Search results for "functional theory"

showing 10 items of 1012 documents

Imidazole-amino acids. Conformational switch under tautomer and pH change.

2022

AbstractReplacement of the main chain peptide bond by imidazole ring seems to be a promising tool for the peptide-based drug design, due to the specific prototropic tautomeric as well as amphoteric properties. In this study, we present that both tautomer and pH change can cause a conformational switch of the studied residues of alanine (1–4) and dehydroalanine (5–8) with the C-terminal peptide group replaced by imidazole. The DFT methods are applied and an environment of increasing polarity is simulated. The conformational maps (Ramachandram diagrams) are presented and the stability of possible conformations is discussed. The neutral forms, tautomers τ (1) and π (2), adapt the conformations…

Density Functional Theory (DFT)Conformational analysisOrganic ChemistryClinical BiochemistryTautomersNon-standard amino acidsRamachandran mapBiochemistryImidazoleAmino acids
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Muscimol hydration and vibrational spectroscopy – The impact of explicit and implicit water

2022

The presented study focuses on the interaction of the well-known neurotoxin muscimol with water. Two approaches for the water solvent are applied – the explicit and the implicit. The muscimol-water clusters were obtained by the molecular dynamics simulations and the first solvation shell was kept for further studies. Implicit water was mimicked via the polarized continuum model (PCM). All three tautomeric forms of the free muscimol molecule are considered in the calculations. The combined theoretical and experimental vibrational IR and Raman studies determined the stability of the prevailing zwitterion form in water. We proved that water molecules in the first solvation shell are crucial fo…

Density Functional Theory (DFT)Hydration energyMuscimolTautomersMolecular Dynamics (MD)Hydrogen bondsJournal of Molecular Liquids
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Response calculations based on an independent particle system with the exact one-particle density matrix: Excitation energies

2012

Adiabatic response time-dependent density functional theory (TDDFT) suffers from the restriction to basically an occupied → virtual single excitation formulation. Adiabatic time-dependent density matrix functional theory allows to break away from this restriction. Problematic excitations for TDDFT, viz. bonding-antibonding, double, charge transfer, and higher excitations, are calculated along the bond-dissociation coordinate of the prototype molecules H2 and HeH+ using the recently developed adiabatic linear response phase-including (PI) natural orbital theory (PINO). The possibility to systematically increase the scope of the calculation from excitations out of (strongly) occupied into wea…

Density matrix/dk/atira/pure/sustainabledevelopmentgoals/affordable_and_clean_energyChemistrytiheysfunktionaaliteoriaGeneral Physics and AstronomyTime-dependent density functional theoryAtomic orbitalExcited stateDensity functional theorySDG 7 - Affordable and Clean EnergyPhysical and Theoretical ChemistryAtomic physicsPhysics::Chemical PhysicsAdiabatic processHOMO/LUMOExcitationdensity functional theoryJournal of Chemical Physics
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Oscillator Strengths of Electronic Excitations with Response Theory using Phase Including Natural Orbital Functionals

2013

The key characteristics of electronic excitations of many-electron systems, the excitation energies ωα and the oscillator strengths fα, can be obtained from linear response theory. In one-electron models and within the adiabatic approximation, the zeros of the inverse response matrix, which occur at the excitation energies, can be obtained from a simple diagonalization. Particular cases are the eigenvalue equations of time-dependent density functional theory (TDDFT), time-dependent density matrix functional theory, and the recently developed phase-including natural orbital (PINO) functional theory. In this paper, an expression for the oscillator strengths fα of the electronic excitations is…

Density matrixta114Chemistryexcitation energytiheysfunktionaaliteoriaGeneral Physics and AstronomyTime-dependent density functional theoryelektronitAdiabatic theoremMatrix (mathematics)Quantum mechanicsExcited stateDensity functional theoryeigenvalues and eigenfunctionsPhysical and Theoretical ChemistryAdiabatic processEigenvalues and eigenvectorsJournal of Chemical Physics
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Remote Modification of Bidentate Phosphane Ligands Controlling the Photonic Properties in Their Complexes: Enhanced Performance of [Cu(RN‐xantphos)(N…

2020

A series of copper(I) complexes of the type [Cu(HN-xantphos)(N^N)][PF6] and [Cu(BnN-xantphos)(N^N)][PF6], in which N^N = bpy, Mebpy and Me2bpy, HN-xantphos = 4,6-bis(diphenylphosphanyl)-10H-phenoxazine and BnN-xantphos = 10-benzyl-4,6-bis(diphenylphosphanyl)-10H-phenoxazine is described. The single crystal structures of [Cu(HN-xantphos)(Mebpy)][PF6] and [Cu(BnN-xantphos)(Me2bpy)][PF6] confirm the presence of N^N and P^P chelating ligands with the copper(I) atoms in distorted coordination environments. Solution electrochemical and photophysical properties of the BnN-xantphos-containing compounds (for which the highest-occupied molecular orbital is located on the phenoxazine moiety) are repor…

DenticityMaterials scienceAbsorption spectroscopyXantphosLigandQuantum yield02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic Materialschemistry.chemical_compoundCrystallographychemistryExcited stateDensity functional theory0210 nano-technologySingle crystalAdvanced Optical Materials
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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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Electronic fluxes during diels-alder reactions involving 1,2-benzoquinones: mechanistic insights from the analysis of electron localization function …

2012

By means of the joint use of electron localization function (ELF) and Thom's catastrophe theory, a theoretical analysis of the energy profile for the hetero-Diels-Alder reaction of 4-methoxy-1,2-benzoquinone 1 and methoxyethylene 2 has been carried out. The 12 different structural stability domains obtained by the bonding evolution theory have been identified as well as the bifurcation catastrophes (fold and cusp) responsible for the changes in the topology of the system. This analysis permits finding a relationship between the ELF topology and the evolution of the bond breaking/forming processes and electron pair rearrangements through the reaction progress in terms of the different ways o…

Diels-Alder reactionsElectron pairElectron localization functionMolecular StructureChemistryCatastrophe theoryRegioselectivityElectronsGeneral ChemistryElectron localization function12-benzoquinonesComputational MathematicsRegioselectivityEnergy profileNucleophileChemical physicsComputational chemistryElectrophileBenzoquinonesQuantum TheoryDensity functional theoryCatastrophe theoryJournal of Computational Chemistry
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Precise Characterization of the Rich Structural Landscape Induced by Pressure in Multifunctional FeVO4

2020

We have studied the high-pressure behavior of FeVO4 by means of single-crystal X-ray diffraction (XRD) and density functional theory (DFT) calculations. We have found that the structural sequence o...

Diffraction010405 organic chemistryChemistryPhysics::Optics010402 general chemistry01 natural sciences0104 chemical sciencesCharacterization (materials science)Inorganic ChemistryCondensed Matter::Materials ScienceCrystallographyDensity functional theoryPhysics::Chemical PhysicsPhysical and Theoretical ChemistrySequence (medicine)Inorganic Chemistry
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Defect interaction and local structural distortions in Mg-doped LaGaO3: A combined experimental and theoretical study

2017

A combined experimental and theoretical study of Mg-doped LaGaO3 electrolyte was carried out, with the aim to unveil the interaction between oxygen vacancy (Vo) and perovskite B site cations. LaGaO3 (LG) and LaGa0.875Mg0.125O2.938 (LGM0125) samples were comprehensively characterized by X-ray absorption spectroscopy (XAS) and X-ray diffraction, in order to investigate short- and long-range structures of both undoped and Mg-doped materials. XAS analysis evidenced a preferential Ga-Vo interaction in LGM0125, confirmed by periodic hybrid density functional theory calculations, which were combined with a symmetry-independent classes (SICs) approach in order to (a) obtain a detailed picture of th…

DiffractionAbsorption spectroscopyGeneral Physics and Astronomy02 engineering and technologyCrystal structure010402 general chemistry01 natural sciencesCHEMISTRY1ST PRINCIPLESRAY-ABSORPTION SPECTROSCOPYBODY DISTRIBUTION-FUNCTIONSPhysical and Theoretical ChemistryOXIDE FUEL-CELLSION CONDUCTIVITYPerovskite (structure)CONDENSED MATTERX-ray absorption spectroscopyELECTROLYTESChemistryDoping021001 nanoscience & nanotechnologyTRANSPORT0104 chemical sciencesCrystallographyX-ray crystallographyDensity functional theory0210 nano-technologyLANTHANUM GALLATE PEROVSKITEThe Journal of Chemical Physics
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Crystal structure of BaCa(CO3)2 alstonite carbonate and its phase stability upon compression

2021

Authors thank the financial support from the Spanish Ministerio de Ciencia, Innovación y Universidades (MICINN) and the Agencia Estatal de Investigación under projects MALTA Consolider Ingenio 2010 network (MAT2015-71070- REDC) and PGC2018-097520-A-I00 (cofinanced by EU FEDER funds) and from the Generalitat Valenciana under project PROMETEO/2018/123. D.S.-P. and A.O.R. acknowledge the financial support of the Spanish MINECO for RyC-2014-15643 and RyC-2016-20301 Ramón y Cajal grants, respectively. C.P. acknowledges the financial support from the Spanish Ministerio de Economia y Competitividad (MINECO project FIS2017-83295-P). Authors also thank Dr. Nicolescu and the Mineralogy and Meteoritic…

DiffractionAtmospheric SciencePhase transitionMaterials scienceCrystal chemistryAstrophysics::Instrumentation and Methods for AstrophysicsPhysics::OpticsCrystal structureengineering.materialAlstonitechemistry.chemical_compoundCrystallographychemistrySpace and Planetary ScienceGeochemistry and PetrologyCompression (functional analysis)engineeringCarbonateDensity functional theory
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