Search results for "Ionic polymerization"

showing 10 items of 481 documents

Rotationsdispersion bei monomerem und polymerem L-(–)-Lactid

1965

Bei der kationischen Polymerisation von L-Lactid entsteht ein hochkristallines, isotaktisches Polymeres. Physikalische Eigenschaften des Monomeren und Polymeren werden mitgeteilt. Fur die Rotationsdispersion von L-Lactid in verschiedenen Losungsmitteln gilt die eintermige DRUDE-Gleichung. Das Polymere hat eine Dispersions-Kurve mit einem ersten Extremum bei 275 mμ. Die Dispersionskurve des Poly-L-lactids last sich durch die MOFFITT-YANG-Gleichung beschreiben. Hieraus werden Schlusse auf die Sekundarstruktur des gelosten Polymeren gezogen. In the cationic polymerization of L-lactide a high cristalline isotactic polymer is obtained. Physical properties of monomer and polymer are reported. The…

chemistry.chemical_classificationchemistry.chemical_compoundMonomerPolymerizationChemistryTacticityPolymer chemistryCationic polymerizationPolymerDispersion (chemistry)Dispersion curveOptical rotatory dispersionDie Makromolekulare Chemie
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Über die polymerisation bei der sublimation des trioxans. 17. Mitt. Über polyoxymethylene

1962

Bei der Sublimation von gereinigtem Trioxan und bei seiner Kristallisation aus der Schmelze erfolgt in der kristallinen Phase eine langsame Polymerisation zu hochmolekularem Polyoxymethylen. Die Ausbeuten an Polymeren sind um so hoher, je trockener das Trioxan ist und je geringer der Fremdgasdruck bei der Sublimation ist. Es wurde festgestellt, das diese Polymerisation durch Spuren von monomerem Formaldehyd ausgelost wird; wenn letzterer durch Silberoxyd zerstort wird, kann Trioxan unverandert sublimiert und kristallisiert werden. Wahrend der Polymerisation wird monomerer Formaldehyd von den wachsenden Polyoxymethylenketten abgespalten und so der Polymerisationskatalysator regeneriert. Desh…

chemistry.chemical_classificationchemistry.chemical_compoundMonomerchemistryPolyoxymethyleneTrioxanePolymerizationPolymer chemistryFormaldehydeCationic polymerizationSublimation (phase transition)PolymerDie Makromolekulare Chemie
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Generalized synthesis of periodic surfactant/inorganic composite materials

1994

THE recent synthesis of silica-based mesoporous materials1,2 by the cooperative assembly of periodic inorganic and surfactant-based structures has attracted great interest because it extends the range of molecular-sieve materials into the very-large-pore regime. If the synthetic approach can be generalized to transition-metal oxide mesostructures, the resulting nanocomposite materials might find applications in electrochromic or solid-electrolyte devices3,4, as high-surface-area redox catalysts5 and as substrates for biochemical separations. We have proposed recently6 that the matching of charge density at the surfactant/inorganic interfaces governs the assembly process; such co-organizatio…

chemistry.chemical_classificationchemistry.chemical_compoundMultidisciplinaryNanocompositePulmonary surfactantchemistryElectrochromismOxideCationic polymerizationCounterionComposite materialMesoporous materialElectrostaticsNature
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Über die möglichkeit der bildung makrocyclischer polyoxyniethylene. 29. mitt über polyoxymethylene1

1966

Bei der kationischen Polymerisation von 1,3,5-Trioxan in Cyclohexan entstehen Polyoxymethylene, welche partiell thermisch stabil und alkalibestandig sind, ohne das irgendwelche bekamiten stabilen Endgruppen nachgewiesen werden konnten. Moglicberweise handelt es sich hierbei um Makrocyclen. Cationic polymerization of 1,3,5-trioxan in cyclohexane yields polyoxymethylene which is partially stable to heat and to alkali but does not contain any of the known stable endgroups. These polymers possibly have a macrocyclic structure.

chemistry.chemical_classificationchemistry.chemical_compoundPolyoxymethylenePolymerizationCyclohexaneChemistryPolymer chemistryCationic polymerizationPolymerAlkali metalDie Makromolekulare Chemie
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Complexes of star-shaped cationic polyelectrolytes with anionic liposomes: Towards multi-liposomal assemblies with controllable stability

2016

Abstract Complexes were formed via the electrostatic interaction between 30–50 nm anionic liposomes and a star-shaped polyelectrolyte, poly{[2-(methacryloyloxy)ethyl]trimethyl ammonium iodide}, having cationic arms that radiate from a silicon-based central core. The complexation was investigated with attention given to assessing the capacity of the cationic stars for the anionic liposomes (both liquid and solid); the integrity of the complexed liposomes; and the stability of the resulting star/liposome complexes in aqueous salt solutions. We have found that by changing the content of anionic groups in the liposomal membrane as well as the phase-state of membrane, the stability of star/lipos…

chemistry.chemical_classificationendocrine systemLiposomeAqueous solutionPolymers and PlasticsChemistryOrganic ChemistryCationic polymerizationSalt (chemistry)02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesPolyelectrolyteAmmonium iodide0104 chemical scienceschemistry.chemical_compoundMembranePolymer chemistryMaterials ChemistryOrganic chemistrySelf-assembly0210 nano-technologyPolymer
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Cationic Au Nanoparticle Binding with Plasma Membrane-like Lipid Bilayers: Potential Mechanism for Spontaneous Permeation to Cells Revealed by Atomis…

2014

Despite being chemically inert as a bulk material, nanoscale gold can pose harmful side effects to living organisms. In particular, cationic Au nanoparticles (AuNP+) of 2 nm diameter or less permeate readily through plasma membranes and induce cell death. We report atomistic simulations of cationic Au nanoparticles interacting with realistic membranes and explicit solvent using a model system that comprises two cellular compartments, extracellular and cytosolic, divided by two asymmetric lipid bilayers. The membrane-AuNP+ binding and membrane reorganization processes are discovered to be governed by cooperative effects where AuNP+, counterions, water, and the two membrane leaflets all contr…

chemistry.chemical_classificationta114ta221Cationic polymerizationNanoparticlePermeationSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyMembranechemistryExtracellularBiophysicsOrganic chemistryPhysical and Theoretical ChemistryCounterionLipid bilayerta116Cellular compartment
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Polymerization of methyl and phenyl oxazoline initiated with alkyl chloroformates

2010

It has been shown that alkyl chloroformates are capable of initiating the polymerization of oxazolines. Esters itself initiate rather slowly and the polymerization proceeds via covalent growing species. Exchange of counter ions with triflate or iodide anions leads to faster initiation and higher reaction rates. The polymerization is of living character.

chemistry.chemical_classificationtechnology industry and agricultureChain transfermacromolecular substancesGeneral ChemistryOxazolinePhotochemistryLiving free-radical polymerizationchemistry.chemical_compoundChain-growth polymerizationchemistryPolymerizationPolymer chemistryReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationAlkylBulletin des Sociétés Chimiques Belges
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1980

chemistry.chemical_compoundAnionic addition polymerizationChemistryKineticsPolymer chemistryMethyl methacrylateIonic polymerizationPhotochemistryDimethoxyethaneLiving anionic polymerizationDie Makromolekulare Chemie, Rapid Communications
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Kinetics of Group Transfer Polymerization

1987

The group transfer polymerization (GTP) of methyl methacrylate (MMA) and tert.-butyl methacrylate (TBMA), catalyzed by bifluoride, is of first order with respect to monomer and catalyst concentrations. A slightly negative order with respect to initiator concentration is observed, indicating an inhibitive function of the initiator. Termination reactions occur at lower catalyst concentrations. They are very pronounced for TBMA and result in incomplete conversions. For MMA, at lower catalyst and higher initiator concentrations, induction periods are observed which increase when lowering the temperature. This is related with the formation of active chains. The Arrhenius plots for the propagatio…

chemistry.chemical_compoundAnionic addition polymerizationPolymerizationchemistryInduction periodPolymer chemistryRadical polymerizationLiving polymerizationChain transferMethyl methacrylateIonic polymerization
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A Straightforward Route to Homoallyl-Homocrotylamines Promoted by a Titanium Complex

2012

I�-Allyltitanium complexes, generated in situ from 1,3-dienes and Cp2TiH, react with benzotriazole derivatives to give homoallylic amines in good yields. Under similar conditions, triple cascade reactions (allyltitanation followed by cationic 2-aza-Cope rearrangement followed by a second allyltitanation) occur from bis(benzotriazolyl) compounds affording a straightforward route to homoallyl-(E)-homocrotylamines. A theoretical study provides further insight into the factors that govern the selectivity of this sequence of reactions. The titanium-promoted reductive coupling of 1,3-dienes with bis(benzotriazolyl) compounds as substrates led selectively to homoallyl-homocrotylamines through a tr…

chemistry.chemical_compoundBenzotriazoleCascade reactionChemistryOrganic ChemistryCationic polymerizationOrganic chemistryPhysical and Theoretical ChemistrySigmatropic reactionSelectivityCombinatorial chemistryA titaniumEuropean Journal of Organic Chemistry
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