Search results for "Material chemistry"

showing 10 items of 413 documents

Effect of temperature and ligand protonation on the electronic ground state in Cu( ii ) polymers having unusual secondary interactions: a magnetic an…

2018

International audience; Two new copper(II) polymeric complexes, {[Cu(HPymat)(H2O)](NO3)}n (1) and [Cu2(Pymat)2(H2O)3]n (2), have been synthesized using the Schiff base ligand H2Pymat [H2Pymat = (E)-2-(1-(pyridin-2-yl)-methyleneamino)terephthalic acid]. Complex 1 is a cationic 1D polymer, whereas complex 2 is a two dimensional polymer. Both complexes were crystallographically, spectroscopically and magnetically characterized. Theoretical studies were performed and the catecholase activity of the complexes was also examined. Complex 1 is a ferromagnetically coupled complex with J = 2.8 cm−1 and 2 shows antiferromagnetic coupling with J = −1.6 cm−1. Both complexes show notable features in the …

Models MolecularPolymerschemistry.chemical_elementProtonation010402 general chemistryCrystallography X-RayLigands01 natural scienceslaw.inventionInorganic Chemistrychemistry.chemical_compoundlawCoordination ComplexesMolecule[CHIM]Chemical SciencesElectron paramagnetic resonanceSchiff baseMolecular Structure010405 organic chemistryLigandMagnetic PhenomenaTemperatureTwo-dimensional polymer[CHIM.MATE]Chemical Sciences/Material chemistryHydrogen-Ion ConcentrationCopper0104 chemical sciencesCrystallography[CHIM.POLY]Chemical Sciences/PolymerschemistryQuantum TheoryProtonsGround stateCatechol OxidaseCopper
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Exploring the redox reactivity of magnesium porphine. Insight into the origins of electropolymerisation.

2010

International audience; Magnesium(II) porphine, MgP (1), was synthesised according to the Lindsey procedure allowing to isolate and crystallise 1-formyldipyrromethane (2) as a synthetic intermediate. Unprecedented Xray diffraction studies revealed multiple intermolecular associations in the crystal between neighbouring units of 2, namely hydrogen bond and CH … π. The electrochemical behaviour of 1 was examined by means of cyclic voltammetry. In oxydation, two well-defined and distinct steps are assigned to macrocycle concerned electron transfers yielding initially the π-cation radical and π dication, respectively. The highly reactive dication condenses neutral magnesium porphine to form a d…

Models MolecularPorphyrinsInorganic chemistrychemistry.chemical_element010402 general chemistryElectrochemistryCrystallography X-Ray01 natural sciencesRedoxOligomerInorganic Chemistrychemistry.chemical_compound[CHIM.ANAL]Chemical Sciences/Analytical chemistryPolymer chemistryElectrochemistryOrganometallic Compounds[CHIM.COOR]Chemical Sciences/Coordination chemistryReactivity (chemistry)Magnesium[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryHydrogen bondChemistryMagnesiumHydrogen Bonding[CHIM.MATE]Chemical Sciences/Material chemistry0104 chemical sciencesDicationCyclic voltammetryOxidation-ReductionDalton transactions (Cambridge, England : 2003)
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The amorphous silica-liquid water interface studied by ab initio molecular dynamics (AIMD): local organization in global disorder

2014

International audience; The structural organization of water at a model of amorphous silica-liquid water interface is investigated by ab initio molecular dynamics (AIMD) simulations at room temperature. The amorphous surface is constructed with isolated, H-bonded vicinal and geminal silanols. In the absence of water, the silanols have orientations that depend on the local surface topology (i.e. presence of concave and convex zones). However, in the presence of liquid water, only the strong inter-silanol H-bonds are maintained, whereas the weaker ones are replaced by H-bonds formed with interfacial water molecules. All silanols are found to act as H- bond donors to water. The vicinal silanol…

Models MolecularProtonSurface Propertiesamorphous silicawatergeminal silanols02 engineering and technologyMolecular Dynamics Simulation010402 general chemistry01 natural sciencesAb initio molecular dynamicsComputational chemistryMoleculeGeneral Materials ScienceQuartzGeminalMolecular StructureChemistryab initio molecular dynamicsHydrogen Bonding[CHIM.MATE]Chemical Sciences/Material chemistrySilanes021001 nanoscience & nanotechnologyCondensed Matter PhysicsSilicon Dioxide0104 chemical sciencesAmorphous solidChemical physicsQuantum TheoryAmorphous silicaProtons0210 nano-technologyVicinal
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Bioinspired manganese(II) complexes with a clickable ligand for immobilisation on a solid support.

2014

International audience; Clickable ligands like N,N′-bis((pyridin-2-yl)methyl)prop-2-yn-1-amine (L1) and N-((1-methyl-1H-imidazol-2-yl)methyl)-N-(pyridin-2-ylmethyl)prop-2-yn-1-amine (L2) have been used to synthesise a series of manganese(II) complexes for grafting onto appropriate solid supports. These ligands mimic the 2-His-1-carboxylate facial chelation present in the active site of the manganese-dependent dioxygenase (MndD), while the alkyne side function allows grafting of the ligand onto an azido-functionalised support using “click chemistry” methodologies. Such synthetic analogues of the MndD crystallise in the solid state as double halide or pseudohalide-bridged dinuclear manganese(…

Models MolecularStereochemistryMolecular ConformationAlkynechemistry.chemical_elementManganese[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryCrystallography X-RayLigands01 natural scienceslaw.inventionDioxygenasesInorganic ChemistrylawCoordination ComplexesCatalytic DomainPolymer chemistryChelationElectron paramagnetic resonanceSolid-Phase Synthesis Techniqueschemistry.chemical_classificationManganesebiology010405 organic chemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryElectron Spin Resonance SpectroscopyActive site[CHIM.CATA]Chemical Sciences/Catalysis[CHIM.MATE]Chemical Sciences/Material chemistrySilicon Dioxide0104 chemical scienceschemistrySuperexchangebiology.proteinClick chemistryClick ChemistryDalton transactions (Cambridge, England : 2003)
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Spherical ordered mesoporous silicas and silica monoliths as stationary phases for liquid chromatography

2006

Ordered mesoporous silicas such as micelle-templated silicas (MTS) feature unique textural properties in addition to their high surface area (approximately 1000 m2/g): narrow mesopore size distributions and controlled pore connectivity. These characteristics are highly relevant to chromatographic applications for resistance to mass transfer, which has never been studied in chromatography because of the absence of model materials such as MTS. Their synthesis is based on unique self-assembly processes between surfactants and silica. In order to take advantage of the perfectly adjustable texture of MTS in chromatographic applications, their particle morphology has to be tailored at the microme…

Monolithic HPLC columnMaterials scienceAnalytical chemistryFiltration and Separation02 engineering and technology010402 general chemistryMolecular sieveMCM-4101 natural sciencesAnalytical Chemistrychemistry.chemical_compoundMCM-41Electrochromatography[CHIM.ANAL]Chemical Sciences/Analytical chemistrychemistry.chemical_classificationChromatographyChromatographySilica gelPolymer[CHIM.MATE]Chemical Sciences/Material chemistryMesoporous silica021001 nanoscience & nanotechnologyMonolithic silica0104 chemical scienceschemistryMCM-480210 nano-technologyMesoporous materialMesoporous silica
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Surface Charge Density and Electrokinetic Potential of Highly Charged Minerals: Experiments and Monte Carlo Simulations on Calcium Silicate Hydrate

2006

International audience; In this paper, we are concerned with the charging and electrokinetic behavior of colloidal particles exhibiting a high surface charge in the alkaline pH range. For such particles, a theoretical approach has been developed in the framework of the primitive model. The charging and electrokinetic behavior of the particles are determined by the use of a Monte Carlo simulation in a grand canonical ensemble and compared with those obtained through the mean field theory. One of the most common colloidal particles has been chosen to test our theoretical approach. That is calcium silicate hydrate (C−S−H) which is the main component of hydrated cement and is known for being re…

Monte Carlo methodAnalytical chemistryCharge density[CHIM.MATE]Chemical Sciences/Material chemistrySurfaces Coatings and Filmschemistry.chemical_compoundElectrophoresisGrand canonical ensembleElectrokinetic phenomena[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]chemistryMean field theoryChemical physics[ CHIM.MATE ] Chemical Sciences/Material chemistryMaterials ChemistrySurface charge[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Physical and Theoretical ChemistryCalcium silicate hydrate
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Elaboration of multimaterial optical fibers with electro-optical functionalities

2022

The emergence of multimaterials optical fibers is of tremendous technological interest in photonics to combine the remarkable properties of glasses with those of other materials such as metals or polymers in order to form a fully integrated fiber optical system with multiple functionalities. Among these hybrid fibers, the development of fibers combining both optical signal and simultaneous electrical transport function could bring alternative interesting solution in many fields such as telecommunications, medicine or sensing. The drawing of architectures merging electrical and optical features in a unique elongated wave-guiding structure will enable to develop electro-optical functionalitie…

MultimatériauxElectro-Optical properties[CHIM.MATE] Chemical Sciences/Material chemistryOptical fiberTelluriteKerr effectChalcogenidePropriétés électro-OptiquesMultimaterialEffet KerrFibre optiqueChalcogénure
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Development of high entropy tungsten-based alloys by powder metallurgy processes

2022

Although metallurgy is a very old research domain, many innovations are still being considered, such as the emergence of high-entropy alloys. These alloys, composed of at least three elements, are characterized by a chemical composition without a majority element and most of the time equimolar. Research in this field is very recent since the first studies concerning these alloys are from the early 2000s. The original chemical compositions of these alloys open the way to many possibilities to obtain unusual properties.In conjunction with these developments, powder metallurgy processes are expanding quickly because of the advantages they offer over more traditional techniques (foundry and for…

Métallurgie des poudres[CHIM.MATE] Chemical Sciences/Material chemistryPowder metallurgyAlliage à Haute EntropieHigh Entropy AlloySpark Plasma Sintering
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Consolidation and densification mechanisms of copper powder during Spark plasma sintering (SPS)

2015

Spark plasma sintering is a manufacturing process that leads to dense materials with fine microstructures. SPS combines heating and uniaxial load as well as the Hot Pressing (HP) process but the material is heated using a pulsed current. The phenomena occurring during SPS are not fully understood and are still an open point: -Which densification and consolidation mechanisms are involved during SPS? -Why is sintering by SPS more efficient than sintering by traditional ways such as HP? –Does electrical current modify the sintering mechanisms? The aim of this work is to answer these questions in the case of spherical copper powder (from 10 to 50 µm). Comparisons between SPS and HP were perform…

Métallurgie des poudres[CHIM.MATE] Chemical Sciences/Material chemistrySinteringPowder metallurgyFrittageHot PressingCuivreSPSCopper[PHYS.PHYS.PHYS-CHEM-PH] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]
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GraftFast Surface Engineering to Improve MOF Nanoparticles Furtiveness

2018

International audience; Controlling the outer surface of nanometric metal–organic frameworks (nanoMOFs) and further understanding the in vivo effect of the coated material are crucial for the convenient biomedical applications of MOFs. However, in most studies, the surface modification protocol is often associated with significant toxicity and/or lack of selectivity. As an alternative, how the highly selective and general grafting GraftFast method leads, through a green and simple process, to the successful attachment of multifunctional biopolymers (polyethylene glycol (PEG) and hyaluronic acid) on the external surface of nanoMOFs is reported. In particular, effectively PEGylated iron trime…

Nanoparticle02 engineering and technologyPolyethylene glycol[CHIM.THER]Chemical Sciences/Medicinal ChemistrySurface engineering010402 general chemistry01 natural sciencesBiomaterialschemistry.chemical_compoundAdsorptionPEG ratio[CHIM]Chemical SciencesGeneral Materials ScienceComputingMilieux_MISCELLANEOUSChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnologyGrafting0104 chemical sciencesChemical engineeringSurface modification0210 nano-technologySelectivityBiotechnology
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