Search results for " copolymers"

showing 10 items of 65 documents

Random Structural Modification of a Low-Band-Gap BODIPY-Based Polymer

2017

International audience; A BODIPY thiophene polymer modified by extending conjugation of the BODIPY chromophore is reported. This modification induces tunability of energy levels and therefore absorption wavelengths in order to target lower energies.

Materials scienceBand gapthin-film transistors02 engineering and technology010402 general chemistryPhotochemistry[ CHIM ] Chemical Sciences01 natural scienceschemistry.chemical_compoundmolecular-orbital methodsorganometallic compounds[CHIM]Chemical SciencesPhysical and Theoretical Chemistrydensity-functional theoryAbsorption (electromagnetic radiation)valence basis-setsdistyryl-boradiazaindaceneschemistry.chemical_classificationPolymer modifiedfield-effect transistorspi-conjugated copolymers[CHIM.MATE]Chemical Sciences/Material chemistryPolymerChromophore021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsWavelengthsolar-cellsGeneral Energychemistry[ CHIM.MATE ] Chemical Sciences/Material chemistryextended basis-setsBODIPY0210 nano-technologyThe Journal of Physical Chemistry C
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Biocompatible micelles based on squalene portions linked to pegylated polyaspartamide as potential colloidal drug carriers

2011

Materials scienceBiomedical EngineeringPharmaceutical ScienceMedicine (miscellaneous)BioengineeringBiocompatible materialMicelleSqualenechemistry.chemical_compoundColloidchemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoOrganic chemistryDrug carrieramphiphilic copolymers drug carriers micelles αβ-poly(N-2-hydroxyethyl)-DLaspartamidesqualene in vitro uptakeBiotechnology
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Hierarchical Self-Assembly of Halogen-Bonded Block Copolymer Complexes into Upright Cylindrical Domains

2017

Summary Self-assembly of block copolymers into well-defined, ordered arrangements of chemically distinct domains is a reliable strategy for preparing tailored nanostructures. Microphase separation results from the system, minimizing repulsive interactions between dissimilar blocks and maximizing attractive interactions between similar blocks. Supramolecular methods have also achieved this separation by introducing small-molecule additives binding specifically to one block by noncovalent interactions. Here, we use halogen bonding as a supramolecular tool that directs the hierarchical self-assembly of low-molecular-weight perfluorinated molecules and diblock copolymers. Microphase separation …

Materials scienceBlock copolymerGeneral Chemical Engineering116 Chemical sciencesSupramolecular chemistryNanotechnologyblock copolymer02 engineering and technologyhierarchical self-assembly010402 general chemistry01 natural sciencesBiochemistryMicelleArticleSDG9: Industry innovation and infrastructuresupramolecular complexesMaterials ChemistryCopolymerEnvironmental ChemistryNon-covalent interactionsMoleculeLamellar structureta116chemistry.chemical_classificationHalogen bondta114Biochemistry (medical)General Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesblock copolymerschemistryChemical engineeringIndustry innovation and infrastructure [SDG9]nanofabricationhalogen bondSettore CHIM/07 - Fondamenti Chimici Delle TecnologieSelf-assembly0210 nano-technology
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Thermal stability of ethylene copolymers with multi-alkenylsilsesquioxane comonomers synthesized by organometallic catalyst - Effect of copolymer str…

2020

Abstract This study was focused on thermal properties of ethylene copolymers with di-, tri- and tetra-alkenylsilsesquioxanes (POSS) synthesized by ansa-metallocene complex. Ethylene copolymers with multi-alkenyl POSS were characterized by different thermal behavior depending on the kind of POSS comonomer and its content, as well as the copolymer structure. The copolymers differed in the incorporation way of POSS into the polymer chain (linear and crosslinked structure), content of specific unsaturation groups, molecular weight, as well as heterogeneity of polymer chain compositions. It was found that the kind and content of unsaturation groups in E/POSS copolymers played a significant role …

Materials scienceEthylenePolymers and Plastics02 engineering and technology010402 general chemistry01 natural sciencesEthylenechemistry.chemical_compoundMulti-alkenyl polyhedral oligomericMaterials ChemistryCopolymerThermal stabilitychemistry.chemical_classificationDegree of unsaturationLinear and crosslinked copolymersComonomerThermal stabilityPolymerPolyethylene021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencessilsesquioxanes (POSS)Chemical engineeringchemistryMechanics of MaterialsNon-isothermal and isothermal conditions0210 nano-technologyHybrid materialPolymer Degradation and Stability
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Enhanced power-conversion efficiency in organic solar cells incorporating copolymeric phase-separation modulators

2018

A new class of copolymers containing oligothiophene moieties with different lengths and fullerene units have been designed and prepared by an easy and inexpensive one-step synthetic approach. The incorporation of small quantities of these copolymers into bulk heterojunction (BHJ) solar cells with donor regioregular polythiophene (P3HT) and an acceptor fullerene derivate (PCBM) results in good control of the phase separation process without further affecting the BHJ optoelectronic properties. Indeed, under thermal annealing these copolymers allow the modulation of the growth of domains whose size depends on the length of the copolymer repetitive units. Domain size on the same length scale as…

Materials scienceFullereneOrganic solar cellRenewable Energy Sustainability and the EnvironmentExcitonEnergy conversion efficiency02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAcceptorPolymer solar cell0104 chemical scienceschemistry.chemical_compoundchemistryChemical engineeringCopolymerPolythiopheneGeneral Materials Science0210 nano-technologyorganic solar cells plastic solar cells phase separation copolymers modulators efficiencyJournal of Materials Chemistry A
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Building Bridges by Blending: Morphology and Mechanical Properties of Binary Tapered Diblock/Multiblock Copolymer Blends

2021

Materials scienceMorphology (linguistics)Polymers and PlasticsOrganic ChemistryMultiblock copolymerBinary numberCondensed Matter Physics540MiscibilityChemical engineeringPolymer chemistryMaterials ChemistryGradient copolymersPolymer blendPhysical and Theoretical Chemistry
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Dynamics of paramagnetic nanostructured rods under rotating field

2011

International audience; The dynamical rotational behavior of magnetic nanostructured rods based on the auto-association of maghemite nanoparticles and block-copolymers is probed by optical microscopy under rotating fields i n a s imple l iquid. The reorientation of the rods by a field rotated by 90° is first studied. The measured relaxation is characteristic of param-agnetic objects. Under a stationnary rotating field, a synchronous rotational regime is observed at low field frequency. Above a frequency threshold which scales as H^2 , the dynamics becomes asynchronous with back-and-forth rotations. These behaviors are well predicted by the presented model.

Materials scienceNanostructureField (physics)Maghemite02 engineering and technologyengineering.material01 natural sciencesRod010305 fluids & plasmaslaw.inventionNanocompositesParamagnetismNuclear magnetic resonanceOptical microscopelaw0103 physical sciencesColloids[PHYS.COND]Physics [physics]/Condensed Matter [cond-mat]8116DnCondensed matter physicsRelaxation (NMR)Self-assembly[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsBlock copolymersElectronic Optical and Magnetic Materials8107-b8380Uv[CHIM.POLY]Chemical Sciences/PolymersengineeringSelf-assembly0210 nano-technology8270Dd[PHYS.COND.CM-SCM]Physics [physics]/Condensed Matter [cond-mat]/Soft Condensed Matter [cond-mat.soft]
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Porphyrins and BODIPY as Building Blocks for Efficient Donor Materials in Bulk Heterojunction Solar Cells

2017

International audience; Advances in the synthesis and application of highly efficient polymers and small molecules over the last two decades have enabled the rapid advancement in the development of organic solar cells and photovoltaic technology as a promising alternative to conventional solar cells, based on silicon and other inorganic semiconducting materials. Among the different types of organic semiconducting materials, porphyrins and BODIPY-based small molecules and conjugated polymers attract high interest as efficient semiconducting organic materials for dye sensitized solar cells and bulk heterojunction organic solar cells. The highest power conversion efficiency exceeding 9% has be…

Materials scienceOrganic solar cellEnergy Engineering and Power Technologypower-conversion efficiency02 engineering and technologydonor materials010402 general chemistryporphyrins7. Clean energy01 natural sciencesPolymer solar cellbulk heterojunction solar cellsphotoinduced electron-transferchemistry.chemical_compoundBODIPYElectrical and Electronic Engineeringsmall-moleculelow-bandgap polymerbusiness.industryfield-effect transistors[CHIM.MATE]Chemical Sciences/Material chemistryHybrid solar cellpi-conjugated copolymersd-a021001 nanoscience & nanotechnologyAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic Materialsphotovoltaic propertieschemistryopen-circuit voltage[ CHIM.MATE ] Chemical Sciences/Material chemistryOptoelectronicsorganic photovoltaicsBODIPY0210 nano-technologybusiness
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Evaluation of biodegradability on polyaspartamide-polylactic acid based nanoparticles by chemical hydrolysis studies

2015

Here, the synthesis of two graft copolymers based on ?,?-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…

Materials sciencePolymers and PlasticsNanoparticlemacromolecular substancesPolyethylene glycolchemistry.chemical_compoundHydrolysispoly(lactic acid) (PLA)Polylactic acid: ?biodegradability.Materials ChemistryOrganic chemistrytechnology industry and agriculturepoly(ethylene glycol) (PEG)BiodegradationCondensed Matter PhysicsLactic acidchemistry?-poly-(N-2-hydroxyethyl)-DL-aspartamide (PHEA)Mechanics of MaterialsYield (chemistry)graft copolymersnanoparticlesChemical stabilityNuclear chemistryPolymer Degradation and Stability
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Hepatocyte-targeted fluorescent nanoparticles based on a polyaspartamide for potential theranostic applications

2015

Abstract Here, the synthesis of a galactosylated amphiphilic copolymer bearing rhodamine (RhB) moieties and its use for the preparation of polymeric fluorescent nanoparticles for potential applications in therapy and diagnosis are described. To do this, firstly, a fluorescent derivative of α,β-poly( N -2-hydroxyethyl)- d , l -aspartamide (PHEA) was synthesized by chemical reaction with RhB, and with polylactic acid (PLA), to obtain PHEA-RhB-PLA. Then, the derivatization of PHEA-RhB-PLA with GAL-PEG-NH 2 allows obtaining PHEA-RhB-PLA-PEG-GAL copolymer, with derivatization degrees in -PLA and -PEG-GAL equal to 1.9 mol% and 4.5 mol%, respectively. Starting from this copolymer, liver-targeted f…

Materials sciencePolymers and PlasticsOrganic Chemistrytechnology industry and agricultureNanoparticlemacromolecular substancesCombinatorial chemistryFluorescenceRhodaminechemistry.chemical_compoundPolylactic acidchemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoPolymer chemistryMaterials ChemistryZeta potentialCopolymerAsialoglycoprotein receptorActive targeting alphabeta-Poly-(N-2-hydroxyethyl)-DL-aspartamide (PHEA) Fluorescence imaging Graft copolymers NanoparticlesDerivatization
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