Search results for "PLASTICS"

showing 10 items of 2724 documents

Poly(1,2-glycerol carbonate): A Fundamental Polymer Structure Synthesized from CO2 and Glycidyl Ethers

2013

The functional, aliphatic poly(1,2-glycerol carbonate) as a fundamental, simple polymer structure based on glycerol and CO2 was prepared by combination of glycidyl ether monomers with carbon dioxide via two different approaches. The material was obtained by two-step procedures either via copolymerization of (i) ethoxy ethyl glycidyl ether (EEGE) or (ii) benzyl glycidyl ether (BGE) with CO2, followed by removal of the respective protecting groups via acidic cleavage for (i) and hydrogenation for (ii). The resulting protected polycarbonate structures and the targeted poly(1,2-glycerol carbonate) were investigated with 1H NMR and 13C NMR spectroscopy as well as 2D-NMR methods. Removal of both …

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryPolymerInorganic Chemistrychemistry.chemical_compoundMonomerchemistryvisual_artPolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumGlycerolCopolymerAlkoxy groupProton NMRCarbonateOrganic chemistryPolycarbonateMacromolecules
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Combining oxyanionic polymerization and click-chemistry: a general strategy for the synthesis of polyether polyol macromonomers

2014

We describe a synthetic pathway to tailor-made amphiphilic macromonomers by a combination of anionic ring-opening polymerization and copper-catalyzed azide–alkyne cycloaddition (CuAAC). Linear polyglycerol and poly(glyceryl glycerol) were synthesized in a controlled manner by anionic ring-opening polymerization of ethoxyethyl glycidyl ether or isopropylidene glyceryl glycidyl ether, respectively, with narrow and monomodal molecular weight distributions (Mw/Mn < 1.20) and molecular weights ranging from 850 g mol−1 to 2500 g mol−1. After end-capping with propargyl bromide and removal of the protecting groups, the hydrophilic precursors were quantitatively clicked to a series of hydrophobic az…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryRadical polymerizationBioengineeringBiochemistryCycloadditionchemistry.chemical_compoundchemistryPolymerizationPolymer chemistryAmphiphileClick chemistryCopolymerOrganic chemistryPropargyl bromideAlkylPolym. Chem.
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RAFT polymerization of activated 4-vinylbenzoates

2009

The reversible addition fragmentation chain transfer (RAFT) polymerization of five active ester monomers based on 4-vinylbenzoic acid had been investigated. Pentafluorophenyl 4-vinylbenzoate could be polymerized under RAFT conditions yielding polymers with very good control over molecular weight and narrow molecular weight distributions. Following the synthesis of diblock copolymers consisting of polystyrene, polypentafluorostyrene, poly(4-octylstyrene), or poly(4-acetoxystyrene) as an inert block and poly(pentafluorophenyl 4-vinylbenzoate) as a reactive block was successfully performed. The diblock copolymer poly(pentafluoro styrene)-block-poly(pentafluorophenyl 4-vinylbenzoate) had been a…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryRadical polymerizationChain transferRaftPolymerchemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerReversible addition−fragmentation chain-transfer polymerizationJournal of Polymer Science Part A: Polymer Chemistry
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Polymeric nitrones, 1. Synthesis and modification of polymeric nitrones derived from polymerizable aldehydes

1999

The model compound N,C-diphenylnitrone[N-(benzylidene)aniline-N-oxide] (3) was prepared by condensation of benzaldehyde with phenylhydroxylamine to study its thermal stability. X-ray diffraction analysis of a single crystal established the conformation of the nitrone group. A new monomer 4-(methacryloyloxy)benzaldehyde-phenylnitrone (8) was also prepared and could not be polymerized with 2,2′-azobisisobutyronitrile (AIBN) as initiator at 70°C. Under these conditions the nitrone reacted exclusively in an intermolecular 1,3-dipolar cycloaddition to give oligomeric tetrahydro-1,2-oxazoline derivates. The kinetics of the cycloaddition was investigated. Additionally, different (meth)acryl- and s…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryRadical polymerizationCondensed Matter PhysicsCondensation reactionAldehydeCycloadditionNitroneBenzaldehydechemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryPhenylhydroxylamineMacromolecular Chemistry and Physics
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Synthesis and polymerization of active ester monomers based on 4-vinylbenzoic acid

2007

Abstract Nine active ester monomers based on 4-vinylbenzoic acid have been synthesized. Under free radical polymerization conditions these monomers could successfully be polymerized yielding reactive polymers with molecular weights of around M n  = 20.000–50.000 g/mol and molecular weight distributions M w / M n of around or below 2 in good yields. Polymer analogous reactions with amines have been investigated by time-resolved FT-IR spectroscopy and it was found that especially poly(pentafluorophenyl 4-vinylbenzoate) featured a significant reactivity, such that polymer analogous reactions proceeded quantitatively with amines within less than 5 min at 0 °C.

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryRadical polymerizationGeneral Physics and AstronomyChemical modificationPolymerRing-opening polymerizationchemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryReactivity (chemistry)Functional polymersEuropean Polymer Journal
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Molecular Parameters of Hyperbranched Copolymers Obtained by Self-Condensing Vinyl Copolymerization, 2. Non-Equal Rate Constants

2001

The kinetics, molecular weight averages, and the average degree of branching, DB, are calculated for the self-condensing vinyl copolymerization (SCVCP) of a vinyl monomer M with an "inimer" AB* in the case of different reactivities of active species. Emphasis is given to two limiting cases: formation of "macroinimers" occurs if the monomer M is more reactive than the vinyl groups of inimers or polymer, and "hyperstars" are formed in the opposite case. It is shown that the kinetics, the molecular weight averages, and the average degree of branching strongly depend on the relative reactivities of monomer and inimer. Comparison with experimental data shows that consistent fits of the reactivit…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryRadical polymerizationKineticsPolymerBranching (polymer chemistry)Inorganic Chemistrychemistry.chemical_compoundReaction rate constantMonomerchemistryPolymer chemistryMaterials ChemistryCopolymerMolar mass distributionMacromolecules
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Poly(4-vinylbenzoyl azide): A New Isocyanato Group Generating Polymer

2007

4-Vinylbenzoyl azide was synthesized from p-vinylbenzoic acid and polymerized by free radical polymerization. The obtained polymer contained acyl azide groups which were thermally transformed to the corresponding isocyanato groups. Reactions on these polymers with ethanol, hydroxyethyl methacrylate and 1-pyrene-butanol proceeded quantitatively. Time-resolved FT-IR studies of the reactions with ethanol were carried out by varying the concentration and temperature. The effect of the solvent polarity on the Curtius rearrangement was investigated.

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryRadical polymerizationPolymer(Hydroxyethyl)methacrylateAcyl azidechemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryAzideSolvent effectsCurtius rearrangementMacromolecular Rapid Communications
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Ion-Induced Stretching of Low Generation Dendronized Polymers with Crown Ether Branching Units

2009

Synthesis of the first (G1) and second generation (G2) dendronized macromonomers MG1 and MG2 with the dibenzo-24-crown-8 moiety as branching unit is reported. The corresponding dendronized polymers, the polymethacrylates PG1 and PG2, were synthesized by free radical polymerization using AIBN as initiator at 60−80 °C. Static and dynamic light scattering revealed a significant chain expansion upon complexation of these polymers’ crown ether side chains with K+ ions. It is concluded that electrostatic repulsion does not significantly contribute to the chain expansion because of excessive counterion binding even well below the Manning limit, as evidenced by 19F NMR and 1H−19F NOE experiments. R…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryRadical polymerizationPolymerBranching (polymer chemistry)MacromonomerInorganic ChemistryDynamic light scatteringchemistryDendrimerPolymer chemistryMaterials ChemistrySide chainCrown etherMacromolecules
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Versatile ω-end group functionalization of RAFT polymers using functional methane thiosulfonates

2009

Five different polymers, poly[methyl methacrylate] (PMMA), poly[lauryl methacrylate] (PLMA), poly[diethylene glycol methacrylate] (PDEGMA), poly[N-iso-propylacrylamide] (PNIPA), and poly[styrene] (PS) prepared by the RAFT process and thus terminated with dithioesters were aminolyzed in the presence of S-3-butynyl methane thiosulfonate (MTS), which was synthesized in two steps. Analysis of the polymers by 2D NMR, UV–vis absorbance, and gel permeation chromatogra-phy revealed them to quantitatively carry acetylene end groups connected with disul-fide bridges, indicating that functional MTS reagents can be employed for end group functionalization of RAFT polymers. This versatile method is of ad…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryRaftPolymerMethacrylateContact anglechemistry.chemical_compoundEnd-groupchemistryPolymer chemistryMaterials ChemistrySurface modificationAzideMethyl methacrylateJournal of Polymer Science Part A: Polymer Chemistry
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Hyperbranched methacrylates by self-condensing group transfer polymerization

1997

The synthesis of hyperbranched methacrylates was achieved by self-condensing group transfer polymerization of 2-(2-methyl-1-triethylsiloxy-1-propenyloxy)ethyl methacrylate (1). “Back-biting” is shown to be the predominant side reaction. In spite of this, the compact nature of the hyperbranched molecules was demonstrated through SEC-viscosity measurements and comparison with a linear analogue. The degree of branching can be controlled by copolymerization with conventional monomers, e.g. MMA, and the living polymers can be used as macroinitiators for star-shaped polymers.

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistrySide reactionPolymerSelf-condensationBranching (polymer chemistry)Methacrylatechemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerMacromolecular Rapid Communications
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