Search results for "Macromonomer"

showing 10 items of 32 documents

Copolymerization of n-Butyl Acrylate with Methyl Methacrylate and PMMA Macromonomers:  Comparison of Reactivity Ratios in Conventional and Atom Trans…

1999

The reactivity ratios of n-butyl acrylate (nBuA) with methyl methacrylate (MMA) and ω-methacryloyl-PMMA macromonomers (MM) in conventional and atom transfer radical copolymerization (ATRP) have been determined. For the copolymerization of nBuA with MMA, good agreement of the ratios is observed between conventional and controlled radical copolymerization, indicating that chemoselectivities in both processes are similar. The relative reactivity of the MM (1/rnBuA) in conventional copolymerization is significantly lower than that of MMA. It depends on the concentration of the comonomers but is not significantly influenced by the length of the MM. At high concentrations the relative reactivity …

AcrylatePolymers and PlasticsDiffusionOrganic ChemistryMacromonomerInorganic Chemistrychemistry.chemical_compoundMonomerchemistryAtomPolymer chemistryMaterials ChemistryCopolymerReactivity (chemistry)Methyl methacrylateMacromolecules
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Towards the Generation of Self-Healing Materials by Means of a Reversible Photo-induced Approach

2011

Photo-induced reversibility as a tool for self-healing: a reversible photo-induced dendritic macromonomer was synthesized and proven to form networks with different features depending on the crosslinking conditions. While networks formed from aqueous systems exhibited a reversible change in their crosslinking degree, networks generated in bulk underwent fully reversibility. The latter was then exploited for generating self-healing materials by means of a photo-induced treatment.

Aqueous solutionMaterials sciencePolymers and PlasticsChemical engineeringDendritic PolymersSelf-healingOrganic ChemistryPolymer chemistryMaterials Chemistrysense organsSelf-healing materialMacromonomerMacromolecular Rapid Communications
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PEG-benzofulvene copolymer hydrogels for antibody delivery.

2010

A new amphiphilic copolymer have been synthesized starting from the hydrosoluble polyaspartylhydrazide (PAHy) polymer, by grafting both hydrophilic PEG(2000) chains and hydrophobic palmitic acid (C(16)) moieties on polymer backbone, and the structure of obtained PAHy-PEG(2000)-C(16) copolymer have been characterized by 2D (1)H/(13)C NMR experiments. PAHy-PEG(2000)-C(16) copolymer showed the ability of self-assembling in aqueous media giving a core-shell structure and resulted potentially useful for encapsulating and dissolving hydrophobic drug. The formation of micellar core-shell structure has been investigated by 2D (1)H NMR NOESY experiments. The presence of cross-peaks for protons of C(…

BiocompatibilityCell SurvivalPolymersSurface PropertiesPEG-benzofulvene immunoglobulin delivery hydrogelsimmunoglobulinsPharmaceutical SciencePolyethylene Glycolschemistry.chemical_compoundDrug Delivery SystemsCell Line TumorPolymer chemistryPEG ratioCopolymerHumansantibody deliverybenzofulvene copolymerschemistry.chemical_classificationChemistrytechnology industry and agricultureHydrogelsantibody delivery; benzofulvene copolymers; hydrogels; immunoglobulinsPolymerMacromonomerIndenesSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoImmunoglobulin GDrug deliverySelf-healing hydrogelsbenzofulvene copolymerhydrogelDrug Screening Assays AntitumorRheologyEthylene glycolInternational journal of pharmaceutics
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MALDI-TOF characterization of macromonomers

1996

Methacryloyl endfunctionalized oligostyrene macromonomers were characterized by matrix assisted laser desorption ionization/time of flight (MALDI-TOF) spectroscopy and by isocratic and gradient high performance liquid chromatography (HPLC). The molar mass distribution derived by the different techniques coincide for the investigated oligomers. Mixing experiments revealed that the MALDI-TOF peak areas do not necessarily represent the mixing ratio of the components. Combination of gradient HPLC and MALDI-TOF has resolved the chemical composition of the coupling products formed by reaction of the living anion with oxygen.

ChromatographyPolymers and PlasticsChemistryOrganic ChemistryMatrix isolationAnalytical chemistryMass spectrometryMacromonomerHigh-performance liquid chromatographyTime of flightMatrix-assisted laser desorption/ionizationMaterials ChemistryMolar mass distributionSpectroscopyMacromolecular Rapid Communications
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Synthesis of hydrophilic polymers in supercritical carbon dioxide in the presence of a siloxane-based macromonomer surfactant: Heterogeneous polymeri…

2003

Batch free radical polymerization of 1-vinyl-2-pyrrolidone (VP) in super- critical carbon dioxide (scCO2) was studied in the presence of a reactive polysiloxane surfactant (PDMS-mMA). Phase behavior investigation showed that when the initial concentration of the surface active macromonomer was higher than 2.5% w/w with respect to the monomer, the reaction mixture, in the absence of efficient stirring, was initially opaque to the visible light, and it slowly turned to an orange tint. Polymeriza- tion experiments carried out with surfactant concentration higher than the aforemen- tioned value proceeded with a fast kinetics, and led to the formation of spherical nanoparticles with almost quant…

Dispersion polymerizationPolymers and PlasticsOrganic ChemistryRadical polymerizationEmulsion polymerizationhydrophilic polymersiloxane-based macromonomer surfactantMacromonomerchemistry.chemical_compoundMonomersupercritical carbon dioxidechemistryPulmonary surfactantPolymerizationPolymer chemistryMaterials ChemistryPrecipitation polymerizationJournal of Polymer Science Part A: Polymer Chemistry
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New approach for synthesis of poly(ethylglyoxylate) using Maghnite-H + , an Algerian proton exchanged montmorillonite clay, as an eco-catalyst

2017

International audience; In this works, we have explored a new method for a green synthesis of poly(ethylglyoxylate) (PEtG). This method consists on using a montmorillonite clay called Maghnite-H+ as an eco-catalyst to replace triethylamine which is toxic. Cationic polymerization experiments are performed in bulk conditions at three temperatures (-40 degrees C, 25 degrees C, 80 degrees C) and in THF solutions at room temperature (25 degrees C). At 25 degrees C, an optimum ratio of 5 wt% of catalyst leads to molar masses up to 22000 g/mol in THF solutions. Polymerizations in bulk conditions lead to slightly lower masses than experiments conducted in THF solutions. However, bulk polymerization…

Green chemistryThermogravimetric analysisMaterials scienceepsilon-caprolactonePolymers and PlasticsBulk polymerizationMaghnite-H+ring-opening polymerization02 engineering and technologyEthylglyoxylate010402 general chemistry7. Clean energy01 natural sciencesalcoholschemistry.chemical_compoundbiodegradable plasticsMaterials Chemistrycationic polymerizationionic polymerizationsThermal stabilityComposite materialsheet silicatespoly(methyl glyoxylate)degradationchemistry.chemical_classificationMolar masscopolymergreen chemistrybis-macromonomersCationic polymerizationbiodegradable polymerGeneral ChemistryPolymer021001 nanoscience & nanotechnology0104 chemical sciences[ CHIM.POLY ] Chemical Sciences/PolymersMontmorillonite[CHIM.POLY]Chemical Sciences/PolymersChemical engineeringchemistryCeramics and Compositeseco-catalyst0210 nano-technology
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Designed biodegradable hydrogel structures prepared by stereolithography using poly(ethylene glycol)/poly(D,L-lactide)-based resins

2010

Designed three-dimensional biodegradable poly(ethylene glycol)/poly(D,L-lactide) hydrogel structures were prepared for the first time by stereolithography at high resolutions. A photo-polymerisable aqueous resin comprising PDLLA-PEG-PDLLA-based macromer, visible light photo-initiator, dye and inhibitor in DMSO/water was used to build the structures. Porous and non-porous hydrogels with well-defined architectures and good mechanical properties were prepared. Porous hydrogel structures with a gyroid pore network architecture showed narrow pore size distributions, excellent pore interconnectivity and good mechanical properties. The structures showed good cell seeding characteristics, and human…

IR-80283Materials scienceStereolithographyPolyestersPharmaceutical ScienceDesigned porous structuresSCAFFOLDSHydrogel Polyethylene Glycol Dimethacrylatelaw.inventionPolyethylene GlycolsMacromer photo-polymerisationCONSTRUCTSchemistry.chemical_compoundMETIS-272859lawPolymer chemistryGLYCOL)Cell Adhesionmacromer photopolymerisationHumansTissue engineeringPorosityStereolithographyAqueous solutiontechnology industry and agricultureMesenchymal Stem CellsMacromonomerResins SyntheticPhotopolymerBiodegradation EnvironmentalchemistryChemical engineeringBiodegradable hydrogelsSelf-healing hydrogelsCELLS090301 BiomaterialsEthylene glycolGyroid
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Nanoparticles Built of Cross-Linked Heterotelechelic, Amphiphilic Poly(dimethylsiloxane)-b-poly(ethylene oxide) Diblock Copolymers

2000

Novel short chain α,ω-heterotelechelic amphiphilic poly(dimethylsiloxane)-b-poly(ethylene oxide) diblock copolymers (PDMS−PEO) with total molecular weights below 10 000 g/mol are synthesized, characterized, and used as basic constituent parts for functionalized nanoparticles. The self-assembly of the amphiphilic diblock copolymer in water as a solvent selective for the PEO block leads to the formation of spherical and cylindrical micellar structures with diameters between 10 and 25 nm. The core of the micelles is built of the hydrophobic PDMS chains, whereas the corona is set up by the hydrophilic PEO blocks. By using α,ω-heterotelechelic diblock copolymers, it is possible to fix the core o…

Materials scienceAqueous solutionPolymers and PlasticsEthylene oxideOrganic ChemistryNanoparticleMacromonomerMicelleInorganic Chemistrychemistry.chemical_compoundEnd-groupchemistryPolymer chemistryAmphiphileMaterials ChemistryCopolymerMacromolecules
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Cylindrical Polypeptide Brushes

2005

Cylindrical brushes with poly(L-lysine) and poly(L-glutamate) side chains were prepared by grafting through and grafting from techniques. Grafting from is shown to be more successful for the synthesis of cylindrical brushes with high molar mass main and side chains.

Materials scienceMolar massPolymers and PlasticsOrganic ChemistryRadical polymerizationChemical modificationCondensed Matter PhysicsGraftingMacromonomerdigestive systemRing-opening polymerizationEnd-groupsurgical procedures operativePolymer chemistryMaterials ChemistrySide chainPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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Acrylic thermoplastic elastomers and comb-shaped poly(methyl methacrylate) via the macromonomer technique

1996

Comb-shaped poly(methyl methacrylate) (PMMA) and poly(butyl acrylate) (PnBuA) grafted with PMMA were prepared by radical copolymerization of ω-methacryloyl-PMMA with MMA and nBuA, respectively. The comb-shaped PMMA is characterized with respect to radius of gyration by using gel permeation chromatography equipped with a multi-angle laser light scattering detector. The radical copolymerization of the macromonomer with nBuA in toluene follows complex kinetics. The dependence of the relative reactivity of the macromonomer on absolute concentration and on the ratio of comonomers may be explained by preferential solvation of comonomers by segments of their own kind (“bootstrap effect”) or even m…

Materials sciencePolymers and PlasticsButyl acrylateOrganic Chemistrytechnology industry and agriculturemacromolecular substancesCondensed Matter PhysicsMacromonomerMicellePoly(methyl methacrylate)chemistry.chemical_compoundchemistryvisual_artPolymer chemistryMaterials ChemistryRadius of gyrationCopolymervisual_art.visual_art_mediumMethyl methacrylateThermoplastic elastomerMacromolecular Symposia
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