Search results for "N compounds"

showing 10 items of 203 documents

Theoretical absorption spectrum of the Ar–CO van der Waals complex

2003

The three-dimensional intermolecular electric dipole moment surface of Ar–CO is calculated at the coupled cluster singles and doubles level of theory with the aug-cc-pVTZ basis set extended with a 3s3p2d1f1g set of midbond functions. Using the rovibrational energies and wave functions of our recent study [J. Chem. Phys. 117, 6562 (2002)], temperature-dependent spectral intensities are evaluated and compared to available experimental data. Based on the theoretical spectrum, alternative assignments of the experimentally observed lines in the fundamental band of CO around 2160 and 2166 cm−1 are suggested. Thomas.Bondo@uv.es

Coupled Cluster CalculationsAbsorption spectroscopyGeneral Physics and AstronomySpectral Line IntensitySpectral linesymbols.namesakePhysics and Astronomy (all)Argon ; Carbon Compounds ; Quasimolecules ; Molecular Moments ; Coupled Cluster Calculations ; Rotational-Vibrational States ; Spectral Line Intensity ; SpectraQuasimoleculesPhysics::Atomic and Molecular ClustersArgonPhysics::Chemical PhysicsPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Rotational-Vibrational StatesBasis setMolecular MomentsChemistryIntermolecular forceRotational–vibrational spectroscopySpectraCarbon CompoundsUNESCO::FÍSICA::Química físicaElectric dipole momentCoupled clusterPhysics::Space Physicssymbolsvan der Waals forceAtomic physics
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Anharmonic force fields from analytic CCSD(T) second derivatives: HOF and F2O

1999

The recent implementation of analytic second derivatives for CCSD(T) (coupled cluster theory with single and double excitations augmented by a perturbational treatment of connected triple excitations) has been combined with a numerical finite difference procedure to calculate cubic and semidiagonal quartic force fields. Computational details of this approach are outlined. Applications are reported for HOF and F2O. The CCSD(T) results are in excellent agreement with experiment and represent a substantial improvement over the results obtained from MP2 (Mo/ller–Plesset second-order perturbation theory).

Coupled clusterHydrogen compoundsChemistryQuartic functionQuantum mechanicsAnharmonicityPhysics::Atomic and Molecular ClustersFinite difference methodFinite differenceGeneral Physics and AstronomyPhysical and Theoretical ChemistryPerturbation theorySecond derivativeThe Journal of Chemical Physics
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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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A DFT study of the vicinal 3J(119Sn,13C) and 3J(119Sn,1H) coupling constants in trimethyl- and chlorodimethyl-stannyl propanoates.

2013

Abstract We have tested the performance of DFT protocols, both at the Scalar relativistic ZORA and non-relativistic level of theory, for the calculation of the 3 J( 119 Sn, 13 C) and 3 J( 119 Sn, 1 H) vicinal couplings for a series of flexible organotin(IV) derivatives with formula XMe2SnCHRCHR′COOMe (X = Me, Cl; R, R′ = Me, Ph). A satisfactory agreement between experimental and calculated vicinal couplings has been obtained by taking into account the conformational behaviour of the compounds investigated. The protocols used, mainly the relativistic one, were found to give a correct picture of the populations and a sufficiently high overall performance in calculating the vicinal couplings, …

Coupling constantheteronuclear NMR spectroscopySeries (mathematics)ChemistryOrganoTin(IV) 119Sn NMR 119Sn couplings Karplus DFT Relativistic ZORAOrganic ChemistryScalar (mathematics)heteronuclear NMR spectroscopy; DFT calculations; tin compoundstin compoundsDFT calculationsBiochemistryInorganic ChemistryComputational chemistrySettore CHIM/03 - Chimica Generale E InorganicaMaterials ChemistryOverall performancePhysical and Theoretical ChemistryVicinal
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The Synthesis and Structure of Palladium 2,4-dimethyl-8-hydroselenoquinolinate

2014

The internal complex palladium 2,4-dimethyl-8- hydroselenoquinolinate Pd[C9H4(CH3)2NSe]2 (I) has been synthesized in the course of study of the complexing activity of 8- hydroselenoquinoline and investigation of the nature of chemical bond metal-selenium in the five-membered metal-containing ring. X-ray diffraction data for I: Monoclinic, space group P21/n, a = 9.0092(4), b = 16.3290(7), c = 14.1073(6) A,  = 106.710(2)o, V = 1987.7(2) A3, Z = 4, R1=0.0477, wR2=0.1182 for 4499 reflections (diffractometer Bruker-Nonius KappaCCD, MoK). The crystal structure of the complex I is formed by neutral asymmetric molecules Pd[C9H4(CH3)2NSe]2 in which the central atom palladium is connected bidentic…

CrystallographyChemical bondCovalent bondChemistrychemistry.chemical_elementMoleculeCrystal structureDihedral anglepalladium 24-dimethyl-8-hydroselenoquinolinate palladium coordination compounds synthesis of 8- hydroselenoquinolinates X-ray diffraction analysisRing (chemistry)PalladiumMonoclinic crystal systemMaterials Science and Applied Chemistry
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Synthesis, chemical characterization, computational studies and biological activity of new DNA methyltransferases (DNMTs) specific inhibitor. Epigene…

2015

This work deals with the synthesis, the chemical characterization of dibutyltin(IV) complex of caffeic acid (Bu2Sn(IV)HCAF, caf1) and its cytotoxic action on tumor cells. The coordination environment at the tin center was investigated by FTIR, (119)Sn{(1)H} cross polarization magic angle spinning, electrospray ionization mass spectroscopy in the solid state and UV-vis, fluorescence and (1)H, (13)C and (119)Sn NMR spectroscopy in solution phases. Density functional theory study confirmed the proposed structures in solution phase and indicated the most probably stable conformation. The effects on viability of breast cancer MDA-MB231, colorectal cancer HCT116, hepatocellular carcinoma HepG2 an…

DNA (Cytosine-5-)-Methyltransferase 1Magnetic Resonance SpectroscopyMethyltransferaseAntineoplastic AgentsBiochemistryEpigenesis GeneticMembrane PotentialsInorganic Chemistrychemistry.chemical_compoundCaffeic AcidsCell Line TumorSettore BIO/10 - BiochimicaSpectroscopy Fourier Transform InfraredOrganotin CompoundsCaffeic acidHumansCytotoxic T cellDNA (Cytosine-5-)-MethyltransferasesEnzyme InhibitorsSettore CHIM/02 - Chimica FisicaChemistryOrganotin(IV) Caffeic acid DNMT1 DNA methylation CancerBiological activityDNA MethylationFlow CytometryMitochondriaModels ChemicalBiochemistryCell cultureSettore CHIM/03 - Chimica Generale E InorganicaDNA methylationHepatic stellate cellDNA
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Cytotoxic Activity of Organotin(IV) Derivatives with Triazolopyrimidine Containing Exocyclic Oxygen Atoms

2020

In this study cytotoxicity of organotin(IV) compounds with 1,2,4-triazolo[1,5-a]pyrimidines, Me3Sn(5tpO) (1), n-Bu3Sn(5tpO) (2), Me3Sn(mtpO) (3), n-Bu3Sn(mtpO) (4), n-Bu3Sn(HtpO2) (5), Ph3Sn(HtpO2) (6) where 5HtpO = 4,5-dihydro-5-oxo-[1,2,4]triazolo-[1,5-a]pyrimidine, HmtpO = 4,7-dihydro-5-methyl-7-oxo-[1,2,4]triazolo-[1,5-a]pyrimidine, and H2tpO2 = 4,5,6,7-tetrahydro-5,7- dioxo-[1,2,4]triazolo-[1,5-a]-pyrimidine, was assessed on three different human tumor cell lines: HCT-116 (colorectal carcinoma), HepG2 (hepatocarcinoma) and MCF-7 (breast cancer). While 1 and 3 were inactive, compounds 2, 4, 5 and 6 inhibited the growth of the three tumor cell lines with IC50 values in the submicromolar …

DenticityCellPharmaceutical Science01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundDrug DiscoveryOrganotin CompoundstriazolopyrimidineCytotoxicityMembrane Potential MitochondrialCytotoxinsapoptosisBiological activityHep G2 CellsG2 Phase Cell Cycle CheckpointsGene Expression Regulation Neoplasticmedicine.anatomical_structureChemistry (miscellaneous)Mitochondrial MembranesMCF-7 CellsMolecular MedicineCyclin-Dependent Kinase Inhibitor p21crystal structurein vitro anticancer activityPyrimidineCell SurvivalStereochemistryorganotin(iv)010402 general chemistryArticlelcsh:QD241-441Inhibitory Concentration 50Structure-Activity Relationshiplcsh:Organic chemistrymedicineHumansPhysical and Theoretical ChemistryMetallodrug010405 organic chemistryLigandOrganic ChemistryTriazolesHCT116 CellsapoptosiG1 Phase Cell Cycle Checkpoints0104 chemical sciencesPyrimidineschemistrymetallodrugsCell cultureApoptosisDrug DesignTumor Suppressor Protein p53Reactive Oxygen SpeciesMolecules
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Characterization of complexes formed between [Me2Sn(IV)]2+ and carboxymethylcelluloses.

2006

Complexes formed between carboxymethylcellulose (CMC) and the [Me(2)Sn(IV)]2+ cation have been prepared in the solid state and characterized by FTIR and Mossbauer spectroscopy. The complexes contained CMC with varying molar weight and degree of carboxylation, and the complexes were isolated both from acidic and from neutral solutions at varying metal-to-ligand ratios. The characteristic vibration bands of the ligands were identified from their pH-dependent FTIR spectra. In the organotin(IV) complexes obtained at pH approximately 2, the -COO- moieties were found to be coordinated in a monodentate manner, and the band characteristic of the protonated (unbound) -COO- group(s) was also identifi…

DenticityMetal ions in aqueous solutionInorganic chemistryInfrared spectroscopyBiochemistryAnalytical ChemistrySpectroscopy MossbauerDeprotonationSpectroscopy Fourier Transform InfraredOrganotin CompoundsCarboxymethylcelluloseValence (chemistry)Sn(IV)Molecular StructureLigandChemistryOrganic ChemistryStructureTin CompoundsGeneral MedicineQuadrupole splittingInfrared spectraTrigonal bipyramidal molecular geometryCrystallographyCarboxymethylcellulose SodiumMössbauer spectraCarbohydrate research
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Determination of inorganic species by thermal lens spectrometry

1997

Abstract The application of thermal lens spectrometry (TLS) to the determination of inorganic species is reviewed. The requirements of a chromogenic reaction to be advantageously adapted to TLS detection, and the necessary conditions for reaching very low limits of detection are discussed. Methods for the determination of metals and P, Si, S and N compounds in several samples are examined. Flow-injection and extraction methods, associated photoinduced reactions and surface phenomena, speciation and equilibrium studies are discussed. Gas phase NO 2 methods are also commented upon. Trends are given.

Detection limitChromogenicChemistryAnalytical chemistryMass spectrometryN compoundsAnalytical ChemistryGas phaselaw.inventionLens (optics)lawThermalExtraction methodsSpectroscopyTrAC Trends in Analytical Chemistry
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Determination of mercury in rice by cold vapor atomic fluorescence spectrometry after microwave-assisted digestion.

2010

Abstract A cold vapor atomic fluorescence spectrometry method (CV-AFS) has been developed for the determination of Hg in rice samples at a few ng g−1 concentration level. The method is based on the previous digestion of samples in a microwave oven with HNO3 and H2O2 followed by dilution with water containing KBr/KBrO3 and hydroxylamine and reduction with SnCl2 in HCl using external calibration. The matrix interferences and the effect of nitrogen oxide vapors have been evaluated and the method validated using a certified reference material. The limit of detection of the method was 0.9 ng g−1 with a recovery percentage of 95 ± 4% at an added concentration of 5 ng g−1. The concentration level …

Detection limitMicrowave ovenAnalytical chemistrychemistry.chemical_elementTin CompoundsOryzaHydrogen PeroxideMercuryBiochemistryNitric AcidAnalytical ChemistryDilutionMercury (element)Cold Temperaturechemistry.chemical_compoundHydroxylamineCertified reference materialsSpectrometry FluorescencechemistryEnvironmental ChemistryNitrogen oxideGasesMicrowave digestionMicrowavesSpectroscopyAnalytica chimica acta
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