Search results for "Ionic polymerization"

showing 10 items of 481 documents

Oligoethyleneoxide spacer groups in polymerizable surfactants

1991

Cationic and zwitterionic polymerizable surfactants bearing tri- and tetraethyleneglycol spacer groups between the polymerizable moiety and the surfactant structure were prepared and polymerized. Monomers and polymers were investigated with respect to their aggregation behavior in aqueous systems and compared to analogous monomers and polymers lacking spacer groups. In the case of the monomeric surfactants, the spacer groups depress both the Kraffttemperature and the critical micelle concentration. the area occupied per molecule at the air-water interface is substantially enlarged by the spacers, whereas the depression of surface tension is nearly constant. Although the monomers with and wi…

chemistry.chemical_classificationPolymers and PlasticsCationic polymerizationPolymerMicelleKrafft temperaturechemistry.chemical_compoundColloid and Surface ChemistryMonomerPulmonary surfactantchemistryCritical micelle concentrationddc:540Polymer chemistryMaterials ChemistryInstitut für ChemieMoietyPhysical and Theoretical ChemistryColloid & Polymer Science
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Poly(2-oxazoline)s Functionalized with Palladium Carbene Complexes: Soluble, Amphiphilic Polymer Supports for C−C Coupling Reactions in Water

2004

This paper describes the synthesis and characterization of a new class of amphiphilic, water-soluble diblock copolymers based on 2-oxazoline derivatives with pendent N-heterocyclic carbene/palladium catalysts in the hydrophobic block. The synthetic strategy involves a four-step synthesis of three functionalized monomers, each composed of a bis(imidazoline-2-ylidene)palladium(II) diiodide derivative that is covalently linked to a 2-oxazoline monomer via a flexible alkyl spacer (alkyl = butyl, hexyl, octyl). The structure of the monomers was analyzed by 1H and 13C NMR spectroscopy, MALDI-TOF, and elemental analysis. Three diblock copolymers P1−P3 with the monomers being part of the hydrophobi…

chemistry.chemical_classificationPolymers and PlasticsChemistryOrganic ChemistryCationic polymerizationchemistry.chemical_elementOxazolineInorganic Chemistrychemistry.chemical_compoundMonomerPolymerizationPolymer chemistryMaterials ChemistryCopolymerCarbeneAlkylPalladiumMacromolecules
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Some examples of the modification of polymers

1986

Reactions avec des groupes amide et amino dans la chaine principale, et avec un groupe terminal bromoacetyl. Polymerisation de la conidine en presence d'un polystyrene vivant

chemistry.chemical_classificationPolymers and PlasticsChemistryOrganic ChemistryPolymer chemistryMaterials ChemistryChemical reductionCationic polymerizationOrganic chemistryChemical modificationPolymerCondensed Matter PhysicsPolyelectrolyteMakromolekulare Chemie. Macromolecular Symposia
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Reactions of Maleisomides with Alcohols

2004

Abstract New surfactants (surfmers) with various amide and ester groups next to C˭C double bonds have been obtained. Maleic acid amidesters (AE) with different hydrophobic groups at the nitrogen atom and hydrophilic substituents at oxygen atoms were synthesized starting with maleic isoimides. 1H KMR and IR spectra were used for their characterization. Some were further characterized for their critical micellar concentration (CMC). A few cationic and zwitterionic surfmers were also prepared from isoimide precursors and characterized. All these surfmers were applied in batch emulsion polymerization of styrene, and in core‐shell seeded copolymerization of styrene and butylacrylate to give late…

chemistry.chemical_classificationPolymers and PlasticsDouble bondMaleic acidCationic polymerizationEmulsion polymerizationSurfaces Coatings and FilmsStyrenechemistry.chemical_compoundchemistryAmideCritical micelle concentrationPolymer chemistryCopolymerOrganic chemistryPhysical and Theoretical ChemistryJournal of Dispersion Science and Technology
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Comparison of living polymerization systems

1994

Recent developments in the field of living polymerization are surveyed. Comparison of the available mechanistic and kinetic information is made for living anionic, cationic, free radical, group transfer, ring-opening metathesis, Ziegler-Natta and immortal polymerizations. This evaluation indicates that the majority of living polymerizations involve quasiliving equilibrium between active (propagating) and dormant (nonpropagating) polymer chains. On the basis of the kinetics of a general model for quasiliving and ideal living polymerizations it is concluded that ideal living polymerization is a special subclass of quasiliving polymerizations. Classification of living polymerization systems is…

chemistry.chemical_classificationPolymers and PlasticsKinetic informationOrganic Chemistrytechnology industry and agricultureCationic polymerizationmacromolecular substancesPolymerCondensed Matter PhysicsMetathesisLiving free-radical polymerizationchemistryPolymer chemistryMaterials ChemistryLiving polymerizationReversible addition−fragmentation chain-transfer polymerizationMacromolecular Symposia
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Cationic copolymers of ?,?-poly-(N-2-hydroxyethyl)-DL-aspartamide (PHEA) and ?,?-polyasparthylhydrazide (PAHy): synthesis and characterization

2000

In the present study the derivatization of two water-soluble synthetic polymers, α,β-poly(N-2-hydroxyethyl)-DL-aspartamide (PHEA) and α,β-polyasparthylhydrazide (PAHy), with glycidyltrimethylammonium chloride (GTA) is described. This reaction permits the introduction of positive charges in the macromolecular chains of PHEA and PAHy in order to make easier the electrostatic interaction with DNA. Different parameters affect the reaction of derivatization, such as GTA concentration and reaction time. PHEA reacts partially and slowly with GTA; on the contrary the reaction of PAHy with GTA is more rapid and extensive. The derivatization of PHEA and PAHy with GTA is a convenient method to introdu…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryCationic polymerizationChemical modificationPolymerPolyelectrolytechemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCopolymerSurface modificationDerivatizationMacromoleculePolymer International
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The role of association/complexation equilibria in the anionic polymerization of (meth)acrylates

1992

The kinetics of the anionic polymerization of methacrylates and acrylates in THF as well as the MWD of the polymers formed depend on the concentration of active centres and of additives, such as lithium halides and lithium alkoxides. These results are discussed on basis of multiple equilibria between non-associated, associated, and complexed ion pairs which are supported by viscosity measurements. The position of these equilibria determines the rate of polymerization, whereas the dynamics of interconversion determine the polydispersity. In the absence of additives the rate of monomer addition to non-associated ion pairs competes with the rate of association. Addition of lithium chloride mai…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryDispersitychemistry.chemical_elementPolymerCondensed Matter Physicschemistry.chemical_compoundAnionic addition polymerizationMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryLithium chlorideLithiumIonic polymerizationMakromolekulare Chemie. Macromolecular Symposia
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Multihydroxyl-Functional Polystyrenes in Continuous Flow

2010

We describe the synthesis of end-functionalized polystyrenes by living anionic polymerization in a microstructured reactor via termination by acetal-protected functional epoxides. Initiation of styrene polymerization by alkyllithium takes place in a micromixing device with efficient heat and mass transfer properties. A newly developed continuous polymerization−termination sequence enabled quantitative functionalization of the living carbanions by nucleophilic displacement with different, specifically designed glycidyl ethers (ethoxy ethyl glycidyl ether (EEGE), 1,2-isopropylidene glyceryl glycidyl ether (IGG), and trans-2-phenyl-1,3-dioxane glycidyl ether (PDGE)). Upon acidic hydrolysis the…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryEpoxidePolymerStyreneInorganic Chemistrychemistry.chemical_compoundEnd-groupAnionic addition polymerizationPolymerizationchemistryPolymer chemistryMaterials ChemistryAlkoxy groupOrganic chemistryLiving anionic polymerizationMacromolecules
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Metal-free anionic polymerization of methyl methacrylate in tetrahydrofuran using bis(triphenylphosphoranilydene)ammonium (PNP+) as counterion

2000

Bis(triphenylphosphoranilydene)ammonium (PNP + ) triphenylmethanide (Ph 3 C - ) is a new metal-free initiator for the living polymerization of methyl methacrylate (MMA). The kinetics of the polymerization strongly depend on the metal counterion the initiator precursor. When the initiator is made from the metathesis reaction of Ph 3 CK and PNPCl, the polymerization follows first-order kinetics up to 0°C with half-lives below 0.1 s. The propagation rate constants are much higher than those obtained with tetraphenylphosphonium (TPP + ) cations, indicating a smaller fraction of dormant ylides. When the initiator is synthesized from Ph 3 CLi, polymerization proceeds much slower and molecular wei…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryInorganic chemistrySolution polymerizationchemistry.chemical_compoundAnionic addition polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryLiving polymerizationCounterionMethyl methacrylateIonic polymerizationTetrahydrofuran
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Living Anionic Polymerization Celebrates 60 Years: Unique Features and Polymer Architectures

2017

chemistry.chemical_classificationPolymers and PlasticsPolymer scienceChemistryOrganic Chemistry02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesPolymer chemistryMaterials ChemistryPhysical and Theoretical Chemistry0210 nano-technologyLiving anionic polymerizationMacromolecular Chemistry and Physics
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