Search results for " polymerization"

showing 10 items of 1054 documents

Room temperature ionic liquids based on cationic porphyrin derivatives and tetrakis(pentafluorophenyl)borate anion

2011

A series of 11 low melting ionic liquids based on meso-substituted A3B -porphyrins and A2B2-porphyrins containing one or two pyridyl substituents have been synthesized in high yields. Three of them are liquids at room temperature. All these porphyrinic salts were characterized by1H NMR,19F NMR, MALDI-TOF mass spectrometry, elemental analysis and UV-visible spectroscopy. The thermal properties and conductivity values of these salt derivatives have been also measured. A specific conductivity value of up to 4 mS.cm-1could be obtained for a compound having the counter-anion B(C6F5)4-.

A(2)B(2)-porphyrinsMediaInorganic chemistrySalt (chemistry)tetrakis(pentafluorophenyl)borate anionExtractionConductivityElectrochemistryCatalysisIonDscchemistry.chemical_compoundElectrolyteElectrochemistryMolten-Saltschemistry.chemical_classificationTgaCationic polymerizationGeneral ChemistryA(3)B-porphyrinsPorphyrinRT ionic liquidschemistrySensitized Solar-CellsIonic liquidProton NMRconductivity
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Reversible isomerization of metal nanoclusters induced by intermolecular interaction

2021

Most inorganic nanoparticles are directly surface-terminated (and -stabilized) by protecting ligands, which could greatly affect the atomic packing and physical/chemical properties of their inorganic cores. Here, we show that the intermolecular interactions between the adsorbed molecules and surface ligands can also affect the core structure of inorganic nanoparticles. Through the coupling/decoupling of cationic surfactants (cetyltrimethylammonium cations, CTA+) and anionic surface ligands (para-mercaptobenzoic acid, p-MBA) in the aqueous phase, we have achieved a reversible transformation between two isomers of [Au25(p-MBA)18]− nanoclusters. The interconversion process between the two isom…

Absorption spectroscopyLigandChemistryGeneral Chemical EngineeringBiochemistry (medical)Intermolecular forceCationic polymerizationGeneral ChemistryPhotochemistryBiochemistryNanoclustersMetalMolecular dynamicsCrystallographyAdsorptionvisual_artMaterials Chemistryvisual_art.visual_art_mediumEnvironmental ChemistryMoleculeDensity functional theoryIsomerizationChem
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Effect of short-chain alcohols on surfactant-mediated reversed-phase liquid chromatographic systems.

2010

The behaviour of β-blockers in a reversed-phase liquid chromatographic (RPLC) column with mobile phases containing a short-chain alcohol (methanol, ethanol or 1-propanol), with and without the surfactant sodium dodecyl sulphate (SDS), was explored. Two surfactant-mediated RPLC modes were studied, where the mobile phases contained either micelles or only surfactant monomers at high concentration. Acetonitrile was also considered for comparison purposes. A correlation was found between the effects of the organic solvent on micelle formation (monitored by the drop weight procedure) and on the nature of the chromatographic system (as revealed by the retention, elution strength and peak shape of…

AcetonitrilesAdrenergic beta-Antagonists1-PropanolBiochemistryMicelleAnalytical ChemistryHydrophobic effectchemistry.chemical_compoundSurface-Active AgentsPulmonary surfactantPhase (matter)AcetonitrileMicellesChromatography Reverse-PhaseChromatographyEthanolElutionChemistryMethanolOrganic ChemistryCationic polymerizationSodium Dodecyl SulfateGeneral MedicineReversed-phase chromatographyAlcoholsData Interpretation StatisticalJournal of chromatography. A
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Submicellar and micellar reversed-phase liquid chromatographic modes applied to the separation of beta-blockers.

2009

The behaviour of a reversed-phase liquid chromatographic (RPLC) system (i.e. elution order, resolution and analysis time), used in the analysis of β-blockers with acetonitrile-water mobile phases, changes drastically upon addition of an anionic surfactant (sodium dodecyl sulphate, SDS). Surfactant monomers cover the alkyl-bonded phase in different extent depending on the concentration of both modifiers, in the ranges 1 × 10-3-0.15 M SDS and 5-50% acetonitrile. Meanwhile, the surfactant is dissolved in the mobile phase as free monomers, associated in small clusters or forming micelles. Four characteristic RPLC modes are yielded, with transition regions between them: hydro-organic, micellar, …

AcetonitrilesAdrenergic beta-AntagonistsAnalytical chemistryBiochemistryMicelleSensitivity and SpecificityAnalytical Chemistrychemistry.chemical_compoundPulmonary surfactantSurfactant-mediated chromatographic systemsPhase (matter)Sodium dodecyl sulphateSelectivityAcetonitrileAcetonitrileMicellesChromatographyElutionChemistryOrganic ChemistryCationic polymerizationAnalysis timeSodium Dodecyl SulfateGeneral MedicineReversed-phase chromatographyDirect transfer mechanismModels ChemicalCritical micelle concentrationSolventsβ-BlockersAlgorithmsChromatography LiquidJournal of chromatography. A
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Performance of different C18 columns in reversed-phase liquid chromatography with hydro-organic and micellar-organic mobile phases

2014

Column selection in reversed-phase liquid chromatography (RPLC) can become a challenge if the target compounds interact with the silica-based packing. One of such interactions is the attraction of cationic solutes to the free silanols in silica-based columns, which is a slow sorption-desorption interaction process that gives rise to tailed and broad peaks. The effect of silanols is minimised by the addition of a competing agent in the mobile phase, such as the anionic surfactant sodium dodecyl sulphate (SDS). In micellar-organic RPLC, the adsorption of an approximately fixed amount of SDS monomers gives rise to a stable modified stationary phase, with properties remarkably different from th…

AcetonitrilesAdrenergic beta-AntagonistsBiochemistryAnalytical ChemistrySurface-Active AgentsAdsorptionPulmonary surfactantPhenolsPhase (matter)Sodium dodecyl sulphateAcetonitrileMicellesChromatography Reverse-PhaseChromatographyElutionChemistryOrganic ChemistryCationic polymerizationC18 columnsSodium Dodecyl SulfateWaterGeneral MedicineReversed-phase chromatographySilanesMicellar liquid chromatographyβ-BlockersAdsorptionSelectivityMicellar liquid chromatography
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Double Thermoresponsive Block Copolymers Featuring a Biotin End Group

2010

A poly(oligo(ethylene glycol) monomethyl ether methacrylate)-block-poly(N-isopropyl methacrylamide) (POEGMA-b-PNIPMAM) block copolymer with a biotin end group on the PNIPMAM block as a biotarget was synthesized as a model system for temperature-controlled polymer immobilization. The synthesis was based on RAFT polymerization followed by postpolymerization modification of an activated ester precursor block and an exchange of the dithioester end group within one step. NMR, differential scanning calorimetry (DSC), dynamic light scattering (DLS), and turbidimetry measurements were performed to investigate the stimulus-responsive properties. The double thermoresponsive POEGMA-b-PNIPMAM with biot…

AcrylamidesMagnetic Resonance SpectroscopyCalorimetry Differential ScanningPolymers and PlasticsPolymersRadical polymerizationTemperaturetechnology industry and agricultureBiotinBioengineeringChain transferLower critical solution temperaturePolymerizationBiomaterialschemistry.chemical_compoundEnd-groupchemistryPolymer chemistryMaterials ChemistryCopolymerMethacrylamideReversible addition−fragmentation chain-transfer polymerizationStreptavidinEthylene glycolMicellesBiomacromolecules
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Anionic Polymerization of (Meth)acrylates in the Presence of Cesium Halide−Trialkylaluminum Complexes in Toluene

2001

The polymerization of methyl methacrylate and various acrylates initiated by ester enolates in the presence of cesium halide-trialkylaluminum complexes, Cs[Al n R 2n X] (n = 1, 2; R = Et, Bu'), in toluene has living and controlled character at -20 °C for methacrylates (X = Cl) and at -65 °C for n-butyl acrylate (X = F). Quantitative monomer conversions are usually reached, leading to polymers with narrow molecular weight distributions (M w /M n < 1.1). Kinetic investigations indicate a rather complex polymerization mechanism, and we assume an equilibrium between at least two active species. With this new initiating system, beside acrylate homopolymers, random and graft copolymers can be syn…

Acrylate polymerAcrylatePolymers and PlasticsOrganic ChemistrySolution polymerizationInorganic Chemistrychemistry.chemical_compoundMonomerAnionic addition polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerMethyl methacrylateMacromolecules
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Darstellung und polymerisation von diestern aus 2,2′-methylendiphenolen und acryl-, methacryl- bzw. Crotonsäure

1984

Several mono- and diesters of four selected 2,2′-methylenediphenols with acrylic, methacrylic, and crotonic acid were synthesized for the first time. Special emphasis was paid to the preparation of diesters with two different acyl groups which could be obtained via the corresponding monoesters. The radical polymerization of these esters with AIBN (mainly in benzene) gave insoluble (crosslinked) products from dimethacrylates and soluble (linear) polymers from mixed diesters with methacrylic and crotonic acid, while the dicrotonates are not reactive.

Acrylate polymerchemistry.chemical_classificationLinear polymerRadical polymerizationSolution polymerizationmacromolecular substancesPolymerchemistry.chemical_compoundchemistryPolymer chemistryCrotonic acidOrganic chemistrySolubilityBenzeneDie Makromolekulare Chemie
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Controlled synthesis of poly(acetone oxime acrylate) as a new reactive polymer: Stimuli-responsive reactive copolymers

2007

Abstract Acetone oxime acrylate has been synthesized as a new active ester monomer. Free radical polymerization yielded a reactive polymer soluble in various organic solvents, such as chloroform, dioxane, DMSO, acetone, methanol, dichloromethane, DMF, and ethanol. Controlled radical polymerization of acetone oxime acrylate was successfully conducted using the RAFT, NMP and Iniferter method. Partly polymer analogous reaction with N-isopropylamine resulted in the reactive copolymer poly(N-isopropylacrylamide-co-acetone oxime acrylate), which featured a lower critical solution temperature (LCST) of 61 °C in water. Further, the reactivity of the copolymer was exemplary proven by complete reacti…

AcrylateChloroformPolymers and PlasticsOrganic ChemistryRadical polymerizationGeneral Physics and AstronomyChain transferLower critical solution temperaturechemistry.chemical_compoundPhotopolymerchemistryPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryAcetone oximeEuropean Polymer Journal
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Interfacial stabilization by soft Janus nanoparticles

2016

Abstract The stabilization of water/air, water/oil and water/solid interfaces by Janus particles with polystyrene (PS) and poly(methacrylic acid) (PMAA) hemispheres was systematically investigated. The stabilization of these interfaces is of relevance for the formulation of foams, emulsions and dispersions. The Janus particles were prepared from micellar solutions of polystyrene-b-polyisoprene-b-poly(tert-butyl methacrylate) (PS-PI-PtBMA) triblock terpolymers by selective cross-linking of the polyisoprene domain on a multi-gram scale, followed by hydrolysis of the PtBMA block. For the investigation of water/oil-emulsions a series of hydrophobic oils (paraffin oil, xylene, peanut oil, isopro…

AcrylateMaterials sciencePolymers and PlasticsOrganic ChemistryEmulsion polymerizationJanus particles02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyMethacrylate01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryMethacrylic acidPolymer chemistryMaterials ChemistryJanusPolystyreneMethyl methacrylate0210 nano-technologyPolymer
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