Search results for "DFT"

showing 10 items of 361 documents

Theoretical study of isomerism in phenoxyimine-based precursors of coordinative olefin polymerization catalysts

2010

Precursors of post-metallocene olefin polymerization catalysts, unlike their predecessors, are usually octahedral transition metal complexes with multidentate ligands. Such ligands may wrap around the central atom in many ways, thus yielding several isomeric species. For a wide range of phenoxyimine (FI) ligands with different substituents, all the theoretically predicted diastereomers of group 4 and 5 complexes are available synthetically. However, only one of the isomers is usually preferred, and this is determined by the nature of the substituents in the FI ligand. The origin and mechanism of such preference has not been completely elucidated. We attempted to describe it quantitatively o…

DenticitySchiff baseLigandStereochemistryProcess Chemistry and TechnologyFI catalystSubstituentDiastereomerDFTCatalysisphenoxyimineCatalysischemistry.chemical_compoundchemistryTransition metalPolymer chemistryDensity functional theoryPhysical and Theoretical Chemistryolefin polymerizationJournal of Molecular Catalysis A-Chemical
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Understanding the participation of 3-nitropyridine in polar Diels–Alder reactions. A DFT study

2015

The reactivity of 3-nitropyridine acting as an electrophilic dienophile in polar Diels-Alder (P-DA) reactions toward three different dienes of increased nucleophilicity has been theoretically studied using DFT methods at the MPWB1K/6-31G(d) level. It has been observed that this aromatic heterocyclic system suffers cycloaddition reactions yielding isoquinoline derivatives. The present DFT study establishes that while the P-DA reactions with isoprene and 1-methoxy-1,3-butadiene take place through a two-stage one-step mechanism, the use of the strong nucleophilic Danishefsky's diene changes the mechanism to a two-step one with formation of a zwitterionic intermediate. These P-DA reactions are …

DieneChemistryPARR FUNCTIONSCiencias QuímicasRegioselectivityREGIOSELECTIVITYCondensed Matter PhysicsBiochemistryCycloaddition3-NITROPYRIDINEchemistry.chemical_compoundQuímica OrgánicaNucleophileMOLECULAR MECHANISMSComputational chemistryDFT INDICESElectrophileOrganic chemistryReactivity (chemistry)Physical and Theoretical ChemistryIsoquinolinePOLAR DIELS-ALDERCIENCIAS NATURALES Y EXACTASIsopreneComputational and Theoretical Chemistry
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Elektrónová a pásová štruktúra CuMnAs študovaná optickou a fotoemissinou spektroskopiou

2017

Tetragonal phase of CuMnAs progressively appears as one of the key materials for antiferromagnetic spintronics due to efficient current-induced spin-orbit torques whose existence can be directly inferred from crystal symmetry. Theoretical understanding of spintronic phenomena in this material, however, relies on the detailed knowledge of electronic structure (band structure and corresponding wave functions) which has so far been tested only to a limited extent. We show that AC permittivity (obtained from ellipsometry) and UV photoelectron spectra agree with density functional calculations. Together with the x-ray diffraction and precession electron diffraction tomography, our analysis confi…

DiffractionCondensed Matter - Materials ScienceMaterials scienceSpintronicsCondensed matter physicsPhotoemission spectroscopyMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesspintronics DFT photoemission optical properties CuMnAs02 engineering and technologyCrystal structureElectronic structure021001 nanoscience & nanotechnology01 natural sciences3. Good healthTetragonal crystal systemCondensed Matter::Materials ScienceSpintronika DFT fotoemissia optické vlastnosti CuMnAs0103 physical sciencesPrecession electron diffraction010306 general physics0210 nano-technologyElectronic band structure
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Controlling the Formation of Sodium/Black Phosphorus IntercalationCompounds Towards High Sodium Content

2021

The solid-state synthesis of pure sodium-black phosphorus intercalation compounds (Na-BPICs) has been optimized in bulk for two stoichiometric ratios. Specifically, in-situ X-Ray diffraction (XRD) allowed the precise identification of the optimal temperature range for the formation of Na-BPICs: 94°C–96°C. Moreover, as the undesired formation of Na3P takes place at this very same range, we succeeded in introducing a new synthetic route based on a fast-thermal ball milling implementation that results in the bulk production of BPIC without Na3P in 9 out of 10 cases. Finally, by combining XRD, Raman spectroscopy, and DFT calculations we developed a new structural model for Na-based BPICs showin…

DiffractionMaterials scienceSodiumIntercalation (chemistry)Energy Engineering and Power Technologychemistry.chemical_element02 engineering and technologyblack phosphorusDFT calculations01 natural sciencessymbols.namesakeElectrochemistryintercalation compoundsElectrical and Electronic EngineeringsodiumBall mill010405 organic chemistryAtmospheric temperature range021001 nanoscience & nanotechnologyX-ray diffraction0104 chemical scienceschemistryChemical engineeringX-ray crystallographysymbols0210 nano-technologyRaman spectroscopyStoichiometryddc:547Batteries & Supercaps
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Mechanism of photoluminescence in intrinsically disordered CaZrO3 crystals: First principles modeling of the excited electronic states

2017

Abstract CaZrO3 (CZO) powders obtained by the polymeric precursor method at 400 °C, and then, the samples were annealed at different temperatures (400, 600, 800, and 1000 °C) and characterized by X-ray diffraction, Raman and ultraviolet–visible spectroscopic methods, along with photoluminescence (PL) emissions. First principle calculations based on the density functional theory (DFT), using a periodic cell models, provide a theoretical framework for understanding the PL spectra based on the localization and characterization of the ground and electronic excited states. Fundamental (singlet, s ) and excited (singlet, s* , and triplet, t* ) electronic states were localized and characterized us…

DiffractionPhotoluminescence02 engineering and technologyPL emissionsorder-disorderDFT calculations010402 general chemistry01 natural sciencessymbols.namesakeAtomic orbitalMaterials ChemistrySinglet stateChemistryMechanical EngineeringMetals and Alloys021001 nanoscience & nanotechnologyexcited electronic states0104 chemical sciencesMechanics of MaterialsExcited statesymbolsFirst principleDensity functional theoryAtomic physics0210 nano-technologyRaman spectroscopyJournal of Alloys and Compounds
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Impact of the ΔPhe configuration on the Boc-Gly-ΔPhe-NHMe conformation: experiment and theory

2019

Conformational propensities of N-t-butoxycarbonyl-glycine-(E/Z)-dehydrophenylalanine N′-methylamides (Boc-Gly-(E/Z)-ΔPhe-NHMe) in chloroform were investigated by NMR and IR techniques. The low-temperature crystal structure of the E isomer was determined by single crystal X-ray diffraction and the experimental data were elaborated by theoretical calculations using DFT (B3LYP, M06-2X) and MP2 approaches. The β-turn tendencies for both isomers were determined in the gas phase and in the presence of solvent. The obtained results reveal that the configuration of ΔPhe residue significantly affects the conformations of the studied dehydropeptides. The tendency to adopt β-turn conformations is sign…

Diffractionβ-turn tendencyCrystal structure010402 general chemistry01 natural sciencesGas phaseX-ray crystal structure analysischemistry.chemical_compoundResidue (chemistry)Peptide conformational analysisZ isomer0103 physical sciencesPhysical and Theoretical Chemistry13C NMRChloroform010304 chemical physicsDehydrophenylalanineE isomer1H NMRCondensed Matter Physics0104 chemical sciencesSolventCrystallographychemistryIR spectroscopyDFT-GIAO calculationsSingle crystalStructural Chemistry
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Experimental and theoretical characterization of chelidonic acid structure

2022

Abstract Chelidonic acid (4-oxo-4H-pyran-2,6-dicarboxylic acid) is present in plants of Papaveraceae family, especially in Chelidonium majus. Due to its anticancer, antibacterial, hepatoprotective, and antioxidant properties, it has been used in medical treatments. In this work, the X-ray structure of methanol solvate of chelidonic acid was determined. Layers of chelidonic acid are held by hydrogen bonds via COOH and C = O fragments and additionally bridged by methanol. The formed H-bond network between two acid units is different from typical –COOH dimers observed, e.g., in crystals of isophtalic acid. The molecular structure of 2,6-dimethyl-γ-pyrone (2Me4PN) and chelidonic acid, a 2,6-dic…

Dipole momentNBO chargesChelidonic acid2γ-Pyrone (4PN)6-Dimethyl-γ-pyrone (2Me4PN)Physical and Theoretical ChemistryCondensed Matter PhysicsDFTMolecular structureStructural Chemistry
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Real-space grids and the Octopus code as tools for the development of new simulation approaches for electronic systems.

2015

This Open Access Article is licensed under a Creative Commons Attribution 3.0 Unported Licence.

DiscretizationComputer sciencephysics.chem-phGeneral Physics and AstronomyFOS: Physical sciencesPhysics and Astronomy(all)Settore FIS/03 - Fisica Della MateriaDevelopment (topology)EngineeringTDDFT/dk/atira/pure/subjectarea/asjc/3100Physics - Chemical Physicsoctopus (software)Code (cryptography)Physical and Theoretical ChemistryQuantumFlexibility (engineering)/dk/atira/pure/subjectarea/asjc/1600/1606Chemical Physics (physics.chem-ph)Chemical PhysicsComputational Physics (physics.comp-ph)GridOptimal controlCondensed Matter - Other Condensed MatterComputer engineeringcond-mat.otherphysics.comp-phddc:540Physical SciencesChemical SciencesPhysics - Computational PhysicsOther Condensed Matter (cond-mat.other)Physical chemistry chemical physics : PCCP
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Molecular Electron Density Theory: A Modern View of Reactivity in Organic Chemistry

2016

A new theory for the study of the reactivity in Organic Chemistry, named Molecular Electron Density Theory (MEDT), is proposed herein. MEDT is based on the idea that while the electron density distribution at the ground state is responsible for physical and chemical molecular properties, as proposed by the Density Functional Theory (DFT), the capability for changes in electron density is responsible for molecular reactivity. Within MEDT, the reactivity in Organic Chemistry is studied through a rigorous quantum chemical analysis of the changes of the electron density as well as the energies associated with these changes along the reaction path in order to understand experimental outcomes. St…

Electron densitymolecular mechanismsChemistry OrganicPharmaceutical ScienceElectronsElectron010402 general chemistry01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-441Electron density distributionlcsh:Organic chemistryComputational chemistryDrug DiscoveryDFT reactivity indicesNon-covalent interactionsOrganic chemistryReactivity (chemistry)Physical and Theoretical Chemistryelectron densityQuantum chemicalchemistry.chemical_classification010405 organic chemistryOrganic Chemistrymolecular electron density theory0104 chemical scienceschemistrynon-covalent interactionsModels ChemicalChemistry (miscellaneous)molecular electron density theory; DFT reactivity indices; electron localisation function; non-covalent interactions; electron density; molecular mechanisms; chemical reactivityMolecular MedicineDensity functional theoryGround stateelectron localisation functionchemical reactivityMolecules; Volume 21; Issue 10; Pages: 1319
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A theoretical study on NHC-catalysed enantioselective cycloaddition of ketenes and 3-aroylcoumarins: mechanism and enantioselectivity.

2018

NHC-catalysed enantioselective cycloaddition of ketenes to 3-aroylcoumarins to yield dihydrocoumarin-fused dihydropyranones has been investigated using DFT methods at the B3LYP/6-31G* and MPWB1K/6-311G** computational levels. Two plausible mechanisms have been studied: the “ketene-first” mechanism A and the “coumarin-first” mechanism B. An analysis of the activation Gibbs free energies involved in the two competitive pathways makes it possible to rule out the pathway associated with the “coumarin-first” mechanism B. The first step of the “ketene-first” mechanism A is the formation of zwitterionic intermediate IN1-Zvia a nucleophilic attack of NHC 1 on ketene 2. A [4 + 2] cycloaddition throu…

Enantioselective010405 organic chemistryStereochemistryOrganic ChemistryEnantioselective synthesisKeteneCarbene010402 general chemistryDFT01 natural sciencesBiochemistryTransition stateCycloaddition0104 chemical sciencesAdductchemistry.chemical_compoundKetenechemistryNucleophileIntramolecular forceAroylcoumarinPhysical and Theoretical ChemistryCarbeneOrganicbiomolecular chemistry
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