Search results for "Spectroscopy"

showing 10 items of 10293 documents

Solid state electrochemical behavior of organosulfur compounds

2017

Abstract The solid-sate electrochemistry of organosulfur compounds existing in petroleum and its derived matrices is described using the voltammetry of immobilized microparticles methodology. Cyclic and square wave voltammogrammetric responses of sulfur compounds responsible of aging of asphalt pavements, namely, thiophenes, disulfides, sulfides, sulfoxides and sulfones were determined at compound-modified graphite electrodes in contact with 0.10 M H2SO4. The electrochemical oxidation/reduction products were characterized by attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) and scanning electron microscopy with energy dispersion x-ray detection (SEM-EDX) couple…

chemistry.chemical_classificationChemistryGeneral Chemical Engineering010401 analytical chemistryInorganic chemistrychemistry.chemical_element02 engineering and technologySulfonic acid021001 nanoscience & nanotechnologyElectrochemistry01 natural sciencesSulfur0104 chemical sciencesAnalytical ChemistrySulfonechemistry.chemical_compoundAttenuated total reflectionElectrochemistryFourier transform infrared spectroscopy0210 nano-technologyDissolutionOrganosulfur compoundsJournal of Electroanalytical Chemistry
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Analysis of adsorption of phospholipids at the 1,2-dichloroethane/water interface by electrochemical impedance spectroscopy: A study of the effect of…

2007

Abstract The adsorption behaviour of a series of phosphatidylcholines (PCs) with saturated carbon chains of different length (DLPC, DPPC, DSPC, DAPC, and DBPC) at the electrified 1,2-dichloroethane/water interface was studied by measuring electrochemical impedance spectroscopy at the polarized interface. Two different trends in the interfacial capacitance were observed for any of the PCs the capacity dependence on the applied potential: strong adsorption occurs at negative potential with a marked decrease of C ( E ); increase of capacity is observed at positive potentials. It is demonstrated that the interfacial lipid adsorption was dependent on phospholipid concentration, applied potential…

chemistry.chemical_classificationChemistryGeneral Chemical EngineeringPhospholipid adsorptionPhospholipidAnalytical chemistryLiquid-liquid interfaceCapacitanceAnalytical ChemistryDielectric spectroscopyDichloroethanechemistry.chemical_compoundAdsorptionInterfacial capacitancePhosphatidylcholineElectrochemistrylipids (amino acids peptides and proteins)ITIESElectrochemical impedance spectroscopyAlkyl
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Conjugation reactions of polyaromatic quinones to mono- and bisglutathionyl adducts: Direct analysis by fast atom bombardment mass spectrometry

1988

The conjugation products of several reactive quinones with glutathione have been identified by fast atom bombardment mass spectrometry. Appropriate conditions have been developed which enabled the direct, dynamic mass spectral analysis of spontaneous, as well as glutathione transferase catalysed conjugation reactions. Applications to a series of quinones provided the direct detection and differentiation of the formation of mono- and bisglutathionyl adducts between regioisomeric quinone substrates in that only 1,4-quinones yielded bisglutathionyl adducts, which were not observed for the 1,2-isomers.

chemistry.chemical_classificationChemistryGlutathioneFast atom bombardmentMass spectrometryPhotochemistryQuinoneAdductchemistry.chemical_compoundHydrocarbonOrganic chemistrySpectral analysisDirect analysisSpectroscopyBiological Mass Spectrometry
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Role of residual water hydrogen bonding in sugar/water/biomolecule systems: a possible explanation fortrehalose peculiarity

2007

We report on the set of experimental and simulative evidences which enabled us to suggest how biological structures embedded in a non-liquid water–saccharide solvent are anchored to the surrounding matrix via a hydrogen bond network. Such a network, whose rigidity increases by decreasing the sample water content, couples the degrees of freedom of the biostructure to those of the matrix and gives place to protein–saccharide–water structures (protein–solvent conformational substates). In particular, the whole set of data evidences that, while the protein–sugar interaction is well described in terms of a water entrapment hypothesis, the water replacement hypothesis better describes the sugar–m…

chemistry.chemical_classificationChemistryHydrogen bondStereochemistryBiomoleculeCondensed Matter PhysicsTrehaloseSolventchemistry.chemical_compoundtrehalose water FTIR spectroscopyRigidity (electromagnetism)MembraneChemical physicsMoleculeGeneral Materials ScienceSupercoolingJournal of Physics: Condensed Matter
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FT-IR investigation of the state of iron (III) chloride clusters confined in AOT reverse micelles dispersed in carbon tetrachloride

2007

The state of the water-soluble salt iron(III) chloride in AOT reverse micelles dispersed in carbon tetrachloride has been investigated by FT-IR spectroscopy. Interestingly, while the entrapment of a lot of water-soluble inorganic salts in AOT reverse micelles requires preliminarily the presence of significant amounts of water within the micellar core, solubilization of FeCl3 occurs without the need to add water in the micellar solution reaching the very high solubility value, expressed as the maximum salt-to-surfactant molar ratio, of 1.30. The analysis of the spectral features of the investigated samples leads to hypothesize that iron(III) chloride is confined within the reverse micellar c…

chemistry.chemical_classificationChemistryInorganic chemistryIonic bondingGeneral ChemistryConductivityCondensed Matter PhysicsBiochemistryChlorideMicelleCrystallographychemistry.chemical_compoundmedicineGeneral Materials ScienceSolubilization Confinement effects Ferric chloride AOT reverse micelles Ionic clustersCounterionSolubilitySpectroscopyIron(III) chloridemedicine.drug
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Synthesis, structure and physical characterization of the dimer {[(bpy)2Co]2(TPOA)}4+ (bpy=2,2′-dipyridyl; H2TPOA=N,N′,N′′,N′′′-tetraphenyl oxalamidi…

2008

Abstract The reaction between CoCl 2 , 2,2′-dipyridyl (bpy) and N , N ′, N ′′, N ′′′-tetraphenyl oxalamidine (H 2 TPOA) in a water/ethanol mixture yields the {[(bpy) 2 Co] 2 (TPOA)} 2+ dimer, that is immediately oxidized in aerobic conditions leading to the Co III species {[(bpy) 2 Co] 2 (TPOA)} 4+ . This cation was isolated as the {[(bpy) 2 Co] 2 (TPOA)}(PF6) 4 ( 1 ) salt, that was characterized by X-ray diffraction on single crystals. The dimer is formed by two Co III ions in octahedral coordination bridged by a deprotonated μ 2 -TPOA ligand. The Co III ions appear in its low spin configuration. Thus, the dimers are essentially diamagnetic, as shown by 1 H NMR and magnetic measurements.

chemistry.chemical_classificationChemistryLigandDimerOrganic ChemistrySalt (chemistry)Analytical ChemistryIonInorganic ChemistryCrystallographychemistry.chemical_compoundDeprotonationOctahedronProton NMRDiamagnetismSpectroscopyJournal of Molecular Structure
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119Sn Mössbauer spectroscopic studies of the products of the reaction of triorganotin(IV) derivatives with 6-thiopurine

1985

Abstract A structural study of the products of the reaction of R 3 Sn IV derivatives (R = Me, Bu n , Ph) with 6-thiopurine, 6-TPH 2 , and its sodium salt, 6-TPHNa, has been undertaken using Mossbauer spectroscopy and the point-charge model rationalization of the Mossbauer parameter nuclear quadrupole splitting. The synthetic reactions have been carried out at ca . 0 °C, 20 °C and 50 °C. The Mossbauer spectra of the complexes AlK 3 Sn(6-TPH) are consistent with the occurrence of two distinct tin(IV) sites in samples prepared at the lower temperature, while one only site appears by increasing the temperature of the reaction. Two tin sites constantly occur in the products of the reactions invo…

chemistry.chemical_classificationChemistryLigandInorganic chemistrychemistry.chemical_elementQuadrupole splittingInorganic ChemistryCrystallographyTrigonal bipyramidal molecular geometryMössbauer spectroscopyMaterials ChemistryMoietyPhysical and Theoretical ChemistryTinInorganic compoundStoichiometryInorganica Chimica Acta
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Alkali metal complexation properties of resorcinarene bis-crown ethers: effect of the crown ether functionality and preorganization on complexation

2008

Abstract The synthesis and characterization of tetramethoxy resorcinarene tribenzo-bis-crown ethers, m - and p -TBBC6 , are described. The effect of the added aromatic functionality in the crown ether bridge on the alkali metal complexation properties was investigated and compared to the properties of tetramethoxy resorcinarene bis-crown-5 ( BC5 ) by means of 1 H NMR spectroscopy and X-ray crystallography. It was found that BC5 and m -TBBC6 were capable of binding alkali metal cations (K + , Rb + , and Cs + ), with the highest affinity toward Cs + cation, while no binding was observed in the case of p -TBBC6 , which confirms the significance of the complementarity and preorganization for co…

chemistry.chemical_classificationChemistryOrganic ChemistryDrug DiscoveryPolymer chemistryInorganic chemistryProton NMRNO bindingResorcinareneAlkali metalSpectroscopyBiochemistryCrown etherTetrahedron
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A Metal-Free, Nonconjugated Polymer for Solar Photocatalysis

2017

Heterogeneous catalysts that can absorb light over the solar range are ideal for green photocatalysis. Recently, attention has been directed towards the generation of novel solar-light photocatalysts, in particular, metal-free polymers. Herein, it is demonstrated that a metal-free, nonconjugated, anthraquinone-based copolymer (poly[1,4-diamine-9,10-dioxoanthracene-alt-(benzene-1,4-dioic acid)] (COP)) with a strong absorption in the visible region is effective as a sunlight heterogeneous photocatalyst. As a proof of concept, it has been used to mineralize 2,5-dichlorophenol (2,5-DCP) in water under air and sunlight irradiation. The photocatalytic efficiency of COP compares well with that of …

chemistry.chemical_classificationChemistryOrganic ChemistryNanotechnology02 engineering and technologyGeneral ChemistryPolymer010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesFluorescenceAnthraquinoneCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundExcited stateUltrafast laser spectroscopyPhotocatalysis0210 nano-technologyAbsorption (electromagnetic radiation)Chemistry - A European Journal
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Syntheses of novelN-([18F]fluoroalkyl)-N-nitroso-4-methyl-benzenesulfonamides and decomposition studies of corresponding19F- and bromo-analogues: pot…

2003

N-([ 18 F]fluoroalkyl)-N-nitroso-4-methyl-benzensulfonamides [n-alkyl = (-CH 2 ) [ 18,19 F]F, n=2-4)] were synthesized in radiochemical yields ranging from 75-90% to provide new secondary labelling precursors for the syntheses of 18 F-labelled compounds. Preliminary decomposition studies utilizing the corresponding non-radioactive 19 F-compounds as well as the bromo containing analogous compounds were performed to evaluate their stability regarding temperature and basicity of the labelling medium. Furthermore, initial difficulties in labelling these compounds led to the development of a modified labelling procedure applying nearly solvent-free conditions. Extensive decomposition experiments…

chemistry.chemical_classificationChemistryOrganic ChemistryNitrosoBiochemistryDecompositionChemical synthesisAnalytical ChemistrySulfonamidechemistry.chemical_compoundLabellingDrug DiscoveryOrganic chemistryRadiology Nuclear Medicine and imagingReactivity (chemistry)SpectroscopyAlkylJournal of Labelled Compounds and Radiopharmaceuticals
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