Search results for "Nuclear magnetic resonance"

showing 10 items of 1743 documents

A novel germacranolide-aminoacid adduct dimer from centaurea aspera

1991

Abstract The novel germacronolide-valine adduct dimer 1 has been isolated from aerial parts of Centaurea aspera var. aspera . Its structure has been determined by spectroscopic methods.

chemistry.chemical_classificationGermacranolideStereochemistryDimerfungiOrganic ChemistryNuclear magnetic resonance spectroscopySesquiterpeneBiochemistryAdductchemistry.chemical_compoundchemistryDrug DiscoveryCentaurea asperaLactoneTetrahedron Letters
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Structural studies of adsorbed protein (betalactoglobulin) on natural clay (montmorillonite)

2014

International audience; In this work, the adsorption of a small globular protein (betalactoglobulin, BLG), on a natural montmorillonite clay (Mt) was investigated in acidic buffer (pH = 3). The combination of different characterization techniques such as zetametry, X-ray diffraction, transmission electronic microscopy, fluorescence and solid state nuclear magnetic resonance spectroscopies shed light on the interaction mechanism between the clay mineral and the proteins. For low BLG concentration, a slight increase of the interlayer spacing of the clay mineral was noticed as well as structural changes of the protein. In contrast, as the concentration of BLG increased, the adsorption led to a…

chemistry.chemical_classificationGlobular proteinGeneral Chemical EngineeringMineralogyGeneral ChemistryExfoliation jointFluorescencechemistry.chemical_compoundAdsorptionMontmorillonitechemistryChemical engineeringSolid-state nuclear magnetic resonance[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyClay mineralsHybrid materialRSC Adv.
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Counterion influence on the N–I–N halogen bond

2015

A detailed investigation of the influence of counterions on the [N–I–N]+ halogen bond in solution, in the solid state and in silico is presented. Translational diffusion coefficients indicate close attachment of counterions to the cationic, three-center halogen bond in dichloromethane solution. Isotopic perturbation of equilibrium NMR studies performed on isotopologue mixtures of regioselectively deuterated and nondeuterated analogues of the model system showed that the counterion is incapable of altering the symmetry of the [N–I–N]+ halogen bond. This symmetry remains even in the presence of an unfavorable geometric restraint. A high preference for the symmetric geometry was found also in …

chemistry.chemical_classificationHalogen bond010405 organic chemistryHydrogen bondcounterion; halogen bond; single crystal X-ray diffraction; DFT computationInorganic chemistryGeneral ChemistryNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciencesN–I–N halogen bond0104 chemical sciencesCrystallographyChemical bondchemistryTransition metalCounterionta116Single crystalBasis setChemical Science
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Dimethoxy aromatic compounds. IV.—determination of stereochemistry of 2,3,6,7-tetraalkoxy-9,10-dihalomethyl-9,10-dihydroanthracenes by13C NMR chemica…

1987

The analysis of the 13C NMR spectra of several 2,3,6,7-tetraalkoxy-9,10-dihalomethyl-9,10-dihydroanthracenes showed a strong dependence of the chemical shift values on the orientation of the halomethyl groups. On this basis it was possible to determine both the configuration (cis or trans) and conformation of the isomers, even if only one isomer was available.

chemistry.chemical_classificationHydrocarbonChemistryStereochemistryChemical shiftChemical solutionGeneral Materials ScienceGeneral ChemistryNuclear magnetic resonance spectroscopyCarbon-13 NMRMagnetic Resonance in Chemistry
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17O NMR study of isomeric monochloro- and monohydroxy-benzaldehydes and chlorinated salicylaldehydes

1991

The 17O NMR chemical shifts of isomeric monochloro- and monohydroxy-benzaldehydes and chlorinated salicylaldehydes were measured at 40°C for 0.25 M CDCI3 solutions. The 17O NMR chemical shift of the carbonyl oxygen of the compounds studied varies from 506 to 573 ppm measured from external D2O. The observed variation is probably mainly due to the intramolecular hydrogen bonding between the adjacent carbonyl and hydroxyl groups. The 17O NMR chemical shift range of the hydroxyl oxygen is from 80 to 98 ppm.

chemistry.chemical_classificationHydrogen bondChemical shiftchemistry.chemical_elementGeneral ChemistryNuclear magnetic resonance spectroscopyAldehydeMedicinal chemistryOxygenchemistryIntramolecular forceOrganic chemistryChemical solutionGeneral Materials ScienceMagnetic Resonance in Chemistry
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Impact of O → S Exchange in Ferrocenyl Amides on the Structure and Redox Chemistry

2014

The conformations and redox chemistry of ferrocenyl amides have been investigated in considerable depth in the last few years, while ferrocenyl thioamides have attracted less interest so far, although distinctly different conformations and reactivity patterns are expected. Monoferrocenyl amides Fc-NHC(O)CH3 (1) and 1,1′-CH3O(O)C-Fn-NHC(O)CH3 (2) and diferrocenyl amides Fc-NHC(O)-Fc (5) and Fc-NHC(O)-Fn-NHC(O)CH3 (6) are easily transformed into the corresponding thioamides (3, 4, 7, 8) by treatment with Lawesson’s reagent (2,4-bis(p-methoxyphenyl)-1,3-dithiaphosphetane-2,4-disulfide) (Fc = Fe(C5H4)(C5H5), Fn = Fe(C5H4)2). The thioamide conformations (cis/trans) in 3, 4, 7, and 8 and the hydr…

chemistry.chemical_classificationHydrogen bondOrganic ChemistryNuclear magnetic resonance spectroscopyRedoxInorganic ChemistryCrystallographychemistryReagentElectronic communicationReactivity (chemistry)Physical and Theoretical ChemistryProtein secondary structureThioamideOrganometallics
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Interactions between 2-Aminobenzothiazole and Natural Organic Matter as Evidenced by CPMAS Nitrogen-15 NMR Spectroscopy

2009

Cross-polarization magic angle spinning (CPMAS) 15N nuclear magnetic resonance (NMR) spectroscopy was used to study the interactions between 2-aminobenzothiazole (ABT) and natural organic matter in the presence of the natural enzyme laccase and synthetic air. Through the use of synthesized model compounds, we were able to confirm previous findings by CPMAS 13C NMR spectroscopy that showed the formation of covalent amide bonds. We also provide evidence of the presence of two additional H bonds between ABT and the natural organic matter. Both H bonds involved the amino and thiazole groups of ABT.

chemistry.chemical_classificationHydrogen bondSettore AGR/13 - Chimica AgrariaHASoil Science2-aminobenzothiazolenuclear magnetic resonance.Nuclear magnetic resonance spectroscopyCPMAShumic acidCarbon-13 NMRABTNMRchemistry.chemical_compoundchemistryCovalent bondMagic angle spinningOrganic chemistryOrganic mattercross-polarization magic angle spinningHPLChigh-performance liquid chromatographyThiazoleSpectroscopy
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The effect of disorder on optical spectra of conjugated polymers

1993

Abstract Using the semi-empirical parametrization of the Pariser-Parr-Pople model we determine the excitonic states in conjugated polymers. The employed parameters correspond to a moderate strength of the long-range Coulomb interaction. In order to take the disorder into account, the nearest-neighbour transfer matrix elements are chosen according to a random distribution. Averaging the results over a large number of chains of 100 sites, which are known to be sufficiently long so that finite-size effects become negligible, we obtain the linear and third-order nonlinear optical susceptibilities. With increasing disorder the linear absorption, the two-photon absorption and the third-harmonic g…

chemistry.chemical_classificationImaginationChemistryMechanical Engineeringmedia_common.quotation_subjectMetals and AlloysPolymerCondensed Matter PhysicsAsymmetryMolecular physicsTransfer matrixSpectral lineElectronic Optical and Magnetic MaterialsNuclear magnetic resonanceMechanics of MaterialsMaterials ChemistryCoulombAbsorption (electromagnetic radiation)Parametrizationmedia_commonSynthetic Metals
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Mononuclear mixed oxosulfidomolybdate(VI) complexes with aminodicarboxylic ligands. Synthesis and spectroscopic characterization by multinulcear magn…

1993

Addition of B2S3 to a methanolic solution of the MoVIO3L2− complex (L=N,N-bis(ethanoic acid)-1-amino-2- methylthio-ethane) results in the formation of two different monomeric oxosulfidomolybdate(VI) complexes, [MoO2SL]2− and [MoOS2L]2− as indicated by 1H, 13C, 17O and 95Mo NMR spectroscopy and by the reaction of these two sulfurated species with triphenylphosphine. The temperature dependences of the 1H NMR spectra indicate exchange processes for both sulfido complexes. Their redox properties are discussed and contrasted with those observed for the parent fac-trioxo molybdenum(VI) complex. The primary synthetic route to mixed oxosulfido [MoO3−nSnL]2− complexes described here can be extended …

chemistry.chemical_classificationIminodiacetic acidStereochemistryCarboxylic acidNuclear magnetic resonance spectroscopyRedoxInorganic Chemistrychemistry.chemical_compoundMonomerchemistryDiaminePolymer chemistryMaterials ChemistryProton NMRPhysical and Theoretical ChemistryTriphenylphosphineInorganica Chimica Acta
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Maghemite polymer nanocomposites with modulated magnetic properties

2007

A method is presented for the production of maghemite polymer nanocomposites with modulated magnetic properties. Magnetic nanocomposites prepared using this method show regular variation in the magnetic blocking temperature from 2 K to 300 K, and variation in the saturation magnetization from 0 to 50 emu g � 1 (Fe2O3). The method is based on the in situ formation of maghemite nanoparticles in nitrogen-base polymer matrixes. The particle size can be varied regularly from 1.5 nm to 16 nm by changing the ratio of iron loading in the polymer and/or the Fe(II)/Fe(III) ratios. The particles are isolated and uniformly distributed within the matrix. The mate

chemistry.chemical_classificationIn situNanocompositeMaterials sciencePolymers and PlasticsPolymer nanocompositeMetals and AlloysMaghemiteNanoparticlePolymerengineering.materialElectronic Optical and Magnetic MaterialsNuclear magnetic resonancechemistryChemical engineeringCeramics and CompositesengineeringParticle sizeActa Materialia
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