Search results for " copolymer"

showing 10 items of 160 documents

Supramolecular Modification of ABC Triblock Terpolymers in Confinement Assembly

2018

The self-assembly of AB diblock copolymers in three-dimensional (3D) soft confinement of nanoemulsions has recently become an attractive bottom up route to prepare colloids with controlled inner morphologies. In that regard, ABC triblock terpolymers show a more complex morphological behavior and could thus give access to extensive libraries of multicompartment microparticles. However, knowledge about their self-assembly in confinement is very limited thus far. Here, we investigated the confinement assembly of polystyrene-block-poly(4-vinylpyridine)-block-poly(tert-butyl methacrylate) (PS-b-P4VP-b-PT or SVT) triblock terpolymers in nanoemulsion droplets. Depending on the block weight fractio…

nanoemulsions3D confinement assemblyMaterials scienceBlock copolymerGeneral Chemical EngineeringChemieSupramolecular chemistryNanoparticle02 engineering and technology010402 general chemistryMethacrylate01 natural sciencesArticlesupramolecular chemistrylcsh:ChemistrymulticompartmentNanoemulsionCopolymerGeneral Materials ScienceMicroparticleAlkylchemistry.chemical_classificationmicroparticlesHydrogen bond021001 nanoscience & nanotechnology0104 chemical sciencesblock copolymersLamella (surface anatomy)Microparticlelcsh:QD1-999Chemical engineeringchemistryhalogen bondSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologyNanomaterials
researchProduct

Facile and efficient chemical functionalization of aliphatic polyesters by cross metathesis

2016

International audience; An effective preparation of new tailor-made macromolecular materials via a combination of two (atom-efficient) catalytic transformations is reported. First, new aliphatic polyesters with alternated composition have been prepared using a salen aluminum catalyst system. Next, the pendant vinyl moieties in those copolymers have been selectively transformed into various functional groups by metathesis in the presence of homogeneous Grubbs catalysts. The latter metathesis reaction has been optimized in terms of catalytic activity and selectivity, to define the conditions for an effective and safe procedure that does not affect the macromolecular architecture. All polymer …

plga microspheresphosphate-buffered solutionin-vivo degradationPolymers and PlasticsBioengineeringmolecular-weight poly(l-lactide)010402 general chemistryMetathesis01 natural sciencesBiochemistry[ CHIM ] Chemical SciencesCatalysisacid) microspheresCopolymerSalt metathesis reactionenzymatic degradation[CHIM]Chemical SciencesOrganic chemistryRing-opening metathesis polymerisationcyclic anhydrides010405 organic chemistryChemistryring-opening copolymerizationOrganic Chemistryrenewable resources0104 chemical sciencesPolyester[ CHIM.POLY ] Chemical Sciences/Polymers[CHIM.POLY]Chemical Sciences/Polymersbiodegradable polymersSelectivityAcyclic diene metathesis
researchProduct

Naturally Occurring Oxazole Structural Units as Ligands of Vanadium Catalysts for Ethylene-Norbornene (Co)polymerization

2021

1,3-Oxazole and 4,5-dihydro-1,3-oxazole are common structural motifs in naturally occurring peptides. A series of vanadium complexes were synthesized using VCl3(THF)3 and methyl substituted (4,5-dihydro-1,3-oxazol-2-yl)-1,3-oxazoles as ligands and analyzed using NMR and MS methods. The complexes were found to be active catalysts both in ethylene polymerization and ethylene-norbornene copolymerization. The position of methyl substituent in the ligand has considerable impact on the performance of (co)polymerization reaction, as well as on the microstructure, and thus physical properties of the obtained copolymers.

polyethyleneEthyleneSubstituentVanadiumchemistry.chemical_elementTP1-1185010402 general chemistry01 natural sciencesCatalysisCatalysischemistry.chemical_compoundPolymer chemistryCopolymervanadium catalystPhysical and Theoretical ChemistryQD1-999polyethylene; norbornene copolymers; oxazole ligand; vanadium catalyNorborneneOxazole010405 organic chemistryChemical technology0104 chemical sciencesChemistrychemistryPolymerizationnorbornene copolymersoxazole ligandCatalysts
researchProduct

Titanium and Vanadium Catalysts with 2-Hydroxyphenyloxazoline and Oxazine Ligands for Ethylene-Norbornene (co)Polymerization

2019

A series of titanium and vanadium complexes with oxazoline 2-(4,5-dihydro-1,3-oxazol-2-yl)phenol (L1), 2-(4-methyl-4,5-dihydro-1,3-oxazol-2-yl)phenol (L2), and oxazine 2-(5,6-dihydro-4H-1,3-oxazin-2-yl)phenol (L3) ligands were synthesized, and their structures were determined by NMR and MS methods as (L)2MtCl2. The vanadium complexes were found to be highly active in ethylene (7300 kgPE/(molV&middot

polyethyleneEthyleneoxazine ligandVanadiumchemistry.chemical_elementPolyethyleneCatalysisCatalysischemistry.chemical_compoundchemistryPolymerizationnorbornene copolymersPolymer chemistryCopolymervanadium catalystMolar mass distributionPhysical and Theoretical Chemistryoxazole ligandNorborneneCatalysts
researchProduct

Block copolymers from ionic liquids for the preparation of thin carbonaceous shells

2017

This paper describes the controlled radical polymerization of an ionic-liquid monomer by RAFT polymerization. This allows the control over the molecular weight of ionic liquid blocks in the range of 8000 and 22000 and of the block-copolymer synthesis. In this work we focus on block copolymers with an anchor block. They can be used to control the formation of TiO2 nanoparticles, which are functionalized thereafter with a block of ionic-liquid polymer. Pyrolysis of these polymer functionalized inorganic nanoparticles leads to TiO2 nanoparticles coated with a thin carbonaceous shell. Such materials may, e.g., be interesting as battery materials.

polymeric ionic liquidRadical polymerizationblock copolymer02 engineering and technology010402 general chemistry01 natural sciencesFull Research Paperlcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryPolymer chemistryCopolymerReversible addition−fragmentation chain-transfer polymerizationlcsh:Scienceionic liquidchemistry.chemical_classificationRAFT polymerizationcarbonOrganic ChemistryPolymer021001 nanoscience & nanotechnologyBlock (periodic table)0104 chemical sciencesChemistryMonomerchemistryIonic liquidlcsh:Q0210 nano-technologyPyrolysisBeilstein Journal of Organic Chemistry
researchProduct

Dexamethasone Dipropionate Loaded Nanoparticles Of -Elastin-G-Plga For Potential Treatment Of Restenosis

2013

restenosisnanoparticlepoly(lactic- co -glycolic) acidα-elastindexamethasone dipropionategraft copolymer
researchProduct

Oil solubilization in copolymer and copolymer covered laponite aqueous dispersion

2007

solubilization copolymer dispersion nanoclaySettore CHIM/02 - Chimica Fisica
researchProduct

Modeling Heterogeneous copolymerization in scCO2

2008

supercritical carbon dioxidemass transferFree radical copolymerizationkinetic model
researchProduct

EVALUATION OF BIODEGRADABILITY ON POLYSPARTAMIDE-POLYLACTIC ACID BASED NANOPARTICLES BY CHEMICAL HYDROLYSIS STUDIES POLYMER DEGRADATION AND STABILITY

2015

Here, the synthesis of two graft copolymers based on α,β-poly(N-2-hydroxyethyl)-D,L-aspartamide (PHEA) and poly(lactic acid) (PLA), the O-(2-aminoethyl)-O′-galactosyl polyethylene glycol (GAL-PEG-NH2) or the methoxypolyethylene glycol amine (H2N-PEG-OCH3) is described. Starting from the obtained PHEA-PLA-PEG-GAL and PHEA-PLA-PEG copolymers, polymeric nanoparticles were prepared by high pressure homogenization–solvent evaporation method. To demonstrate their biodegradability as a function of the matrix composition, a chemical stability study was carried out until 21 days by incubating systems in two media mimicking physiological compartments (pH 7.4 and pH 5.5). The degradability of both nan…

αβ-poly-(N-2-hydroxyethyl)-DL-aspartamide (PHEA) poly(lactic acid) (PLA) poly(ethylene glycol) (PEG) graft copolymers nanoparticles biodegradability
researchProduct

Evaluation of biodegradability of novel polymeric nanoparticles based on amphiphilic polylactide-polyaspartamide derivatives.

2015

αβ-poly-(N-2-hydroxyethyl)-DL-aspartamide (PHEA) poly(lactic acid) (PLA) poly(ethylene glycol) (PEG) graft copolymers nanoparticles biodegradability.
researchProduct