Search results for " DFT."

showing 10 items of 87 documents

Palladium clusters on BNNT as catalysts for biomass conversion

2015

The construction of a heterogeneous catalytic systems by a bottom-up approach is a fascinating strategy well assisted by molecular level characterizations. In this sense, DFT investigations can be used with predictive and descriptive purposes both for the treatment of the catalyst/support and for the substrate/catalyst characterization. This should be particularly useful for highly perspective but scarcely treated systems such as boron nitride based supports. Among these, boron nitride nanotubes (BNNT) have been demonstrated to have high chemical and thermal stability as well as great mechanical strength and high thermal conductivity.[1] Moreover, a high affinity toward hydrogen [2] as well…

Settore CHIM/03 - Chimica Generale E InorganicaBoron Nitride Nanotube DFT Biomass Conversion
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NAOs and vdW‐DF for simulating co‐adsorption of water and polyols on metal surfaces

2015

The computational approach employed in this study is based on the combined use of numerical atomic orbitals (NAOs), which are recognized as highly efficient basis sets, and different parameterization of vdW-DF exchange-correlation functionals, namely DRSLL and KBM as implemented in the SIESTA code.

Settore CHIM/03 - Chimica Generale E InorganicaPolyols metal surface DFT
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Reactivity of antitumor coinage metal-based N-heterocyclic carbene complexes with cysteine and selenocysteine protein sites

2021

Abstract The reaction of the antitumor M(I)-bis-N-heterocyclic carbene (M(I)-NHC) complexes, M = Cu, Ag, and Au, with their potential protein binding sites, i.e. cysteine and selenocysteine, was investigated by means of density functional theory approaches. Capped cysteine and selenocysteine were employed to better model the corresponding residues environment within peptide structures. By assuming the neutral or deprotonated form of the side chains of these amino acids and by considering the possible assistance of an external proton donor such as an adjacent acidic residue or the acidic component of the surrounding buffer environment, we devised five possible routes leading to the binding o…

SilverAnticancer; Copper(I) complexes; DFT calculations; Gold(I) complexes; N-heterocyclic carbenes; Silver(I) complexesStereochemistryCoinage metalsAntineoplastic AgentsProtonationLigandsDFT calculationsBiochemistrySilver(I) complexesInorganic Chemistrychemistry.chemical_compoundDeprotonationProtein structureCoordination ComplexesCysteineN-heterocyclic carbenesDensity Functional Theorychemistry.chemical_classificationMolecular StructureSelenocysteineCopper(I) complexesSelenocysteineAmino acidAnticancerGold(I) complexesModels ChemicalchemistryThermodynamicsGoldCarbeneCopperCysteineJournal of Inorganic Biochemistry
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Straightforward Regio- and Diastereoselective Synthesis, Molecular Structure, Intermolecular Interactions and Mechanistic Study of Spirooxindole-Engr…

2021

Straightforward regio- and diastereoselective synthesis of bi-spirooxindole-engrafted rhodanine analogs 5a–d were achieved by one-pot multicomponent [3 + 2] cycloaddition (32CA) reaction of stabilized azomethine ylide (AYs 3a–d) generated in situ by condensation of L-thioproline and 6-chloro-isatin with (E)-2-(5-(4-chlorobenzylidene)-2,4-dioxothiazolidin-3-yl)-N-(2-morpholinoethyl)acetamide. The bi-spirooxindole-engrafted rhodanine analogs were constructed with excellent diastereo- and regioselectivity along with high chemical yield. X-ray crystallographic investigations for hybrid 5a revealed the presence of four contiguous stereocenters related to C11, C12, C19 and C22 of the spiro struct…

StereochemistryHirshfeld DFTPharmaceutical ScienceAzomethine ylideOrganic chemistryArticleAnalytical ChemistryStereocenterchemistry.chemical_compoundQD241-441spirooxindole; rhodanine; azomethine ylides; [3 + 2] cycloaddition (32CA) reactions; hydrogen bonding; Hirshfeld DFT; supernucleophilesNucleophileDrug DiscoveryrhodanineReactivity (chemistry)Physical and Theoretical Chemistryheterosykliset yhdisteetsupernucleophilesvetysidoksettiheysfunktionaaliteoriaRegioselectivityazomethine ylidesspirooxindolehydrogen bondingCycloaddition[3 + 2] cycloaddition (32CA) reactionsRhodaninechemistryChemistry (miscellaneous)Molecular MedicineDerivative (chemistry)Molecules; Volume 26; Issue 23; Pages: 7276
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Matrix isolation studies on the co-condensation reactions of molecular SiO and GeO: the characterisation of the novel cyclic species SiGeO(2), Si(2)G…

2010

Matrix isolation IR studies, together with DFT calculations, have established that the co-condensation of molecular SiO and GeO in low temperature (12 K) nitrogen matrices leads to the formation of the novel silicon germanium oxide species SiGeO(2), Si(2)GeO(3) and SiGe(2)O(3) analogous to the known dimer and trimer species M(2)O(2) and M(3)O(3) (M = Si, Ge). Controlled diffusion studies in the temperature range 20-34 K result in a significant increase in trimer formation, which implies a very low activation energy for this oligomerisation step. Characteristic IR modes are assigned for all three novel mixed oxide molecules, and the DFT calculations establish that these species have cyclic C…

StereochemistryMatrix isolation new molecular species DFTMatrix isolationOxideGeneral Physics and AstronomyTrimerActivation energyAtmospheric temperature rangechemistry.chemical_compoundchemistryMoleculePhysical chemistryMixed oxidePhysical and Theoretical ChemistryGermanium oxidePhysical chemistry chemical physics : PCCP
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A density functional theory study of uranium(VI) nitrate monoamide complexes.

2011

Density functional theory calculations were performed on uranyl complexed with nitrate and monoamide ligands (L) [UO(2)(NO(3))(2)·2L]. The obtained results show that the complex stability is mainly governed by two factors: (i) the maximization of the polarizability of the coordinating ligand and (ii) the minimization of the steric hindrance effects. Furthermore, the electrostatic interaction between ligands and uranium(vi) was found to be a crucial parameter for the complex stability. These results pave the way to the definition of (quantitative) property/structure relationships for the in silico screening of monoamide ligands with improved extraction efficiency of uranium(vi) in nitrate ac…

Steric effectsLigandExtraction (chemistry)Inorganic chemistryGeneral Physics and Astronomychemistry.chemical_elementUraniumUranylUranium complexes DFT nitrate acidic solutionchemistry.chemical_compoundchemistryNitrateComputational chemistryPolarizabilitySettore CHIM/03 - Chimica Generale E InorganicaDensity functional theoryPhysical and Theoretical ChemistryPhysical chemistry chemical physics : PCCP
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Synthesis, spectroscopic characterization and in vitro antimicrobial activity of diorganotin(IV) dichloride adducts with [1,2,4]triazolo-[1,5-a]pyrim…

2006

Abstract The heterocyclic ligands [1,2,4]triazolo-[1,5-a]pyrimidine (tp) and 5,7-dimethyl-[1,2,4]triazolo-[1,5-a]pyrimidine (dmtp), react with diorganotin dichlorides giving the addition compounds Me2SnCl2(tp)2, Et2SnCl2(tp)2, Me2SnCl2(dmtp)2, Et2SnCl2(dmtp)2, Bu2SnCl2(dmtp), Ph2SnCl2(dmtp). The organotin:ligand stoichiometry goes from 1:2 to 1:1 by increasing the steric hindrance of the organic groups bound to tin. The compounds have been characterized by means of infrared, 119Sn Mossbauer and 1H AND 13C NMR spectroscopy. The ligands presumably coordinate to tin classically through the nitrogen atom at the position 3. The 1:1 complexes adopt trigonal bipyramidal structures, with the organi…

Steric effectsPyrimidineLigandStereochemistryOrganic ChemistryDFT calculationchemistry.chemical_elementAntimicrobial activityBiochemistryMedicinal chemistryTriazolopyrimidine; Diorganotin(IV); Mossbauer; DFT calculations; Antimicrobial activityAdductMossbauerInorganic ChemistryTrigonal bipyramidal molecular geometrychemistry.chemical_compoundchemistryOctahedronMössbauer spectroscopyMaterials ChemistryTriazolopyrimidinePhysical and Theoretical ChemistryTinDiorganotin(IV)Journal of Organometallic Chemistry
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α-d-Glucopyranose Adsorption on a Pd30 Cluster Supported on Boron Nitride Nanotube

2016

Boron nitride nanotube (BNNT) as an innovative support for carbohydrate transformation processes was evaluated, using density functional theory. The α-d-glucopyranose adsorption on a Pd30 cluster, supported on BNNT, was used to check both the local activity of topologically different metallic sites and the effects of the proximity of the BNNT surface to the same metallic sites. Detailed geometrical and electronic analyses performed on Pd30/BNNT and α-d-glucopyranose/Pd30/BNNT systems were discussed. It was observed that the deposition of the Pd30 cluster onto the BNNT support gives rise to an electronic rearrangement, determining a charge transfer from the support to the adsorbed metal clus…

Surface site reactivityChemical substanceNanotechnologyElectron donor02 engineering and technology010402 general chemistryDFT01 natural sciencesBoron nitride nanotubeCatalysisCatalysiCatalysisMetalchemistry.chemical_compoundAdsorptionSupported palladium catalystCluster (physics)Chemistry (all)Molecular electrostatic potentialGeneral Chemistry021001 nanoscience & nanotechnologyBoron nitride nanotube; DFT; Molecular electrostatic potential; Supported palladium catalyst; Surface site reactivity; α-d-Glucopyranose adsorption; Catalysis; Chemistry (all)0104 chemical scienceschemistryChemical physicsvisual_artα-d-Glucopyranose adsorptionvisual_art.visual_art_mediumDensity functional theory0210 nano-technologyScience technology and societyTopics in Catalysis
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Calculations Yb [Dataset]

2022

Orca outputs of TDDFT and DFT calculations on a Yb complex Archivos OUT. Abrir con Windows Notepad, WordPad, TextEdit o Text editor. Archivos OUT. Abrir con Windows Notepad, WordPad, TextEdit o Text editor.

TDDFT DFT Calculation with OrcaUNESCO::QUÍMICAcalculations
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Dimensionality of the Superconductivity in the Transition Metal Pnictide WP

2020

We report theoretical and experimental results on the transition metal pnictide WP. The theoretical outcomes based on tight-binding calculations and density functional theory indicate that WP is a three-dimensional superconductor with an anisotropic electronic structure and nonsymmorphic symmetries. On the other hand, magnetoresistance experimental data and the analysis of superconducting fluctuations of the conductivity in external magnetic field indicate a weakly anisotropic three-dimensional superconducting phase.

TechnologyFOS: Physical sciencesDFTSuperconductivity (cond-mat.supr-con)Condensed Matter - Strongly Correlated ElectronsSuperconducting fluctuationsCondensed Matter::SuperconductivityPnictidesGeneral Materials ScienceMicroscopyQC120-168.85Strongly Correlated Electrons (cond-mat.str-el)MagnetoresistanceCondensed Matter - SuperconductivityTQH201-278.5Nonsymmorphic symmetriesWPTransition metalEngineering (General). Civil engineering (General)TK1-9971Descriptive and experimental mechanicstransition metal; pnictides; WP; pnictide superconductors; superconducting fluctuations; magnetoresistance; DFT; nonsymmorphic symmetriesDFT; Magnetoresistance; Nonsymmorphic symmetries; Pnictide superconductors; Pnictides; Superconducting fluctuations; Transition metal; WPPnictide superconductorsElectrical engineering. Electronics. Nuclear engineeringTA1-2040
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