Search results for "Proton"

showing 10 items of 5886 documents

2-Acylamino- and 2,4-bis(acylamino)pyrimidines as supramolecular synthons analysed by multiple non-covalent interactions. DFT, X-ray diffraction, and…

2012

Intermolecular interactions of ten 2-acylamino and 2,4-bis(acylamino)pyrimidines (7 of which are previously unknown) have been investigated by X-ray structural, quantum chemical (DFT), and NMR spectral methods. Especially the concentration dependencies of the (1)H NMR chemical shifts and titrations with other molecules capable of multiple hydrogen bonding provided useful information regarding their association via triple or quadruple hydrogen bonding, which is controlled by the conformational preferences of 2-acylamino- and 2,4-bis(acylamino)pyrimidines. On comparison of the properties of 2-acylamino- and 2,4-bis(acylamino)pyrimidines with the corresponding pyridines, an additional nitrogen…

chemistry.chemical_classificationMagnetic Resonance SpectroscopyHydrogen bondStereochemistryOrganic ChemistrySubstituentSupramolecular chemistryMolecular ConformationHydrogen BondingNuclear magnetic resonance spectroscopyCrystallography X-Raychemistry.chemical_compoundCrystallographyPyrimidineschemistryX-Ray DiffractionProton NMRMoleculeNon-covalent interactionsQuantum TheoryConformational isomerismta116Journal of Organic Chemistry
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Conformational studies of hexapeptides containing two dehydroamino acid residues in positions 2 and 5 in peptide chain

2008

Conformational preferences of a group of hexapeptides containing two dehydroamino acid residues in Positions 2 and 5 in peptide chain were investigated by means of spectroscopic methods (NMR and CD) and theoretical calculations. In the case of dimethylsulfoxide (DMSO) solution, only peptide with free N-termini adopted rigid 310-helical conformation, for the rest of examined peptides extended and “zig-zag” conformers were predominant. CD measurements showed that only in chloroform solution the conformational freedom of investigated peptides was restricted. © 2008 Wiley Periodicals, Inc. Biopolymers 89: 691–699, 2008. This article was originally published online as an accepted preprint. The “…

chemistry.chemical_classificationMagnetic Resonance SpectroscopyProtein ConformationStereochemistryCircular DichroismMolecular Sequence DataOrganic ChemistryTemperatureBiophysicsPeptideGeneral MedicineAmidesBiochemistryProtein Structure SecondaryBiomaterialschemistry.chemical_compoundChain (algebraic topology)chemistryDehydroalanineAmino Acid SequenceAmino AcidsProtonsPeptidesConformational isomerismBiopolymers
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Design and characterization of bi-functional electrocatalytic layers for application in PEM unitized regenerative fuel cells

2010

Abstract Results concerning the development and characterization of bi-functional electrocatalytic layers for application in unitized regenerative fuel cells (URFCs) based on proton exchange membrane (PEM) technology are reported. Carbon-supported hydrophobic (10 wt.% of PTFE) Pt catalysts (40 wt.% of Pt), and Pt and Ir black powders of large specific areas have been synthesized. Their structure, morphology and electrochemical properties have been investigated using SEM, TEM, XRD analysis, and by measurements of polarization curves and cyclic voltammograms. Current–voltage curves have been recorded during water electrolysis and H 2 /O 2 fuel cell experiments to evaluate their performances a…

chemistry.chemical_classificationMaterials scienceElectrolysis of waterRenewable Energy Sustainability and the EnvironmentAnalytical chemistryEnergy Engineering and Power TechnologyProton exchange membrane fuel cellPolymerCondensed Matter PhysicsElectrochemistryAnodeCatalysisFuel TechnologyMembraneChemical engineeringchemistryPolarization (electrochemistry)International Journal of Hydrogen Energy
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Proton Conducting Membrane Prepared by Cross-Linking Highly Sulfonated Peek for PEMFC Application

2009

The proton conducting membrane was prepared by cross-linking highly sulfonated and sulfinated poly(etheretherketone) (SsPEEK). The cross-linked membrane is low cost due to its use of non-expensive chemical and simple production procedure. The membrane exhibited high proton conductivity (0.04 S/cm at 60 °C), extremely reduced water uptake, enhanced strength and stability compared with that of non-cross-linked membrane. These results suggested that the cross-linked PEEK membrane is a suitable candidate of proton conducting membranes for polymer electrolyte membrane fuel cell (PEMFC) applications, particularly promising to be used in direct methanol fuel cell (DMFC) due to its lower methanol c…

chemistry.chemical_classificationMaterials scienceProton exchange membrane fuel cellElectrolytePolymerConductivitychemistry.chemical_compoundDirect methanol fuel cellMembranechemistryChemical engineeringPeekMethanolNuclear chemistryASME 2009 7th International Conference on Fuel Cell Science, Engineering and Technology
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Insights into the Dynamics of Grotthuss Mechanism in a Proton-Conducting Chiral bioMOF

2016

Proton conduction in solids attracts great interest, not only because of possible applications in fuel cell technologies, but also because of the main role of this process in many biological mechanisms. Metal–organic frameworks (MOFs) can exhibit exceptional proton-conduction performances, because of the large number of hydrogen-bonded water molecules embedded in their pores. However, further work remains to be done to elucidate the real conducting mechanism. Among the different MOF subfamilies, bioMOFs, which have been constructed using biomolecule derivatives as building blocks and often affording water-stable materials, emerge as valuable systems to study the transport mechanisms involve…

chemistry.chemical_classificationMaterials scienceProtonGeneral Chemical EngineeringBiomoleculeNanotechnology02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistryMaterials ChemistryMoleculeFuel cellsGrotthuss mechanism0210 nano-technologyPorosityChemistry of Materials
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The deprotonative metalation of [1,2,3]triazolo[1,5-a]quinoline. Synthesis of 8-haloquinolin-2-carboxaldehydes

2009

New highly functionalized triazoloquinolines were synthesized by applying polar organometallic methods. Double metalation and functionalization provided 3,9-dihalogenated triazoloquinolines. Ring opening of the triazole with loss of nitrogen has been performed for the first time with 3,9-dihalogenated triazoloquinolines allowing the access toward 8-haloquinolin-2-carboxaldehydes under oxidant-free conditions. This approach demonstrates that the triazole ring can be used as protecting group of 2-quinolinecarboxaldehydes, activating the C9-position for lithiation and functionalization by triazole ring opening. 8-Haloquinoline-2-carbaldehydes become in this way readily available.

chemistry.chemical_classificationMetalationOrganic ChemistryQuinolineTriazoleRing (chemistry)BiochemistryCombinatorial chemistryChemical synthesisAldehydechemistry.chemical_compoundDeprotonationchemistryDrug DiscoveryOrganic chemistryProtecting groupTetrahedron
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FT-IR and nuclear overhauser enhancement study of the state of urea confined in AOT-reversed micelles

2003

Abstract The system urea/sodium-bis(2-ethylhexyl)sulfosuccinate (AOT) dispersed in CCl 4 and benzene-d6 was investigated by viscosimetry, FT-IR and high-resolution 1 H NMR spectroscopy, as a function of urea/AOT molar ratio ( R urea ) at fixed AOT molal concentration (0.3467 mol kg −1 ) and as a function of AOT concentration at fixed R urea (0.5) at 25 °C. The experimental data are consistent with the hypothesis that urea is encapsulated as small-size hydrogen-bonded cluster in the hydrophilic micellar core of the AOT-reversed micelles and that this structure is maintained well above the volume fraction of the dispersed phase, where a percolative transition occurs. Intermolecular nuclear ov…

chemistry.chemical_classificationMolalityInorganic chemistryMicellechemistry.chemical_compoundColloid and Surface ChemistrySulfonatechemistryPulmonary surfactantUreaProton NMRPhysical chemistryAlkylMethyl groupColloids and Surfaces A: Physicochemical and Engineering Aspects
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Normal-phase (temperature gradient) interaction chromatography – A powerful tool for the characterisation of high molecular weight chain-end function…

2015

Abstract We report here, for the first time, quantitative analysis of end-group functionalisation and the extent of end-group modification of polymers with molar mass up to 200,000 g mol −1 , using a combination of isothermal and temperature gradient interaction chromatography. At such high molecular weights, other common analytical techniques such as MALDI-ToF-MS and NMR spectroscopy are simply unable to offer any quantitative insight into the end-group functionality of polymers. Thus, normal phase isothermal interaction chromatography (NP-IIC) has been used to characterise a series of polystyrene samples, with identical molar mass (c. 90,000 g mol −1 ), each carrying a single chain-end fu…

chemistry.chemical_classificationMolar massChromatographyPolymers and PlasticsResolution (mass spectrometry)ChemistryElutionOrganic ChemistryAnalytical chemistryGeneral Physics and AstronomyPolymerNuclear magnetic resonance spectroscopyTemperature gradient interaction chromatography (TGIC)Primary alcoholEnd-functionalised polymers.Anionic polymerisationIsothermal processMaterials ChemistryProton NMRPolymer characterisation
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Mn(II) complexes with sulfonamides as ligands.

2012

Abstract Sulfonamides derived from 8-aminoquinoline react with Mn(II) and Mn(III) salts to form Mn(II) complexes; the Mn(III) species are reduced to the divalent state in the presence of 1,10 phenanthroline and bipyridine. Their molecular structure, determined by single crystal X‐ray diffraction, show that all the complexes present a distorted octahedral geometry, in which the deprotonated sulfonamide acts as a bidentate ligand. UV–visible spectroscopy and changes in the melting temperature (Tm) of calf thymus DNA show a strong interaction of these complexes with DNA. The significant hypochromicity of the charge transfer transition at 370 nm without an appreciable change in wavelength and t…

chemistry.chemical_classificationNucleasebiologyStereochemistryPhenanthrolineBiochemistryDivalentInorganic Chemistrychemistry.chemical_compoundBipyridineCrystallographyDeprotonationchemistryOctahedral molecular geometrybiology.proteinMoleculeDNAJournal of Inorganic Biochemistry
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Reactivity of the di-μ-hydroxo-complexes [{Pd(NN)}2(μ-OH)2][ClO4]2 (NN=bis(pyrazol-1-yl)alkanes) towards protic electrophiles. Hydration of coordin…

2000

Abstract The hydroxo-complexes [{Pd(μ-OH)(NN)}2][ClO4]2 (NN=bpzm:bis(pyrazol-1-yl) methane: a-compounds, bpzm*:bis(3,5-dimethylpyrazol-1-yl)methane; b-compounds) react with a wide variety of weak protic electrophiles H(LL) in a 1:2 molar ratio to give the mononuclear cationic palladium(II) derivatives of general formula [Pd(LL)(NN)][ClO4] [LL=2-pyridine-methoxo (OCH2-py) (1a,b); picolinate (pic) (2a,b); 8-hydroxiquinolinate (oxin) (3a,b)] or the dinuclear complexes [{Pd(NN)}2(μ-ox)][ClO4]2 [ox=oxalate: (4a,b)] and [{Pd(μ-LL)(NN)}2][ClO4]2 [LL=pyrazolate (pz) (5a,b); p-thiocresolate (SC6H4Me-p) (6a,b); triazolate (tz) (7b); thiophenolate (SPh) (8b)] when reacting with oxalic acid, azole…

chemistry.chemical_classificationNucleophilic additionStereochemistrychemistry.chemical_elementCrystal structureMedicinal chemistryOxalateInorganic Chemistrychemistry.chemical_compoundDeprotonationchemistryElectrophileMaterials ChemistryReactivity (chemistry)Physical and Theoretical ChemistryDithiocarbamatePalladiumPolyhedron
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