Search results for "liquid"

showing 10 items of 4351 documents

Self-Assembled Molecular Rafts at Liquid|Liquid Interfaces for Four-Electron Oxygen Reduction

2011

The self-assembly of the oppositely charged water-soluble porphyrins, cobalt tetramethylpyridinium porphyrin (CoTMPyP(4+)) and cobalt tetrasulphonatophenyl porphyrin (CoTPPS(4-)), at the interface with an organic solvent to form molecular "rafts", provides an excellent catalyst to perform the interfacial four-electron reduction of oxygen by lipophilic electron donors such as tetrathiafulvalene (TTF). The catalytic activity and selectivity of the self-assembled catalyst toward the four-electron pathway was found to be as good as that of the Pacman type cofacial cobalt porphyrins. The assembly has been characterized by UV-visible spectroscopy, Surface Second Harmonic Generation, and Scanning …

inorganic chemicals2Nd-Harmonic Generationchemistry.chemical_elementPhotochemistryBiochemistryOxygenCatalysisCatalysischemistry.chemical_compoundWater-Soluble PorphyrinsColloid and Surface ChemistryCobalt Porphyrinsheterocyclic compoundsLiquid/Liquid Interface2Nd DerivativesEnergyDioxygenPolarizable Continuum ModelGeneral ChemistryPorphyrinRadical CationchemistryRadical ionSurface second harmonic generationDensity functional theoryImmiscible Electrolyte-SolutionsCobaltTetrathiafulvalene
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Cross-Linked Imidazolium Salts as Scavengers for Palladium.

2014

Five imidazolium-based materials have been synthesised and used for the first time as palladium scavengers. Radical reactions of suitable bis-vinylimidazolium salts led to a series of insoluble materials through homo-polymerisation, immobilisation with a 3-mercaptopropyl-modified silica gel or co-polymerisation with ethylene glycol dimethylacrylate. These materials were screened as palladium scavengers with a set of palladium(0) and palladium(II) compounds in different solvents and at different starting amounts of palladium. In many cases, residual amounts of palladium were lower than 5 ppm, as requested for the manufacture of active pharmaceutical ingredients and fine chemicals. The applic…

inorganic chemicalsActive ingredientSilica gelchemistry.chemical_elementGeneral ChemistrySettore CHIM/06 - Chimica OrganicaScavenger (chemistry)chemistry.chemical_compoundchemistrySuzuki reactionIonic liquidOrganic chemistryEthylene glycolcross-coupling imidazolium salts ionic liquids palladium supported catalystsPalladiumChemPlusChem
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Supported Ionic Liquid Asymmetric Catalysis. A New Method for Chiral Catalysts Recycling. The Case of Proline-Catalyzed Aldol Reaction.

2004

A new method for chiral catalysts recycling, based on the supported ionic liquid asymmetric catalysis concept, has been developed. This concept involves the treatment of a monolayer of covalently attached ionic liquid on the surface of silica gel with additional ionic liquid. These layers serve as the reaction phase in which the homogeneous chiral catalyst is dissolved. As first application of this concept the L-proline-catalyzed aldol reaction has been carried out. Good yields and ee values, comparable with those obtained under homogeneous conditions have been obtained. Moreover, this material shows high regenerability.

inorganic chemicalsChemistrySilica gelorganic chemicalsOrganic ChemistryInorganic chemistryEnantioselective synthesisGeneral MedicineBiochemistryCombinatorial chemistryCatalysischemistry.chemical_compoundAldol reactionCovalent bondPhase (matter)Drug DiscoveryMonolayerIonic liquidChemInform
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[35] Determination of oxidized glutathione in blood: High-performance liquid chromatography

1994

Publisher Summary The measurement of glutathione status is important in determining oxidative stress in tissues and biological fluids. The ratio of reduced to oxidized glutathione (GSH/GSSG) is a good indicator of the oxidative stress that may occur under physiological and pathological conditions. Changes in GSSG levels have been considered as intracellular signals able to modulate enzyme activity. Thus, it is important to have accurate methods to determine GSSG in biological fluids and in cells. In many cases, it is possible to use tissues, such as liver, muscle, or brain to determine GSH/GSSG. However, especially in human studies, samples from these tissues are not readily available; the …

inorganic chemicalsHuman studiesbiologyChemistryGlutathionemedicine.disease_causeHigh-performance liquid chromatographyEnzyme assayOxidized Glutathionechemistry.chemical_compoundfluids and secretionsBiochemistrymedicinebiology.proteinChelationIntracellularOxidative stress
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Trace Analysis of Plutonium and Technetium by Resonance Ionization Mass Spectrometry Using an Atomic Beam and a Laser Ion Source

1990

A method for low level detection of plutonium and technetium is described with a detection limit of less than 107 atoms. Plutonium is a very toxic element due to its radioactive decay as well as its chemical behaviour. It was released to the environment in large amounts during the fifties and sixties of his century, principally by nuclear-weapon tests and some accidents. As a result about 0.4 − 4 mBq per gram 239Pu(T1/2 = 24390 y), corresponding to 4 × 108 − 4 × 109 atoms, can be found in the Northern Hemisphere in soil samples.

inorganic chemicalsStatic secondary-ion mass spectrometryMaterials scienceRadiochemistryAnalytical chemistryThermal ionizationchemistry.chemical_elementThermal ionization mass spectrometryMass spectrometryIon sourceAtmospheric-pressure laser ionizationPlutoniumchemistryDirect electron ionization liquid chromatography–mass spectrometry interface
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Electronic and Steric Effects: How Do They Work in Ionic Liquids? The Case of Benzoic Acid Dissociation

2010

The need to have a measure of the strength of some substituted benzoic acids in ionic liquid solution led us to use the protonation equilibrium of sodium p-nitrophenolate as a probe reaction, which was studied by means of spectrophotometric titration at 298 K. In order to evaluate the importance of electronic effect of the substituents present on the aromatic ring, both electron-withdrawing and -donor substituents were taken into account. Furthermore, to have a measure of the importance of the steric effect of the substituents both para- and ortho-substituted benzoic acids were analyzed. The probe reaction was studied in two ionic liquids differing for the ability of the cation to give hydr…

inorganic chemicalsSteric effectsionic liquids ion pair formation carboxylic acidsChemistryHydrogen bondorganic chemicalsOrganic ChemistryInorganic chemistryProtonationSettore CHIM/06 - Chimica OrganicaDissociation (chemistry)chemistry.chemical_compoundIonic liquidElectronic effectEquilibrium constantBenzoic acidThe Journal of Organic Chemistry
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Hydration dependence of myoglobin dynamics studied with elastic neutron scattering, differential scanning calorimetry and broadband dielectric spectr…

2014

In this work we present a thorough investigation of the hydration dependence of myoglobin dynamics. The study is performed on D2O-hydrated protein powders in the hydration range 0<h<0.5 (h≡gr[D2O]/gr[protein]) and in the temperature range 20-300K. The protein equilibrium fluctuations are investigated with Elastic Neutron Scattering using the spectrometer IN13 at ILL (Grenoble), while the relaxations of the protein + hydration water system are investigated with Broadband Dielectric Spectroscopy; finally, Differential Scanning Calorimetry is used to obtain a thermodynamic description of the system. The effect of increasing hydration is to speed up the relaxations of the myoglobin + hydration …

inorganic chemicalsWork (thermodynamics)BiophysicsNeutron scatteringMolecular Dynamics SimulationBiochemistryPhase Transitionchemistry.chemical_compoundDifferential scanning calorimetryAnimalsHorsesRange (particle radiation)Calorimetry Differential ScanningMyoglobinProtein dynamicsOrganic ChemistryDynamics (mechanics)WaterSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Neutron DiffractionMyoglobinchemistryChemical physicsDielectric SpectroscopyPhysical chemistryGlass transition•Protein dynamics •Equilibrium fluctuations •Protein/hydration water relaxations •Glass transition •Hydration water liquid-liquid transitionBiophysical chemistry
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Enantioselective transport of amino acid through supported chiral liquid membranes

1993

Abstract Two chiral alcohols, nopol and (2S)-(−)-methyl-1-butanol, immobilized in the pores of a polyethylene film were used for the anantioselective transport of amino acid hydrochloride. The degree of stereoselectivity of the permeation process varied from 0.39 to 1.52 depending on both the type of the chiral membrane phase and the properties of the amino acid. The evaluation of the membrane ability to separate stereoisomers was performed by the step-by-step analysis by considering the effect of amino acids' hydrophobicity, polarity and degree of chirality. For the purpose of this paper, the chirality measure was introduced. It was demonstrated that the enantioselectivity was affected mai…

inorganic chemicalschemistry.chemical_classificationamino acidschiral discriminationStereochemistryHydrochlorideorganic chemicalsEnantioselective synthesisFiltration and SeparationPermeationBiochemistryAmino acidsupported liquid membraneschemistry.chemical_compoundMembranechemistryPhase (matter)Organic chemistryheterocyclic compoundsGeneral Materials ScienceStereoselectivityPhysical and Theoretical ChemistryChirality (chemistry)Journal of Membrane Science
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Linear Triphosphines as Ligands for Metal Complexes Immobilization in Ionic Liquids: Palladium-Catalyzed Methoxylation of Alkynes

2012

Several novel palladium triphosphine complexes have been synthesized and tested as recyclable catalysts for the methoxylation of alkynes into acetals in ionic liquids. A complete conversion of phenylacetylene was achieved with only 0.2% of (Pd(Triphos)NCMe)((PF6)2) in a methanol/(BMIM)(BF4) mixture. We discovered that the addition of an ionic liquid to methanol allowed not only to increase the activity of the palladium catalyst but also to provide a recyclable catalyst which can be reused several times with a weaker drop of activity. To complete these catalytic studies, we describe the synthesis of the first poor -electron-donating/strong -electron-acceptor linear Triphosphine which, afte…

inorganic chemicalschemistry.chemical_elementCombinatorial chemistryTriphosCatalysisMetalchemistry.chemical_compoundchemistryPhenylacetylenevisual_artIonic liquidvisual_art.visual_art_mediumOrganic chemistryMethanolSelectivityPalladiumThe Open Organic Chemistry Journal
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An Interview with Zygmunt Bauman: How to Turn the Word into Flesh

2017

Deceased in January this year, the Polish-British sociologist Zygmunt Bauman has left an extremely rich scholarly legacy. In one of his last academic interviews, he refers to the key issues which had been the subject of his in-depth analysis for many years. Bauman starts with reflections on the gap between political authority and power. Next, given his long-standing research into ‘liquid modernity’, he focuses on the vitality of capitalism, which has now adopted a lighter, consumer form. Another thread of the interview is Bauman’s own research attitude, which he refers to as ‘sociological hermeneutics’. It is characterized by his reluctance to use any ‘-isms’ and a profound mistrust of all…

intellectualsSociology and Political Sciencemedia_common.quotation_subjectCreative freedomPolitical authority0507 social and economic geographyVitalityKey issuesacademicSociologymedia_commonLiteraturebusiness.industryModernity05 social sciencesliquid modernirty050301 educationGeneral Social SciencesCapitalismPostmodernismexpertAestheticsHermeneuticsbusiness050703 geography0503 educationZygmunt BaumanTheory, Culture &amp; Society
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