Search results for "Reactivity"

showing 10 items of 880 documents

Study of the fuel/clad bonding of pressurized water reactors fuel rods

2017

Durability and integrity of materials used in nuclear power plants is a continuous concern of the nuclear power plant owners and developers. During the fuel irradiation in pressurised water reactors (PWR), the whole fuel-clad assembly is subjected to several irradiation-induced modifications. In particular, the fuel element expansion concomitant to the cladding creeping, leads to the contacting of both materials, allowing the oxidation of the inner side of the clad, locally at first, then tending to affect the overall cladding inner surface. At high burnup, a bonding of the fuel periphery with the metallic cladding can be observed, forming the fuel-clad bonding phenomenon, which conditions …

Zirconium alloysReactivityInterfacesCombustible nucléaireCladSolid state oxidationRéactivitéAlliages de Zirconium[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistryNuclear fuel[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryGaineOxydation en phase solide
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Zirconium, hafnium and yttrium complexes containing two linked amido— tetramethylcyclopentadienyl ligands: Synthesis, reactivity and molecular struct…

1998

Abstract Zirconium and hafnium complexes M(η5: η1−C5Me4SiMe2NR′)xCl(4−2x) (M = Zr, Hf; x = 1, 2; R′ = iPr, tBu) containing one or two linked amido-tetramethylcyclopentadienyl ligands C5Me4SiMe2NR′ have been synthesized by the reaction of the dilithium derivative Li2(C5Me4SiMe2NR′) with MCl4(THF)2. The crystal structure of the hafnium complex Hf(η5: η1−C5Me4SiMe2NiPr)2 has been determined by a single-crystal X-ray diffraction study and shows a C2-symmetric helical metallocene, in which the amido ligands are bonded as π-donor ligands with Hf—N bond lengths of 2.115(2) A. The isoelectronic heterobimetallic yttrium complex Li[Y(η5: η1−C5Me4SiMe2NCH2CH2OMe)2] reacts with phenylacetylene to give …

ZirconiumInorganic chemistrychemistry.chemical_elementYttriumCrystal structureInorganic ChemistryDilithiumchemistry.chemical_compoundCrystallographychemistryPhenylacetyleneMaterials ChemistryReactivity (chemistry)Physical and Theoretical ChemistryMetalloceneDerivative (chemistry)Polyhedron
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Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory

2018

Después de la primera clasificación de las reacciones 32CA en reacciones de tipo zw y pr, establecidas en el año 2014, la estructura y reactividad de los TACs más importantes utilizados en las reacciones 32CA ha sido completamente caracterizado en base a la MEDT propuesta recientemente. Entre la gran cantidad de trabajo desarrollado a lo largo de la presente tesis doctoral, se han seleccionado y discutido ocho publicaciones representativas, que permitieron caracterizar dos nuevos tipos de reactividad y consolidar la reactividad original de tipo zw. Así, dependiendo de las cuatro estructuras electrónicas diferentes de los TACs, es decir, pseudodiradical, pseudoradical, carbenoide y zwitterió…

[3+2] Cycloaddition ReactionsMolecular Electron Density TheoryMolecular MechanismsTheoretical Organic ChemistryOrganic Reactivity
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Perfluoroketene dithioacetals and perfluorodithiocarboxylic acid derivatives: Versatile tools for organofluorine synthesis

2007

Perfluoroketene dithioacetals are simple and versatile compounds that can be transformed into a large variety of trifluoromethyl derivatives, in particular aza- and thiaheterocycles, perhalodithiocrotonic esters, and fluorinated dithiol thiones. These unsaturated perfluorodithioesters and analogs give interesting polar cycloaddition reactions whose mechanism is strongly influenced by the fluorine substitution. This substitution plays an important role in the reactivity of saturated perfluorodithiocarboxylic acids as well. Except for the carbophilic addition of allyl Grignard reagents to perfluorocarboxamides, a domino thiophilic addition-fluoride elimination was the main reaction process. I…

[CHIM.MATE] Chemical Sciences/Material chemistryTrifluoromethyl010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistrychemistry.chemical_elementDithiolGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistry[CHIM.ORGA] Chemical Sciences/Organic chemistry01 natural sciencesCombinatorial chemistryDominoCycloaddition0104 chemical scienceschemistry.chemical_compoundchemistryCascade reactionReagentFluorineOrganic chemistryReactivity (chemistry)ComputingMilieux_MISCELLANEOUS
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Initial stages of metal oxides thin films growth by MOCVD: physicochemical characterisation of the film/substrate interface

2006

The initial stages of Metalorganic Chemical Vapour Deposition (MOCVD) of TiO2 thin films on Si(100) were studied in situ by surface analyses (XPS, ARXPS, AES). An original experimental set-up was built for this purpose and developed. Information obtained from these in situ experiments was completed by ex situ characterisations (HRTEM, SIMS, GIXRD...).The formation of an interfacial SiOy<2 layer resulting of the interaction of the precursor Ti(OCH(CH3)2)4 with the substrate takes place before the formation of stoichiometric TiO2 and leads to the presence of carbon at the interface. At the deposition temperature, 675 °C, silicon diffusion within the TiO2 external layer was also revealed. Conc…

[CHIM.MATE] Chemical Sciences/Material chemistryinterfacial reactivityin situ surface analysisARXPScrystalline structure[ CHIM.MATE ] Chemical Sciences/Material chemistryMOCVDTEMXPSstructure cristallineMETréactivité interfacialeanalyse de surfaces in situTiO2/Si
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Fabrication and characterization of barium silicate ultrathin films as an alternative gate oxide

2008

Down-scaling of elementary CMOS elements requires the replacement of SiO2 as a gate oxide. By the identification of the formation conditions of barium silicate in direct contact of a silicon substrate, this study revealed a potential candidate. First of all, a reaction between Ba and SiO2 leading to the formation of barium silicate as been evidenced by in-situ XPS and SR-PES analyses. Then, barium silicate films have been elaborated by oxygen and barium co-deposition at 580 °C. Thermal treatments under vacuum showed that barium silicate was thermally stable up to 900 °C. TEM and SIMS ex-situ analyses revealed a sharp interface with the substrate. Finally, an experimental setup dedicated to …

[CHIM.MATE] Chemical Sciences/Material chemistrysilicate de baryuminterfacial reactivity[ CHIM.MATE ] Chemical Sciences/Material chemistrybarium silicateXPS[CHIM.MATE]Chemical Sciences/Material chemistry[PHYS.COND]Physics [physics]/Condensed Matter [cond-mat]SR-PESréactivité interfaciale[PHYS.COND] Physics [physics]/Condensed Matter [cond-mat]high-k[ PHYS.COND ] Physics [physics]/Condensed Matter [cond-mat]
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Are hedonic responses to food odours linked to food liking in infants at 12 and 22 months?

2013

Communication orale (résumé 1 p.) ; http://www.pangborn2013.com/; International audience

[SDV.AEN] Life Sciences [q-bio]/Food and Nutritionolfactory reactivityodours[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutritionfood likingodourtoddlertoddlers[SDV.AEN]Life Sciences [q-bio]/Food and NutritionComputingMilieux_MISCELLANEOUS
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Variability in olfactory reactivity in 7-8 month-old infants

2006

To determine the origin of early food preference variability, an Observatory of Food Preference in Infants and Children (Opaline) was set up. One of its objectives is to relate hedonic reaction to odours to previous exposures (via amniotic fluid and/or breast milk) and to understand the role of hedonic reaction to odours on food rejections or preferences. To answer this question, we developed an instrument to measure and to compare olfactory reactivity in 7-8 month-old infants.

[SDV] Life Sciences [q-bio][SDE] Environmental Sciences[SPI.GPROC] Engineering Sciences [physics]/Chemical and Process Engineering[SDV]Life Sciences [q-bio][SDV.IDA]Life Sciences [q-bio]/Food engineering[SDE]Environmental SciencesOLFACTION[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringINFANT[SDV.IDA] Life Sciences [q-bio]/Food engineeringREACTIVITY
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Unveiling the Unexpected Reactivity of Electrophilic Diazoalkanes in [3+2] Cycloaddition Reactions within Molecular Electron Density Theory

2021

The [3+2] cycloaddition (32CA) reactions of strongly nucleophilic norbornadiene (NBD), with simplest diazoalkane (DAA) and three DAAs of increased electrophilicity, have been studied within the Molecular Electron Density Theory (MEDT) at the MPWB1K/6-311G (d,p) computational level. These pmr-type 32CA reactions follow an asynchronous one-step mechanism with activation enthalpies ranging from 17.7 to 27.9 kcal&middot

analytical_chemistryExergonic reactiondiazoalkanes010405 organic chemistryNorbornadienemolecular electron density theoryGeneral Medicine010402 general chemistry01 natural sciencesCycloadditionElectron localization function3. Good health0104 chemical scienceslcsh:Chemistrychemistry.chemical_compoundlcsh:QD1-999conceptual DFTchemistryNucleophileComputational chemistryelectron localization functionElectrophilenorbornadieneReactivity (chemistry)Acetonitrile
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Unveiling the Different Reactivity of Bent and Linear Three-Atom-Components Participating in [3 + 2] Cycloaddition Reactions

2021

The reactivity of a series of pairs of bent and linear three-atom-component (B-TACs and L-TACs) participating in [3 + 2] cycloaddition (32CA) reactions towards ethylene and electrophilic dicyanoethylene (DCE) have been studied within the Molecular Electron Density Theory. While the pseudodiradical structure of B-TACs changes to that of pseudoradical or carbenoid L-TACs upon dehydrogenation, zwitterionic B-TACs remain unchanged. Conceptual Density Functional Theory (CDFT) indices characterize five of the nine TACs as strong nucleophiles participating in polar reactions towards electrophilic ethylenes. The activation energies of the 32CA reactions with electrophilic DCE range from 0.5 to 22.0…

analytical_chemistry[3 + 2] cycloaddition reactionsOrganic chemistrychemical and pharmacologic phenomena010402 general chemistry01 natural sciencesQD241-441stomatognathic systemNucleophileComputational chemistrySingle bondReactivity (chemistry)skin and connective tissue diseasesCarbenoid010405 organic chemistryChemistrymolecular electron density theoryRegioselectivity16. Peace & justiceCycloaddition0104 chemical sciencesreactivitystomatognathic diseasesbent and linear three-atom-componentsregioselectivityElectrophileDensity functional theoryOrganics
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