Search results for "bonding"

showing 10 items of 996 documents

Quantitative retention—structure and retention—activity relationship studies of ionic and non-ionic catecholamines by micellar liquid chromatography

1997

When ionic surfactants are used as mobile phases in micellar liquid chromatography, MLC, the retention of compounds is governed by hydrophobic and electrostatic forces. In the absence of electrostatic effects, the hydrophobicity of a compound is the predominant factor affecting its retention and its interaction with micelles. Because both interactions should be considered for ionic compounds, a novel retention model is proposed which includes the hydrophobicity of a compound and the molar fraction of its charged form. High correlations between the logarithm of the capacity factors and structural parameters were obtained for ionic compounds with different degrees of ionization. The effect of…

ChromatographyChemistryOrganic ChemistryClinical BiochemistryIonic bondingMole fractionBiochemistryMicelleMicellar electrokinetic chromatographyCapacity factorAnalytical ChemistryPulmonary surfactantMicellar liquid chromatographyPhase (matter)Chromatographia
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Micellar versus hydro-organic reversed-phase liquid chromatography: a solvation parameter-based perspective.

2007

The performance of the solvation parameter model is examined for micellar liquid chromatography. The results are compared with those offered with hydro-organic eluents, intending to reveal the properties that influence the retention and distinguish the particular behaviour of micellar systems. The retention data of several series of non-ionisable and ionisable compounds (mainly steroids, polyaromatic hydrocarbons, phenols, sulfonamides, beta-blockers, phenethylamines, antihistamines, and diuretics) were used as probe compounds. The micellar mobile phases contained an anionic (sodium dodecyl sulphate), non-ionic (Brij-35), or cationic (cetyltrimethylamonium bromide) surfactant, with or witho…

ChromatographyChemistryOrganic ChemistrySolvationIonic bondingGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryPropanolchemistry.chemical_compoundSurface-Active AgentsMicellar liquid chromatographyBromideSolventsAcetonitrileMicellesChromatography LiquidJournal of chromatography. A
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Retention mechanisms in micellar liquid chromatography.

2008

Micellar liquid chromatography (MLC) is a reversed-phase liquid chromatographic (RPLC) mode with mobile phases containing a surfactant (ionic or non-ionic) above its critical micellar concentration (CMC). In these conditions, the stationary phase is modified with an approximately constant amount of surfactant monomers, and the solubilising capability of the mobile phase is altered by the presence of micelles, giving rise to diverse interactions (hydrophobic, ionic and steric) with major implications in retention and selectivity. From its beginnings in 1980, the technique has evolved up to becoming a real alternative in some instances (and a complement in others) to classical RPLC with hydro…

ChromatographyChemistryOrganic ChemistrySolvationIonic bondingGeneral MedicineReversed-phase chromatographyHydrogen-Ion ConcentrationBiochemistryMicelleAnalytical ChemistrySilanolchemistry.chemical_compoundSurface-Active AgentsModels ChemicalSolubilityMicellar liquid chromatographyPhase (matter)Critical micelle concentrationSolventsAdsorptionHydrophobic and Hydrophilic InteractionsAlgorithmsMicellesChromatography LiquidJournal of chromatography. A
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Ionomers in solution: 1. Viscometric and chromatographic studies in cononsolvent and cosolvent mixtures

1997

Abstract The viscosity and elution behaviour of polystyrene sulfonate ionomers with varying ionic content has been studied in the pure solvents chloroform (CHL), tetrahydrofuran (THF), dioxan (DIO), ethyl acetate (EA) and dimethylformamide (DMF) as well as in their cononsolvent mixtures CHL/THF (50:50), DIO/CHL (75:25) and in the cosolvent mixture EA/DMF (50:50). In the pure solvents with low dielectric constant the reduced viscosities of ionomers are lower at low concentrations and higher at moderate ones than the respective viscosities of the polystyrene precursor. These results can be explained by formation of intramolecular and intermolecular associations. Moreover, differences in visco…

ChromatographyPolymers and PlasticsOrganic ChemistryConcentration effectIonic bondingPolyelectrolytePolystyrene sulfonatechemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryDimethylformamidePolystyreneIonomerTetrahydrofuranPolymer
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Assessment and optimization of system parameters in size exclusion separation of proteins on diol-modified silica columns

1981

Abstract On diol-modified silica columns the retention of proteins is governed by a size exclusion effect, but superimposed on this are some secondary effects, i.e. , ionic and diol-ligand interactions which can be controlled and adjusted reproducibly by varying the eluent composition. The eluent composition also affects the column efficiency and peak shape. Both dependences can be employed to obtain a better resolution of proteins than can be expected from size exclusion alone.

ChromatographyResolution (mass spectrometry)fungiOrganic ChemistrySize-exclusion chromatographyDiolAnalytical chemistryfood and beveragesIonic bondingGeneral MedicineBiochemistryAnalytical Chemistrychemistry.chemical_compoundColumn chromatographychemistrySystem parametersJournal of Chromatography A
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Diastereoselective Insertion of Isocyanide into the Alkyl−Metal Bond of Methylbenz[ e ]indenyl ansa ‐Zirconocene Complexes

2004

Alkylation of ansa-zirconocene [Zr{(η5-C5H5)SiMe2(MBI)}Cl2] (MBI = η5-2-Me−C13H7) with MgRCl gave the dimethyl complex [Zr{(η5-C5H5)SiMe2(MBI)}Me2], but unresolvable mixtures containing mono-alkylated compounds were obtained when bulkier alkyls were used. However pure dialkyl complexes [Zr{(η5-C5H5)SiMe2(MBI)}R2] (R = CH2Ph, CH2SiMe3) were easily obtained using K(CH2Ph) and Li(CH2SiMe3) as alkylating agents. Diastereoselective insertion into the MBI-unprotected Zr−R bond was observed when all of these dialkyl complexes were treated with 2,6-xylyl isocyanide to give the iminoacyl compounds [Zr{(η5-C5H5)SiMe2(MBI)}R{CR[η2-N-(2,6-xylyl)]}] (R = Me, CH2Ph, CH2SiMe3). All of the new complexes we…

Cienciachemistry.chemical_classificationZirconiumMetallocenesStereochemistryScienceIsocyanidechemistry.chemical_elementSCIENCEIsocyanidesAlkylationMedicinal chemistryQuímica inorgánicaPolymerizationInorganic Chemistrychemistry.chemical_compoundchemistryPolymerizationCIENCIAZirconiumInsertionChemistry inorganicAlkylMetallic bondingEuropean Journal of Inorganic Chemistry
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Carnosine Inhibits Aβ42Aggregation by Perturbing the H-Bond Network in and around the Central Hydrophobic Cluster

2013

Aggregation of the amyloid-β peptide (Aβ) into fibrillar structures is a hallmark of Alzheimer's disease. Thus, preventing self-assembly of the Aβ peptide is an attractive therapeutic strategy. Here, we used experimental techniques and atomistic simulations to investigate the influence of carnosine, a dipeptide naturally occurring in the brain, on Aβ aggregation. Scanning force microscopy, circular dichroism and thioflavin T fluorescence experiments showed that carnosine does not modify the conformational features of Aβ42 but nonetheless inhibits amyloid growth. Molecular dynamics (MD) simulations indicated that carnosine interacts transiently with monomeric Aβ42 by salt bridges with charge…

Circular dichroismMagnetic Resonance Spectroscopy1303 BiochemistryStereochemistryStatic ElectricityCarnosinePeptideMolecular Dynamics SimulationBiochemistryproteinprotein interactionsProtein–protein interactionchemistry.chemical_compoundMolecular dynamicsnutraceutical compounds10019 Department of Biochemistry1312 Molecular BiologyMolecular Biologychemistry.chemical_classificationAmyloid beta-PeptidesDipeptideHydrogen bondOrganic ChemistryIntermolecular forceTemperatureneuroprotective agentHydrogen BondingAlzheimer's diseasePeptide Fragmentsmolecular dynamicscarnosinechemistry1313 Molecular Medicine570 Life sciences; biologyMolecular MedicineHydrophobic and Hydrophilic Interactionsprotein aggregation fibrillogenesis carnosine AFM1605 Organic ChemistryChemBioChem
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Circular dichroism of polynucleotides: Interactions of NiCl2 with poly(dA-dT).poly(dA-dT) and poly(dG-dC).poly(dG-dC) in a water-in-oil microemulsion.

2008

The thermal behavior of the synthetic, high molecular weight, double stranded polynucleotides poly(dA-dT)·poly(dA-dT) [polyAT] and poly(dG-dC)·poly(dG-dC) [polyGC] solubilized in the aqueous core of the quaternary water-in-oil cationic microemulsion CTAB|n-pentanol|n-hexane|water in the presence of increasing amounts of NiCl2 at several constant ionic strength values (NaCl) has been studied by means of circular dichroism and electronic absorption spectroscopies. In the microemulsive medium, both polynucleotides show temperature-induced modifications that markedly vary with both Ni(II) concentration and ionic strength. An increase of temperature causes denaturation of the polyAT duplex at lo…

Circular dichroismPolynucleotidesAnalytical chemistryIonic bondingchemistry.chemical_elementmodel polynucleotideCatalysisAnalytical ChemistryNickelthermal denaturationDrug DiscoveryMicroemulsionSpectroscopyPharmacologyAqueous solutionChemistryCircular DichroismOrganic ChemistryCationic polymerizationTemperatureWaterCD and UV spectroscopiesnickel (II) ionNickelCrystallographywater-in-oil microemulsionPolynucleotideIonic strengthEmulsionsOilsChirality
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Surfactant Association: Recent Theoretical and Experimental Developments

1991

A theoretical model describing the association of ionic surfactants into rod-shaped micelles is combined with an approximate formula for the viscosity increase induced by rod-shaped aggregates. It is shown that most of the thermodynamic parameters of the association model can be obtained from viscosity measurements. The approach is applied to micellar solutions of hexadecylpyridinium salts. The pronounced effect of counter-ion concentration on the growth of rod-shaped micelles can be attributed to a slightly higher degree of counter-ion association in the cylindrical part than in the end portions. An attempt is made to explain the finding that the degree of counter-ion association is virtua…

Cloud pointViscosityPulmonary surfactantChemistryCritical micelle concentrationAssociation (object-oriented programming)Micellar solutionsIonic bondingThermodynamicsMicelle
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Thermodynamics of ABO3-Type Perovskite Surfaces

2011

The ABO3-type perovskite manganites, cobaltates, and ferrates (A= La, Sr, Ca; B=Mn, Co, Fe) are important functional materials which have numerous high-tech applications due to their outstanding magnetic and electrical properties, such as colossal magnetoresistance, half-metallic behavior, and composition-dependent metal-insulator transition (Coey et al., 1999; Haghiri-Gosnet & Renard, 2003). Owing to high electronic and ionic conductivities. these materials show also excellent electrochemical performance, thermal and chemical stability, as well as compatibility with widely used electrolyte based on yttrium-stabilized zirconia (YSZ). Therefore they are among the most promising materials as …

Colossal magnetoresistanceMaterials scienceThermodynamicsIonic bondingPrimitive cell02 engineering and technologyCrystal structure021001 nanoscience & nanotechnology01 natural sciences7. Clean energy0103 physical sciencesPhysical chemistryCubic zirconiaOrthorhombic crystal system010306 general physics0210 nano-technologyYttria-stabilized zirconiaPerovskite (structure)
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