Search results for "Reactivity"

showing 10 items of 880 documents

Reversible coordination of dioxygen by tripodal tetraamine copper complexes incorporated in a porous silica framework.

2010

The present study reports the synthesis and rational design of porous structured materials by using a templating method. A tetraethoxysilylated tripodal tetraamine (TREN) was covalently incorporated in a silica framework with a double imprint: A surfactant template and a metal ion imprint. The presence of a cationic surfactant (CTAB) endowed the material with a high porosity, and the tripodal or square-pyramidal topology of the ligand was preserved thanks to the use of the silylated Cu(II) complex. After removal of the surfactant and de-metalation, the incorporated tetraamine was quantitatively complexed by CuCl(2) and the material has shown after thermal activation that a reversible bindin…

Carbon MonoxideSilicon dioxideLigandNitrogenMetal ions in aqueous solutionOrganic ChemistryInorganic chemistryCationic polymerizationElectron Spin Resonance Spectroscopychemistry.chemical_elementGeneral ChemistrySilicon DioxideCopperCatalysisAdductOxygenchemistry.chemical_compoundchemistryCoordination ComplexesTripodal ligandPolymer chemistryReactivity (chemistry)AminesPorosityCopperChemistry (Weinheim an der Bergstrasse, Germany)
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Effect of electron-withdrawing substituents on the electrophilicity of carbonyl carbons

2005

Indexación: Scopus The substituent effects on the carbonyl carbon atom for a series of twelve substituted phenyl acetates have been rationalized using a global electrophilicity index. This index is linearly correlated with the experimental reaction rate coefficients. We found that, in contrast to the proposed interpretation based on experimental 13C NMR chemical shifts and ground state destabilization calculations, the electrophilicity of carbonyl compounds increases due to the effect promoted by electron-withdrawing groups in these systems. https://www.sciencedirect.com/science/article/pii/S0040402004018046?via%3Dihub

Carbon atomChemistryChemical shiftOrganic ChemistrySubstituentcarbonyl derivativecarbonylCarbon-13 NMRcarbon nuclear magnetic resonancePhotochemistryDFT calculationsBiochemistryMedicinal chemistryParrReaction rateElectron-withdrawing effectschemistry.chemical_compoundElectronegativityDrug DiscoveryElectrophilePolar effectChemical Reactivityphenylacetic acid derivativeElectrophilicityGround state
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Carbon Nanostructures: Covalent and Macromolecular Chemistry

2012

The aim of this introductory chapter is to bring to the attention of the readers the achievements made in the chemistry of carbon nanostructures and, mostly, in the chemistry of fullerenes, carbon nanotubes (CNTs), and the most recent graphenes. Since the discovery of fullerenes in 1985 and their further preparation in multigram amounts, the chemistry and reactivity of thesemolecular carbon allotropes have been well established. Actually, this chemical reactivity has been used as a benchmark for further studies carried out in the coming carbon nanotubes (single andmultiple wall) and graphenes. Assuming that the fundamental chemistry of fullerenes is known and basically corresponds to that o…

Carbon nanostructuresMaterials scienceFullereneSupramolecular chemistrychemistry.chemical_elementCarbon nanotubelaw.inventionchemistrylawCovalent bondPolymer chemistrySurface modificationReactivity (chemistry)CarbonSupramolecular Chemistry of Fullerenes and Carbon Nanotubes
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Selective photocatalytic oxidation of 5-hydroxymethyl-2-furfural in aqueous suspension of polymeric carbon nitride and its adduct with H2O2 in a sola…

2018

Abstract This work reports a study on the reactivity of polymeric carbon nitride (PCN) and PCN-H2O2 adduct samples for sunlight photocatalytic selective oxidation reactions. The characterization of these materials was reported in a previous paper where the reactivity towards the partial oxidation of 5-hydroxymethylfurfural (HMF) was studied by using two different laboratory scale photoreactors; one irradiated by UV lamps and the other one by natural sunlight. In the present study it has been confirmed the effectiveness of these C3N4 based materials for the selective partial oxidation of HMF to FDC (2,5-furandicarboxaldehyde) in aqueous medium in a pilot plant photoreactor irradiated by natu…

Carbon nitrideoxidation010402 general chemistry01 natural sciencesCatalysisAdductCatalysisBenzaldehydechemistry.chemical_compoundReaction rate constantBenzyl alcoholReactivity (chemistry)Partial oxidation4-Methoxy-benzyl alcohol010405 organic chemistryGeneral Chemistry0104 chemical scienceschemistryBenzyl alcoholSolar photocatalysis25-FurandicarboxaldehydePhotocatalysisSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie5-Hydroxymethyl-2-furfuralSelective photocatalyticNuclear chemistry
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Chemistry and reactivity of dinuclear manganese oxamate complexes: Aerobic catechol oxidation catalyzed by high-valent bis(oxo)-bridged dimanganese(I…

2006

[EN] The high-valent bis(oxo)-bridged dimanganese(IV) complexes with the series of binucleating 4.5-X-2-o-phenylenebis(oxamate) ligands (opbaX(2); X = H, Cl, Me) (1a-c) have been synthesized and characterized structurally, spectroscopically and magnetically. Complexes la-c possess unique Mn-2(mu-O)(2) core structures with two o-phenylenediamidate type additional bridges which lead to exceptionally short Mn-Mn distances (2.63-2.65 angstrom) and fairly bent Mn-O-Mn angles (94.1 degrees-94.6 degrees). The cyclovoltammograms of la-c in acetonitrile (25 degrees C, 0.1 M Bu4NPF6) show an irreversible one-electron oxidation peak at moderately high anodic potentials (E-ap = 0.50-0.85 V versus SCE),…

CatecholManganeseLigandStereochemistryProcess Chemistry and TechnologyCatecholschemistry.chemical_elementElectron donorManganeseMedicinal chemistryCatalysisQuinonechemistry.chemical_compoundHomologous serieschemistryO-O Bond activationOxidationsFISICA APLICADAReactivity (chemistry)Physical and Theoretical ChemistryAcetonitrileRedox properties
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Powerful Fluoroalkoxy Molybdenum(V) Reagent for Selective Oxidative Arene Coupling Reaction

2013

We introduce the novel fluoroalkoxy molybdenum(V) reagent 1 which has superior reactivity and selectivity in comparison to MoCl5 or the MoCl5 /TiCl4 reagent mixture in the oxidative coupling reactions of aryls. Common side reactions, such as chlorination and/or oligomer formation, are drastically diminished creating a powerful and useful reagent for oxidative coupling. Theoretical treatment of the reagent interaction with 1,2-dimethoxybenzene-type substrates indicates an inner-sphere electron transfer followed by a radical cationic reaction pathway for the oxidative-coupling process. EPR spectroscopic and electrochemical studies, X-ray analyses, computational investigations, and the experim…

Cationic polymerizationGeneral ChemistryPhotochemistryCombinatorial chemistryOligomerCatalysisCoupling reactionchemistry.chemical_compoundElectron transferchemistryReagentReactivity (chemistry)Oxidative coupling of methaneSelectivityAngewandte Chemie International Edition
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Exceptional affinity of nanostructured organic-inorganic hybrid materials towards dioxygen: confinement effect of copper complexes

2007

We report the exceptional reactivity towards dioxygen of a nanostructured organic-inorganic hybrid material due to the confinement of copper cyclam within a silica matrix. The key step is the metalation reaction of the ligand, which can occur before or after xerogel formation through the sol-gel process. The incorporation of a Cu(II) center into the material after xerogel formation leads to a bridged Cu(I)/Cu(II) mixed-valence dinuclear species. This complex exhibits a very high affinity towards dioxygen, attributable to auto-organization of the active species in the solid. The remarkable properties of these copper complexes in the silica matrix demonstrate a high cooperative effect for O(2…

Cations DivalentMetalationInorganic chemistrychemistry.chemical_elementLigands010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundAdsorptionHeterocyclic CompoundsCyclamPolymer chemistryOrganometallic CompoundsLamellar structureReactivity (chemistry)ComputingMilieux_MISCELLANEOUSdioxygen bindingBinding Sites010405 organic chemistryLigandsol-gel processesSpectrum AnalysisOrganic ChemistryTemperatureGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistrySilicon DioxideCopperEnzymesNanostructuresPeroxides0104 chemical sciencesOxygenchemistrytetraazamacrocyclesMultiprotein Complexescopper[ CHIM.MATE ] Chemical Sciences/Material chemistryAnisotropyAdsorptionHybrid materialGelsorganic-inorganic hybrid composites
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Natural fluorapatite as a raw material for Portland clinker

2018

Abstract The present work focuses on the mineralogy and the reactivity of clinkers made from the integration of natural fluorapatite in the raw meals with percentages ranging from 0 up to15%. The samples were characterized by infrared spectrometry, X-ray diffraction and microscopy techniques. The distribution of phosphorous and fluorine into clinkers minerals was determined by MEB/EDS mapping. The mineralogical composition was determined by XRD/Rietveld and the samples reactivity followed by isothermal microcalorimetry. It has been found that fluorine stabilizes C3S and β-C2S which still are found with high levels of P2O5. Cements obtained from up to 8% natural fluorapatite incorporation st…

CementIsothermal microcalorimetryMaterials scienceMetallurgyFluorapatite0211 other engineering and technologieschemistry.chemical_elementInfrared spectroscopy02 engineering and technologyBuilding and ConstructionRaw material021001 nanoscience & nanotechnologyClinker (cement)chemistry021105 building & constructionFluorineGeneral Materials ScienceReactivity (chemistry)0210 nano-technologyCement and Concrete Research
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Does phosphorus affect the industrial Portland cement reactivity?

2018

Abstract The effect of phosphorous on the mineralogy and reactivity of Portland cement has been investigated through an industrial clinkers series. The samples were collected from the same Tunisian cement plant and classified according to the content of P2O5 from 0.5% to 1.1%. All samples were manufactured at the same thermal and cooling conditions as well as possible. The specimens were characterized by X-ray fluorescence spectrometry and optical microscopy techniques and their mineralogy was determined by X-ray powder diffraction coupled to the Rietveld analysis. The cements reactivity prepared from the clinkers was followed by means of isothermalcalorimetry. The compressive strength of t…

CementMaterials scienceRietveld refinementPhosphorusMetallurgy0211 other engineering and technologiesFluorescence spectrometrychemistry.chemical_element02 engineering and technologyBuilding and Construction021001 nanoscience & nanotechnologylaw.inventionPortland cementCompressive strengthchemistrylaw021105 building & constructionGeneral Materials ScienceReactivity (chemistry)0210 nano-technologyPowder diffractionCivil and Structural EngineeringConstruction and Building Materials
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Nonlocal (Pair Site) Reactivity from Second-Order Static Density Response Function:  Gas- and Solution-Phase Reactivity of the Acetaldehyde Enolate a…

1999

A nonlocal (pair site) reactivity scheme is developed and tested. The theory is cast in terms of the first-order Fukui response function f(r,r‘), previously proposed by Fuentealba and Parr [J. Chem. Phys. 1991, 94, 5559]. A change of variables is introduced by using the softness s(r) and t(r) = [∂s(r)/∂N]υ(r) (the variation of softness with respect to the changes in the total number of electrons N at constant external potential υ(r)) that leads to a simple expression for the variation of the Fukui function at site k, namely = − for an electrophilic attack. The first term describes a local contribution, proportional to the variation of the electrostatic potential that can be induced, for exa…

Change of variables (PDE)Computational chemistryChemistryOrder (group theory)ThermodynamicsReactivity (chemistry)ElectronFunction (mathematics)Physical and Theoretical ChemistryConstant (mathematics)Fukui functionVariable (mathematics)The Journal of Physical Chemistry A
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