Search results for " copolymers"

showing 10 items of 65 documents

Synthesis of polybutadiene-polycaprolactone multi-blokcs based on hydroxyl telechelic polybutadiene. Composition and kinetic study

2009

International audience

[ CHIM.POLY ] Chemical Sciences/Polymersthermoplastic block copolymerspoly(butadiene[CHIM.POLY] Chemical Sciences/Polymers[CHIM.POLY]Chemical Sciences/PolymersComputingMilieux_MISCELLANEOUSpoly(e-caprolactone)
researchProduct

Janus Nanostructures from ABC/B Triblock Terpolymer Blends

2019

Lamella-forming ABC triblock terpolymers are convenient building blocks for the synthesis of soft Janus nanoparticles (JNPs) by crosslinking the B domain that is &ldquo

bulk morphologiestechnology industry and agricultureChemiemacromolecular substancesArticlelcsh:QD241-441block copolymersForschungszentren » Center for Nanointegration Duisburg-Essen (CENIDE)lcsh:Organic chemistryddc:540DPD simulationspolymer blendingddc:541Janus nanostructuresFakultät für Chemie » Physikalische ChemiePolymers
researchProduct

Biocompatible polymeric micelles with polysorbate 80 for use in brain targeting.

2008

In this paper, the synthesis and characterization of novel amphiphilic graft copolymers based on an alpha,beta-poly(N-2-hydroxyethyl)-D, L-aspartamide (PHEA) backbone and D, L-polylactic acid (PLA) hydrophobic side chains are reported. These copolymers were obtained starting from PHEA-ethylenediamine (PHEA-EDA), which was functionalized with polysorbate 80 (PS(80)) and/or PLA in order to obtain the PHEA-EDA-PS(80)-PLA and PHEA-EDA-PLA samples, respectively. The degrees of derivatization, DD(PS80) and DD(PLA), of PHEA-EDA-PS80-PLA, calculated by (1)H-NMR, resulted in being 1.2 +/- 0.03 mol% and 0.54 +/- 0.05 mol%, respectively, while that of PHEA-EDA-PLA was found to be 0.60 +/- 0.05 mol%. S…

chemistry.chemical_classificationChromatographyMaterials scienceMechanical EngineeringSize-exclusion chromatographyBioengineeringGeneral ChemistryPolymerMicelleAMPHIPHILIC COPOLYMERS MICELLES BRAIN TARGETING POLYSORBATE 80chemistry.chemical_compoundchemistryMechanics of MaterialsSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoAmphiphileSide chainZeta potentialCopolymerGeneral Materials ScienceElectrical and Electronic EngineeringDerivatizationNuclear chemistryNanotechnology
researchProduct

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
researchProduct

Monomer Sequence Distribution Monitoring in Living Carbanionic Copolymerization by Real-Time 1H NMR Spectroscopy

2013

Detailed understanding of the monomer sequence distribution in carbanionic copolymerization was achieved by direct online monitoring of copolymerizations in an NMR tube. Obtaining detailed knowledge of the changing monomer concentration in stock during the reaction, this technique permits to determine the incorporation probability for each monomer at every position of the polymer chain. An in situ kinetic study of two different carbanionic copolymerizations has been carried out. On the one hand, the copolymerization of the structurally similar, protected hydroxystyrene derivatives, p-(1-ethoxy ethoxy)styrene (pEES) and 4-tert-butoxystyrene (tBuOS), and on the other hand the copolymerization…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryNMR tubeNuclear magnetic resonance spectroscopyPolymerStyreneInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistryAlkoxy groupCopolymerGradient copolymersMacromolecules
researchProduct

New amphiphilic conjugates of mono- and bis(carboxy)-PEG(2,000) polymers with lipoamino acids as surface modifiers of colloidal drug carriers

2010

chemistry.chemical_classificationamphiphilesPolymers and Plasticspoly(ethylene glycol)Organic Chemistrylipoaminoacids copolymers surface modifiers drug carrierslipoamino acidslong-circulating drug-delivery systemsPolymerCondensed Matter PhysicsColloidMatrix-assisted laser desorption/ionizationchemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoPolymer chemistryAmphiphileamphiphiles; conjugated polymers; lipoamino acids; long-circulating drug-delivery systems; MALDI-TOF MS; poly(ethylene glycol)Materials Chemistryconjugated polymersMALDI-TOF MSPhysical and Theoretical ChemistryDrug carrierConjugate
researchProduct

Hydrophilic and hydrophobic copolymers of a polyasparthylhydrazide bearing positive charges as vector for gene therapy

2008

BACKGROUND: The design of polymeric vectors for gene delivery provided with specific properties is one of the most critical aspects for a successful gene therapy. These polymers should be biocompatible as well as able to carry efficiently DNA to target tissues and to transfect it into cells. RESULTS: The formation of complexes of poly[(α,β-asparthylhydrazide)–poly(ethylene glycol)] and poly[(α,β-asparthylhydrazide)–hexadecylamine] copolymers functionalised with glycidyltrimethylammonium chloride (PAHy–PEG-GTA and PAHy–C16-GTA, respectively) with DNA was studied. The effects of the introduction of hydrophilic (PEG) or hydrophobic (C16) moieties on the chains of PAHy–GTA copolymers, such as t…

chemistry.chemical_classificationcationic polyaminoacidMaterials sciencePolymers and PlasticsPAHy-GTA copolymers polyaspartylhydrazidefungiOrganic ChemistrySupramolecular chemistryDNA protectionPolymerGene deliveryPolyelectrolytechemistry.chemical_compoundpolyion complexchemistryPolymer chemistryPEG ratioMaterials ChemistrySide chainEthylene glycolDNA
researchProduct

Synthesis and characterization of poly(L,L-lactide)-b-polyethylene glycol) diblock copolymers as plasticizers and their effect on the hydrophilicity …

2011

diblock copolymers synthesis PLA PEG
researchProduct

Vanadium catalysts for ethylene-norbornene copolymerization

2020

Kopolimery cyklicznych olefin (COCs) stanowią obiecującą grupę materiałów o specyficznych, możliwych do zaprojektowania właściwościach. Szczególnym zainteresowaniem w tej grupie związków cieszą się kopolimery etylenu z norbornenem. Do ich syntezy stosuje się różnorodne kompleksy metali przejściowych, przede wszystkim pierwiastków z grupy 4. Artykuł stanowi przegląd literatury dotyczącej wykorzystania katalizatorów wanadowych z różnego rodzaju ligandami w syntezie kopolimerów etylenu z norbornenem. Opisano wpływ ligandów i warunków prowadzenia reakcji na aktywność oraz wybrane właściwości otrzymanych kopolimerów.

kopolimery cyklicznych olefinVanadium catalystCopolymerizationkatalizator wanadowyeNorbornenekopolimeryzacjaetylenCyclic olefin copolymersEthylennorbornenPolimery
researchProduct

Studies of ethylene/1-hexene copolymerization over zirconocene catalyst supported on MAO-modified MgCl2(THF)2. The effect of copolymerization conditi…

2003

Composition of catalytic system and copolymerization reaction conditions influence on heterogeneity of ethylene/1-hexene copolymers obtained over MgCI2(THF)2/MAO/Cp2ZrCl2/MAO catalyst was studied. One of the DSC techniques, i.e. successive self-nucleation/annealing (SSA) method allowing separation of the polymer into fractions with differing chemical composition in result of alternating crystallization and melting cycles was applied. It was found that the intermolecular heterogeneity exists inside all studied samples irrespective of the reaction conditions (temperature and time) and the catalyst composition (Al/Zr molar ratio). It was also confirmed that catalyst composition has a considera…

lamella thicknessintermolecular heterogeneityethylene/1-hexene copolymerszirconocene catalystSSA methodPolimery
researchProduct