Search results for "cationic polymerization"

showing 10 items of 441 documents

Hydroxyfunctional oxetane-inimers with varied polarity for the synthesis of hyperbranched polyether polyols via cationic ROP

2014

Polymers and PlasticsChemistryOrganic ChemistryCationic polymerizationChain transferOxetaneRing-opening polymerizationchemistry.chemical_compoundChain-growth polymerizationPolymerizationPolymer chemistryMaterials ChemistryOrganic chemistryReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationJournal of Polymer Science Part A: Polymer Chemistry
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Group transfer and anionic polymerization: A critical comparison

1990

The mechanism of group transfer polymerization (GTP) of methacrylates in THF is investigated by using data on kinetics of homo- and copolymerization, polymer microstructure and molecular weight distribution. By comparison with corresponding data on anionic polymerization it is concluded that the mechanisms of monomer addition to the active chain end is very similar for both anionic and group transfer polymerization and that GTP is ionic in character. On the other hand, GTP uniquely is characterized by the existence of a catalyst exchange equilibrium. The position of this equilibrium determines the rates of polymerization, and the dynamics determine the molecular weight distribution.

Polymers and PlasticsChemistryOrganic ChemistryRadical polymerizationtechnology industry and agricultureCationic polymerizationChain transfermacromolecular substancesCondensed Matter PhysicsChain-growth polymerizationAnionic addition polymerizationPolymerizationPolymer chemistryMaterials ChemistryLiving polymerizationIonic polymerizationMakromolekulare Chemie. Macromolecular Symposia
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Preparation of Hyperbranched Polyacrylates by Atom Transfer Radical Polymerization. 2. Kinetics and Mechanism of Chain Growth for the Self-Condensing…

1997

The self-condensing vinyl polymerization (SCVP) of 2-((2-bromopropionyl)oxy)ethyl acrylate (BPEA) has resulted in the formation of hyperbranched polyacrylates. The polymerization mechanism used to polymerize the BPEA was atom transfer radical polymerization (ATRP), a “living”/controlled radical polymerization. This paper details the study of the kinetics of polymerization and the growth of the macromolecule during the polymerization. The results obtained in the polymerization were compared to the theoretical predictions for SCVP. It was determined that the polymerization deviated from the ideal case, as a consequence of the establishment of a dynamic equilibrium in ATRP resulting in the add…

Polymers and PlasticsChemistryOrganic ChemistryRadical polymerizationtechnology industry and agricultureCationic polymerizationChain transfermacromolecular substancesPhotochemistryInorganic ChemistryLiving free-radical polymerizationChain-growth polymerizationPolymerizationPolymer chemistryMaterials ChemistryReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationMacromolecules
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Synthesis and characterization of optically active 2,4-disubstituted-2-oxazolines and their polymerization

1994

Four different optically active 2,4-disubstituted-2-oxazolines were synthesized and characterized. Cationic polymerization of these oxazolines were studied. Three of the oxazolines could be polymerized using methyl trifluoromethanesulfonate as initiator. S-(–)-2-Phenyl-4-isopropyl-2-oxazoline could not be polymerized under the conditions used.

Polymers and PlasticsChemistryOrganic Chemistrytechnology industry and agricultureCationic polymerizationmacromolecular substancesOptically activeRing-opening polymerizationCharacterization (materials science)chemistry.chemical_compoundPolymerizationPolymer chemistryMaterials ChemistryOrganic chemistryMethyl trifluoromethanesulfonatePolymer International
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Poly(THF-co-cyano ethylene oxide): Cyano Ethylene Oxide (CEO) Copolymerization with THF Leading to Multifunctional and Water-Soluble PolyTHF Polyelec…

2016

Cyano-functional polyether copolymers based on THF were prepared via cationic ring-opening copolymerization of THF with cyano ethylene oxide (CEO). The CEO content of poly(tetrahydrofuran) (polyTHF) based copolymers varied from 3.3 to 29.3%, and molecular weights ranged from 5100 to 31900 g·mol–1 with Mw/Mn in the range of 1.31 to 1.74 (SEC in THF, PS standards). The polymerization was conducted with methyl trifluoromethanesulfonate (MeOTf) as an initiator. Kinetic studies concerning incorporation of both monomers were performed via NMR spectroscopy. The cyano groups at the poly(THF-co-CEO) copolymers enable direct access to amino (polyTHF–NH2) and carboxyl groups (polyTHF–COOH) in facile o…

Polymers and PlasticsEthylene oxideOrganic ChemistryCationic polymerization02 engineering and technologyNuclear magnetic resonance spectroscopy010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesPolyelectrolyte0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymer0210 nano-technologyTetrahydrofuranMethyl trifluoromethanesulfonateMacromolecules
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Maleimide Glycidyl Ether: A Bifunctional Monomer for Orthogonal Cationic and Radical Polymerizations.

2015

A novel bifunctional monomer, namely maleimide glycidyl ether (MalGE), prepared in a four-step reaction sequence is introduced. This monomer allows for selective (co)polymerization of the epoxide group via cationic ring-opening polymerization, preserving the maleimide functionality. On the other hand, the maleimide functionality can be copolymerized via radical techniques, preserving the epoxide moiety. Cationic ring-opening multibranching copolymerization of MalGE with glycidol was performed, and a MalGE content of up to 24 mol% could be incorporated into the hyperbranched polymer backbone (Mn = 1000-3000 g mol(-1)). Preservation of the maleimide functionality during cationic copolymerizat…

Polymers and PlasticsFree RadicalsChemistryPolymersPropanolsOrganic ChemistryRadical polymerizationCationic polymerizationChain transferPolymerizationMaleimideschemistry.chemical_compoundPolymerizationCationsMaterials ChemistryCopolymerOrganic chemistryEpoxy CompoundsReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationMaleimideEthersMacromolecular rapid communications
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Size-dependent knockdown potential of siRNA-loaded cationic nanohydrogel particles.

2014

To overcome the poor pharmacokinetic conditions of short double-stranded RNA molecules in RNA interference therapies, cationic nanohydrogel particles can be considered as alternative safe and stable carriers for oligonucleotide delivery. For understanding key parameters during this process, two different types of well-defined cationic nanohydrogel particles were synthesized, which provided nearly identical physicochemical properties with regards to their material composition and resulting siRNA loading characteristics. Yet, according to the manufacturing process using amphiphilic reactive ester block copolymers of pentafluorophenyl methacrylate (PFPMA) and tri(ethylene glycol)methyl ether m…

Polymers and PlasticsNanogelsBioengineeringEtherMethacrylateProtein Structure SecondaryPolyethylene GlycolsBiomaterialschemistry.chemical_compoundCationsAmphiphilePolymer chemistryMaterials ChemistryCopolymerHumansPolyethyleneimineParticle SizeRNA Small InterferingRNA Double-StrandedOligonucleotideCationic polymerizationHydrogelschemistryChemical engineeringGene Knockdown TechniquesEthylene glycolNanogelHeLa CellsBiomacromolecules
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Lanthanides benzimidinates: initiators or real catalysts for theɛ-caprolactone polymerization

2000

Polymers and PlasticsOrganic ChemistryCationic polymerizationSolution polymerizationRing-opening polymerizationchemistry.chemical_compoundLiving free-radical polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryLiving polymerizationOrganic chemistryIonic polymerizationCaprolactoneMacromolecular Rapid Communications
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Ionic Hydrogel Based on Chitosan Cross-Linked with 6-Phosphogluconic Trisodium Salt as a Drug Delivery System.

2018

[EN] In this work, 6-phosphogluconic trisodium salt (6-PG(-)Na(+)) is introduced as a new aqueous and nontoxic cross-linking agent to obtain ionic hydrogels. Here, it is shown the formation of hydrogels based on chitosan cross-linked with 6-PG(-)Na(+). This formulation is obtained by ionic interaction of cationic groups of polymer with anionic groups of the cross linker. These hydrogels are nontoxic, do not cause dermal irritation, are easy to extend, and have an adequate adhesion force to be applied as polymeric film over the skin. This AWN formulation exhibits a first order release kinetic and can be applied as drug vehicle for topical administration or as wound dressing for wound healing…

Polymers and PlasticsPolymersAdministration TopicalIonic bondingSalt (chemistry)Bioengineering02 engineering and technology010402 general chemistry01 natural sciencesGluconatesHydrogel Polyethylene Glycol DimethacrylateBiomaterialsChitosanchemistry.chemical_compoundQUIMICA ORGANICADrug Delivery SystemsMaterials ChemistryHumanschemistry.chemical_classificationChitosanWound HealingAqueous solutionWound Closure TechniquesSodiumCationic polymerization021001 nanoscience & nanotechnology0104 chemical sciencesDrug vehicleKineticsCross-Linking ReagentsChemical engineeringchemistrySelf-healing hydrogelsDrug delivery0210 nano-technologyBiomacromolecules
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Cationic Copolymerization of 3,3-Bis(hydroxymethyl)oxetane and Glycidol: Biocompatible Hyperbranched Polyether Polyols with High Content of Primary H…

2015

The cationic ring-opening copolymerization of 3,3-bis(hydroxymethyl)oxetane (BHMO) with glycidol using different comonomer ratios (BHMO content from 25 to 90%) and BF3OEt2 as an initiator has been studied. Apparent molecular weights of the resulting hyperbranched polyether copolymers ranged from 1400 to 3300 g mol(-1) (PDI: 1.21-1.48; method: SEC, linear PEG standards). Incorporation of both comonomers is evidenced by MALDI-TOF mass spectroscopy. All hyperbranched polyether polyols with high content of primary hydroxyl groups portray good solubility in water, which correlates with an increasing content of glycerol units. Detailed NMR characterization was employed to elucidate the copolymer …

Polymers and PlasticsPropanolsProton Magnetic Resonance SpectroscopyComonomerGlycidolCationic polymerizationBiocompatible MaterialsBioengineeringOxetanePolymerizationBiomaterialschemistry.chemical_compoundchemistryPolymerizationEthers CyclicCationsSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationPolymer chemistryMaterials ChemistryCopolymerEpoxy CompoundsOrganic chemistryHydroxymethylCarbon-13 Magnetic Resonance SpectroscopySolubilityBiomacromolecules
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