Search results for "infrared"

showing 10 items of 2110 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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Complexes of organometallic compounds XXXIII. The coordination chemistry of dimethyl and diphenylthallium(III) ith tridentate ligands

1973

Summary Several novel complexes Na[Me 2 TIL] and Na[Ph 2 TIL] (L 2− =dianion tridentate ligands with S, N, and O donor atoms) were synthesized, and investigated by infrared spectroscopy in the solid state, and by electronic and PMR spectroscopy in solution. Suggestions for the configuration of the complex anions are advanced and the nature of species present in solution is discussed.

chemistry.chemical_classificationChemistryStereochemistryOrganic ChemistrySolid-stateInfrared spectroscopyBiochemistryCoordination complexInorganic ChemistryPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistrySpectroscopyGroup 2 organometallic chemistryJournal of Organometallic Chemistry
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Near infrared dyes by combination of squaraine and ferrocene chromophores

2000

Abstract Squaraines represent a class of compounds which attracts a lot of attention in materials science. A synthetic sequence for the preparation of the symmetrical squaraines 12a , b , which contain ferrocene units as electron donors, is described. The compounds exhibit, in dichloromethane or chloroform, two intense absorption bands. One of them is located at 641/650 nm—a normal region for squaraines; however, the other band is strongly shifted to long wavelengths and has its maximum at 921/961 nm. Alkyl sidechains enhance the solubility of 12a , b , which represent a new type of NIR dyes.

chemistry.chemical_classificationChloroformOrganic ChemistryNear-infrared spectroscopyChromophorePhotochemistryBiochemistrychemistry.chemical_compoundchemistryFerroceneDrug DiscoveryAbsorption (chemistry)SolubilityAlkylDichloromethaneTetrahedron Letters
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Characterization of aquatic humic substances and their metal complexes by immobilized metal-chelate affinity chromatography on iron(III)-loaded ion e…

2001

The analytical fractionation of aquatic humic substances (HS) by means of immobilized metal-chelate affinity chromatography (IMAC) on metal-loaded chelating ion exchangers is described. The cellulose HYPHAN, loaded with different trivalent ions, and the chelate exchanger Chelex 100, loaded to 90% of its capacity with Fe(III), were used. The cellulose HYPHAN, loaded with 2% Fe(III), resulted in HS distribution coefficients Kd of up to 10(3.7) mL/g at pH 4.0 continuously decreasing down to 10(1.5) at pH 12, which were appropriate for HS fractionation by a pH-depending chromatographic procedure. Similar distribution coefficients Kd were obtained for HS sorption onto Fe(III)-loaded Chelex 100. …

chemistry.chemical_classificationChromatographyIon exchangeElutionIronSorptionFractionationReference StandardsChromatography Ion ExchangeBiochemistryChromatography Affinitychemistry.chemical_compoundChelex 100chemistryMetalsSpectroscopy Fourier Transform InfraredHumic acidSpectrophotometry UltravioletChelationCelluloseHumic SubstancesWater Pollutants ChemicalChelating AgentsFresenius' Journal of Analytical Chemistry
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Conformational characteristics of homo-oligopeptides of O-benzyl-L-tyrosine+

1983

Conformational studies of X[-L-Tyr(Bzl)-]n-series bound to polyethyleneglycol (X = H2, Nps; n = 3-8) in the solid state and in solvents of different polarities and capabilities of forming hydrogen bonds are reported. By using i.r. absorption, the occurrence of the beta-structure in the higher oligomers in the solid state was established. By means of i.r. absorption and CD the onset of that ordered conformation in solution was assessed as a function of chain length. The effects induced by the presence of the N-protecting group and added base, and by changing the nature of solvent on the conformational preferences of the [-L-Tyr(Bzl)-]n homo-peptides were also examined. The 2-nitrophenylsulph…

chemistry.chemical_classificationCircular dichroismChemical PhenomenaSpectrophotometry InfraredBase (chemistry)Protein ConformationStereochemistryHydrogen bondCircular DichroismInfrared spectroscopyBiochemistryPeptide ConformationSolutionsSolventChemistrychemistry.chemical_compoundchemistryTyrosineAbsorption (chemistry)OligopeptidesDerivative (chemistry)International Journal of Peptide and Protein Research
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Enantioselektive Trifluoracetylierung mit Hilfe chiraler Polyamide

1980

(S)-Poly(2-aminobutyric acid) (1) [(S)-poly(imino-1-methyl-3-oxotrimethylene)] was transformed into its N-trifluoroacetyl derivative 4. The IR spectra and the circular dichroism of both substances were compared. In addition, (S)-poly[N-(1-phenylethyl)acrylamide] (2) ((S)-poly-[1-(1-phenylethylaminocarbonyl)ethylene]) was trifluoroacetylated leading to polymer 5. 4 was found to react as trifluoroacetylating agent with L-1-phenylethylamine (L-3) twice as fast as it reacts with D-3. Accordingly, the reaction of 4 with D,L-3 leads preferentially to the L-form of N-(1-phenylethyl)trifluoroacetamide with optical yields up to 6%. The reaction of 5 with D,L-3 affords the D-form of N-(1-phenylethyl)…

chemistry.chemical_classificationCircular dichroismchemistry.chemical_compoundEthylenechemistryAcrylamidePolymer chemistryInfrared spectroscopyPolymerDerivative (chemistry)Die Makromolekulare Chemie
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Synthesis of new electroactive polymers by ion-exchange replacement of Mg(II) by 2H+ or Zn(II) cations inside Mg(II) polyporphine film, with their su…

2014

Abstract It has been demonstrated that the treatment of the magnesium polyporphine of type I, pMgP-I, by trifluoroacetic acid in acetonitrile may be used to replace initial central Mg(II) cations inside the monomeric macrocycle units by protons, to get a new electroactive polymer, “free-base polyporphine of type I”, pH2P-I. In its turn, these inserted protons may be replaced by Zn(II) cations via the film treatment with zinc acetate in organic solvent, to get another new electroactive polymer, “zinc polyporphine of type I”, pZnP-I. These changes of central ions inside monomer units manifest themselves by characteristic modifications of their electroactive properties as well as of UV–visible…

chemistry.chemical_classificationConductive polymerGeneral Chemical EngineeringInorganic chemistryInfrared spectroscopychemistry.chemical_elementPolymerZincElectrochemistrychemistry.chemical_compoundMonomerchemistryElectrochemistryElectroactive polymersAcetonitrileElectrochimica Acta
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Electropolymerization of N-methylanthranilic acid and spectroelectrochemical characterization of the formed film

2009

Abstract The electropolymerization of N-methylanthranilic acid (NMAA) is reported in this paper. The monomer is substituted both at ortho- and N-position and, to the best of our knowledge, it has not been previously electropolymerized. Electropolymerization of NMAA was done on glassy carbon and optically transparent (indium) tin oxide electrodes. The obtained films, which are probably of an oligomeric nature (oligoNMMA), were characterized with cyclic voltammetry (CV), in situ UV–vis and Raman spectroscopy, ex situ FTIR spectroscopy and scanning electron microscopy (SEM). Our results show that NMAA can be electropolymerized as thin films in 1.0 M HClO4, but the oxidation and reduction peak …

chemistry.chemical_classificationConductive polymerMaterials scienceMechanical EngineeringCarboxylic acidMetals and AlloysGlassy carbonCondensed Matter PhysicsTin oxideElectronic Optical and Magnetic Materialssymbols.namesakeUltraviolet visible spectroscopychemistryMechanics of MaterialsPolymer chemistryMaterials ChemistrysymbolsFourier transform infrared spectroscopyCyclic voltammetryRaman spectroscopySynthetic Metals
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In-situ polymerization of polyaniline in radiation functionalized polypropylene films

2015

Abstract In-situ generation of a nanodispersed conductive polymer within a polypropylene matrix has been pursued in order to obtain flexible, conductive films. Radiation grafting of acrylic acid to polypropylene (PP) has been applied to insert carboxyl functionalities on PP. The radiation-grafted films have been further derivatized with a variety of diamines and used as substrates for in-situ chemical oxidative polymerization of polyaniline (PANI). PANI grows as a thin skin from the surface of the film as well as an interpenetrated network in its interiors. Evidence of chemical attachment of PANI to PP has been sought by performing FTIR and XPS analyses after extraction of the unbound polym…

chemistry.chemical_classificationConductive polymerPolypropyleneMaterials sciencePolymers and PlasticsPolyanilineOrganic ChemistryConductive filmsConductive filmRadiation graftingPolymerSettore ING-IND/27 - Chimica Industriale E Tecnologicachemistry.chemical_compoundchemistryPolymerizationPolyanilinePolymer chemistryMaterials ChemistrySettore CHIM/07 - Fondamenti Chimici Delle TecnologieIn situ polymerizationFourier transform infrared spectroscopyAcrylic acidPolymer
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Chemical characterization of peat fulvic acid fractions

1993

Abstract Milled peat fulvic acid (FA) preparation was fractionated by XAD-8 and conventional extraction methods. The fractions were further analyzed by IR and NMR and subjected to cupric oxide (CuO) oxidation. Carbohydrates of polydisperse FA were mostly not retained in the XAD-8 fractionation. The intensity of the signals due to double bonded carbons was much greater in the 13 C and proton NMR spectrum of the XAD-8 retained fraction than in the spectra of the XAD-8 non-retained or XAD-8 non-treated fractions. In CuO oxidation the main products of all FA fractions were 4-hydroxybenzaldehyde and 4-hydroxyacetophenone, both indicators of 4-hydroxyphenylpropane building blocks. Their concentra…

chemistry.chemical_classificationDegree of unsaturationEnvironmental EngineeringDouble bondChemistryHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthAnalytical chemistryInfrared spectroscopyAromaticityFraction (chemistry)General MedicineGeneral ChemistryFractionationPollutionNMR spectra databaseProton NMREnvironmental ChemistryNuclear chemistryChemosphere
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