Search results for "Proton"

showing 10 items of 5886 documents

Pseudo-solid echoes of proton and deuteron NMR in polyethvlene melts

1981

The solid echo technique is applied to determining residual dipolar and quadrupolar couplings in molten polyethylene (PE) and deuterated PE, respectively. The residual coupling defined by the square root of the second moment is about 1% of the corresponding quantity in the solid. It increases with molecular weight, and decreases with rising temperature. A theoretical treatment of time dependent residual couplings yields a decay time that is found experimentally to be about 0.1 ms in molten PE, and independent of molecular weight and temperature within our limits of accuracy. The residual coupling is discussed in relation with chain entanglement in PE. Measurements of the spin-lattice and sp…

chemistry.chemical_classificationCouplingPolymers and PlasticsProtonSecond moment of areaPolymerPolyethyleneResidualMolecular physicschemistry.chemical_compoundDipoleColloid and Surface ChemistryNuclear magnetic resonancechemistryDeuteriumMaterials ChemistryPhysical and Theoretical ChemistryColloid and Polymer Science
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Binding properties of heptakis-(2,6-di-O-methyl)-β-cyclodextrin and mono-(3,6-anhydro)-β-cyclodextrin: a polarimetric study

2011

The binding constants for the inclusion complexes formed between heptakis-(2,6-di-O-methyl)-β-cyclodextrin (MβCD) and mono-(3,6-anhydro)-β-cyclodextrin (AβCD) with a set of suitably selected organic guests, were measured by means of polarimetry. Measurements were carried out at various pH values in order to ensure the correct protonation state for ionizable guests. Experimental data suggest that the binding properties of MβCD may be rationalized considering the less polar and more hydrophobic character of the cavity, although similar variations in conformational/dynamic behaviour occur as for native βCD. On the other hand, AβCD shows some similarities with αCD, due to the significant distor…

chemistry.chemical_classificationCrystallographyCyclodextrins host-guest complexes polarimetric measurementsCyclodextrinChemistryBinding propertiesSupramolecular chemistryPolarProtonationSettore CHIM/06 - Chimica OrganicaGeneral ChemistryCondensed Matter PhysicsFood ScienceJournal of Inclusion Phenomena and Macrocyclic Chemistry
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Cation and Anion Coordination Chemistry of Palladium(II) with Polyazacycloalkanes. Thermodynamic and Structural Studies

1992

The interaction of PdCI2 4 - with the macrocyclic ligands of the series [3k]aneNk has been studied both in solution and in the solid state. [18]aneN6 and [21]aneN7 form both mono- and binuclear Pd2+ complexes, whose stability constants have been determined in 0.5 mol dm-3 NaCI at 298.15 K. [21]aneN7 also forms, in solution, a trinuclear species in which an amino group deprotonates to bridge two Pd2+ ions, as observed in the solid state. The crystal structure of the complexes [Pd2([18]aneN6)Cl2][CIO4]2 and [Pd3[21]aneN7)CI3][CIO4]2 ⋅ H2O have been solved by single crystal X-ray analysis. C12H30N6CI4O8Pd2: monoclinic, space group C2/m, a = 10.876(2), b = 18.117(2), c = 7.043(2) A, s = 113.78(…

chemistry.chemical_classificationCrystallographyDeprotonationchemistryStereochemistryX-ray crystallographyOrthorhombic crystal systemCrystal structureTriclinic crystal systemSingle crystalCoordination complexMonoclinic crystal system
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Two-Component Hydrogels Formed by Cyclodextrins and Dicationic Imidazolium Salts

2013

In the framework of our recent interest in studying the gelling behaviour of imidazolium salts, we took into account the possibility of obtaining two-component hydrogels by combining cyclodextrins and dicationic imidazolium salts. In particular, we used diimidazolium salts differing in the alkyl chain length and in the size, shape, and coordination ability of the anion, namely the 3,3′-di-n-decyl- and 3,3′-di-n-dodecyl-1,1′-(1,4-phenylenedimethylene)diimidazolium dibromide, and 3,3′-di-n-dodecyl-1,1′-(1,4-phenylenedimethylene)diimidazolium ditetrafluoroborate and dihexafluorophosphate. As far as cyclodextrins are concerned, to gain information on the effects of different sized cyclic oligos…

chemistry.chemical_classificationCyclodextrinOrganic ChemistryResonance (chemistry)FluorescencechemistryChemical engineeringSelf-healing hydrogelsProton NMROrganic chemistryChemical stabilityPhysical and Theoretical ChemistrySpectroscopyAlkylEuropean Journal of Organic Chemistry
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Protein Unfolding:1H-NMR Studies of Paramagnetic Ferricytochrome c-550 from Horse Heart

2005

Electronic transfer protein cytochrome c-550 from horse heart is studied in the unfolded state by means of paramagnetic 1H NMR. The protein contains 104 aminoacid residues and a heme group with low spin FeIII ion in the oxidized form of protein. The global secondary structure is of the α-helix type as occurs in the case of very other cytochromes c investigated such as cyt c-550 from Thiobacillus versutus or cyt c-551 from Pseudomonas aeruginosa. We have studied the coordination characteristic and electronic properties of heme iron horse heart ferricytochrome c-550 at increasing denaturing conditions (up to 3.1 M GuHCl and 288-323 K). The 1H T1 values of the signals were measured and some re…

chemistry.chemical_classificationCytochromebiologyLigandSpin transitionNuclear magnetic resonance spectroscopyInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryProton NMRMetalloproteinbiology.proteinProtein secondary structureHemeZeitschrift für anorganische und allgemeine Chemie
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1H NMR studies of paramagnetic ferricytochrome c-551 from Pseudomonas aeruginosa at high pH: The role of histidine 16 in the spin transition

2005

Abstract Cytochrome c-551 from the mesophile Pseudomonas aeruginosa is an electronic transfer protein that contains 82 amino-acid residues and a c-type heme as the prosthetic group with low spin Fe(II) in the reduced form and low spin Fe(III) in the oxidized form of cytochrome c-551. We have studied the electronic properties of ferricytochrome c-551 from P. aeruginosa at high pH (9–11.4) by means of paramagnetic 1H NMR spectra and the T1 and T2 values of isotropically shifted proton resonances. We have also analyzed the temperature dependence of the hyperfine-shifts. Resonance assignment of some signals was based on 2D saturation transfer experiments, EXSY. These results indicate the existe…

chemistry.chemical_classificationCytochromebiologySpin transitionAnalytical chemistryInorganic Chemistrychemistry.chemical_compoundCrystallographyDeprotonationchemistrySpin crossoverMaterials ChemistryMetalloproteinbiology.proteinProton NMRPhysical and Theoretical ChemistryHemeTwo-dimensional nuclear magnetic resonance spectroscopyPolyhedron
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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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CuIIand ZnIICoordination Chemistry of Pyrazole‐Containing Polyamine Receptors − Influence of the Hydrocarbon Side Chain Length on the Metal Coordinat…

2004

The synthesis of a new macrocyclic receptor (L 4 ) containing two 3,5-dimethylpyrazole units connected by dipropylenetriamine bridges is reported for the first time; pH-metric titrations indicate that L 4 shows six protonation steps in the pH range 2-11. In the absence of metal ions, the pyrazole moieties are not involved in acid-base processes in this pH range. Addition of Cu I I and Zn I I results in deprotonation of the pyrazole moieties which act as bis(monodentate) η 1 :η 1 ligands. This induced deprotonation occurs at higher pH values than in the complexes of the analogous ligand containing diethylenetriamine bridges (L 1 ). The crystal structures of [Cu 2 (H - 2 L 4 )](ClO 4 ) 2 and …

chemistry.chemical_classificationDenticityChemistryStereochemistryLigandPyrazoleCoordination complexInorganic ChemistryCrystallographyTrigonal bipyramidal molecular geometrychemistry.chemical_compoundDeprotonationDiethylenetriamineCoordination geometryEuropean Journal of Inorganic Chemistry
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Solvation chemistry of water-soluble thiol-protected gold nanocluster Au102 from DOSY NMR spectroscopy and DFT calculations

2014

The hydrodynamic diameter of Aum(pMBA)n [(m, n) = (102, 44) and (144, 60)] clusters in aqueous media was determined via DOSY NMR spectroscopy. The apparent size of the same (n, m) cluster depends on the counter ion of the deprotonated pMBA− ligand as explained by the competing ion-pair strength and hydrogen bonding interactions studied in DFT calculations. The choice of the counter ion affects the surface chemistry and molecular structure at the organic/water interface, which is relevant for biological applications.

chemistry.chemical_classificationDeprotonationchemistryHydrogen bondComputational chemistryLigandSolvationCluster (physics)MoleculeGeneral Materials ScienceNuclear magnetic resonance spectroscopyCounterionNanoscale
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Synthesis of γ-Amino Acid Esters by 1,4-Addition of Deprotonated α-Aminonitriles and α-(Alkylideneamino)nitriles to α,β-Unsaturated Esters.

2007

α-Aminonitriles and α-(alkylideneamino)nitriles can serve as readily available α-aminocarbanion equivalents. Their conjugate addition to α,β-unsaturated esters followed by reduction furnishes polysubstituted γ-amino acid esters in moderate to high yield.

chemistry.chemical_classificationDeprotonationchemistryYield (chemistry)fungiOrganic chemistryGeneral MedicineAmino acidConjugateChemInform
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