Search results for "ionic"

showing 10 items of 2016 documents

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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Polymerization of 3-alkylthiophenes with FeCl3

1992

We report on the mechanism of direct oxidation of 3-alkylthiophenes using ferric chloride (FeCl3) as the polymerization oxidant/catalyst to produce high molecular weight poly(3-alkylthiophenes) (P3ATs), conjugated polymers that have potential as electrically and optically active polymers. This study shows that the FeCl3 must exist in the solid state in the reaction mixture to be active as an oxidant in the polymerization of P3AT. A feasible polymerization mechanism for 3-alkylthiophene was developed on the basis of the crystal structure of FeCl3 and quantum chemical computations of thiophene derivatives. The polymerization is hypothesized to proceed through a radical mechanism rather than a…

Polymers and PlasticsChemistryOrganic ChemistryRadical polymerizationtechnology industry and agricultureChain transferPhotochemistryLiving free-radical polymerizationChain-growth polymerizationCobalt-mediated radical polymerizationPolymerizationPolymer chemistryMaterials ChemistryReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationPolymer
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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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Ionic tactile sensors as promising biomaterials for artificial skin: Review of latest advances and future perspectives

2021

Abstract Ionic tactile sensors (ITS) are an emerging subfield of wearable electronics, capable of mimicking the human skin, including not only the typical anisotropic structure, mechanical behaviour, and tactile functions but even the mechanosensitive ionic channels that are crucial for the human sense of touch. With the rapid development of intelligent technology, such bioinspired materials constitute the core foundation of intelligent systems and are a candidate to be the next generation e-skins, offering a more accurate and evolved biointerface. In the latest years, a wealth of novel ultra-stretchable ITS was proposed, progressively refining the choice of soft materials, including ion ge…

Polymers and PlasticsComputer sciencebusiness.industryOrganic ChemistryIntelligent decision support systemGeneral Physics and AstronomyIonic bondingRoboticsNanotechnologyBiointerface02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesHydrogel Ion gel Ionic liquid Pressure sensor Strain sensor Stretchable sensor Tactile sensorArtificial skin0104 chemical sciencesSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiSelf-healing hydrogelsMaterials ChemistryArtificial intelligence0210 nano-technologybusinessTactile sensorWearable technology
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PEG-based Multifunctional Polyethers with Highly Reactive Vinyl-Ether Side Chains for Click-Type Functionalization

2011

Introduction of highly reactive vinyl ether moieties along a poly(ethylene-glycol) (PEG) backbone has been realized by copolymerization of the novel epoxide monomer ethoxy vinyl glycidyl ether (EVGE) with ethylene oxide (EO). A series of copolymers with varying structure (block and random) as well as EVGE comonomer content (5-100%) with molecular weights in the range of 3,900-13,200 g/mol and narrow molecular weight distributions (M-w/M-n = 1.06-1.20) has been synthesized and characterized with respect to their microstructure and thermal properties. The facile transformation of the vinyl ether side chains in click type reactions was verified by two different post polymerization modification…

Polymers and PlasticsCyanideEpoxideRing-opening polymerizationPolymerizationInorganic Chemistrychemistry.chemical_compoundThiolsPolymer chemistryMaterials ChemistrymedicineOrganic chemistryPoly(Ethylene Glycol) CopolymersOxide)Ethylene oxideMonomersOrganic Chemistrytechnology industry and agricultureVinyl etherAnionic addition polymerizationchemistryPolymerizationGlycidolBlock-CopolymersFree-Radical AdditionAlkoxy groupEthylene glycolDerivativesmedicine.drugMacromolecules
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Amphiphilic Linear-Hyperbranched Block Copolymers with Linear Poly(ethylene oxide) and Hyperbranched Poly(carbosilane) Block

2008

The synthesis of amphiphilic linear-hyperbranched block copolymers with a linear poly(ethylene oxide) (PEO) segment and a hyperbranched poly(carbosilane)s (PCS) block in a rapid three-step strategy is described, combining oxyanionic polymerization with carbosilane chemistry. A linear precursor block copolymer was synthesized via anionic polymerization of allyl glycidyl ether onto a commercial hydroxyl-terminated PEO, using its cesium alkoxide as macro-initiator. The resulting linear AB or ABA-type di- or triblock copolymers serve as polymer cores for the subsequent hydrosilylation polyaddition of an AB2-type carbosilane monomer. Di(allyl)methylsilane or methyldi(undec-10-enylsilane) were em…

Polymers and PlasticsEthylene oxideHydrosilylationAllyl glycidyl etherOrganic ChemistryRing-opening polymerizationInorganic Chemistrychemistry.chemical_compoundMonomerAnionic addition polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryMacromolecules
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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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Synthesis and properties of amphiphilic “dumbbell”-shaped grafted block copolymers, 1. Anionic synthesis via a polyfunctional initiator

1994

Two poly(ethylene oxide) stars linked by a long polystyrene chain represent a novel amphiphilic architecture (dumbbell), which is available by anionic grafting of ethylene oxide from a hydroxylated polybutadiene-block-polystyrene-block-polybutadiene triblock copolymer. The short butadiene end-blocks (DPB = 36) of a BSB triblock copolymer with a long styrene middle block (DPS = 650) was first modified by hydroboration and oxidation. A multifunctional alkoxide initiator is thus prepared by titration of the hydroxyl groups of the “polybutadiene” end-block with cumylpotassium. Gelation and precipitation of the polyfunctional initiator in THF could be avoided by complexing the cation (K+) with a…

Polymers and PlasticsEthylene oxideOrganic ChemistryCondensed Matter PhysicsRing-opening polymerizationStyrenechemistry.chemical_compoundAnionic addition polymerizationPolybutadienechemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerPolystyrenePhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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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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Hydrogen Production from Methanol-Water Solution and Pure Water Electrolysis Using Nanocomposite Perfluorinated Sulfocationic Membranes Modified by P…

2022

In this work, we report the preparation of Nafion membranes containing two different nanocomposite MF-4SC membranes, modified with polyaniline (PANI) by the casting method through two different polyaniline infiltration procedures. These membranes were evaluated as a polymer electrolyte membrane for water electrolysis. Operating conditions were optimized in terms of current density, stability, and methanol concentration. A study was made on the effects on the cell performance of various parameters, such as methanol concentration, water, and cell voltage. The energy required for pure water electrolysis was analyzed at different temperatures for the different membranes. Our experiments showed …

Polymers and PlasticsGeneral ChemistryQuímicawater electrolysis; methanol electrolysis; perfluorinated sulfocationic membranes; polyaniline; PEMWE; hydrogen productionQuímica orgànicaPolymers
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