Search results for " polymers"

showing 10 items of 465 documents

Electrical conductivity and strong luminescence in copper Iodide double chains with isonicotinato derivatives

2015

Direct reactions between CuI and isonicotinic acid (HIN) or the corresponding esters, ethyl isonicotinate (EtIN) or methyl isonicotinate (MeIN), give rise to the formation of the coordination polymers [CuI(L)] with L=EtIN (1), MeIN (2) and HIN (3). Polymers 1-3 show similar structures based on a CuI double chain in which ethyl-, methyl isonicotinate or isonicotinic acid are coordinated as terminal ligands. Albeit, their supramolecular architecture differs considerably, affecting the distances and angles of the central CuI double chains and thereby their physical properties. Hence, the photoluminescence shows remarkable differences; 1 and 2 show a strong yellow emission, whereas 3 displays a…

Models MolecularThermogravimetric analysisPhotoluminescenceLuminescencePolymersInorganic chemistrySupramolecular chemistrychemistry.chemical_elementConductivityIsonicotinic acidLigandsNiacinCatalysisCopper iodidechemistry.chemical_compoundCoordination ComplexesElectrical conductivityCarboxylateMolecular StructureStructure elucidationOrganic ChemistryElectric ConductivityGeneral ChemistryIodidesCopperCoordination polymersCrystallographychemistryLuminescenceCopper
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Scaffold and scaffold-free self-assembled systems in regenerative medicine.

2016

Self-assembly in tissue engineering refers to the spontaneous chemical or biological association of components to form a distinct functional construct, reminiscent of native tissue. Such self-assembled systems have been widely used to develop platforms for the delivery of therapeutic and/or bioactive molecules and various cell populations. Tissue morphology and functional characteristics have been recapitulated in several self-assembled constructs, designed to incorporate stimuli responsiveness and controlled architecture through spatial confinement or field manipulation. In parallel, owing to substantial functional properties, scaffold-free cell-assembled devices have aided in the developm…

Modular engineeringTissue EngineeringTissue ScaffoldsCell-assembled devicesSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoBiomimetic MaterialsGuided Tissue RegenerationHumansSelf-assemblyRegenerative MedicineDelivery of biologicsStimuli-responsive polymersExtracellular MatrixBiotechnology and bioengineering
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A new route for the preparation of flexible skin–core poly(ethylene-co-acrylic acid)/polyaniline functional hybrids

2011

Abstract Surface modification of polymeric films is a way to obtain final products with high performance for many specific and ad hoc tailored applications, e.g. in functional packaging, tissue engineering or (bio)sensing. The present work reports, for the first time, on the design and development of surface modified ethylene–acrylic acid copolymer (EAA) films with polyaniline (PANI), with the aim of inducing electrical conductivity and potentially enable the electronic control of a range of physical and chemical properties of the film surface, via a new “grafting from” approach. In particular, we demonstrate that PANI was successfully polymerized and covalently grafted onto flexible EAA su…

MorphologyMaterials Chemistry2506 Metals and AlloysMaterials sciencePolymers and PlasticsPolyanilineGeneral Chemical EngineeringHybrid polymersBiochemistrychemistry.chemical_compoundX-ray photoelectron spectroscopyPolyanilinePolymer chemistryChemical surface modificationElectrical conductivityPolyaniline Chemical surface modification Hybrid polymers Morphology Electrical conductivityMaterials ChemistryCopolymerEnvironmental ChemistryChemical Engineering (all)Fourier transform infrared spectroscopyAcrylic acidChemistry (all)General ChemistryChemical engineeringchemistryPolymerizationSurface modificationSettore CHIM/07 - Fondamenti Chimici Delle TecnologieChemical surface modification; Electrical conductivity; Hybrid polymers; Morphology; Polyaniline; Materials Chemistry2506 Metals and Alloys; Polymers and Plastics; Chemistry (all); Chemical Engineering (all); Environmental Chemistry; BiochemistryHybrid materialReactive and Functional Polymers
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Tuning the magneto-structural properties of non-porous coordination polymers by HCl chemisorption.

2011

Responsive materials for which physical or chemical properties can be tuned by applying an external stimulus are attracting considerable interest in view of their potential applications as chemical switches or molecular sensors. A potential source of such materials is metal-organic frameworks. These porous coordination polymers permit the physisorption of guest molecules that can provoke subtle changes in their porous structure, thus affecting their physical properties. Here we show that the chemisorption of gaseous HCl molecules by a non-porous one-dimensional coordination polymer instigates drastic modifications in the magnetic properties of the material. These changes result from profoun…

MultidisciplinaryMaterials science010405 organic chemistryCoordination polymerPorous Coordination PolymersGeneral Physics and AstronomyGeneral Chemistry010402 general chemistry01 natural sciencesGeneral Biochemistry Genetics and Molecular Biology0104 chemical scienceschemistry.chemical_compoundchemistryChemisorptionChemical physicsNature communications
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Polyamide/carbonaceous particles nanocomposites fibers: Morphology and performances

2015

In this work, the influence of carbonaceous particles with different sizes and shapes on the morphology and mechanical performances of polyamide (PA)-based fibers was investigated. Graphene nanoplatelets (GNP) are compared with spherical and rod-like carbon fillers such as carbon black (CB) and multiwall carbon nanotubes (CNTs). The increments of the complex viscosity as well as elastic and loss moduli, in the melt state, assessed by rheological analysis, are reduced by modifying polyamide (PA) matrix with nanofillers in a following order: CNTs > GNP > CB. All the nanocomposites, however, show viscosity and moduli higher than those of neat PA. The CB loading causes a mere increase of the vi…

NanocompositeMaterials sciencePolymers and PlasticsRheometryChemistry (all)Metals and AlloysGeneral ChemistryCarbon nanotubeCarbon blackfibersnanocomposites fiberslaw.inventionViscosityRheologylawPolyamideCeramics and Composites; Chemistry (all); Polymers and Plastics; Materials Chemistry; 2506; Metals and AlloysPolyamideMaterials ChemistryCeramics and Composites2506Composite materialcarbonaceous particleDispersion (chemistry)Polymer Composites
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On the role of multi-functional polyhedral oligomeric silsesquioxane in polystyrene-zinc oxide nanocomposites

2014

Abstract Multi-functional trisilanol phenyl (TSPH) and trisilanol isobutyl (TSIB) polyhedral oligomeric silsesquioxane (POSS) have been used in the formulation of advanced polystyrene (PS)-zinc oxide (ZnO) nanocomposites. The neat matrix and PS/ZnO-based nanocomposites have been characterized through rheological, morphological, mechanical, and dynamic thermo-mechanical analysis. Both TSPH and TSIB are able to improve the dispersion of ZnO into the polystyrene matrix; furthermore, adding TSIB leads to better results because it facilitates better solubility into the PS matrix and interaction/reaction with the ZnO nanopowder. Finally, the optical properties and photo-oxidative resistance of th…

NanocompositeMaterials sciencePolymers and PlasticsnanocompositeGeneral Chemical Engineeringdispersant agentMetals and Alloyschemistry.chemical_elementZincSilsesquioxanechemistry.chemical_compounddispersant agent; nanocomposites; photo-oxidative resistance; POSS; UV shielding; Chemical Engineering (all); Polymers and Plastics; Materials Chemistry; 2506; Metals and AlloysUV shieldingchemistryphoto-oxidative resistancePolymer chemistrynanocompositesMaterials ChemistryChemical Engineering (all)Polystyrene2506POSS
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Biomolecular conjugation inside synthetic polymer nanopores via glycoprotein-lectin interactions

2011

We demonstrate the supramolecular bioconjugation of concanavalin A (Con A) protein with glycoenzyme horseradish peroxidase (HRP) inside single nanopores, fabricated in heavy ion tracked polymer membranes. Firstly, the HRP-enzyme was covalently immobilized on the inner wall of the pores using carbodiimide coupling chemistry. The immobilized HRP-enzyme molecules bear sugar (mannose) groups available for the binding of Con A protein. Secondly, the bioconjugation of Con A on the pore wall was achieved through its biospecific interactions with the mannose residues of the HRP enzyme. The immobilization of biomolecules inside the nanopore leads to the reduction of the available area for ionic tran…

NanometresSynthetic membraneTransport equationNanoporesInformation processingRectification propertiesCylinders (shapes)Materials TestingConcanavalin AGeneral Materials ScienceFunctional polymersConical nanoporeschemistry.chemical_classificationChemistryBlocking effectElectric rectifiersComputer simulationEnzymesData processingNanoporeEnzyme moleculesFunctional polymersMolecular imprintingPorosityBio-molecularInner wallsMolecular imprintingSupramolecular chemistryNanotechnologyHorseradish peroxidaseIonic transportsNanocapsulesBio-conjugationMoleculeParticle SizeAqueous solutionsGlycoproteinsBiomoleculesBioconjugationBiomoleculeNanostructuresModel simulationChemical engineeringModels ChemicalPolymer membraneConductance stateFISICA APLICADABiospecific interactionSynthetic polymersSugarsSupramolecular chemistryPore wallCarbodiimide-coupling chemistry
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Orthogonal functionalisation of upconverting NaYF4 nanocrystals.

2013

A simple and straightforward method for the orthogonal functionalisation of upconverting NaYF4 nanocrystals (UCNCs)-doped withYb(3+) and Er(3+)-based on N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide/N-hydroxysuccinimide (EDC/NHS) selective reactions between two dyes and two different reactive groups present at the periphery of the upconverting nanocrystals is reported. Organic-soluble UCNCs of 10 and 50 nm in size are encapsulated efficiently in a 1:1 mixture of two commercial 3000 Da poly(ethylene glycol) derivatives with two different reactive groups (amino and carboxylic groups). The water-dispersible UCNCs are non-cytotoxic, stable in the physiological environment, and present free ami…

NanoparticleSuccinimideslanthanides; nanocrystals; nanoparticles; polymersCatalysislaw.inventionPolyethylene Glycolschemistry.chemical_compoundFluoridesDynamic light scatteringnanocrystalsConfocal microscopylawOrganic chemistryReactivity (chemistry)lanthanidesYttriumpolymerschemistry.chemical_classificationMolecular StructureOrganic ChemistryGeneral ChemistryPolymerCombinatorial chemistrychemistryCovalent bondNanoparticlesAmine gas treatingEthylene glycolChemistry (Weinheim an der Bergstrasse, Germany)
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Polynitrile anions as ligands: From magnetic polymeric architectures to spin crossover materials

2010

International audience; The use of polynitrile anions as ligands (L) either alone or in combination with neutral co-ligands (L′) is a very promising and appealing strategy to get molecular architectures with different topologies and dimensionalities thanks to their ability to coordinate and bridge metal ions in many different ways. The presence of several potentially coordinating nitrile groups (or even other donor groups as –OH, –SH or –NH2), their rigidity and their electronic delocalization allow the synthesis of original magnetic high dimensional coordination polymers with transition metals ions. Furthermore, these ligands have shown coordinating and bridging capabilities in novel discr…

NitrileMetal ions in aqueous solutionMetal(II) complexesInorganic chemistry[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesCoordination complexInorganic ChemistryDelocalized electronchemistry.chemical_compoundTransition metalSpin crossoverMagnetic propertiesMagnetic transitionMaterials Chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistrychemistry.chemical_classificationThermochromismThermochromism010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryPolymer0104 chemical sciencesCoordination polymersCrystallographyPolynitrilechemistryStructural transitionNitrile ligandCyano ligand
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Magneto-structural and theoretical study of the weak interactions in a Mn(II) complex with a very unusual N,O-chelating coordination mode of 2-aminot…

2017

International audience; The Mn(II) complex {[Mn(atpa)(H2O)2]·H2O}n (1),with the dicarboxylate ligand 2-aminoterephthalic acid (H2atpa), has been synthesized and crystallographically, spectroscopically and magnetically characterized. Complex 1 shows a very unusual 1κ2N,O coordination mode of the aminoterephthalate dianion with the Mn(II) ion. One of the carboxylate groups shows a syn-anti-μ2-η1:η1 binding mode to form a 2D square grid. The magnetic properties of this compound can be very well reproduced with a regular S = 5/2 chain model with a very weak antiferromagnetic coupling constant of J = −0.2 cm−1 through the single syn-anti carboxylate bridges. EPR measurement also supports the exp…

Noncovalent interactionsDihedral angle010402 general chemistry01 natural scienceslaw.inventionIonHydrogen bondsInorganic Chemistrychemistry.chemical_compoundlawComputational chemistryMaterials Chemistry[CHIM.CRIS]Chemical Sciences/CristallographyNon-covalent interactions[CHIM]Chemical SciencesChelationCarboxylatePhysical and Theoretical ChemistryElectron paramagnetic resonancechemistry.chemical_classification010405 organic chemistryHydrogen bondLigand0104 chemical sciencesCoordination polymersCrystallographyDensity functional calculationschemistryπ-Interactions
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