Search results for "Solvents"

showing 10 items of 291 documents

The fractal calibration method applied to the characterization of polymers in solvent mixtures and in mixed gel packings by SEC.

2007

The size-exclusion chromatographic (SEC) behaviour of different solvent/polymer systems in three packing sets has been analysed from fractal considerations. The three-column sets studied are specifically formed by: (i) 'pure' micro-styragel, (ii) 'mixed' TSK Gel H(HR + XL + HR) and (iii) mixed TSK Gel H(XL + HR + XL). The experimental data reveals that in most of the systems assayed the classical universal calibration (UC) is not fulfilled, denoting the existence of secondary effects accompanying the main SEC mechanism. In order to obtain an accurate characterization of different polymers eluted in solvent mixtures and/or mixed packings, the use of a reliable and trusted calibration curve i…

chemistry.chemical_classificationMolar massChemistryElutionCalibration curvePolymersAnalytical chemistryFiltration and SeparationPolymerAnalytical ChemistryGel permeation chromatographyMolecular WeightFractalCalibrationMaterials TestingCalibrationChromatography GelSolventsMolar mass distributionParticle SizeGelsPorosityMathematicsJournal of separation science
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Influence of solvents on the antioxidant property of flavonoids.

2003

In polyphenols redox systems, the solvent plays a fundamental role in the chemical behaviour of these compounds. Antioxidants can react in different ways with the prooxidant molecules. We have found differences in the antioxidant capacity of flavonoids such as naringin, neohesperidin, neoericitrin, hesperidin, narirutin didymin and the related flavones naringenin, hesperetin eriodictyol and isosakuratenin, when they are in the presence of radicals and solved in water or in an alcohol mixture.

chemistry.chemical_classificationNeohesperidinNaringeninFlavonoidsNarirutinFree RadicalsHesperetinEriodictyolFlavonesAntioxidantschemistry.chemical_compoundHesperidinchemistrySolventsOrganic chemistryReactive Oxygen SpeciesNaringinOxidation-ReductionFood ScienceDie Nahrung
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Spectroscopic and structural characterization of pure and FeCl3-containing tri-n-butyl phosphate

2014

The spectroscopic properties and liquid structure of pure tri-n-butyl phosphate (TBP) and FeCl3/TBP solutions have been investigated by Uv–Vis and Raman spectroscopies, X-ray diffraction and conductometry. Uv–Vis and Raman spectra, supported by conductometric measurements, consistently indicate that the solubilized salt is present mostly as TBP n [FeCl3 − n ] n+ and FeCl4 − complex ions due to specific interaction with the TBP phosphate group. Thanks to this interaction, a high amount of salt (up to 13 % w/w) can be dissolved despite the relatively low dielectric constant of TBP. The X-ray diffractogram of pure TBP has been interpreted in terms of three main contributions which can be attri…

chemistry.chemical_classificationPolymers and PlasticsConductometryChemistryInorganic chemistryTri-N-butyl PhosphateFeCl3 . Tri-n-butyl phosphate . Self-assembling . Local structures .Amphiphilic solventsNanoparticleSalt (chemistry)Ionic bondingTri-n-butyl phosphatePhosphatesymbols.namesakechemistry.chemical_compoundColloid and Surface ChemistryFeCl3Materials ChemistrysymbolsMoleculeSelf-assemblingAmphiphilic solventsPhysical and Theoretical ChemistryLocal structuresRaman spectroscopy
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7-Amino-2-methylsulfanyl-1,2,4-triazolo[1,5-a]pyrimidine-6-carboxylic acid as the dimethylformamide and water monosolvates at 293 K.

2010

The molecular structure of 7-amino-2-methylsulfanyl-1,2,4-triazolo[1,5-a]pyrimidine-6-carboxylic acid is reported in two crystal environments, viz. as the dimethylformamide (DMF) monosolvate, C(7)H(7)N(5)O(2)S·C(3)H(7)NO, (I), and as the monohydrate, C(7)H(7)N(5)O(2)S·H(2)O, (II), both at 293 (2) K. The triazolo[1,5-a]pyrimidine molecule is of interest with respect to the possible biological activity of its coordination compounds. While the DMF solvate exhibits a layered structural arrangement through N...O hydrogen-bonding interactions, the monohydrate displays a network of intermolecular O...O and N...O hydrogen bonds assisted by cocrystallized water molecules and weak π-π stacking intera…

chemistry.chemical_classificationPyrimidineMolecular StructureHydrogen bondStereochemistryCarboxylic acidStackingCarboxylic AcidsWaterDimethylformamideHydrogen BondingGeneral MedicineCrystal structureCrystallography X-RayGeneral Biochemistry Genetics and Molecular BiologyCoordination complexchemistry.chemical_compoundCrystallographyPyrimidineschemistrytriazolo- [15-a]pyrimidineSettore CHIM/03 - Chimica Generale E InorganicaSolventsDimethylformamideMoleculeActa crystallographica. Section C, Crystal structure communications
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Influence of chain stiffness on knottedness in single polymers.

2013

In the present article, we investigate and review the influence of chain stiffness on self-entanglements and knots in a single polymer chain with Monte Carlo simulations spanning good solvent, theta and globular phases. The last-named are of particular importance as a model system for DNA in viral capsids. Intriguingly, the dependence of knot occurrence and complexity with increasing stiffness is non-trivial, but can be understood with a few simple concepts outlined in the present article.

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceMonte Carlo methodMolecular ConformationStiffnessModel systemNanotechnologyPolymerDNABiochemistryMolecular conformationKnot (unit)BiopolymerschemistrymedicineSolventsNucleic Acid ConformationStatistical physicsmedicine.symptomBiochemical Society transactions
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Biomolecular-solvent stereodynamic coupling probed by deuteration.

1983

Thermodynamic interpretation of experiments with isotopically perturbed solvent supports the view that solvent stereodynamics is directly relevant to thermodynamic stability of biomolecules. According with the current understanding of the structure of the aqueous solvent, in any stereodynamic configuration of the latter, connectivity pathways are identifiable for their topologic and order properties. Perturbing the solvent by isotopic substitution or, e.g., by addition of co-solvents, can therefore be viewed as reinforcing or otherwise perturbing these topologic structures. This microscopic model readily visualizes thermodynamic interpretation. In conclusion, the topologic stereodynamic str…

chemistry.chemical_classificationQuantitative Biology::BiomoleculesPhysics::Biological PhysicsAqueous solutionBiomoleculeMolecular ConformationStereoisomerismGeneral MedicineDeuteriumCondensed Matter::Soft Condensed MatterSolventCoupling (physics)Order (biology)chemistryModels ChemicalStructural BiologyComputational chemistryPhase spaceSolventsMoleculeThermodynamicsChemical stabilityPhysics::Chemical PhysicsMolecular BiologyJournal of biomolecular structuredynamics
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Solvent-Free Synthesis of a Pillared Three-Dimensional Coordination Polymer with Magnetic Ordering

2015

A new magnetic coordination polymer, [Fe(bipy)(im)2] (bipy = 4,4-bipyridine and im = imidazole), has been synthesized in a solvent-free reaction. Structural analysis reveals a pillared 3D coordination polymer composed by neutral layers, formed by iron(II) and imidazolate linkers, interconnected by bipy ligands which serve as pillars. Magnetic measurements show that the material magnetically orders at low temperatures (Tc = 14.5 K) as a weak ferromagnet, likely due to a spin canting.

chemistry.chemical_classificationSolvent freePolymersCoordination polymerInorganic chemistryPolymerCrystallography X-RayInorganic ChemistryThermogravimetryMagneticschemistry.chemical_compoundCrystallographychemistryFerromagnetismThermogravimetryImidazolateSolventsImidazolePhysical and Theoretical ChemistrySpin cantingInorganic Chemistry
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On the determination of underivatised fatty alcohol ethoxylates by electrospray ionisation–mass spectrometry

2006

Abstract The oligomers of fatty alcohol ethoxylates (FAEs) exhibit large sensitivity differences in mass spectrometry with electrospray ionisation (ESI–MS) and atmospheric pressure chemical ionization (APCI). Standards of the oligomers from m = 1 to 7 ethylene oxide units (EOs) and linear alkyl chains from n = 10 to 18 carbon atoms were infused to examine the relative sensitivities or response factors in several media. The response factors of the [M + H]+ and [M + Na]+ peaks in 9:1 acetonitrile/water and methanol/water media containing acid buffers increased following irregular patterns when n and m increased. In methanol/water the response factors depended on the parity of m, being larger …

chemistry.chemical_classificationSpectrometry Mass Electrospray IonizationElectrosprayChromatographyEthylene oxideOrganic ChemistryAnalytical chemistryFatty alcoholAtmospheric-pressure chemical ionizationGeneral MedicineBuffersReference StandardsMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistrySolventsMethanolFatty AlcoholsChromatography High Pressure LiquidAlkylJournal of Chromatography A
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Mechanism of the Oxidation of Sulfides by Dioxiranes. 1. Intermediacy of a 10-S-4 Hypervalent Sulfur Adduct

2002

Earlier studies established that dimethyldioxirane (1a) reacts with sulfides 2 in two consecutive concerted electrophilic oxygen-transfer steps to give first sulfoxides 3 and then sulfones 4. The same sequential electrophilic oxidation model was assumed for the reaction of sulfides 2 with the strongly electrophilic methyl(trifluoromethyl)dioxirane (1b). In this paper we report on a systematic and general study on the mechanism of the reaction of simple sulfides 2 with DMDO (1a) and TFDO (1b) which provides clear evidence for the involvement of hypervalent sulfur species in the oxidation process. In the oxidation of sulfides 2a-c, diphenyl sulfide (2d), para-substituted aryl methyl sulfides …

chemistry.chemical_classificationSulfideTemperatureHypervalent moleculechemistry.chemical_elementSulfoxideGeneral ChemistryReaction intermediateSulfidesBiochemistryMedicinal chemistrySulfurCatalysisSulfonechemistry.chemical_compoundColloid and Surface ChemistrychemistryDioxiraneOxygen RadioisotopesSolventsEpoxy CompoundsOrganic chemistryDimethyldioxiraneOxidation-ReductionSulfurJournal of the American Chemical Society
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Heterogeneous oxidation of pyrimidine and alkyl thioethers in ionic liquids over mesoporous Ti or Ti/Ge catalysts.

2004

Heterogeneous catalytic oxidation of a series of thioethers (2-thiomethylpyrimidine, 2-thiomethyl-4,6-dimethyl-pyrimidine, 2-thiobenzylpyrimidine, 2-thiobenzyl-4,6-dimethylpyrimidine, thioanisole, and n-heptyl methyl sulfide) was performed in ionic liquids by using MCM-41 and UVM-type mesoporous catalysts containing Ti, or Ti and Ge. A range of triflate, tetrafluoroborate, trifluoroacetate, lactate and bis(trifluoromethanesulfonyl)-imide-based ionic liquids were used. The oxidations were carried out by using anhydrous hydrogen peroxide or the urea-hydrogen peroxide adduct and showed that ionic liquids are very effective solvents, achieving greater reactivity and selectivity than reactions p…

chemistry.chemical_classificationTitaniumMolecular StructureChemistryGermaniumOrganic ChemistryThioanisoleInorganic chemistryGeneral ChemistrySulfidesHeterogeneous catalysisSilicon DioxidePeroxideCatalysisCatalysischemistry.chemical_compoundPyrimidinesCatalytic oxidationIonic liquidSolventsParticle SizeTrifluoromethanesulfonateOxidation-ReductionPorosityAlkylChemistry (Weinheim an der Bergstrasse, Germany)
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