Search results for "Spectroscopy"

showing 10 items of 10293 documents

Chalcogenide-capped triiron clusters [Fe3(CO)9(μ3-E)2], [Fe3(CO)7(μ3-CO)(μ3-E)(μ-dppm)] and [Fe3(CO)7(μ3-E)2(μ-dppm)] (E = S, Se) as proton-reduction…

2019

Chalcogenide-capped triiron clusters [Fe3(CO)7(μ3-CO)(μ3-E)(μ-dppm)] and [Fe3(CO)7(μ3-E)2(μ-dppm)] (E = S, Se) have been examined as proton-reduction catalysts. Protonation studies show that [Fe3(CO)9(μ3-E)2] are unaffected by strong acids. Mono-capped [Fe3(CO)7(μ3-CO)(μ3-E)(μ-dppm)] react with HBF4.Et2O but changes in IR spectra are attributed to BF3 binding to the face-capping carbonyl, while bicapped [Fe3(CO)7(μ3-E)2(μ-dppm)] are protonated but in a process that is not catalytically important. DFT calculations are presented to support these protonation studies. Cyclic voltammetry shows that [Fe3(CO)9(μ3-Se)2] exhibits two reduction waves, and upon addition of strong acids, proton-reducti…

SulfideInfrared spectroscopyProtonationorganometalliyhdisteetSulfonic acid010402 general chemistryElectrochemistry01 natural sciencesBiochemistryMedicinal chemistryCatalysisInorganic Chemistrychalcogenidechemistry.chemical_compoundSelenideElectrochemistryMaterials ChemistryPhysical and Theoretical Chemistryclusterta116proton-reductionchemistry.chemical_classification010405 organic chemistryChalcogenideOrganic Chemistrytriironsähkökemia0104 chemical scienceselectrochemistrychemistryClusterTriironProton-reductionCyclic voltammetryJournal of Organometallic Chemistry
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1H NMR and UV-vis spectroscopic characterization of sulfonamide complexes of nickek(II)-carbonic anhydrase. Resonance assignments based on NOE effects

1992

The binding of acetazolamide, p-fluorobenzensulfonamide, p-toluenesulfonamide, and sulfanilamide to nickel(II)-substituted carbonic anhydrase II has been studied by 1H NMR and electronic absorption spectroscopies. These inhibitors bind to the metal ion forming 1:1 complexes and their affinity constants were determined. The 1H NMR spectra of the formed complexes show a number of isotropically shifted signals corresponding to the histidine ligands. The complexes with benzene-sulfonamides gave rise to very similar 1H NMR spectra. The NMR data suggest that these aromatic sulfonamides bind to the metal ion altering its coordination sphere. In addition, from the temperature dependence of 1H NMR s…

SulfonamidesConformational changeMagnetic Resonance SpectroscopyCoordination sphereProtein ConformationCarbon-13 NMR satelliteChemistryStereochemistryCarbonic anhydrase IINuclear magnetic resonance spectroscopy of nucleic acidsNuclear magnetic resonance spectroscopyBiochemistryAdductAcetazolamideInorganic ChemistryCrystallographyNickelSpectrophotometryProton NMRAnimalsCattleSpectrophotometry UltravioletCarbonic AnhydrasesProtein BindingJournal of Inorganic Biochemistry
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DNA cleavage reaction induced by dimeric copper(II) complexes of N-substituted thiazole sulfonamides

2005

A new dinuclear copper(II) complex has been synthesised and structurally characterised: [Cu2(tz-ben)4] (Htz-ben = N-thiazol-2-yl-benzenesulfonamide). Its crystal structure, magnetic properties and electronic paramagnetic resonance (EPR) spectra were studied in detail. In the compound the metal centres are bridged by four non-linear triatomic NCN groups. The coordination geometry of the copper ions in the dinuclear entity is distorted square pyramidal (4+1). Two thiazole N and two sulfonamido N atoms occupy the equatorial positions and one sulfonamido O atom is in the axial position. Magnetic susceptibility data show a strong antiferromagnetic coupling, -2J = 114.1 cm(-1). The EPR spectra of…

SulfonamidesSpectrophotometry InfraredStereochemistryElectron Spin Resonance SpectroscopyDNACrystal structureZero field splittingCrystallography X-RayBiochemistryMagnetic susceptibilityMass SpectrometrySquare pyramidal molecular geometrylaw.inventionInorganic ChemistryThiazolesCrystallographychemistry.chemical_compoundchemistrylawOrganometallic CompoundsSinglet stateThiazoleElectron paramagnetic resonanceCopperCoordination geometryJournal of Inorganic Biochemistry
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Isolation, dynamic NMR study and X-ray characterisation of a bis sulfonium zirconocene-ate dimer.

2004

The novel dimer [Cp(2)Zr[upper bond start]([minus sign in circle])S([plus sign in circle])CH(Ph)CH[double bond]C[upper bond end]PPh(2)](2), the first example of a structurally characterised sulfur-bridged binuclear zirconathiolane complex, was prepared, characterised by NMR spectroscopy and X-ray crystallography, and some aspects of its solution behaviour were studied.

SulfoniumStereochemistryDimerMetals and AlloysX-rayGeneral ChemistryNuclear magnetic resonance spectroscopyCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryMaterials ChemistryCeramics and CompositesChemical communications (Cambridge, England)
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Aqua complex of iron(III) and 5-chloro-3-(2-(4,4-dimethyl-2,6- dioxocyclohexylidene) hydrazinyl)-2-hydroxybenzenesulfonate: Structure and catalytic a…

2013

Abstract A water-soluble iron(III) complex [Fe(H2O)3(L)]·5H2O (1) was prepared by reaction of iron(III) chloride with 5-chloro-3-(2-(4,4-dimethyl-2,6-dioxocyclohexylidene)hydrazinyl)-2-hydroxy-benzenesulfonic acid (H3L). The complex was characterized by IR, 1H NMR and ESI-MS spectroscopies, elemental and X-ray crystal structural analyses. The coordination environment of the central iron(III) is a distorted octahedron, three sites being occupied by L3− ligand, which chelates in O,N,O fashion, while three other sites are filled with the water molecules. The uncoordinated water molecules are held in the channels of the overall 3D supramolecular structure by the carbonyl and sulfonyl groups of …

Sulfonylchemistry.chemical_classificationNitroaldol reactionHalogen bondStereochemistryLigandHydrogen bondOrganic ChemistrySupramolecular chemistryMedicinal chemistryAnalytical ChemistryCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryNitroethaneta116SpectroscopyJournal of molecular structure
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Synthesis, Optical and Electrical Properties of Oligo(phenylenevinylene)s Substituted with Electron-Accepting Sulfonyl Groups

2010

Oligo(phenylenevinylene)s (OPV) composed of five rings and electron donating or withdrawing sulfonyl substituents on the central and lateral rings have been investigated. Two strategies were used for the syntheses of the C2-symmetrical OPVs both include PO-activated olefinations as central steps. Six flexible side chains guarantee good solubility in toluene or dichloromethane. In solution and in films stabilised by polystyrene (60%), the chromophores are strongly fluorescent, with emissions in the violet-blue domain from solutions and in the green to orange region from solid films. The redox potentials, determined by cyclic voltammetry, and the optical properties are strongly depending on t…

Sulfonylchemistry.chemical_classificationchemistry.chemical_compoundMaterials scienceUltraviolet visible spectroscopychemistrySide chainPolystyreneSolubilityChromophoreCyclic voltammetryPhotochemistryAcceptorAdvances in Science and Technology
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Diode laser spectroscopy of the nu(8) band of the SF(5)Cl molecule.

2003

Abstract Diode laser spectra of SF 5 Cl have been recorded in the ν 8 band region at a temperature of ca. 240 K, a pressure of 0.25 mbar and an instrumental bandwidth of ca. 0.001 cm −1 . Four regions have been studied: a first one in the P -branch (906.849–907.687 cm −1 ), a second one in the Q -branch (910.407–910.944 cm −1 ), and two other ones in the R -branch (913.957–914.556 and 917.853–918.705 cm −1 ). The whole ν 1 / ν 8 dyad of SF 5 35 Cl has been previously recorded in the group of Professor H. Burger in Wuppertal, thanks to a Fourier transform infrared spectrometer [J. Mol. Spectrosc. 208 (2001) 169]. These data have thus been combined with our diode laser ones in the aim of refi…

Sulfur CompoundsChemistryLasersFluorine CompoundsAnalytical chemistryInfrared spectroscopyLaserAtomic and Molecular Physics and OpticsSpectral lineAnalytical Chemistrylaw.inventionsymbols.namesakeFourier transformChlorideslawSpectrophotometryData Interpretation StatisticalsymbolsAtomic physicsFourier transform infrared spectroscopyGround stateHamiltonian (quantum mechanics)InstrumentationSpectroscopyDiodeSpectrochimica acta. Part A, Molecular and biomolecular spectroscopy
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Resolving the forbidden band of SF6

2013

Sulfur hexafluoride is an important molecule for modeling thermophysical and polarizability properties. It is also a potent greenhouse gas of anthropogenic origin, whose concentration in the atmosphere, although very low is increasing rapidly; its global warming power is mostly conferred by its strong infrared absorption in the ν3 S-F stretching region near 948 cm(-1). This heavy species, however, features many hot bands at room temperature (at which only 31% of the molecules lie in the ground vibrational state), especially those originating from the lowest, v6 = 1 vibrational state. Unfortunately, the ν6 band itself (near 347 cm(-1)), in the first approximation, is both infrared- and Raman…

Sulfur hexafluoridechemistry.chemical_compoundDipolechemistryInfraredPolarizabilityGeneral Physics and AstronomyInfrared spectroscopySynchrotron radiationRotational–vibrational spectroscopyPhysical and Theoretical ChemistryAtomic physicsHot bandPhys. Chem. Chem. Phys.
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Micrometer-size crystalline monolayer MoS2 domains obtained by sulfurization of molybdenum oxide ultrathin films

2023

In this work, the formation of micrometer-size crystalline monolayer (1L) MoS2 flakes with triangular shape and a central multilayer core is obtained by the sulfurization at 800 °C of pre-deposited ultrathin MoOx films (1.2–1.8 nm) on c-sapphire substrates. The thickness uniformity, crystalline quality, doping and strain distribution in the MoS2 flakes as a function of the initial MoOx thickness was evaluated by micro-Raman (μR) mapping. The excellent crystalline quality of the triangular 1L-MoS2 flakes was confirmed by micro-photoluminescence (μPL) maps, showing a very intense peak at ∼1.85 eV, that decreases in the central part, as expected for multilayers MoS2. A biaxial strain of ∼0.38–…

SulfurizationRaman spectroscopySettore FIS/01 - Fisica SperimentaleElectrical and Electronic EngineeringCondensed Matter PhysicsMoS2PhotoluminescenceAtomic and Molecular Physics and OpticsTransmission electron microscopySurfaces Coatings and FilmsElectronic Optical and Magnetic Materials
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Structure of nanoporous carbon materials for supercapacitors

2012

Activated carbons with highly developed porous structure and nanosized pores (8 - 11 A) were prepared from alder wood using thermochemical activation method with sodium hydroxide. Properties of the obtained activated carbons were examined by benzene and nitrogen sorption, X-Ray diffraction and Raman spectroscopy. Tests of activated carbons as electrodes in supercapacitors were performed as well. It was found that specific surface area of above mentioned activated carbons was 1800 m 2 /g (Dubinin - Radushkevich). Raman spectroscopy demonstrated the presence of ordered and disordered structures of graphite origin. The performance of activated carbons as electrodes in supercapacitors have show…

SupercapacitorMaterials scienceInorganic chemistrychemistry.chemical_elementSorptionchemistry.chemical_compoundsymbols.namesakechemistrySodium hydroxideSpecific surface areasymbolsGraphiteBenzeneRaman spectroscopyCarbonIOP Conference Series: Materials Science and Engineering
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