Search results for "Protonation"

showing 10 items of 583 documents

Proton-Induced Multiple Changes of the Absorption and Fluorescence Spectra of Amino-Aza-Oligo(Phenylenevinylene)s

2008

Fluorescent dyes with a high sensitivity of their optical spectra towards changes of the environment were prepared via aldol condensation or Horner olefinations. The main chromophore is a quadrupolar N-substituted 1,4-distyrylbenzene which allows protonation and complexation at various positions resulting in a series of different and significant changes of the optical spectra. The sensitivity of the absorption and emission spectra on solvent polarity, acid, and cations is reported.

ProtonChemistrySolvatochromismProtonationChromophorePhotochemistryFluorescence spectraFluorescenceAtomic and Molecular Physics and OpticsAldol condensationsense organsEmission spectrumElectrical and Electronic EngineeringAbsorption (chemistry)Advances in Science and Technology
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The ins and outs of proton complexation

2009

Proton complexation differs from simple protonation by the fact that the coordinated hydrogen atom is bound intramolecularly to more than one donor atom. This is usually achieved by covalent bonding supplemented by hydrogen bonding. In a few cases, however, the complexed proton is hydrogen-bound to all donor atoms, which gives rise to single well (SWHB) and low barrier (LBHB) hydrogen bonds. This tutorial review highlights a full range of proton complexes formed with chelating and "proton-sponge"-type ligands, cryptand-like macropolycycles, and molecules of topological relevance, such as rotaxanes and catenanes. The concept of proton complexation can explain how the smallest cation possible…

ProtonStereochemistryLow-barrier hydrogen bondreviewProtonation010402 general chemistry01 natural sciencescovalent bonding[ CHIM.ORGA ] Chemical Sciences/Organic chemistryMoleculePhysics::Atomic PhysicsPhysics::Chemical Physicsproton complexationNuclear ExperimentComputingMilieux_MISCELLANEOUSQuantitative Biology::Biomolecules[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryChemistryHydrogen bondGeneral ChemistryHydrogen atomhydrogen bonding3. Good health0104 chemical sciencesCrystallographyCovalent bondIntramolecular forceChemical Society Reviews
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Dependence of enzyme reaction mechanism on protonation state of titratable residues and QM level description: lactate dehydrogenase

2005

We have studied the dependence of the chemical reaction mechanism of L-lactate dehydrogenase (LDH) on the protonation state of titratable residues and on the level of the quantum mechanical (QM) description by means of hybrid quantum-mechanical/molecular-mechanical (QM/MM) methods; this methodology has allowed clarification of the timing of the hydride transfer and proton transfer components that hitherto had not been possible to state definitively. Ferrer Castillo, Silvia, Silvia.Ferrer@uv.es, Silla Santos, Estanislao, Estanislao.Silla@uv.es ; Tuñon Garcia de Vicuña, Ignacio Nilo, Ignacio.Tunon@uv.es

ProtonStereochemistryUNESCO::QUÍMICATitratable acidDehydrogenaseProtonationChemical reactionQM/MM:QUÍMICA [UNESCO]CatalysisSubstrate Specificitychemistry.chemical_compoundComputational chemistryLactate dehydrogenaseMaterials ChemistryDependenceEnzyme reaction mechanismchemistry.chemical_classificationL-Lactate DehydrogenaseMolecular StructureChemistryHydrideUNESCO::QUÍMICA::Química analíticaMetals and AlloysTitrimetryGeneral ChemistryNADL-Lactate dehydrogenaseSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDependence ; Enzyme reaction mechanism ; Titratable residues ; L-Lactate dehydrogenase ; QM/MMEnzymeCeramics and Composites:QUÍMICA::Química analítica [UNESCO]Titratable residuesProtons
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Molecular orbital studies on the mechanism of catalytic isomerization of xylenes III. Protonation channels

1981

Abstract The isoenergetic lines of the interaction energy between a bare proton and ortho-, meta- , and para -xylene have been calculated in order to detect both the best approaching channel and the preferred protonation positions. The channels found direct the protonation to the following ring positions: 4 and 5 for o -xylene, 4 and 6 for m -xylene, and 2 equivalents for p -xylene. The overall interaction energy determines the protonation positions on each isomer and the most important contributions to it are the electrostatic term in o -xylene, the polarization term in p -xylene, and both terms equally in m -xylene. These results are in agreement with the experimental findings and appear …

ProtonXyleneProtonationInteraction energyRing (chemistry)PhotochemistryCatalysisCatalysischemistry.chemical_compoundchemistryComputational chemistryMolecular orbitalPhysical and Theoretical ChemistryIsomerizationJournal of Catalysis
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Charge-Neutral Constant pH Molecular Dynamics Simulations Using a Parsimonious Proton Buffer

2016

In constant pH molecular dynamics simulations, the protonation states of titratable sites can respond to changes of the pH and of their electrostatic environment. Consequently, the number of protons bound to the biomolecule, and therefore the overall charge of the system, fluctuates during the simulation. To avoid artifacts associated with a non-neutral simulation system, we introduce an approach to maintain neutrality of the simulation box in constant pH molecular dynamics simulations, while maintaining an accurate description of all protonation fluctuations. Specifically, we introduce a proton buffer that, like a buffer in experiment, can exchange protons with the biomolecule enabling its…

ProtonprotonationAnalytical chemistryProtonationBuffersMolecular Dynamics Simulation010402 general chemistry01 natural sciencesBuffer (optical fiber)Molecular dynamics0103 physical sciencesPhysical and Theoretical ChemistryNuclear Experimentta116chemistry.chemical_classificationQuantitative Biology::Biomolecules010304 chemical physicspHQuantitative Biology::Molecular NetworksBiomoleculeProteinsCharge (physics)molecular dynamics simulationselectrostatic environmentHydrogen-Ion Concentration0104 chemical sciencesComputer Science ApplicationschemistryChemical physicsThermodynamicsTitrationbufferProtonsConstant (mathematics)Journal of Chemical Theory and Computation
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Regioselective C–H amination of free base porphyrins via electrogenerated pyridinium-porphyrins and stabilization of easily oxidized amino-porphyrins…

2020

Four free base aminoporphyrins were synthesized in two steps via regioselective anodic nucleophilic substitution with pyridine followed by ring opening of the electrogenerated pyridinium with piperidine. The X-ray crystallographic structure of the unstable 2-aminotetraphenylporphyrin was solved. Protonation of this latter compound leads to the stable diiminium porphyrin salt.

Protonation010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compound[CHIM.ANAL]Chemical Sciences/Analytical chemistryPyridinePolymer chemistryMaterials ChemistryNucleophilic substitution[CHIM.COOR]Chemical Sciences/Coordination chemistryAmination[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryMetals and AlloysFree base[CHIM.MATE]Chemical Sciences/Material chemistryGeneral ChemistryPorphyrin0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCeramics and CompositesPyridiniumPiperidineChemical Communications
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ChemInform Abstract: Auxiliary-Controlled Stereoselective Enolate Protonation: Enantioselective Synthesis of cis and trans Annulated Decahydroquinoli…

2010

Abstract The diastereoselective synthesis of the octahydroquinoline enone precursor of pumiliotoxin C is achieved via tandem Mannich-Michael reaction on N-galactosyl imines. Conjugate cuprate addition to the bicyclic enone stereoselectively forms the trans annulated 4a- epi -pumiliotoxin C skeleton in the presence of the carbohydrate auxiliary, and the cis annulated pumiliotoxin C skeleton in its absence.

Pumiliotoxin Cchemistry.chemical_compoundBicyclic moleculeChemistryStereochemistryEnantioselective synthesisStereoselectivityProtonationGeneral MedicineEnoneCis–trans isomerismConjugateChemInform
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Linear, tripodal, macrocyclic: Ligand geometry and ORR activity of supported Pd(II) complexes

2021

Abstract The novel ligand H3L designed to spontaneously adsorb onto MWCNT via electron-deficient pyrimidine residues and bind metal cations is used to prepare an oxygen reduction reaction (ORR) cathode catalyst based on supported Pd(II) complexes. Herein we report the synthesis of the ligand, its solution behaviour (protonation constants, binding constants for the test cation Cu(II), UV evidence of Cu(II) and Pd(II) complexes formation) and ORR performances together with XPS and STEM characterization. Tripodal nature of the H3L ligand frame it in-between previously studied macrocyclic and linear open chain ligands, allowing to draw meaningful comparisons.

Pyrimidine010405 organic chemistryLigandProtonation010402 general chemistry01 natural sciences0104 chemical sciencesCathode catalystInorganic ChemistryMetalchemistry.chemical_compoundAdsorptionX-ray photoelectron spectroscopychemistryvisual_artPolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumMacrocyclic ligandPhysical and Theoretical ChemistryInorganica Chimica Acta
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Degrees of freedom effect on fragmentation in tandem mass spectrometry of singly charged supramolecular aggregates of sodium sulfonates

2013

The characteristic collision energy (CCE) to obtain 50% fragmentation of positively and negatively single charged non-covalent clusters has been measured. CCE was found to increase linearly with the degrees of freedom (DoF) of the precursor ion, analogously to that observed for synthetic polymers. This suggests that fragmentation behavior (e.g. energy randomization) in covalent molecules and clusters are similar. Analysis of the slope of CCE with molecular size (DoF) indicates that activation energy of fragmentation of these clusters (loss of a monomer unit) is similar to that of the lowest energy fragmentation of protonated leucine-enkephalin. Positively and negatively charged aggregates b…

Quantitative Biology::BiomoleculesPhysics::Instrumentation and DetectorsChemistryAnalytical chemistrySupramolecular chemistryProtonationActivation energyIonchemistry.chemical_compoundMonomerFragmentation (mass spectrometry)Covalent bondMoleculeSpectroscopyJournal of Mass Spectrometry
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ChemInform Abstract: The Ins and Outs of Proton Complexation

2009

Proton complexation differs from simple protonation by the fact that the coordinated hydrogen atom is bound intramolecularly to more than one donor atom. This is usually achieved by covalent bonding supplemented by hydrogen bonding. In a few cases, however, the complexed proton is hydrogen-bound to all donor atoms, which gives rise to single well (SWHB) and low barrier (LBHB) hydrogen bonds. This tutorial review highlights a full range of proton complexes formed with chelating and “proton-sponge”-type ligands, cryptand-like macropolycycles, and molecules of topological relevance, such as rotaxanes and catenanes. The concept of proton complexation can explain how the smallest cation possible…

Quantitative Biology::BiomoleculesProtonHydrogen bondChemistryLow-barrier hydrogen bondProtonationGeneral MedicineHydrogen atomCrystallographyCovalent bondIntramolecular forceMoleculePhysics::Atomic PhysicsPhysics::Chemical PhysicsNuclear ExperimentChemInform
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