Search results for "polymers"

showing 10 items of 3567 documents

Mechanism of Anionic Polymerization of (Meth)acrylates in the Presence of Aluminium Alkyls IV. Formation of a Co-ordinative Polymer Network via the L…

1996

The polymerization of methyl methacrylate in the presence of aluminium alkyls in toluene deviates from conventional kinetics. This results predominantly from the formation and precipitation of a co-ordinative polymer gel or network. Due to the lower reactivity and accessibility of the living chains in the gel, they are regarded as ’dormant’ and thus the concentration of active species decreases during polymerization. The network formation occurs via co-ordination of the living aluminate chain end group with in-chain ester carbonyl groups. Part of the chains are deactivated by a termination process but they are free of cyclic β-ketoesters which would result from the common ’back-biting’ reac…

Polymers and PlasticsChemistryAluminateSolution polymerizationPoly(methyl methacrylate)End-groupchemistry.chemical_compoundAnionic addition polymerizationPolymerizationvisual_artPolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumLiving polymerizationLiving anionic polymerizationPolymer Journal
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Heparin-Based Nanocapsules as Potential Drug Delivery Systems

2015

Herein, the synthesis and characterization of heparin-based nanocapsules (NCs) as potential drug delivery systems is described. For the synthesis of the heparin-based NCs, the versatile method of miniemulsion polymerization at the droplets interface was achieved resulting in narrowly distributed NCs with 180 nm in diameter. Scanning and transmission electron microscopy images showed clearly NC morphology. A highly negative charge density for the heparin-based NCs was determined by measuring the electro-kinetic potential. Measuring the activated clotting time demonstrated the biological intactness of the polymeric shell. The ability of heparin-based NCs to bind to antithrombin (AT III) was i…

Polymers and PlasticsChemistryAnalytical chemistryBioengineeringIsothermal titration calorimetrybehavioral disciplines and activitiesNanocapsulesBiomaterialsMiniemulsionPolymerizationChemical engineeringDynamic light scatteringTransmission electron microscopymental disordersDrug deliveryMaterials ChemistryChemical stabilityBiotechnologyMacromolecular Bioscience
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New hyaluronic acid based brush copolymers synthesized by atom transfer radical polymerization.

2013

Abstract In this work, an efficient method for the synthesis of hyaluronic acid based brush copolymers using atom transfer radical polymerization (ATRP) has been reported. At first, two different hyaluronic acid (HA) based macroinitiators have been prepared and then they have been used for the polymerization via ATRP of hydrophilic or hydrophobic molecules carrying vinyl portions. In particular, by linking 2-bromo-2-methylpropionic acid (BMP) to the primary hydroxyl groups of tetrabutyl ammonium salt of HA (HA–TBA) or to amino groups of the ethylenediamino derivative of HA–TBA (HA–TBA–EDA), two macroinitiators (HA–TBA–BMP and HA–TBA–EDA–BMP) have been obtained. Then they have been used for …

Polymers and PlasticsChemistryAtom-transfer radical-polymerizationPolymersOrganic ChemistrySize-exclusion chromatographyBiocompatible MaterialsChemistry Techniques SyntheticMethacrylateEthylenediaminesPolymerizationMolecular Weightchemistry.chemical_compoundLiving free-radical polymerizationPolymerizationPolymer chemistryMaterials ChemistryCopolymerReversible addition−fragmentation chain-transfer polymerizationHyaluronic AcidPropionatesEthylene glycolCarbohydrate polymers
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Polymerization of styrene

1979

Polymers and PlasticsChemistryChain transferGeneral ChemistryCondensed Matter PhysicsChain-growth polymerizationAnionic addition polymerizationPolymerizationPolymer chemistryMaterials ChemistryCopolymerLiving polymerizationReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationPolymer Bulletin
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Copolymerization of Isoprene with p-Alkylstyrene Monomers: Disparate Reactivity Ratios and the Shape of the Gradient

2019

The statistical copolymerization of isoprene with p-ethyl- (p-ES), p-isopropyl- (p-iPS), and p-tert-butylstyrene (p-tBS) initiated by sec-butyllithium in cyclohexane was investigated with respect to kinetics, reactivity ratios, and formation of tapered block copolymers with pronounced monomer gradient. An efficient synthetic route to the monomers was developed on a multigram scale, relying on the precipitation of the side-product triphenylphosphine oxide at low temperature. The copolymerization kinetics and resulting molecular weight distributions were analyzed. The dispersity, Đ, of the copolymers depends on the p-alkyl substituent, the the degree of polymerization Pn and the comonomer mol…

Polymers and PlasticsChemistryComonomerOrganic ChemistryDispersity02 engineering and technologyDegree of polymerization010402 general chemistry021001 nanoscience & nanotechnologyMole fraction01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundMonomerPolymer chemistryMaterials ChemistryCopolymerReactivity (chemistry)0210 nano-technologyIsopreneMacromolecules
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Hyperbranched Polyols via Copolymerization of 1,2-Butylene Oxide and Glycidol: Comparison of Batch Synthesis and Slow Monomer Addition

2015

Hyperbranched poly(butylene oxide) polyols have been synthesized by multibranching anionic ring-opening copolymerization of 1,2-butylene oxide and glycidol. Systematic variation of the composition from 24 to 74% glycidol content resulted in a series of moderately distributed copolymers (Đ = 1.41–1.65, SEC), albeit with limited molecular weights in the solvent-free batch process in the range of 900–1300 g mol–1 (apparent Mn determined by SEC with PEG standards). In situ monitoring of the copolymerization kinetics by 1H NMR showed a pronounced compositional drift with respect to the monomer feed, indicating a strongly tapered microstructure caused by the higher reactivity of glycidol. In the …

Polymers and PlasticsChemistryComonomerOrganic ChemistryGlycidolOxide02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundMonomerPolymer chemistryPEG ratioMaterials ChemistryCopolymerReactivity (chemistry)0210 nano-technologyGlass transitionMacromolecules
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Die vielfältigen additionsprodukte von phenylen-, naphthylen-, biphenylylen- und methylendiphenylendimethacrylaten mit radikalen aus 2,2'-azoisobutyr…

1976

Die Reaktionen von Phenylen-, Naphthylen-, Biphenylylen- und Methylendiphenylendimethacrylaten (1–4) wurden teils mit 2,2'-Azoisobutyronitril (AIBN) in Substanz oder anionisch in Losung mit Butyllithium oder Natriumdihydronaphthylid (Naphthalinnatrium), teils mit grosem Uberschus an AIBN stark verdunnt in siedendem Benzol durchgefuhrt. Neben unloslichen (vernetzten) Polymeren wurden losliche erhalten, darunter Cyclopolymere vom Typ 9, wie die Ergebnisse der Hydrolyse und anschliesende Umsetzung mit Diazomethan zu Poly(methacrylsaure-methylester)n zeigten. Die Verdunnungsreaktion ergab die Produkte 5 der unterdruckten Polymerisation, der innermolekularen Addition mit Kopf/Schwanz- und Schwan…

Polymers and PlasticsChemistryDiazomethaneMedicinal chemistrySolventchemistry.chemical_compoundHydrolysisColloid and Surface ChemistryPolymerizationMethacrylic acidPhenylenePolymer chemistryMaterials ChemistryButyllithiumPhysical and Theoretical ChemistryMethyl methacrylateDie Makromolekulare Chemie
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Ordering and mobility of ferroelectric liquid crystal dimer as studied by FT-IR spectroscopy with 2D-IR correlation analysis

1997

Both a conservative rapid-scan FT-IR technique and a novel step-scan FT-IR technique with 2D correlation analysis were used to study the orientation and the mobility ofa ferroelectric liquid crystal dimer during switching under an electric field. The detailed mutual arrangements of different molecular segments (mesogen, poly(methylene) chain, polysiloxane chain) in a smectic C* phase were derived from the static spectra. It was shown that the long mesogen axis, the average poly(methylene) and the average polysiloxane chain axes do not coincide with each other. The hindered rotation of the carbonyl group is confirmed. Time-resolved FT-IR technique was used to follow the segmental motion with…

Polymers and PlasticsChemistryDimerMesogenOrganic ChemistryCondensed Matter PhysicsFerroelectricityEnd-groupchemistry.chemical_compoundCrystallographyLiquid crystalPhase (matter)Electric fieldPolymer chemistryMaterials ChemistryMethyleneMacromolecular Symposia
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Colloidal crystallization dynamics

1997

At sufficiently strong interparticle interaction, colloidal particles may form ordered crystalline arrays much in analogy to atomic systems. Well characterized model colloidal suspensions have therefore become valuable model systems for the study of the kinetics of crystal nucleation, growth and ripening. Significant progress has been made in this area throughout the past few years. Precise control of interaction parameters and new instrumental developments have allowed for quantitative determination of nucleation rate densities and growth velocities in monodisperse ‘hard’ and ‘soft sphere’ systems. Results confirm classical theories of nucleation and growth adapted to colloidal systems. Th…

Polymers and PlasticsChemistryDispersityKineticsDynamics (mechanics)NucleationNanotechnologySurfaces and InterfacesQuantitative determinationlaw.inventionCrystalColloidColloid and Surface ChemistryChemical physicslawPhysical and Theoretical ChemistryCrystallizationCurrent Opinion in Colloid & Interface Science
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Single-chain conformations in symmetric binary polymer blends: Quantitative comparison between self-consistent field calculations and Monte Carlo sim…

1998

Single-chain properties in a symmetric binary polymer blend are studied by self-consistent field calculations and Monte Carlo simulations. Within the self-consistent field scheme, the statistical mechanics of a cluster of neighboring polymers is solved. Interactions among the polymers of a cluster and composition fluctuations within a cluster are incorporated exactly, a mean field approximation is invoked for intercluster interactions and long-range fluctuations. The results are compared to large scale Monte Carlo simulations for a broad range of chain lengths. While we find nearly quantitative agreement for single chain propertiese.g., the reduction of the chain dimensions of the minority …

Polymers and PlasticsChemistryEntropy (statistical thermodynamics)Organic ChemistryIntermolecular forceMonte Carlo methodStatistical mechanicsMolecular physicsInorganic ChemistryMean field theoryMaterials ChemistryRadius of gyrationPolymer blendStatistical physicsPhase diagram
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