_classificationHalogen bond010405 organic chemistryHydrogen bondcounterion; halogen bond; single crystal X-ray diffraction; DFT computationInorganic chemistryGeneral ChemistryNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciencesN–I–N halogen bond0104 chemical sciencesCrystallographyChemical bondchemistryTransition metalCounterionta116Single crystalBasis setChemical Science
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