Search results for "Reversible addition−fragmentation chain-transfer polymerization"

showing 10 items of 69 documents

Langmuir-Blodgett films of biocompatible poly(HPMA)-block-poly(lauryl methacrylate) and poly(HPMA)-random-poly(lauryl methacrylate): influence of pol…

2010

Membranes based on functional biocompatible polymers can be regarded as a useful model system to study biological interactions, e.g. antibody-antigen interactions or protein polymer interactions. These model systems may give a better insight into these processes and may help to find suitable polymeric structures offering biocompatibility as well as reduced polymer protein interaction. In this respect, Langmuir-Blodgett (LB) layer formation at the air/water (A/W) interface is studied in respect to polymer architecture in this article. For this purpose, narrowly distributed N-(2-hydroxypropyl)-methacrylamide (HPMA) random and block copolymers have been prepared by the RAFT polymerization meth…

chemistry.chemical_classificationAqueous solutionMaterials scienceMagnetic Resonance SpectroscopyBiocompatibilityPolymersPolymer architectureBiocompatible MaterialsMembranes ArtificialSurfaces and InterfacesPolymerCondensed Matter PhysicsMicroscopy Atomic ForceLangmuir–Blodgett filmMembranechemistryPolymer chemistryElectrochemistryCopolymerMethacrylatesGeneral Materials ScienceReversible addition−fragmentation chain-transfer polymerizationSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Radioactive labeling of defined HPMA-based polymeric structures using [18F]FETos for in vivo imaging by positron emission tomography.

2009

During the last decades polymer-based nanomedicine has turned out to be a promising tool in modern pharmaceutics. The following article describes the synthesis of well-defined random and block copolymers by RAFT polymerization with potential medical application. The polymers have been labeled with the positron-emitting nuclide fluorine-18. The polymeric structures are based on the biocompatible N-(2-hydroxypropyl)-methacrylamide (HPMA). To achieve these structures, functional reactive ester polymers with a molecular weight within the range of 25,000-110,000 g/mol were aminolyzed by 2-hydroxypropylamine and tyramine (3%) to form (18)F-labelable HPMA-polymer precursors. The labeling procedure…

chemistry.chemical_classificationBiodistributionAcrylamidesFluorine RadioisotopesPolymers and PlasticsPolymersRadical polymerizationSize-exclusion chromatographyRadiochemistryBioengineeringChain transferPolymerPolymerizationRatsBiomaterialsPolymerizationchemistryIsotope LabelingPositron-Emission TomographyPolymer chemistryMaterials ChemistryAnimalsReversible addition−fragmentation chain-transfer polymerizationPreclinical imagingBiotransformationBiomacromolecules
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Functionalization of TiO2Nanoparticles with Semiconducting Polymers Containing a Photocleavable Anchor Group and Separation via Irradiation Afterward

2014

The controlled radical polymerization (RAFT polymerization) of semiconducting polymers based on poly(4,4′-dimethyl-triphenylamine) is described. These polymers are afterward end-functionalized with a photocleavable group and an anchor unit (catechol) for oxidic nanoparticles (NPs). Serving as a reference, polystyrene oligomers with the same end groups are also synthesized. Using these polymers allows functionalization of the TiO2-NPs, leading to an improved solubility and miscibility in organic solvents or polymer matrices. Irradiation in the UV region is used to split the photocleavable group and remove the polymer chains from the NPs, which leads to their aggregation.

chemistry.chemical_classificationCatecholPolymers and PlasticsOrganic ChemistryRadical polymerizationtechnology industry and agricultureNanoparticlePolymerCondensed Matter PhysicsMiscibilitychemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistrySurface modificationReversible addition−fragmentation chain-transfer polymerizationPolystyrenePhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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Liquid crystalline phases from polymer functionalized ferri-magnetic Fe3O4nanorods

2017

Here, we present the surface functionalization of anisotropic in form ferri-magnetic Fe3O4-nanorods (NRs) with a diblock copolymer, having a PMMA- or PDEGMEMA-block, for solubilization, and a dopamine anchor block. These polymers were synthesized through RAFT polymerization via a macro-initiator approach. The successful surface functionalization, performed via a grafting-to method, was monitored using TGA, IR and TEM measurements. The NRs were very soluble in organic solvents after functionalization. Afterwards, the liquid crystalline (LC) behavior was investigated. During solvent evaporation, birefringent domains were formed. The self-assembly into lyotropic LC structures could be observed…

chemistry.chemical_classificationMaterials scienceNanoparticle02 engineering and technologyGeneral ChemistryPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistryChemical engineeringPhase (matter)LyotropicMaterials ChemistryCopolymerSurface modificationOrganic chemistryReversible addition−fragmentation chain-transfer polymerizationNanorod0210 nano-technologyJournal of Materials Chemistry C
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Temperature-Responsive Surface Coatings Based on Poly(methylsilsesquioxane)-hybrid Polymers

2007

The present paper presents a new method to build up temperature-responsive surfaces. First a poly(silsesquioxane)-block-poly(N-isopropyl-acrylamide) (PMSSQ-b-PNIPAM) was successfully synthesized using RAFT polymerization. Spin-coating or dip-coating of PMSSQ-b-PNIPAM onto glass surfaces resulted in temperature-responsive surfaces. Surface ATR FT-IR measurements proofed the successful surface modification using PMSSQ-b-PNIPAM. IR fine structures of PNIPAM and PMSSQ could be assigned, respectively. In capillary rise experiments a change of the meniscus height measured at temperatures below or above LCST was observed, indicating a different wetting behavior. Thus, a simple spin- or dip-coating…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsCapillary actionOrganic ChemistryPolymerCondensed Matter PhysicsLower critical solution temperatureSilsesquioxanechemistry.chemical_compoundchemistryChemical engineeringPolymer chemistryMaterials ChemistryCopolymerSurface modificationReversible addition−fragmentation chain-transfer polymerizationWettingMacromolecular Symposia
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Synthesis of well-defined polymeric activated esters

2008

Monomers bearing an activated ester group can be polymerized under various controlled polymerization techniques, such as ATRP, NMP, RAFT polymerization, or ROMP. Combining the functionalization of polymers via polymeric activated esters with these controlled polymerization techniques generate possibilities to realize highly functionalized polymer architectures. Within this highlight two different research areas of activated esters in polymer science will be discussed: (i) the preparation of defined reactive polymer architectures by controlled polymerization techniques and (ii) the preparation of defined reactive thin films. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 6…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryRadical polymerizationtechnology industry and agricultureChain transfermacromolecular substancesPolymerChain-growth polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationJournal of Polymer Science Part A: Polymer Chemistry
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Synthesis of Functional Inorganic−Organic Hybrid Polymers Based on Poly(silsesquioxanes) and Their Thin Film Properties

2008

New stable and adherent coating materials have been synthesized on the basis of inorganic/organic hybrid polymers. As the inorganic part, different poly(silsesquioxanes) (PSSQ) have been functionalized to act as polymeric chain transfer agents (CTAs) for a reversible addition fragmentation chain transfer polymerization, thereby determining the starting point of a controlled radical polymerization of vinyl-type monomers. Using two different CTAs acrylates, we have successfully polymerized methacrylates and styrene under RAFT polymerization conditions. Different monomers were copolymerized in such an organic block to incorporate multiple functionalities. The variation of the block ratios and …

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryRadical polymerizationtechnology industry and agricultureChain transfermacromolecular substancesPolymerMethacrylateInorganic ChemistrySurface coatingPolymerizationchemistryPolymer chemistryMaterials ChemistrySurface modificationReversible addition−fragmentation chain-transfer polymerizationMacromolecules
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Well-defined carbohydrate-based polymers in calcium carbonate crystallization: Influence of stereochemistry in the polymer side chain on polymorphism…

2015

Abstract In this work we demonstrate the remarkable phase control on the crystallization of calcium carbonate by the stereochemistry of carbohydrate-based polymers. The polymers (poly(2-(2,3,4,6-tetra-O-acetyl-β- d -glucosyloxy)ethyl methacrylate) and poly(2-(2,3,4,6-tetra-O-acetyl-β- d -galactosyloxy)ethyl methacrylate)) have been synthesized from the respective glucose or galactose containing monomers (3 step synthesis) by RAFT polymerization leading to well-defined carbohydrate-based polymers with number averages of the molecular weights (Mw) of 10,000–18,000 g/mol and a dispersities (Đ) from 1.1 to 1.2. For the deprotected polymers we found differences in the phase selection of calcium …

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsStereochemistryOrganic ChemistryGeneral Physics and AstronomyPolymerMethacrylatelaw.inventionchemistry.chemical_compoundCalcium carbonateMonomerchemistryPolymorphism (materials science)lawPolymer chemistryMaterials ChemistrySide chainOrganic chemistryReversible addition−fragmentation chain-transfer polymerizationCrystallizationEuropean Polymer Journal
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Synthesis, Characterization and Preliminary Biological Evaluation of P(HPMA)-b-P(LLA) Copolymers: A New Type of Functional Biocompatible Block Copoly…

2010

We describe a synthetic pathway to functional P(HPMA)-b-P(LLA) block copolymers. The synthesis relies on a combination of ring-opening polymerization of L-lactide, conversion into a chain transfer agent (CTA) for the RAFT polymerization of pentafluorophenyl methacrylate. A series of block copolymers was prepared that exhibited molecular weights $\overline M _{\rm n}$ ranging from 7 600 to 34 300 g · mol(-1) , with moderate PDI between 1.3 and 1.45. These reactive precursor polymers have been transformed into biocompatible P(HPMA)-b-P(LLA) copolymers and their fluorescently labeled derivatives by facile replacement of the pentafluorophenyl groups. The fluorescence label attached to this new …

chemistry.chemical_classificationMaterials scienceRAFT polymerizationPolymers and PlasticssynthesisStereochemistryOrganic ChemistryFluorescence correlation spectroscopyfluorescence correlation spectroscopyPolymerchainMethacrylatebiocompatible block copolymerspolylactide block copolymersTransfer agentchemistryPolymerizationPolymer chemistryAmphiphileHPMA block copolymersMaterials ChemistryCopolymerReversible addition−fragmentation chain-transfer polymerization
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Nonlinear Macromolecules by Ring-Opening Polymerization

2012

Ring-opening polymerization (ROP) is a well-established method for the controlled synthesis of linear polymers, which can be found in various everyday applications. However, during the past decades, there has been an increasing interest in the generation of nonlinear highly branched polymers, profiting from the fascination created by the structurally perfect dendrimers. The applicability of various heterocyclic monomers renders the ring-opening multibranching polymerization (ROMBP), a versatile tool for the generation of multifunctional hyperbranched polymers. First, the historical key steps leading to the development of ROMBP are described, which is the basis for the controlled synthesis o…

chemistry.chemical_classificationMaterials sciencechemistryPolymerizationDendrimerCationic polymerizationLiving polymerizationOrganic chemistryNanotechnologyReversible addition−fragmentation chain-transfer polymerizationPolymerRing-opening polymerizationMacromolecule
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