Search results for "Density Functional Theory."

showing 10 items of 935 documents

Kompleksy metali przejściowych z zasadami Lewisa jako prekursory katalizatorów polimeryzacji olefin. Cz. II. Postęp w komputerowym projektowaniu kata…

2001

Dokonano przeglądu prac dotyczących komputerowego projektowania katalizatorów do polimeryzacji olefin z punktu widzenia wpływu katalizatorów na przebieg tego procesu. Omówiono osiągnięcia w teoretycznym przewidywaniu katalitycznych właściwości kompleksów metali przejściowych, które dokonały się dzięki zrozumieniu mechanizmu polimeryzacji, charakteru centrów aktywnych, przyczyn aktywności takich katalizatorów oraz roli poszczególnych ich składników. Przedstawiono również zagadnienia, na których prawdopodobnie skupią się obecne i przyszłe prace teoretyczne w dziedzinie polimeryzacji koordynacyjnej (rola kokatalizatorów i zasad Lewisa dodawanych do układów katalitycznych, wpływ warunków doświa…

komputerowe modelowanie molekularnemolecular modelingmetalocenyteoria funkcjonału gęstościowegopolimeryzacja etylenu i propylenuZiegler-Natta catalystsmetalloceneskatalizatory Zieglera-Nattydensity functional theorypolymerization of ethylene and propylenePolimery
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Prompt and delayed spectroscopy of 203At : Observation of a shears band and a 29/2+ isomeric state

2018

Using fusion-evaporation reactions, a gas-filled recoil separator, recoil-gating technique and recoil-isomer decay tagging technique we have extended the level scheme of 203 At ( N = 118 ) significantly. We have observed an isomeric [ τ = 14.1 ( 3 ) μ s ] state with a spin and parity of 29 / 2 + . The isomeric state is suggested to originate from the π ( h 9 / 2 ) ⊗ ∣ ∣ 202 Po ; 11 − ⟩ coupling, and it is depopulated through 286 keV E 2 and 366 keV E 3 transitions. In addition, we have observed a cascade of magnetic-dipole transitions which is suggested to be generated by the shears mechanism. peerReviewed

level densitiesnuclear spinelectromagnetic transitionsnuclear density functional theorytiheysfunktionaaliteoriaspektroskopialifetimeswidthsenergy levelsNuclear Experimentisomer decaysydinfysiikkanuclear parity
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Computational Criteria for Hydrogen Evolution Activity on Ligand-Protected Au25-Based Nanoclusters

2023

The hydrogen evolution reaction (HER) is a critical reaction in addressing climate change; however, it requires catalysts to be generated on an industrial scale. Nanomaterials offer several advantages over conventional HER catalysts, including the possibility of atomic precision in tailoring the intrinsic activity. Ligand-protected metal clusters, such as the thiolate-protected MAu24(SR)18 (where M is Au, Cu, Pd), are of particular interest as not only are they electrocatalytically active toward HER, but the charge state and composition can be precisely tuned. Here, we present a comprehensive computational study examining how the charge state and dopants affect the catalytic activity of [MA…

ligand protected clusterelektrokatalyysinanorakenteetgold nanoclustertiheysfunktionaaliteoriaelectrocatalysisHERdopingdensity functional theoryredox potential
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Dicyclopentaannelated Hexa-peri-hexabenzocoronenes with a Singlet Biradical Ground State

2021

Abstract Synthesis of two dicyclopentaannelated hexa‐peri‐hexabenzocoronene (PHBC) regioisomers was carried out, using nonplanar oligoaryl precursors with fluorenyl groups: mPHBC 8 with two pentagons in the “meta”‐configuration was obtained as a stable molecule, while its structural isomer with the “para”‐configuration, pPHBC 16, could be generated and characterized only in situ due to its high chemical reactivity. Both PHBCs exhibit low energy gaps, as reflected by UV‐vis‐NIR absorption and electrochemical measurements. They also show open‐shell singlet ground states according to electron paramagnetic resonance (EPR) measurements and density functional theory (DFT) calculations. The use of…

low energy gapnot-fully benzenoid PAH010402 general chemistryPhotochemistry01 natural sciencesCatalysislaw.inventiondicyclopentaannelationopen-shell biradicallawStructural isomerMoleculeSinglet stateElectron paramagnetic resonance010405 organic chemistryChemistryCommunicationAromaticityGeneral ChemistryCommunications0104 chemical sciencesDensity functional theoryPolycyclic Aromatic Hydrocarbons | Hot Paperhexa-peri-hexabenzocoroneneGround stateAntiaromaticityAngewandte Chemie International Edition
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When the Grafting of Double Decker Phthalocyanines on Si(100)-2 × 1 Partly Affects the Molecular Electronic Structure

2016

International audience; A combined X-ray photoelectron spectroscopy (XPS), scanning tunneling microscopy (STM), and density functional theory (DFT) study has been performed to characterize the adsorbate interaction of lutetium biphthalocyanine (LuPc2) molecules on the Si(100)-2 × 1 surface. Large molecule–substrate adsorption energies are computed and are found to compete with the molecule–molecule interactions of the double decker molecules. A particularly good matching between STM images and computed ones confirms the deformation of the molecule upon the absorption process. The comparison between DFT calculations and XP spectra reveals that the electronic distribution in the two plateaus …

lutetium bi-phthalocyanineSiliconXASAtom and Molecular Physics and OpticsSTMAnalytical chemistrychemistry.chemical_element02 engineering and technology010402 general chemistryDFT[ CHIM ] Chemical Sciences01 natural sciencesSi(100)law.inventionAdsorptionX-ray photoelectron spectroscopyscanning tunneling microscopelawbasis-setXPS[CHIM]Chemical SciencessurfaceMoleculePhysical and Theoretical ChemistryBasis setmetal-free phthalocyaninefield-effect transistorsPhthalocyaninebis-phthalocyanine021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialstotal-energy calculationsGeneral EnergyElectronic Structurechemistrysi(001)Chemical physicsthin-filmsaugmented-wave methodAtom- och molekylfysik och optikDensity functional theoryScanning tunneling microscopeAbsorption (chemistry)0210 nano-technologyThe Journal of Physical Chemistry C
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Ligand mediated evolution of size dependent magnetism in cobalt nanoclusters.

2018

We use density functional theory to model the impact of a ligand shell on the magnetic properties of CoN (15 ≤ N ≤ 55) nanoclusters. We study three different ligand shells on each nanocluster core size, each known to have different electronic interactions with the surface: pure Cl ligand shells (X-type), pure PH3 ligand shells (L-type), and two component ligand shells with mixtures of Cl and PH3 ligands. The simulations show that the identity, arrangement, and total coverage of the ligand shell controls the distribution of local magnetic moments across the CoN core. On the surface of an unpassivated CoN nanocluster, the Co-Co coordination number (CN) is known to determine the local magnetic…

magneettiset ominaisuudetMaterials scienceMagnetismCoordination numberShell (structure)General Physics and Astronomychemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesNanoclustersnanorakenteetnanostructureskobolttiPhysical and Theoretical Chemistryta116ta114Magnetic momentLigand021001 nanoscience & nanotechnologycobalt0104 chemical sciencesCrystallographychemistryDensity functional theorymagnetic properties0210 nano-technologyCobaltPhysical chemistry chemical physics : PCCP
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Functional Extrapolations to Tame Unbound Anions in Density-Functional Theory Calculations

2019

Standard flavors of density-functional theory (DFT) calculations are known to fail in describing anions, due to large self-interaction errors. The problem may be circumvented using localized basis sets of reduced size, leaving no variational flexibility for the extra electron to delocalize. Alternatively, a recent approach exploiting DFT evaluations of total energies on electronic densities optimized at the Hartree-Fock (HF) level has been reported, showing that the self-interaction-free HF densities are able to lead to an improved description of the additional electron, returning affinities in close agreement with the experiments. Nonetheless, such an approach can fail when the HF densitie…

molecular-dynamicsforce-fieldExtrapolationFOS: Physical sciencesElectron01 natural sciencesForce field (chemistry)IonMolecular dynamicsDelocalized electronPhysics - Chemical Physics0103 physical sciences[CHIM]Chemical SciencesPhysical and Theoretical ChemistryapproximationComputingMilieux_MISCELLANEOUSChemical Physics (physics.chem-ph)PhysicsCondensed Matter - Materials Scienceelectron-affinitiesatoms010304 chemical physicsMaterials Science (cond-mat.mtrl-sci)energiesComputational Physics (physics.comp-ph)Computer Science ApplicationsComputational physics[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryEmbeddingDensity functional theoryPhysics - Computational PhysicsJournal of Chemical Theory and Computation
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Comparison of different theory models and basis sets in the calculation of 13C NMR chemical shifts of natural products.

2004

The influence of the calculation method in mimicking experimental 13C NMR chemical shifts of 15 low-polarity natural products singularly containing 10–20 carbon atoms was investigated by employing different quantum chemistry approaches and basis sets, both in the preliminary geometry optimizations and in the following single-point 13C GIAO calculations of the NMR chemical shifts. The geometries of the involved species were optimized at the PM3, HF, B3LYP and mPW1PW91 levels whereas the 13C NMR parameters were determined at the HF, B3LYP and mPW1PW91 levels. Different combinations of basis sets were also tested. The consistency and efficiency of the considered combinations of geometry optimi…

natural productBiological ProductsMagnetic Resonance SpectroscopyBasis (linear algebra)Databases FactualChemistryChemical shiftstructure elucidationStatistical parameterGeneral ChemistryGIAOCarbon-13 NMRQuantum chemistryNMRModels ChemicalComputational chemistryAb initio quantum chemistry methodsab initiocalculationData Interpretation Statistical13CNMRQuantum TheoryGeneral Materials ScienceDensity functional theorydensity functional theorySoftwareMagnetic resonance in chemistry : MRC
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Four-Component Relativistic DFT Calculations of C-13 Chemical Shifts of Halogenated Natural Substances

2015

We have calculated the (13) C NMR chemical shifts of a large ensemble of halogenated organic molecules (81 molecules for a total of 250 experimental (13) C NMR data at four different levels of theory), ranging from small rigid organic compounds, used to benchmark the performance of various levels of theory, to natural substances of marine origin with conformational degrees of freedom. Carbon atoms bonded to heavy halogen atoms, particularly bromine and iodine, are known to be rather challenging when it comes to the prediction of their chemical shifts by quantum methods, due to relativistic effects. In this paper, we have applied the state-of-the-art four-component relativistic density funct…

natural productBromineChemistrynatural productsChemical shiftOrganic Chemistrychemistry.chemical_elementorganohalidesGeneral ChemistryNuclear magnetic resonance spectroscopydensity functional calculationCarbon-13 NMRhalogenCatalysisNMR spectroscopyComputational chemistryHalogendensity functional calculationshalogensMoleculeDensity functional theoryRelativistic quantum chemistrySettore CHIM/02 - Chimica Fisica
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Blends of Semiflexible Polymers: Interplay of Nematic Order and Phase Separation

2021

Mixtures of semiflexible polymers with a mismatch in either their persistence lengths or their contour lengths are studied by Density Functional Theory and Molecular Dynamics simulation. Considering lyotropic solutions under good solvent conditions, the mole fraction and pressure is systematically varied for several cases of bending stiffness κ (the normalized persistence length) and chain length N. For binary mixtures with different chain length (i.e., NA=16, NB=32 or 64) but the same stiffness, isotropic-nematic phase coexistence is studied. For mixtures with the same chain length (N=32) and large stiffness disparity (κB/κA=4.9 to 8), both isotropic-nematic and nematic-nematic unmixing oc…

nematic orderMaterials sciencePolymers and PlasticsTriple pointThermodynamicsOrganic chemistry02 engineering and technology01 natural sciencesArticleliquid crystalsQD241-441Critical point (thermodynamics)Liquid crystalsemiflexible polymersPhase (matter)0103 physical sciencesLyotropicphase behaviormacromolecules010306 general physicsdensity functional theoryPhase diagramPersistence lengthGeneral Chemistry021001 nanoscience & nanotechnologymolecular dynamicsCondensed Matter::Soft Condensed MattermixturesBending stiffnessddc:540blends0210 nano-technology
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