Search results for " Spectroscopy"

showing 10 items of 6851 documents

Electrosynthesis of Poly(alanine)-Like Peptides in Concentrated Alanine Based Electrolytes, Characterization Coupled to DFT Study and Application to …

2014

The anodic oxidation of concentrated l-alanine on smooth electrodes such as platinum and glassy carbon electrodes was studied. Contrary to the previous studies performed up to now with diluted l-alanine, the electrochemical process generated here results in a completely different situation. The oxidation on smooth platinum was carried out by electrochemical quartz crystal microbalance (EQCM) coupled to cyclic voltammetry technique. The effects of concentration, scan rate, and pH (zwitterion at pH = 6 and alkaline media at pH = 13) on potential values were examined. Glassy carbon and smooth gold electrodes showed the same behavior as on smooth platinum electrode. Spectroscopic analysis such …

ChemistryInorganic chemistrychemistry.chemical_elementInfrared spectroscopyQuartz crystal microbalanceGlassy carbonElectrosynthesisElectrochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyAttenuated total reflectionPhysical and Theoretical ChemistryCyclic voltammetryPlatinumThe Journal of Physical Chemistry C
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Mössbauer spectroscopic studies on compounds containing tin-cadmium and tin-zinc bonds

1975

The Mossbauer parameters of compounds Ph3Sn MCl · TMED (M = Cd, Zn; TMED = N,N,N′,N′-tetramethylethylenediamine), (Ph3Sn)2CdL2 (L2 = TMED, 2,2′-bipyridine and o-phenanthroline) and (Ph3Sn)2 Zn · TMED have been determined and are discussed in connection with Mossbauer data concerning Ph3SnIV derivatives with other Sn-metal bonds. The isomer shift values suggest a high s character in SnCd and SnZn bonds resulting in deviations from regular tetrahedral environments around tin. Experimental quadrupole splittings and calculated partial quadrupole splitting values indicate reduced donor abilities towards the tin atom of an individual Ph3SnIV moiety by Cd-and Zn(Ph3Sn)1−nClnL2 (i.e., the remaini…

ChemistryInorganic chemistrychemistry.chemical_elementQuadrupole splittingZincInorganic ChemistryMetalCrystallographyvisual_artMössbauer spectroscopyQuadrupoleMaterials Chemistryvisual_art.visual_art_mediumMoietyMoleculePhysical and Theoretical ChemistryTinInorganica Chimica Acta
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Low-temperature methyl group dynamics of hexamethylbenzene in crystalline and glassy matrices as studied by 2H NMR

1991

Abstract 2 H NMR spectra of hexamethylbenzene (HMB) in protonated crystalline and amorphous matrices at low temperatures are presented. All spectra reveal lineshape changes which can be attributed to methyl group tunnelling. Compared to neat HMB, a drastic increase of the tunnelling frequency is found for all systems. This indicates that the hindering potential originates predominantly from intermolecular forces. We studied the temperature dependence of these spectra and the spin-lattice relaxation in order to exclude a distribution of motional correlation times describing a thermally activated process. In addition, we find a distortion of the methyl tetrahedron.

ChemistryIntermolecular forceRelaxation (NMR)Spin–lattice relaxationGeneral Physics and AstronomyNuclear magnetic resonance spectroscopyAmorphous solidchemistry.chemical_compoundNuclear magnetic resonanceProton NMRHexamethylbenzenePhysical chemistryPhysical and Theoretical ChemistryMethyl groupChemical Physics Letters
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Investigations of TiO2 films deposited by different techniques

1991

High refractive TiO2 films deposited by reactive electron beam evaporation, reactive ion plating and dip coating have been characterized by optical spectroscopy, electron spectroscopy for chemical analysis, Rutherford backscattering spectroscopy, nuclear reaction analysis and Raman spectroscopy. The spectral refractive index n exhibits a strong dependence on the deposition conditions. These findings will be connected to variations in density, stoichiometry, hydrogen content (H2O) and binding structure of the layers. A strong correlation is found between optical quantities and microscopic properties of TiO2 films.

ChemistryIon platingMetals and AlloysAnalytical chemistryPhysics::OpticsSurfaces and InterfacesDip-coatingElectron spectroscopyElectron beam physical vapor depositionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCondensed Matter::Materials Sciencesymbols.namesakeNuclear reaction analysisMaterials ChemistrysymbolsThin filmSpectroscopyRaman spectroscopyThin Solid Films
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Application of solid-state electrochemistry techniques to polyfunctional organic–inorganic hybrid materials: The Maya Blue problem

2013

Abstract The time evolution of indigo plus palygorskite powdered mixtures during isothermal heating at different temperatures between 120 and 180 °C to form Maya Blue-type materials has been monitored by means of infrared spectrometry, diffuse reflectance spectrometry in the visible region and solid state electrochemical techniques. The kinetics of the formation process of such materials can be described in terms of two consecutive reactions, the first one consisting of the loss of zeolitic water of the palygorskite coupled with clay-indigo attachment and partial indigo to denydroindigo oxidation. The palygorskite dehydration acts as a rate-determining step fitting to a 3D Avrami-Erofe’ev k…

ChemistryKineticsInfrared spectroscopyPalygorskiteGeneral ChemistryCondensed Matter PhysicsElectrochemistryIndigoIsothermal processChemical engineeringMechanics of MaterialsmedicineOrganic chemistryGeneral Materials ScienceDiffuse reflectionHybrid materialmedicine.drugMicroporous and Mesoporous Materials
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Reactions of Carbonyl Compounds in Basic Solutions. Part 351: The Alkaline Hydrolysis and Reactivity – Structure – Spectra Correlations of (Z)-4-(Sub…

2002

The kinetics of the alkaline hydrolysis and the configuration, conformation and electronic structure were studied using IR, NMR spectroscopy, X-ray analysis and AM1 theoretical calculations for a series of (Z)-4-(substituted benzylidene)-2-phenyl-4H-oxazol-5-ones (1) and compared with analogous results reported for (E)-4-benzylidene-2-phenyl-4H-furan-5-ones (5) and related compounds.

ChemistryKineticsOrganic chemistryReactivity (chemistry)General ChemistryElectronic structureNuclear magnetic resonance spectroscopyAlkaline hydrolysis (body disposal)Medicinal chemistrySpectral lineJournal of Chemical Research
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Femtosecond Transient Absorption Study of the Dynamics of Acrylodan in Solution and Attached to Human Serum Albumin

2003

The excited-state relaxation dynamics of the protein-labeling dye acrylodan in solution and attached to human serum albumin has been studied by femtosecond transient absorption spectroscopy. Time-resolved spectra and kinetics of stimulated emission and excited-state absorption in the wavelength region from 400 to 800 nm were studied in ethanol and dimethylformamide. The excited-state solvation dynamics is characterized by multiexponential behavior in both solvents. In ethanol solution, the time dependence of the transient spectra is interpreted in terms of fast solvent relaxation followed by excited-state isomerization of the dye. Acrylodan attached to the protein shows a relaxation compone…

ChemistryKineticsSolvationAnalytical chemistryHuman serum albuminPhotochemistryFluorescenceSurfaces Coatings and FilmsFemtosecondUltrafast laser spectroscopyMaterials ChemistrymedicineRelaxation (physics)Physical and Theoretical ChemistryAbsorption (chemistry)medicine.drugThe Journal of Physical Chemistry B
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Hypervalent tin-organic compounds: Vibrational spectroscopy in the solid as a tool for structure determination

1997

Abstract A full set of IR- and Raman spectra down from 600 cm1 has been determined and assigned for 60 penta- or hexacoordinated tin-compounds in the groups RSn(CH2CH2CH2)3N (R = Cl, Br, I, Me), RR'Sn(MCH2CH2)2X (R,R′ = Cl, Br, I, Me, Ph, M = CH2 S; X = NMe, O, S), RPh2SnCH2CH2CH2NMe2 (R = Cl, Br, I) and RMe2Sn—CHD—COOMe (R = F, Cl, Br, I, Me). In these hypervalent compounds an approach of the donor atom X to the central atom tin outlines a ‘path’ of nucleophilic attack from a tetrahedron to a trigonal bipyramid. Along this ‘reaction path’ the bond lengths of the axial ligand increase continuously while the bond lengths of the equatorial ligands slightly decrease. The number of similar hype…

ChemistryLigandHypervalent moleculechemistry.chemical_elementInfrared spectroscopyAtomic and Molecular Physics and OpticsAnalytical ChemistryBond lengthTrigonal bipyramidal molecular geometryCrystallographysymbols.namesakeComputational chemistryAtomsymbolsTinRaman spectroscopyInstrumentationSpectroscopySpectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
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3D-transition metal mono-substituted Keggin polyoxotungstate with an antenna molecule: synthesis, structure and characterization

2008

Three new organic-inorganic hybrid complexes based on 3d-transition metal monosubstituted Keggin polyoxometalates (POMs) with imidazole (Im) as pendant ligands, formulated as (HIm)(6-)[SiW11O39NiIm]0.8[SiW11O39Ni(H2O)]0.2.7H2O (1), (Im)4Na6[SiW11O39MnIm]0.69[SiW11O39Mn(H2O)]0.31.7.5H2O (2) and (HIm)6[SiW11O39CoIm]0.63[SiW11O39Co(H2O)]0.37.7H2O (3), have been synthesized and characterized by IR spectroscopy, UV-visible spectroscopy, elemental analysis, TG analysis, cyclic voltammetry, magnetic properties, EPR and single-crystal/powder X-ray diffraction. The structural analyses indicate that the 3d metal atoms are incorporated into the vacancy of the alpha-[SiW11O39](8-) (SiW11). Complexes 1-…

ChemistryLigandInorganic chemistryInfrared spectroscopylaw.inventionInorganic ChemistryMetalCrystallographychemistry.chemical_compoundTransition metallawvisual_artvisual_art.visual_art_mediumMoleculeImidazoleCyclic voltammetryElectron paramagnetic resonanceDalton Transactions
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Synthesis and X-ray structure of cationic β-diimine palladium complexes containing π-methallyl ligand

2005

High yield of cationic palladium β-diimine complexes [(CH 2 (MeCNAr) 2 )Pd(η 3 -C 4 H 7 )][Y] (Ar = C 6 H 5 , Y = PF 6 (8); 2-Me-C 6 H 4 , Y = PF 6 (9); 2,6-Me 2 -C 6 H 3 , Y = PF 6 (10); 2,6-iPr 2 -C 6 H 3 , Y = PF 6 (11), Y = B(3,5-(CF 3 ) 2 -C 6 H 3 ) 4 (12)) have been obtained by an oxidative addition of the methallyloxyphosphonium salts (5, 6) to a preformed complex Pd(dba) 2 (7) in the presence of the β-iminoamine ligands (1-4). These complexes are thermally stable and have been characterized by 'H and 1 3 C{ 1 H} NMR as well as IR spectroscopy. The structure of the cationic allyl palladium complex (12) has been solved by X-ray crystallography.

ChemistryLigandOrganic ChemistryX-rayCationic polymerizationInfrared spectroscopychemistry.chemical_elementPhotochemistryBiochemistryMedicinal chemistryOxidative additionInorganic ChemistryYield (chemistry)Materials ChemistryPhysical and Theoretical ChemistryDiiminePalladiumJournal of Organometallic Chemistry
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