Search results for "solvent"

showing 10 items of 1395 documents

Factors influencing the transport of tryptophan hydrochloride through supported liquid membranes containing macrocyclic carriers

1997

Commercially available PTFE membranes were used as a support for liquid membranes in amino acid transport. Using tryptophan as a model amino acid, the influence of the type of organic liquid, kind of macrocyclic carrier and counter-ion on transport efficiency was examined. These studies show the strong influence of the kind of the counter-ion co-transported with amino acid cation, and the type of macrocyclic carrier used on the transport efficiency. The transport efficiency depends also on the pH of the source phase and on the nature of the organic liquid used as a membrane solvent. Liquid membranes supported on commercial porous-PTFE-membranes with hydrophobic solvents are stable for more …

chemistry.chemical_classificationamino acidsFacilitated diffusionHydrochlorideInorganic chemistryTryptophanFiltration and SeparationBiochemistrysupported liquid membranesAmino acidmembrane stabilitySolventPartition coefficientchemistry.chemical_compoundMembranechemistryOrganic chemistryGeneral Materials Sciencefacilitated transportPhysical and Theoretical ChemistryCounterionJournal of Membrane Science
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π-Conjugated diimidazolium salts: rigid structure to obtain organized materials.

2015

Phenylene ethynylene based diimidazolium salts differing in the alkyl chain length borne on the imidazolium ion and anion nature were synthesized. Their properties were studied both in solution and in the solid state. Salts obtained were able to aggregate in organic solvent solution. Aggregate formation was studied by performing concentration dependent measurements using UV-vis, fluorescence and Resonance Light Scattering. Furthermore, features of the aggregates were also investigated in the solid state by means of fluorescence and Scanning Electron Microscopy measurements. Finally, Density Functional Theory calculations were performed to obtain insights into the interaction geometry in the…

chemistry.chemical_classificationdiimidazolium salts self-assembly DFT investigationChemistryGeneral Physics and AstronomySalt (chemistry)Settore CHIM/06 - Chimica OrganicaConjugated systemResonance (chemistry)IonSolventPhenylenePhysical chemistryOrganic chemistryDensity functional theoryPhysical and Theoretical ChemistryAlkylSettore CHIM/02 - Chimica FisicaPhysical chemistry chemical physics : PCCP
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ChemInform Abstract: Hydrophobically Directed Aldol Reactions: Polystyrene-Supported L-Proline as a Recyclable Catalyst for Direct Asymmetric Aldol R…

2008

A simple synthetic methodology for the preparation of a polystyrene-supported L-proline material is reported, and this material has been used as catalyst in direct asymmetric aldol reactions between several ketones and arylaldehydes to furnish aldol products in high yields and stereoselectivities. Screening of solvents showed that these reactions take place only in the presence of water or methanol, at lower levels of conversion in the latter case. This solvent effect, coupled with the observed high stereoselectivities, has been explained in terms of the formation of a hydrophobic core in the inner surface of the resin, whereas the hydrophilic proline moiety lies at the resin/water interfac…

chemistry.chemical_compoundAldol reactionChemistryMoietyOrganic chemistryStereoselectivityGeneral MedicineProlinePolystyreneMethanolSolvent effectsCatalysisChemInform
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Electrochemical synthesis of diaryl dichalcogenides in acetonitrile, with two sacrificial electrodes: diseleno and ditelluro derivatives of quinolones

1993

chemistry.chemical_compoundAqueous solutionChemistryGeneral Chemical EngineeringOrganic solventKineticsElectrodeInorganic chemistryElectrochemistryElectrochemistryAcetonitrileAnalytical ChemistryJournal of Electroanalytical Chemistry
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Understanding the kinetic solvent effects on the 1,3-dipolar cycloaddition of benzonitrile N-oxide: a DFT study

2011

JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, ISSN : 0894-3230, DOI : 10.1002/poc.1858, Issue : 7, Volume : 24, pp. 611 – 618, JUILLET 2011.

chemistry.chemical_compoundBenzonitrilechemistryVolume (thermodynamics)Computational chemistryOrganic Chemistry13-Dipolar cycloadditionPhysical organic chemistryOxideDensity functional theoryPhysical and Theoretical ChemistrySolvent effectsElectron localization functionJournal of Physical Organic Chemistry
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Membrane Lipid-Polypeptide Molecular Associations in Non Aqueous Solvent. Effect of Phosphatidylcholine Concentration and Temperature and their Influ…

1986

Abstract The use of an Ultrastyragel 500 A column for the study of interactions between phosphatidylcholine and gramicidin A in tetra-hydrofuran is described. Analysis of vacant peak has allowed to establish the influence that eluent lipid composition, concentration of injected gramicidin and temperature have on the interaction. At 20[ddot] C, for the assayed phospholipid concentration range (0.04 to 0.14 %, w/v), the lipid/polypeptide molar binding ratio, BR, varies from 1.3 to 6.9. An increase in temperature from 20 to 40[ddot] C causes a decrease in BR of about 20 %. On the other hand, the interaction releases some of the water bound to the lipid polar head, suggesting that the binding i…

chemistry.chemical_compoundMembraneChromatographyAqueous solutionchemistryPhosphatidylcholineDimerPhospholipidGramicidinMolecular MedicineBound waterlipids (amino acids peptides and proteins)Solvent effectsJournal of Liquid Chromatography
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CO2 switchable nanoparticles: reversible water/organic-phase exchange of gold nanoparticles by gas bubbling

2013

Gold nanoparticles capped with oleylamine can be effectively transferred from an organic solvent to water in the presence of an acetamidine surfactant by CO2 bubbling and then effectively reverted back to the organic phase by N2 bubbling.

chemistry.chemical_compoundPulmonary surfactantChemistryOleylamineColloidal goldGeneral Chemical EngineeringOrganic solventPhase (matter)Inorganic chemistryfood and beveragesNanoparticleGeneral ChemistryRSC Advances
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Mechanism of the oxidation of sulfides by dioxiranes: conformational mobility and transannular interaction in the oxidation of thianthrene 5-oxide.

2004

The detailed study of the oxidation of thianthrene 5-oxide (1) with methyl(trifluoromethyl)dioxirane (5b) in different solvents and in the presence of (18)O isotopic tracers is reported. Thianthrene 5-oxide (1) is a flexible molecule in solution, and this property allows for transannular interaction of the sulfoxide group with the expected zwitterionic 7 and hypervalent 10-S-4 sulfurane 9 intermediates formed in the oxidation and biases the course of the reaction toward the monooxygenation pathway.

chemistry.chemical_compoundReaction mechanismTrifluoromethylchemistryDioxiraneZwitterionOrganic ChemistryHypervalent moleculeSulfoxideSolvent effectsPhotochemistryThianthreneThe Journal of organic chemistry
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1990

Intrinsic viscosities, [η], second virial coefficients, A2, and interaction potentials, g12, for the ternary systems alcohol (1)/3-heptanone (2)/poly(1-vinyl-2-pyrrolidone) (3), with the unbranched alcohols methanol, ethanol and 1-propanol, were determined at 25°C. Taking into account the dependence of the viscometric interaction parameter, B, with the molecular weight of the polymer, the unperturbed dimensions parameter, KΘ, of the polymer was unambiguously obtained. Relationships between ΔKΘ (defined as ΔKΘ = ΔK − KΘ) and excess Gibbs energies, GE, and between excess viscosity, Δ[η], and GE allow to obtain equations relating A2 to ΔKΘ or to Δ[η]. Therefore, A2 can be evaluated from experi…

chemistry.chemical_compoundVirial coefficientChemistryIntrinsic viscosityPolymer chemistryMethanolFlory–Huggins solution theorySolvent effectsTernary operationHeptanone3-HeptanoneDie Makromolekulare Chemie
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Why Do Five-Membered Heterocyclic Compounds Sometimes Not Participate in Polar Diels–Alder Reactions?

2013

The reactions of bicyclic enone (BCE, 1) with cyclopentadiene (Cp, 2) and the five-membered heterocyclic compounds (FHCs) furan 3 and N-methyl pyrrole 4 for the construction of polycyclic heterocyclic compounds have been studied at the B3LYP/6-31G* level. No reaction takes place in the absence of Lewis acid (LA) catalysts as a consequence of the high activation energy associated with these reactions. Electrophilic activation of BCE 1 by formation of a complex with the BF3 LA, 1-BF3, and solvent effects favor the reactions. However, a different reactivity is manifested by Cp 2 and FHCs 3 and 4. Thus, while the reaction of 1-BF3 with Cp 2 yields the expected exo [4 + 2] cycloadduct, the react…

chemistry.chemical_compoundchemistryBicyclic moleculeNucleophileStereochemistryFuranOrganic ChemistryElectrophileLewis acids and basesSolvent effectsEnonePyrroleThe Journal of Organic Chemistry
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