Search results for "ionic"

showing 10 items of 2016 documents

Polymerization with heterogeneous metalorganic catalysts. VI. Differences in polymerization activity of α-olefins and some kinetic results on butene-…

1967

Relative changes in polymerization activity of ethylene, propylene, and butene-1 in Ziegler-Natta polymerization were compared by use of TiCl3 samples contaminated with O2 and H2O to various extents. Catalyst depletion varied for the three monomers which supported the existence of different active centers. In butene-1 polymerizations with the system Al(C2H5)2Cl–TiCl3, the formation of active centers involves an irreversible and a reversible (adsorption) reaction, the former pertaining to the formation of Al(C2H5)Cl2 and dependent upon the purity of the TiCl3. The kinetic treatment of the rate curves suggests a mixed order of catalyst deactivation and again points to the importance of Al(C2H…

Anionic addition polymerizationChain-growth polymerizationBulk polymerizationPolymerizationChemistryPolymer chemistryGeneral EngineeringCationic polymerizationPrecipitation polymerizationCoordination polymerizationPhotochemistryIonic polymerizationJournal of Polymer Science Part A-1: Polymer Chemistry
researchProduct

Some New Copolymers by Ionic Polymerization

1980

In the first part the cationic polymerization of a homologous series of cyclic ether–acetals with ring sizes of 11, 14, and 17 atoms is described. During the polymerization of triethylene glycol formal (TGF) an equilibrium is reached and besides high polymers cyclic oligomers are formed. The oligomers and the polymers are built up of a regular sequence of one oxymethylene unit and three oxyethylene units –[–(OCH2) (OC2H4)3–]–x. They are therefore be labelled a “sequenced copolymer.” The equilibrium concentrations of the cyclic oligomers with a polymerization degree from 2 to 15 follow the Jacobson–Stockmayer equation. The 14- and 17-membered monomers POC and HOC forms cyclic oligomers and h…

Anionic addition polymerizationChain-growth polymerizationPolymers and PlasticsPolymerizationChemistryPolymer chemistryMaterials ChemistryCationic polymerizationCopolymerLiving polymerizationIonic polymerizationRing-opening polymerizationPolymer Journal
researchProduct

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
researchProduct

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
researchProduct

Liquid structure of a water-in-salt electrolyte with a remarkably asymmetric anion

2021

Water-in-salt systems, i.e., super-concentrated aqueous electrolytes, such as lithium bis(trifluoromethanesulfonyl)imide (21 mol/kgwater), have been recently discovered to exhibit unexpectedly large electrochemical windows and high lithium transference numbers, thus paving the way to safe and sustainable charge storage devices. The peculiar transport features in these electrolytes are influenced by their intrinsically nanoseparated morphology, stemming from the anion hydrophobic nature and manifesting as nanosegregation between anions and water domains. The underlying mechanism behind this structure-dynamics correlation is, however, still a matter of strong debate. Here, we enhance the apol…

AnionsDYNAMICSLI+MOLECULAR-FORCE FIELDLOCAL-STRUCTUREWaterLithiumMolecular Dynamics Simulationmolecular-force field; particle meshewald; local-structure; ionic liquids; dynamics; viscosity; conductivity dependence; LI+PARTICLE MESH EWALElectrolytesIONIC LIQUIDSDEPENDENCECONDUCTIVITYVISCOSITY
researchProduct

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
researchProduct

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
researchProduct

Micro magnetofluidics: droplet manipulation of double emulsions based on paramagnetic ionic liquids

2013

The ability to control and manipulate discrete fluid droplets by magnetic fields offers new opportunities in microfluidics. A surfactant-free and easy to realize technique for the continuous generation of double emulsion droplets, composed of an organic solvent and a paramagnetic ionic liquid, is applied. The inner phase of the emulsion droplet consists of imidazolium-based ionic liquids with either iron, manganese, nickel or dysprosium containing anions which provide paramagnetic behaviour. The double emulsion droplets are dispersed in a continuous phase of FC-40. All substances - the organic phase, the paramagnetic ionic liquid and the continuous phase -are immiscible. The magnetic proper…

AnionsIronMicrofluidicsMicrofluidicsBiomedical EngineeringMixing (process engineering)Analytical chemistryIonic LiquidsBioengineeringBiochemistryPhysics::Fluid DynamicsMagneticsParamagnetismchemistry.chemical_compoundNickelPhase (matter)DysprosiumPhysics::Atomic and Molecular ClustersCoalescence (physics)ManganeseChemistryImidazolesGeneral ChemistryMagnetic fieldCondensed Matter::Soft Condensed MatterChemical engineeringMagnetIonic liquidEmulsionshuman activitiesLab on a Chip
researchProduct

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
researchProduct

Thermo-responsive hydrogels from cellulose-based polyelectrolytes and catanionic vesicles for biomedical application.

2016

In this study, negatively charged catanionic vesicles/hydrophobically modified hydroxyethylcellulose polymers thermo-responsive hydrogels have been fabricated. Vesicular aggregates were found to act as multifunctional junctions for networking of modified-cellulose water solutions. The contributions of the electrostatic and hydrophobic interactions were evaluated by changing either vesicles composition or the polymer hydrophobic substitution. Thermal-induced size and lamellarity of hydrogel-enclosed vesicles were detected, with further polygonal shape changes induced by cellulose-based polymer addition. The thermal transition was also found to tune hydrogel mechanical behaviour. The network …

AnionsProton Magnetic Resonance SpectroscopyBiomedical EngineeringBiomedical TechnologyCeramics and CompositeBiomaterialsDiffusioncatanionic vesicleTheophyllineCationsCellulosecatanionic vesicles; cellulose; diffusion; hydrogel; NMR; rheology; Ceramics and Composites; Biomaterials; Biomedical Engineering; 2506ViscositydiffusionTemperatureHydrogelsBiomaterialPolyelectrolytescelluloseNMRElasticityDrug LiberationSettore CHIM/09 - Farmaceutico Tecnologico Applicativocatanionic vesiclesCeramics and Compositesrheologyhydrogel2506RheologyJournal of biomedical materials research. Part A
researchProduct