Search results for "Dft"

showing 10 items of 361 documents

Indefinitely stable iron(IV) cage complexes formed in water by air oxidation

2017

In nature, iron, the fourth most abundant element of the Earth's crust, occurs in its stable forms either as the native metal or in its compounds in the +2 or +3 (low-valent) oxidation states. High-valent iron (+4, +5, +6) compounds are not formed spontaneously at ambient conditions, and the ones obtained synthetically appear to be unstable in polar organic solvents, especially aqueous solutions, and this is what limits their studies and use. Here we describe unprecedented iron(IV) hexahydrazide clathrochelate complexes that are assembled in alkaline aqueous media from iron(III) salts, oxalodihydrazide and formaldehyde in the course of a metal-templated reaction accompanied by air oxidation…

ClathrochelateScienceInorganic chemistryFormaldehydeSolid-stateGeneral Physics and Astronomy010402 general chemistryDFT01 natural sciencesArticleGeneral Biochemistry Genetics and Molecular BiologyInorganic Chemistrychemistry.chemical_compoundhigh-valent ironNative metalOorganisk kemiMultidisciplinaryAqueous solution010405 organic chemistryQGeneral ChemistryDecompositionCoordination chemistry3. Good health0104 chemical scienceschemistryCageEarth (classical element)Nature Communications
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A computational and experimental investigation of halloysite silicic surface modifications after alkaline treatment

2023

Density functional theory calculations were performed in order to investigate the formation of silanol groups on the outer surface of halloysite nanotubes, as possible products of the reactions with water in alkaline environments. The results, discussed in terms of energy release and structural properties of the modified surface, suggest that the formation of various kinds of silanol group constellations, and even the extraction of orthosilicic acid, are highly exothermic reaction in the presence of hydroxide ions. Thermogravimetric analysis, FT-IR, XRD and X-ray fluorescence spectrometry performed on halloysite treated at high pH conditions indicate that the adsorption of water on the oute…

Clay materialsGeochemistry and PetrologySpiral nanotubesGeologyFunctionalizationDFTApplied Clay Science
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Generation and Evolution of Spin-, Valley-, and Layer-Polarized Excited Carriers in Inversion-Symmetric WSe2

2016

We report the spin-selective optical excitation of carriers in inversion-symmetric bulk samples of the transition metal dichalcogenide (TMDC) WSe2. Employing time- and angle-resolved photoelectron spectroscopy (trARPES) and complementary time-dependent density functional theory (TDDFT), we observe spin-, valley-, and layer-polarized excited state populations upon excitation with circularly polarized pump pulses, followed by ultrafast ( < 100     fs ) scattering of carriers towards the global minimum of the conduction band. TDDFT reveals the character of the conduction band, into which electrons are initially excited, to be two-dimensional and localized within individual layers, whereas at t…

Condensed Matter - Materials Sciencetr-ARPESCondensed Matter - Mesoscale and Nanoscale PhysicsTDDFT530 PhysicsMesoscale and Nanoscale Physics (cond-mat.mes-hall)Materials Science (cond-mat.mtrl-sci)FOS: Physical sciences10192 Physics Institute2D materialsSettore FIS/03 - Fisica Della Materia3100 General Physics and Astronomy
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Organoplatinum(II) Complexes Self-Assemble and Recognize AT-Rich Duplex DNA Sequences

2021

The specific recognition of AT-rich DNA sequences opens up the door to promising diagnostic and/or therapeutic strategies against gene-related diseases. Here, we demonstrate that amphiphilic PtII complexes of the type [Pt(dmba)(N∧N)]NO3 (dmba = N,N-dimethylbenzylamine-κN, κC; N∧N = dpq (3), dppz (4), and dppn (5)) recognize AT-rich oligonucleotides over other types of DNA, RNA, and model proteins. The crystal structure of 4 shows the presence of significant π-stacking interactions and a distorted coordination sphere of the d8 PtII atom. Complex 5, containing the largest π-conjugated ligand, forms supramolecular assemblies at high concentrations under aqueous environment. However, its aggreg…

Coordination sphereOrganoplatinum CompoundsStereochemistrySupramolecular chemistryDMBAElectrophoretic Mobility Shift Assay010402 general chemistryCrystallography X-RayLigands01 natural sciencesArticleInorganic Chemistrychemistry.chemical_compoundCoordination ComplexesHumansPhysical and Theoretical ChemistryDNA • light-switch • platinum • pseudo-tetrahedral • antitumor agent • DFTOrganoplatinumGel electrophoresisMolecular Structure010405 organic chemistryChemistryOligonucleotideLigandSpectrum AnalysisStereoisomerismDNAIntercalating Agents0104 chemical sciencesA549 CellsSettore CHIM/03 - Chimica Generale E InorganicaDNA
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Solvent directs the dimensionality of Cu-dicyanoimidazoles

2022

In this paper, we report one-pot reactions of the same reactants 4,5-dicyanoimidazole and CuI in different solvents. In pure MeCN, the reaction resulted in previously reported MOF structure [Cu(4,5-dicyanoimidazole)]n.(MeCN)0.5n (1). On the other hand, when MeCN/MeOH solvent mixture was used, a new coordination polymer [Cu(4,5-dicyanoimidazole)(MeCN)(CuI)]n (2) was formed. The crystallization yielded very different structures as determined by X-ray crystallography. In 1, the solvent molecule acetonitrile occupies the MOF pores via weak interactions, but in 2 it is coordinated to the metal center. Computational DFT calculations and topological charge density analysis were utilized to explore…

Copper complextiheysfunktionaaliteoriakupariGeneral ChemistrykompleksiyhdisteetSolvent effectCondensed Matter PhysicsDFTQTAIMCyanoGeneral Materials ScienceImidazolekristallisaatioliuottimet
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Karplus-Type Dependence of Vicinal119Sn-13C and119Sn-1H Spin-Spin Couplings in Organotin(IV) Derivatives: A DFT Study

2009

The empirical Karplus-type dependence of (3)J((119)Sn,(13)C) and (3)J((119)Sn,(1)H) couplings in organotin(IV) derivatives has been computationally validated by DFT methods both at the nonrelativistic and scalar ZORA relativistic level. A preliminary calibration of the computational protocols, by comparing experimental and calculated couplings for a Set Of Suitable rigid molecules, revealed their high predictive power: in particular, relativistic results for (3)J((119)Sn,(13)C) have a mean absolute error of just above 2 Hz, over a range of values up to about 70 Hz. The latter protocol has then been used to study in detail the influence of substituents and multiple paths connecting the coupl…

Coupling constantChemistryKarplus equationOrganic ChemistryCarbon-13Scalar (mathematics)Relativistic effectsNuclear magnetic resonance spectroscopyRelativistic effects DFT NMR spectroscopy tinMolecular physicsDensity functional calculations; NMR spectroscopy; Relativistic effects; TinDensity functional calculationsNMR spectroscopyNuclear magnetic resonanceTinMoleculePhysical and Theoretical ChemistryRelativistic quantum chemistryorganotinVicinalSpin-½European Journal of Organic Chemistry
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A DFT study of the Karplus-type dependence of vicinal 3J(Sn-C-X- C), X=N,O,S, in organotin(iv) compounds: Application to conformationally flexible sy…

2010

ZORA relativistic and non-relativistic DFT protocols have been used to investigate vicinal coupling constants, (3)J(Sn-C-X-C), in several organotin(iv) compounds, with particular emphasis on cyclic alpha-aminoorganostannanes. The dependence of the coupling constant on the heteroatom X (X = N,O,S) in the coupling path, and, for X = N, its substituents, has been studied in detail. The electron-withdrawing strength of the N-substituents has been found to strongly affect the magnitude and shape of the Karplus-type curve. The results obtained for the simple model systems, having no or little conformational flexibility, have helped in rationalizing the data concerning real flexible cyclic systems…

Coupling constantCouplingeducation.field_of_study119Tin NMR vicinal coupling constants DFTChemistryOrganic ChemistryHeteroatomPopulationType (model theory)BiochemistryComputational chemistryPhysical and Theoretical ChemistryeducationConformational isomerismVicinal
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One-bond 1 J (15 N,H) coupling constants at sp2 -hybridized nitrogen of Schiff bases, enaminones and similar compounds: A theoretical study

2020

1 J(15 N,H) coupling constants for enaminones and NH-forms of intramolecularly hydrogen-bonded Schiff bases as model compounds for sp2 -hybridized nitrogen atoms are evaluated using density functional theory (DFT) to find the optimal functionals and basis sets. Ammonia is used as a test molecule and its one-bond coupling constant is compared with experiment. A methylamine Schiff base of a truncated molecule of gossypol is used for checking the performance of selected B3LYP, O3LYP, PBE, BHandH, and APFD density functionals and standard, modified, and dedicated basis sets for coupling constants. Both in vacuum and in chloroform, modeled by the simple continuum model of solvent, the modified b…

Coupling constantNH‐formsSchiff baseone‐bond NH coupling constants010405 organic chemistryHydrogen bondMethylamineGeneral ChemistryDFT calculations010402 general chemistry01 natural sciencesTautomer0104 chemical sciencesBond lengthSSCCchemistry.chemical_compoundchemistryPhysical chemistryMoleculeSchiff basesGeneral Materials ScienceDensity functional theoryTautomerismMagnetic Resonance in Chemistry
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Prediction of water's isotropic nuclear shieldings and indirect nuclear spin–spin coupling constants (SSCCs) using correlation‐consistent and polariz…

2009

Density functional theory (DFT) was used to estimate water's isotropic nuclear shieldings and indirect nuclear spin-spin coupling constants (SSCCs) in the Kohn-Sham (KS) complete basis set (CBS) limit. Correlation-consistent cc-pVxZ and cc-pCVxZ (x = D, T, Q, 5, and 6), and their modified versions (ccJ-pVxZ, unc-ccJ-pVxZ, and aug-cc-pVTZ-J) and polarization-consistent pc-n and pcJ-n (n = 0, 1, 2, 3, and 4) basis sets were used, and the results fitted with a simple mathematical formula. The performance of over 20 studied density functionals was assessed from comparison with the experiment. The agreement between the CBS DFT-predicted isotropic shieldings, spin-spin values, and the experimenta…

Coupling constantSOPPA(CCSD)Condensed matter physicsChemistryIsotropywaterKohn–Sham equationsPropagatorspin–spin coupling constantsGeneral ChemistryPolarization (waves)DFT‐NMRnuclear isotropic shieldingsSSCCSOPPAGeneral Materials ScienceDensity functional theoryAtomic physicscomplete basis set limitSpin (physics)Basis setMagnetic Resonance in Chemistry
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Relativistic DFT Calculation of (119)Sn Chemical Shifts and Coupling Constants in Tin Compounds.

2006

The nuclear shielding and spin-spin coupling constants of (119)Sn in stannane, tetramethylstannane, methyltin halides Me4-nSnXn (X = Cl, Br, I; n = 1-3), tin halides, and some stannyl cations have been investigated computationally by DFT methods and Slater all-electron basis sets, including relativistic effects by means of the zeroth order regular approximation (ZORA) method up to spin-orbit coupling. Calculated (119)Sn chemical shifts generally correlate well with experimental values, except when several heavy halogen atoms, especially iodine, are bound to tin. In such cases, calculated chemical shifts are almost constant at the scalar (spin-free) ZORA level; only at the spin-orbit level i…

Coupling constantchemistry.chemical_classificationNMR spectroscopy; computational chemistry; tin compounds; tin-119Chemical shifttin compoundsHalidechemistry.chemical_elementOrganotin(IV) NMR DFT coupling constantstin-119Stannanecomputational chemistryComputer Science Applicationschemistry.chemical_compoundNMR spectroscopychemistryComputational chemistryHalogenPhysics::Atomic and Molecular ClustersPhysics::Chemical PhysicsPhysical and Theoretical ChemistryTinRelativistic quantum chemistryAlkylJournal of chemical theory and computation
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