Search results for "Meri"

showing 10 items of 7596 documents

Homogeneous Langmuir-Blodgett Film of Double-Chain Ammonium Amphiphile Complexed with Anionic Polymer

1988

Heterogeneous textures suggesting the coexistence of a fluid and a solid phase were found both in a surface monolayer and in a deposited Langmuir-Blodgett (LB) film of double-chain ammonium amphiphiles by fluorescence microscopy. Although an annealing of the surface monolayer at 40°C allowed crystal growth, the heterogeneous phase separation remained in the LB film. A drastic change of the fluorescence image shows that the recrystallization of the complexed monolayer with anionic polymers conducted the homogeneous monolayer.

Anionic addition polymerizationChemical engineeringAnnealing (metallurgy)ChemistryPhase (matter)AmphiphileMonolayerGeneral EngineeringGeneral Physics and AstronomyOrganic chemistryCrystal growthLangmuir–Blodgett filmPolyelectrolyteJapanese Journal of Applied Physics
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Über zwei formen des initiators Na-naphthalin und die bestimmung der „lebenden” kettenenden bei der anionischen polymerisation

1969

Na-Naphthalin in THF kommt in (mindestens) 2 Formen I und I' vor, die sich beim Start der anionischen Polymerisation von Styrol sehr verschieden verhalten. Ohne Zusatg von NaBPh4 wirken beide Formen als Initiatoren. Bei Zusatz von NzBPh4 wird die From I' desktiviert, wobei auf ein Molekul I' zwei Molekule NaBPh4 entfallen. Die hierbei entstehende inaktive Verbindung hat in der Umgebung der Wellenlange 350 nm fast den gleichen Extinktionskoeffizienten wie die “lebenden” Enden. Bei Nichtberucksichtigung dieses Effektes erhalt man daher fur die Konzentration der “lebenden” enden aus Absorptionsmessungen einen zu hohen Wert und fur die Geschwindigkeitskonstante kw(±) der Polymerisaton uber das …

Anionic addition polymerizationChemistryPolymer chemistryDie Makromolekulare Chemie
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Hyperbranched Polyglycerol-Based Lipids via Oxyanionic Polymerization: Toward Multifunctional Stealth Liposomes

2010

We describe the synthesis of linear-hyperbranched lipids for liposome preparation based on linear poly(ethylene glycol) (PEG) and hyperbranched polyglycerol (PG). Molecular weights were adjusted to values around 3000 g/mol with varying degrees of polymerization of the linear and the branched segments in analogy to PEG-based stealth lipids; polydispersities were generally low and below 1.3. The hydrophobic anchors were introduced into the lipid structures as initiators for the anionic polymerization of ethylene oxide and are either based on cholesterol or on different aliphatic glyceryl ethers. Complete incorporation of the apolar initiators was evidenced by MALDI-ToF analysis at all stages …

AnionsGlycerolLiposomeMagnetic Resonance SpectroscopyPolymers and PlasticsEthylene oxidePolymerstechnology industry and agricultureBioengineeringLipidsSmall-angle neutron scatteringBiomaterialschemistry.chemical_compoundEnd-groupAnionic addition polymerizationchemistryDynamic light scatteringPolymerizationSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationLiposomesSpectroscopy Fourier Transform InfraredPolymer chemistryMaterials Chemistrylipids (amino acids peptides and proteins)Ethylene glycolBiomacromolecules
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Chiral Monofluorobenzyl Carbanions: Synthesis of Enantiopure β‐Fluorinated β‐Phenylethylamines

2011

The preparation of a stabilized monofluorobenzyl carbanion by means of a remote homochiral sulfinyl group and its completely stereoselective reactions with N-p-tolylsulfinylimines are described. The use of these reactions followed by the simultaneous removal of both chiral auxiliaries with tBuLi, which occurs without epimerization at the benzylic position, provides the quickest entry to enantiomerically pure β-fluorinated β-phenylethylamines.

AnionsHalogenationStereochemistryOrganic ChemistryMolecular ConformationEnantioselective synthesisStereoisomerismGeneral ChemistryCatalysischemistry.chemical_compoundEnantiopure drugchemistryBenzyl CompoundsPhenethylaminesIonic liquidStereoselectivityEpimerIminesCarbanionChemistry – A European Journal
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Dynamic magnetic materials based on the cationic coordination polymer [Cu(btix)2]n(2n+) [btix = 1,4-bis(triazol-1-ylmethyl)benzene]: tuning the struc…

2012

A three-dimensional coordination polymer, [Cu(btix)(2)(BF(4))(2)](n) [btix = 1,4-bis(triazol-1-ylmethyl)benzene], with antiferromagnetic interactions occurring via the organic ligand, has been prepared and characterized. It has been shown to permit the exchange of anionic species in the crystalline network with modification of the magnetic properties. Coordinated BF(4)(-) can be reversibly exchanged by different anions with (NO(3)(-) and Cl(-)) or without (PF(6)(-) and ClO(4)(-)) dynamic response of the organic ligand, which acts as the only linker between the metal centers. Interestingly, an irreversible exchange occurs with N(3)(-) anions to generate a new coordination polymer, [Cu(btix)(…

AnionsModels MolecularIon exchangeMolecular StructureLigandCoordination polymerPolymersInorganic chemistryCationic polymerizationAb initioCrystallography X-RayMagnetic susceptibilitylaw.inventionInorganic Chemistrychemistry.chemical_compoundCrystallographyMagnetic FieldschemistrylawCationsOrganometallic CompoundsAntiferromagnetismPhysical and Theoretical ChemistryElectron paramagnetic resonanceCopperInorganic chemistry
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A highly enantioselective abiotic receptor for malate dianion in aqueous solution

2006

The highly enantioselective molecular recognition of the malate dianion by a synthetic receptor in aqueous solution has been studied by potentiometric titrations, mass spectrometry (ESI-MS), diffusion measurements (PGSE NMR) and molecular modeling. Garcia-España Monsonis, Enrique, Enrique.Garcia-Es@uv.es

AnionsModels MolecularMalate dianionSpectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyMolecular modelUNESCO::QUÍMICADiffusionPotentiometric titrationMalatesMolecular modelingAbiotic receptorMass spectrometry:QUÍMICA [UNESCO]CatalysisSubstrate SpecificityMolecular recognitionComputational chemistryMaterials ChemistryOrganic chemistryAqueous solutionReceptorAbiotic componentEnantioselectiveAqueous solutionMolecular StructureChemistrySpectrometryMeasurementsMetals and AlloysEnantioselective synthesisWaterHydrogen BondingStereoisomerismGeneral ChemistryGeneral MedicineUNESCO::QUÍMICA::Química macromolecularCombinatorial chemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSolutionsCeramics and CompositesPotentiometryEnantioselective ; Abiotic receptor ; Malate dianion ; Aqueous solution ; Spectrometry ; Measurements ; Molecular modeling:QUÍMICA::Química macromolecular [UNESCO]
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The Radical Trap in Atom Transfer Radical Polymerization Need Not Be Thermodynamically Stable. A Study of the MoX3(PMe3)3 Catalysts

2005

The molybdenum(III) coordination complexes MoX(3)(PMe(3))(3) (X = Cl, Br, and I) are capable of controlling styrene polymerization under typical atom transfer radical polymerization (ATRP) conditions, in conjunction with 2-bromoethylbenzene (BEB) as an initiator. The process is accelerated by the presence of Al(OPr(i))(3) as a cocatalyst. Electrochemical and synthetic studies aimed at identifying the nature of the spin trap have been carried out. The cyclic voltammogram of MoX(3)(PMe(3))(3) (X = Cl, Br, I) shows partial reversibility (increasing in the order ClBrI) for the one-electron oxidation wave. Addition of X(-) changes the voltammogram, indicating the formation of MoX(4)(PMe(3))(3) f…

AnionsReaction mechanismRadical polymerization010402 general chemistryPhotochemistry01 natural sciencesBiochemistryRedoxCatalysisStyreneCatalysisStyreneschemistry.chemical_compoundColloid and Surface ChemistryRadical polymerizationOxidationOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryRedox reactions010405 organic chemistryAtom-transfer radical-polymerizationGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymersPolymerizationchemistryCyclic voltammetry
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Surface-anchored counterions on weak chiral anion-exchangers accelerate separations and improve their compatibility for mass-spectrometry-hyphenation

2017

In the present work we propose new variants of chiral stationary phases (CSP) with tert-butylcarbamoylquinine (tBuCQN) as chiral selector molecule. Four tBuCQN-CSPs with distinct bonding chemistries are compared in terms of their pH-dependent surface charge by ζ-potential determinations, by achiral and chiral liquid chromatographic tests and LC-ESI-MS hyphenation. In one embodiment tBuCQN was immobilized on 3-mercaptopropylmethylsilyl-modified silica by thiol-ene click reaction (brush type CSP with selector coverage of 0.38mmol/g). In another embodiment, poly-(3-mercaptopropyl)-methylsiloxane was coated onto vinylized silica particles in presence of tBuCQN and radical initiator. The tBuCQN …

AnionsSiloxanesSulfonic acid010402 general chemistry01 natural sciencesBiochemistryMass SpectrometryAnalytical ChemistryEndcappingMoleculeSulfhydryl CompoundsSurface chargeIonschemistry.chemical_classificationChromatographyQuinineElutionOsmolar Concentration010401 analytical chemistryOrganic ChemistryStereoisomerismGeneral MedicineSilicon Dioxide0104 chemical scienceschemistryIonic strengthCounterionEnantiomerChromatography LiquidJournal of Chromatography A
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Comparative analysis of the electrostatics of the binding of cationic proteins to vesicles: Asymmetric location of anionic phospholipids

2009

The role of electrostatics is studied in the adsorption of cationic proteins to zwitterionic phosphatidylcholine (PC) and anionic PC/phosphatidylglycerol (PG) mixed small unilamellarvesicles (SUVs). For model proteins the interaction is monitored vs. PG content at low ionic strength. The adsorption of lysozyme and myoglobin (isoelectric point, pl 7-11) is investigated in SUVs, along with changes of the fluorescence emission spectra of the cationic proteins, via their adsorption on SUVs. In the Gouy-Chapman formalism, the activity coefficient goes with the square of charge number. Deviations from the ideal model could indicate the asymmetric location of the anionic phospholipid in the bilaye…

AnionsStatic ElectricityFluorescence spectrometryAnalytical chemistryBiochemistryAnalytical Chemistrychemistry.chemical_compoundCationsEnvironmental ChemistryProtein–lipid interactionPhospholipidsUnilamellar LiposomesSpectroscopyMyoglobinChemistryBilayerOsmolar ConcentrationCationic polymerizationProteinsCharge numberPhosphatidylglycerolsCrystallographySpectrometry FluorescenceIsoelectric pointMyoglobinIonic strengthPhosphatidylcholinesMuramidaseProtein BindingAnalytica Chimica Acta
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Anionic-anionic asymmetric tandem reactions: one-pot synthesis of optically pure fluorinated indolines from 2-p-tolylsulfinyl alkylbenzenes.

2008

Anionsgamma-sulfinyl carbanionsIndolesTandemChemistryindolinesOne-pot synthesisasymmetric synthesisEnantioselective synthesisBenzeneStereoisomerismGeneral ChemistryGeneral MedicineFluorineCatalysisfluorine chemistrychemistry.chemical_compoundIndolineOrganic chemistryAlkylbenzenesAngewandte Chemie (International ed. in English)
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