Search results for " and optics"

showing 10 items of 4468 documents

Theoretical electronic spectra of 2-aminopurine in vapor and in water

2006

The accurate quantum chemical CASSCF and CASPT2 methods combined with a Monte Carlo procedure to mimic solvation effects have been used in the calculation of the spectroscopic properties of two tautomers of 2-aminopurine (2AP). Absorption and emission spectra have been simulated both in vacuum and in aqueous environment. State and transition energies and properties have been obtained with high accuracy, leading to the assignment of the most important spectroscopic features. The lowest-lying 1 (,*) ( 1 La) state has been determined as responsible for the first band in the absorption spectrum and also for the strong fluorescence observed for the system in water. The combined approach used in …

Aqueous solutionAbsorption spectroscopyChemistryMonte Carlo methodSolvationAnalytical chemistryCondensed Matter PhysicsTautomerMolecular physicsAtomic and Molecular Physics and OpticsSpectral lineEmission spectrumPhysical and Theoretical ChemistryAbsorption (electromagnetic radiation)International Journal of Quantum Chemistry
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Enthalpic and entropic contributions of water molecules to the functional T → R transition of human hemoglobin in solution

1992

Generalized solvent-mediated forces contribute to free energy at the functional T → R transition of human hemoglobin A (HbA). Their contribution is here sorted out quantitatively in both its enthalpic and entropic parts, along with the average number of water molecules involved. The latter (about 75 waters in average) must be considered together with HbA as one statistically defined functional unit for oxygen transport. Their configurations are expected to undergo frequent structural rearrangements. Lifetimes of statistically relevant configurations do not need to (although, of course, they may) exceed by more than a factor 5 the normal H-bond lifetimes of the pure solvent. Compared to the …

Aqueous solutionChemistryStereochemistryEnthalpyOxygen transportThermodynamicsCondensed Matter PhysicsAtomic and Molecular Physics and OpticsGeneralized forcesPhase spaceMoleculePhysical and Theoretical ChemistrySolvent effectsCurse of dimensionalityInternational Journal of Quantum Chemistry
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Sequestration of alkyltin(IV) cations by complexation with amino-polycarboxylic chelating agents

2013

Abstract The binding capacity of four amino-polycarboxylic ligands (APCs) [nitrilotriacetate (NTA), ethylenediamine- N , N , N′ , N′ -tetraacetate (EDTA), (S,S)-ethylenediamine- N , N ′-disuccinic acid (S,S-EDDS) and diethylenetriamine- N , N , N′ , N″ , N″ -pentaacetate (DTPA)] towards mono-, di- and tri-alkyltin(IV) cations [(CH 3 )Sn 3 + , (CH 3 ) 2 Sn 2 + , (C 2 H 5 ) 2 Sn 2 + , (CH 3 ) 3 Sn + or (C 2 H 5 ) 3 Sn + ] was studied, in aqueous solutions, by ISE-H + potentiometry, at I  = 0.1 mol L − 1 (NaCl) and at T  = 298.15 K. In all the systems R x Sn (4 − x)+  − APC (R = CH 3 or C 2 H 5 ) a strong 1:1 species is formed together with protonated, hydroxo and dinuclear complexes. The valu…

Aqueous solutionComplexation in aqueous solutionStereochemistryLigandEthylenediamineProtonationAlkyltin(IV) cations; Amino-polycarboxylic ligands; Complexation in aqueous solution; Sequestration ability of complexones;Condensed Matter PhysicsMedicinal chemistryAtomic and Molecular Physics and OpticsAlkyltin(IV) cationElectronic Optical and Magnetic MaterialsIonAmino-polycarboxylic ligandchemistry.chemical_compoundSequestration ability of complexoneschemistryDiethylenetriamineMaterials ChemistryChelationSettore CHIM/01 - Chimica AnaliticaPhysical and Theoretical ChemistrySimple correlationSpectroscopy
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Interaction of quinine with negatively charged lipid vesicles studied by fluorescence spectroscopy Influence of the pH

1997

Abstract The interaction of quinine with dimyristoylphosphatidic acid (DMPA) and dimyristoylphosphatidyl glycerol (DMPG) small unilamellar vesicles in the gel phase was studied by steady-state fluorescence spectroscopy at pHs 7, 6, 5 and 4 and 20°C. In aqueous solution, with excitation at 335 nm, the emission fluorescence spectrum of quinine varied with pH reflecting the occurrence of different charged species of the drug. In all cases, the emission maximum centered at 383 or 443 nm shifted to lower wavelength in the presence of vesicles. This indicates that the membrane-bound state quinine is in an environment of low polarity. Drug monocationic species were deeply buried in DMPG relative t…

Aqueous solutionFluorophoreChemistryVesicleAnalytical chemistryFluorescenceAtomic and Molecular Physics and OpticsFluorescence spectroscopyAnalytical ChemistryPartition coefficientchemistry.chemical_compoundMembranePhase (matter)InstrumentationSpectroscopySpectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
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Physical origin of Na+/Cl− selectivity of tight junctions between epithelial cells. Nonlocal electrostatic approach

2020

Abstract Tight junctions (TJs) of epithelial cells play a key role in regulation of the ion exchange between NaCl solutions separated by the layer of these cells. Their functioning is based on a strong difference in the permeabilities of these channels for Na+ and Cl− ion migrational fluxes owing to specific properties of the protein network inside TJs. It has been assumed in this study that this phenomenon originates from combination of two effects related to this specific TJ protein (claudin) which segments are partially located inside the TJ space. First, their ionogenic groups create a negative charge distributed inside TJs, thus inducing a difference between the Na+ and Cl− concentrati…

Aqueous solutionIon exchangeTight junctionChemistrySolvation02 engineering and technologyDielectric010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsElectrostatics01 natural sciencesAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsIonChemical physicsMaterials ChemistryMolecule[CHIM]Chemical SciencesPhysical and Theoretical Chemistry0210 nano-technologySpectroscopy
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A simple model for barrier frequencies for enzymatic reactions.

2010

We present a simple model to rationalize the effects of environment on the reaction barrier frequencies derived from free energy profiles. These frequencies are relevant in deviations of a rate constant from its transition state theory value and in determining which environmental dynamics participate in the reaction. In particular, this simple model can be used to understand the changes in the reaction barrier frequencies of an enzymatic catalyzed reaction and the corresponding uncatalyzed process in aqueous solution, a change which has implications for dynamical environmental effects on the enzymatic reaction. Two possible cases are analyzed, in which the polarity (charge separation/locali…

Aqueous solutionMolecular StructureChemistryPolarity (physics)ThermodynamicsInverseAtomic and Molecular Physics and OpticsTransition stateEnzyme catalysisCatalysisEnzymesTransition state theoryReaction rate constantModels ChemicalBiocatalysisPhysical chemistryThermodynamicsPhysical and Theoretical ChemistryNuclear ExperimentChemphyschem : a European journal of chemical physics and physical chemistry
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Dioxygen reduction by cobalt(II) octaethylporphyrin at liquid|liquid interfaces.

2010

Oxygen reduction catalyzed by cobalt(II) (2,3,7,8,12,13,17,18-octaethylporphyrin) [Co(OEP)] at soft interfaces is studied by voltammetry and biphasic reactions. When Co(OEP) is present in a solution of 1,2-dichloroethane in contact with an aqueous acidic solution, oxygen is reduced if the interface is positively polarized (water phase versus organic phase). This reduction reaction is facilitated when an additional electron donor, here ferrocene, is present in excess in the organic phase.

Aqueous solutionPorphyrinsSurface PropertiesInorganic chemistrychemistry.chemical_elementElectron donorOxygenRedoxAtomic and Molecular Physics and OpticsCatalysisCatalysisOxygenchemistry.chemical_compoundchemistryPhase (matter)Organometallic CompoundsPhysical and Theoretical ChemistryCobaltVoltammetryOxidation-ReductionChemphyschem : a European journal of chemical physics and physical chemistry
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Design, Synthesis and Evaluation of Enzyme-Responsive Fluorogenic Probes Based on Pyridine-Flanked Diketopyrrolopyrrole Dyes

2020

The ever-growing demand for fluorogenic dyes usable in the rapid construction of analyte-responsive fluorescent probes, has recently contributed to a revival of interest in the chemistry of diketopyrrolopyrrole (DPP) pigments. In this context, we have explored the potential of symmetrical and unsymmetrical DPP derivatives bearing two or one 4-pyridyl substituents acting as optically tunable group(s). The unique fluorogenic behavior of these molecules, closely linked to N-substitution/charge state of their pyridine unit (i.e., neutral pyridine or cationic pyridinium), has been used to design DPP-based fluorescent probes for detection of hypoxia-related redox enzymes and penicillin G acylase …

Aqueous solutionPyridinesCationic polymerizationContext (language use)02 engineering and technologyKetones010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesFluorescenceCombinatorial chemistryAtomic and Molecular Physics and Optics0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundchemistryPyridineMoleculePyrrolesPyridinium0210 nano-technologyInstrumentationBiosensorSpectroscopyFluorescent Dyes
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Study of separation of water + 2-propanol mixture using different ionic liquids: 1-Butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide or 1-b…

2018

Abstract The liquid–liquid equilibria data of water (1) + 2-propanol (2) + [bmim][Tf2N] (3) and water (1) + 2-propanol (2) + [bmp][Tf2N] (3) at 283.2, 303.2 and 323.2 K and atmospheric pressure were measured with the objective of understanding the behavior of these two systems and to try to improve the extraction of 2-propanol from water from economical and environmental points of view. The thermodynamic parameters were determined using the non-random two-liquid (NRTL) and universal quasichemical (UNIQUAC) models, and excellent results were achieved in both cases (the maximum root-mean-square deviation was 0.433%). Lastly, the capability of the two ionic liquids to separate 2-propanol from …

Aqueous solutionUNIQUACAtmospheric pressureInorganic chemistryExtraction (chemistry)02 engineering and technology010402 general chemistry01 natural sciencesAtomic and Molecular Physics and Optics0104 chemical sciencesPropanolchemistry.chemical_compound020401 chemical engineeringchemistryIonic liquidNon-random two-liquid modelPhysical chemistryGeneral Materials Science0204 chemical engineeringPhysical and Theoretical ChemistryImideThe Journal of Chemical Thermodynamics
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Measurements of transition probabilities for two N I infrared transitions and their application for diagnostics of low temperature plasmas

2010

Abstract Spectra emitted from a wall-stabilized arc, running in a gas mixture of helium, argon, nitrogen, oxygen and traces of hydrogen have been studied. Intensities of selected spectral transitions of neutral nitrogen and oxygen have been measured. Applying the Boltzmann plot method and using a reliable set of O I transition probabilities of spectral lines, originating from levels considerably spread in excitation energies, the temperatures of arc plasmas have been determined. Line intensities of two N I infrared transitions, originating from doubly excited terms 3p′ 2 F o and 3p′ 2 G have been measured. In order to obtain the corresponding transition probabilities ( A ki ) for these line…

ArgonInfraredchemistry.chemical_elementAtomic and Molecular Physics and OpticsSpectral lineAnalytical Chemistrysymbols.namesakechemistryExcited stateIonizationBoltzmann constantsymbolsAtomic physicsInstrumentationSpectroscopyExcitationHeliumSpectrochimica Acta Part B: Atomic Spectroscopy
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