Search results for "Spectroscopy"

showing 10 items of 10293 documents

Dicopper(II) Metallacyclophanes with N,N'-2,6-Pyridinebis(oxamate): Solution Study, Synthesis, Crystal Structures, and Magnetic Properties.

2016

The complexing ability of copper(II) in solution by the ligand N,N'-2,6-pyridinebis(oxamic acid) (H4mpyba, H4L) was determined through potentiometric and UV-vis spectroscopy at 25 °C and 0.15 M NaCl. The logarithms of the equilibrium constants for its copper(II) complexes according to the eqs 2H2L + 2Cu ⇆ [Cu2(H2L)2], 2H2L + 2Cu ⇆ [Cu2(H2L) (HL)] + H, 2H2L + 2Cu ⇆ [Cu2(HL)2] + 2H, 2H2L + 2Cu ⇆ [Cu2(HL)(L)] + 3H, and 2H2L + 2Cu ⇆ [Cu2L2] + 4H were 12.02(7), 8.04(5), 1.26(6), -7.51(6), and -16.36(6), respectively. The knowledge of the solution behavior has supported the synthesis of three new compounds bearing the common building block Cu2L2(4-). Their formulas are (Me4N)4[Cu2(mpyba)2(H2O)2]·…

Tetramethylammonium010405 organic chemistryStereochemistryLigandPotentiometric titrationOxamic acidchemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciencesCopper0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryPhysical and Theoretical ChemistrySpectroscopyEquilibrium constantInorganic chemistry
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Aromatic Bridged Bis-phenol A Derived Cyclophanes. Synthesis, Molecular Structure and Binding Properties Toward Quats

2003

Three novel polyoxyethylene bridged bis phenol A derived cyclophanes, {\rm 2 -- 4,} with additional aromatic units in the bridge to increase the number of cation–π interactions with guest cations, were synthesized and characterized by means of X-ray crystal structure determinations. The binding properties of these receptors toward tetramethylammonium (TMA), N-methylpyridinium (NMP), acetylcholine (ACh) and N-methylquinolinium (NMQ) salts were evaluated by means of 1H NMR spectroscopy and compared with those of the previously reported receptor 1.

Tetramethylammonium1h nmr spectroscopychemistry.chemical_compoundMolecular recognitionchemistryStereochemistryBinding propertiesSupramolecular chemistryPhenolMoleculeGeneral ChemistryCrystal structureMedicinal chemistrySupramolecular Chemistry
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Organotin(IV) azido and mixed azidothiocyanato complex anions; A Mössbauer and vibrational spectroscopic study

1975

Abstract Tetraphenylarsonium and tetramethylammonium salts of the complex anions Ph 3 Sn(N 3 ) − 2 , Ph 3 Sn(N 3 )(NCS) − , Me 2 Sn(N 3 ) 2− 4 and Ph 2 Sn(N 3 ) 2 (NCS) 2− 2 have been synthesized, and the solid state configuration of the complex anions has been studied by Mossbauer and vibrational spectroscopies. Trigonal bipyramidal structures are advanced for the Ph 3 Sn IV derivatives, with equatorial SnC 3 and apical pseudohalide ligands, while the R 2 Sn IV compounds are assumed to be trans -octahedral species. The NCS − ligands are observed to be N-bonded to Sn IV . Conductance and PMR (for the Me 2 Sn IV compound) data suggest the presence of the complex anions also in solution phase…

TetramethylammoniumStereochemistryOrganic ChemistrySolid-stateConductanceBiochemistryInorganic ChemistryTrigonal bipyramidal molecular geometrychemistry.chemical_compoundCrystallographyOctahedronchemistryMössbauer spectroscopyMaterials ChemistryPhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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Screening of some banned aromatic amines in textile products from Indian bandhani and gamthi fabric and in human sweat using micellar liquid chromato…

2021

Certain dyes in textile products, which are capable of reductively splitting into carcinogenic aromatic amines, are strictly controlled in many countries. A simple, rapid, sensitive and green chromatographic method has been developed and validated for the simultaneous determination of 4-aminophenol (4-AMP), p-phenylenediamine (p-PPD) and benzidine (BNZ), banned aromatic amines in dyeing clothes and human sweat. The separation was achieved using a micellar mobile phase of 0.1 M SDS, 4% 1- butanol (v/v) buffered to pH 7 with sodium dihydrogen phosphate, flowing under isocratic mode at 1 mL/min through a C18 column. Photodiode array detector was set at 210 nm. Using the above chromatographic c…

TextileCalibration curve02 engineering and technologydyes01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundSpectroscopyvalidationChromatographytextilebusiness.industryChemistryElutionButanol010401 analytical chemistry021001 nanoscience & nanotechnologyBenzidine0104 chemical sciencessweatMicellar liquid chromatographychromatographyDyeing0210 nano-technologySelectivitybusinesscarcinogenicMicrochemical Journal
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Sulfur isotope ratio measurements of individual sulfate particles by NanoSIMS

2008

Abstract The sulfur isotopic compositions of barite (BaSO4), anhydrite (CaSO4), gypsum (CaSO4·2H2O), mascagnite ((NH4)2SO4), thenardite (Na2SO4), boetite (K2SO4), epsomite (MgSO4·7H2O), magnesium sulfate (MgSO4·xH2O) and cysteine (an amino acid) were determined with a Cameca NanoSIMS 50 ion microprobe employing a Cs+ primary ion beam and measuring negative secondary ions. This ion microprobe permits the analysis of sulfur isotope ratios in sulfates on 0.001–0.5 ng of sample material, enabling the analysis of individual S-bearing particles with diameters as small as 500 nm. The grain-to-grain reproducibility of measurements is typically 5‰ (1σ) for micron-sized grains,

ThenarditeMicroprobeAnhydriteIon beamMagnesiumEpsomiteAnalytical chemistrychemistry.chemical_elementCondensed Matter PhysicsSulfurchemistry.chemical_compoundchemistryPhysical and Theoretical ChemistrySulfateInstrumentationSpectroscopyInternational Journal of Mass Spectrometry
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IR fingerprints of U(VI) nitrate monoamides complexes: a joint experimental and theoretical study.

2010

Infrared spectra of 0.5 mol·L-1 uranium(VI) nitrate monoamide complexes in toluene have been recorded and compared with infrared spectra calculated by DFT. The investigated monoamides were N,N- dimethylformamide (DMF), N,N-dibutylformamide (DBF), and N,N- dicyclohexylformamide (DcHF). The validity of DFT calculations for describing uranium nitrate monoamide complexes has been confirmed as a fair agreement between experimental and calculated spectra was obtained. Furthermore, a topological analysis of the electron density has been carried out to characterize monoamide-uranium interactions. From this work, it appears that the increase of stability of uranylmonoamide complexes may be directly …

Theoretical studyElectron densityTopological analysis Engineering controlled terms: DimethylformamideInorganic chemistryDFT calculationStrontium compoundchemistry.chemical_elementInfrared spectroscopyLigand010402 general chemistryTopology01 natural sciencesElectrostatic interactionSpectral linechemistry.chemical_compoundDelocalized electronNitratePositive charge[CHIM]Chemical SciencesPhysical and Theoretical ChemistryElectron densitieInfrared spectrumSpectroscopyComputingMilieux_MISCELLANEOUSLigand molecule010405 organic chemistrySulfur compoundUraniumTolueneN N-Dimethylformamide0104 chemical sciencesStable complexe[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistryOrganic solventUraniumPhysical chemistryDegree of polarizationDegree of polarizationMonoamideUranium compounds Engineering main heading: ComplexationTolueneThe journal of physical chemistry. A
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Optimizing the Binding Energy of the Surfactant to Iron Oxide Yields Truly Monodisperse Nanoparticles.

2018

Despite the great progress in the synthesis of iron oxide nanoparticles (NPs) using a thermal decomposition method, the production of NPs with low polydispersity index is still challenging. In a thermal decomposition synthesis, oleic acid (OAC) and oleylamine (OAM) are used as surfactants. The surfactants bind to the growth species, thereby controlling the reaction kinetics and hence playing a critical role in the final size and size distribution of the NPs. Finding an optimum molar ratio between the surfactants oleic OAC/OAM is therefore crucial. A systematic experimental and theoretical study, however, on the role of the surfactant ratio is still missing. Here, we present a detailed exper…

Thermal decompositionDispersityIron oxideNanoparticle02 engineering and technologySurfaces and Interfaces010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical scienceschemistry.chemical_compoundOleic acidPulmonary surfactantchemistryChemical engineeringOleylamineElectrochemistryGeneral Materials Science0210 nano-technologySpectroscopyIron oxide nanoparticlesLangmuir : the ACS journal of surfaces and colloids
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Adsorption of m-Xylene on Prehydrated Zeolite BaX:  Correlation between Temperature-Programmed Desorption and Low-Temperature Neutron Powder Diffract…

1999

Adsorption of m-xylene on partially hydrated zeolite BaX is studied by thermogravimetry, mass spectrometry, temperature-programmed desorption and neutron diffraction for different m-xylene loadings of the zeolite. Macroscopic and microscopic measurements, for both molecules, were correlated and relationships were found between the crystallographic positions of the adsorbed molecules on the zeolite and macroscopic properties such as the number and the area of the peaks in the desorption spectra for m-xylene or water. The influence of water molecules on the adsorption phenomenon of m-xylene on BaX zeolite was characterized. In particular, it was shown that the increase of the filling of the p…

Thermal desorption spectroscopyNeutron diffractionAnalytical chemistrySurfaces and InterfacesActivation energyCondensed Matter Physicsm-XyleneThermogravimetrychemistry.chemical_compoundAdsorptionchemistryDesorptionElectrochemistryGeneral Materials ScienceZeoliteSpectroscopyLangmuir
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Surface properties and catalytic performance for ethane combustion of La1−xKxMnO3+δ perovskites

2001

Abstract The influence of K substitution in LaMnO3 perovskite on the surface properties and catalytic oxidation of ethane has been studied. La1−xKxMnO3+δ perovskites (x=0.05, 0.10, 0.15, 0.20 and 0.25) with BET surface area of 20–26 m2 g−1 have been prepared by the freeze-drying method and characterized by X-ray diffraction patterns (XRD), TPR, TPD and XPS. The XRD analyses showed the presence of a single crystalline phase (x≤0.15) with the linear increase of the lattice parameter corroborating the incorporation of potassium in the perovskite structure. The XPS studies revealed an enrichment of the perovskite surface with potassium accompanied by an increase in the surface Mn4+/Mn3+ ratio. …

Thermal desorption spectroscopyProcess Chemistry and TechnologyInorganic chemistrychemistry.chemical_elementOxygenCatalysisPotassium oxideCatalysischemistry.chemical_compoundCatalytic oxidationchemistryDesorptionPerovskite (structure)BET theoryApplied Catalysis A: General
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Biomass-based composite catalysts for catalytic wet peroxide oxidation of bisphenol A : preparation and characterization studies

2019

Abstract The wet granulation process was used to prepare new, efficient, and cost-effective granular biomass-based composite catalysts for catalytic wet peroxide oxidation (CWPO) of bisphenol A (BPA). The most stable composite granules was prepared by mixing biomass-based carbon residue (CR) with metakaolin (MK) combined with calcium oxide (CaO) or cement and a solvent (NaOH or KOH). For all the prepared composite granules, the optimized binding agents to carbon ratio was 0.3, the solvent to carbon ratio 1.2, and the agitation rate 1200 rpm. The specific surface area of the prepared catalysts was 152–205 m2/g. The composite granular catalyst (CR + MK + CaO + NaOH) had the most durable and s…

Thermal desorption spectroscopybiomassacomposite catalystComposite numbergranular activated carbon02 engineering and technologyjätevesi010501 environmental sciences01 natural sciencesPeroxidewastewater purificationCatalysisGranulationchemistry.chemical_compoundSpecific surface areaChemical Engineering (miscellaneous)Calcium oxideWaste Management and Disposalta116komposiitit0105 earth and related environmental sciencesjäteveden käsittelybiomassProcess Chemistry and Technology021001 nanoscience & nanotechnologyPollutionSolventchemistryaktiivihiilioxidation of bisphenol A0210 nano-technologyNuclear chemistryJournal of Environmental Chemical Engineering
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