Search results for "Proton"

showing 10 items of 5886 documents

Synthesis and Structures of Two Triorganotin(IV) Polymers R3Sn{O2CC6H4[N=C(H)}{C(CH3)CH(CH3)-3-OH]-p} n (R = Me and Ph) Containing a 4-[(2Z)-(3-Hydro…

2009

Two new polymeric triorganotin(IV) complexes R3Sn{O2CC6H4[N=C(H)}{C(CH3)CH(CH3)-3-OH]-p} n ([Me3Sn(LH)] n : 1) and ([Ph3Sn(LH)] n : 2) containing a 4-[(2Z)-(3-hydroxy-1-methyl-2-butenylidene)amino]benzoate (LH) framework were prepared. Both compounds have been characterized by 1H, 13C, 119Sn NMR, IR and 119Sn Mossbauer spectroscopic techniques in combination with elemental analyses. The crystal structures of complexes 1 and 2 reveal that they exist as polymeric zig-zag chains in which the LH-bridged Sn-atoms adopt a trans-R3SnO2 trigonal bipyramidal configuration with R groups in the equatorial positions and the axial sites occupied by an oxygen atom from the carboxylate ligand and the alco…

chemistry.chemical_classificationPolymers and PlasticsProtonLigandStereochemistryCrystal structureCrystal structurePolymerMedicinal chemistryNMRchemistry.chemical_compoundTrigonal bipyramidal molecular geometry4-[(2Z)-(3-Hydroxy-1-methyl-2- butenylidene)amino]benzoatechemistrySettore CHIM/03 - Chimica Generale E InorganicaTriorganotin carboxylateMössbauer spectroscopyOrganometallic polymerMössbauerMaterials ChemistryCarboxylateBenzoic acidJournal of Inorganic and Organometallic Polymers and Materials
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Binding ability of N-Para-amino-phenylsulfonyl derivatives of amino acids. Potentiometric and spectroscopic studies of Cu(II) complexes

1995

Abstract N-Para-amino-phenylsulfonyl derivatives of amino acids are very effective ligands for Cu(II) ions. Potentiometric and spectroscopic results have shown that Cu(II) ions are able to deprotonate and bind to sulfonamide nitrogen below pH 5 to form stable mono- and bis-[N − , COO − ] chelates. The basicity of sulfonamide nitrogen is lower than peptide amide nitrogen and no distinct anchoring site is necessary to promote the amide nitrogen deprotonation.

chemistry.chemical_classificationPotentiometric titrationchemistry.chemical_elementPeptideBiochemistryNitrogenMedicinal chemistrySulfonamideAmino acidInorganic Chemistrychemistry.chemical_compoundDeprotonationchemistryAmideOrganic chemistryChelationJournal of Inorganic Biochemistry
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Protonation and rearrangement of the tricyclo[4.2.2.22,5]dodeca-3,7,9,11-tetraene scaffold

2006

The biplanemers 2a,b contain enol ether substructures, which permit facile protonations of the π electron system. The subsequent ether cleavage is characterized by rearrangements of the polycyclic scaffold of the carbenium ions or the electroneutral primary products. Apart from the expected products 3a and 5a, a series of unexpected ketones and diketones (4a′, 9b, 10b, 11b, and 12b) were obtained.

chemistry.chemical_classificationPrimary (chemistry)ChemistryStereochemistryOrganic ChemistryProtonationElectron systemBiochemistryMedicinal chemistryIonHydrolysisDrug DiscoveryEnol etherEther cleavageTetrahedron Letters
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Determination of Amino Acids by Micellar High-Performance Liquid Chromatography and Pre-column Derivatization withO-Phthalaldehyde and N-Acetyl-L-cys…

1995

Abstract Micellar liquid chromatography of proteic primary amino acids with pre-column derivatization with o-phthalaldehyde (OPA) and N-acetyl-L-cysteine was studied, using mobile phases containing a short-chain alcohol. The modification of pH gave a large variation of the retention as a result of the protonation of the carboxylate group of amino acids. Maximum resolution and adequate retentions were achieved with a 0.05 M sodium dodecyl sulphate/3% propanol mobile phase at pH 3. The reproducibility was lower than 1.0% at a 1 × 10−4 M concentration level and between 0.6 and 2.2% for 1 × 10−6 M. The determination of glycine, lysine, methionine and threonine in pharmaceutical formulations gav…

chemistry.chemical_classificationPropanolO-Phthalaldehydechemistry.chemical_compoundChromatographychemistryMicellar liquid chromatographyMolecular MedicineProtonationCarboxylateDerivatizationHigh-performance liquid chromatographyAmino acidJournal of Liquid Chromatography
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PBI-based composite membranes for polymer fuel cells

2010

Abstract In the present study poly(2,2-(2,6-pyridin)-5,5-bibenzimidazole) was used for the preparation of novel MEAs for high-temperature polymer fuel cells (HT-PEMFCs). We prepared hybrid materials with two types of silica fillers in order to increase the MEA performances using this polymer. The membranes were characterized in terms of their microstructure and thermal stability. Cell operation tests and Electrochemical Impedance Spectroscopy were used for the characterization of the MEAs. A maximum power density of about 80 mW cm−2 was obtained at 300 mA cm−2 by using an imidazole-modified silica filler. The EIS technique showed that the fillers chiefly help to reduce the charge transfer r…

chemistry.chemical_classificationProton exchange membrane PBI Electrochemical Impedance SpectroscopyFiller (packaging)Materials scienceRenewable Energy Sustainability and the EnvironmentAnalytical chemistryEnergy Engineering and Power TechnologyProton exchange membrane fuel cellPolymerMicrostructureDielectric spectroscopyMembranechemistryChemical engineeringProton exchange membrane PBI Electrochemical Impedance SpectroscopyThermal stabilityElectrical and Electronic EngineeringPhysical and Theoretical ChemistryHybrid material
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Coordination of copper(II) ions by α,β-dehydro-dipeptides. Potentiometric and spectroscopic study

1991

Abstract Potentiometric and spectroscopic data have shown that the double bond within dehydro-peptides considerably affects their behaviour as ligands relative to their saturated parents, with proton and copper(II) ions.

chemistry.chemical_classificationProtonDouble bondPotentiometric titrationInorganic chemistrychemistry.chemical_elementPeptideProtonationCopperIonInorganic ChemistrychemistryMaterials ChemistryPhysical and Theoretical ChemistryChemical equilibriumPolyhedron
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Enzyme molecular mechanism as a starting point to design new inhibitors: a theoretical study of O-GlcNAcase.

2011

O-Glycoprotein 2-acetamino-2-deoxy-β-d-glucopyranosidase (O-GlcNAcase) hydrolyzes O-linked 2-acetamido-2-deoxy-β-d-glucopyranoside (O-GlcNAc) residues from post-translationally modified serine/threonine residues of nucleocytoplasmic protein. The chemical process involves substrate-assisted catalysis, where two aspartate residues have been identified as the two key catalytic residues of O-GlcNAcase. In this report, the first step of the catalytic mechanism used by O-GlcNAcase involving substrate-assisted catalysis has been studied using a hybrid quantum mechanical/molecular mechanical (QM/MM) Molecular Dynamics (MD) calculations. The free energy profile shows that the formation of the oxazol…

chemistry.chemical_classificationProtonStereochemistryClostridium perfringensOxazolineMolecular Dynamics Simulationbeta-N-AcetylhexosaminidasesSurfaces Coatings and FilmsCatalysisSubstrate SpecificitySerinechemistry.chemical_compoundHydrolysisMolecular dynamicsEnzymechemistryMaterials ChemistryQuantum TheoryThermodynamicsPhysical and Theoretical ChemistryThreonineEnzyme InhibitorsOxazolesThe journal of physical chemistry. B
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Electronic Perspective on the Electrochemistry of Prussian Blue Films

2009

The derivative of the voltabsommetric scans, together with previous nano-electrogravimetric and X-ray diffraction results, allow different electrochemical processes to be distinguished during the Prussian blue (PB) voltammetric scan. Potassium, proton, and hydrated proton counterions involved in PB electrochemistry are related here to the electrochemical reactions of specific Fe sites. Potassium counterions show two different sites for their insertion: one located in the crystalline framework and another in ferrocyanide vacancies. From the monitoring of electroactive Fe sites, the covalent-exchange model is suggested as one of the first approaches to explain the origin of the PB magnetic or…

chemistry.chemical_classificationPrussian blueProtonIon exchangeRenewable Energy Sustainability and the EnvironmentPotassiumInorganic chemistrychemistry.chemical_elementCondensed Matter PhysicsElectrochemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryX-ray crystallographyMaterials ChemistryElectrochemistryCounterionFerrocyanideJournal of The Electrochemical Society
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Zero-field NMR of urea : spin-topology engineering by chemical exchange

2021

Well-resolved and information-rich J-spectra are the foundation for chemical detection in zero-field NMR. However, even for relatively small molecules, spectra exhibit complexity, hindering the analysis. To address this problem, we investigate an example biomolecule with a complex J-coupling network─urea, a key metabolite in protein catabolism─and demonstrate ways of simplifying its zero-field spectra by modifying spin topology. This goal is achieved by controlling pH-dependent chemical exchange rates of 1H nuclei and varying the composition of the D2O/H2O mixture used as a solvent. Specifically, we demonstrate that by increasing the proton exchange rate in the [13C,15N2]-urea solution, the…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceZero field NMRLetterMagnetic Resonance SpectroscopyProtonBiomoleculeWaterHydrogen-Ion ConcentrationTopologySmall moleculeSpectral linechemistryUreaGeneral Materials ScienceIsotopologuePhysical and Theoretical ChemistryDeuterium OxideTopology (chemistry)Spin-½
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Cyclodextrins in Polymer Synthesis: Enantiodiscrimination in Free-Radical Polymerization of Cyclodextrin-Complexed Racemic N -Methacryloyl-D,L -pheny…

2003

The enantiodiscriminating polymerization of racemic cyclodextrin-complexed N-methacryloylphenylalanine methyl ester is investigated 1 H NMR spectra of the complexes with methylated β-cyclodextrin in D 2 O manifest splittings due to chiral recognition. The different stabilities of the diastereomeric complexes influence the kinetics of the homopolymerization, particularly at 0°C. An enrichment of the residual N-methacryloyl-L-phenylalanine methyl ester of 14% was achieved after 21 h of polymerization.

chemistry.chemical_classificationReaction mechanismPolymers and PlasticsCyclodextrinOrganic ChemistryRadical polymerizationtechnology industry and agricultureDiastereomerPolymerchemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistrypolycyclic compoundsMaterials ChemistryProton NMRMacromolecular Rapid Communications
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