Search results for "C-S"

showing 10 items of 151 documents

Ovine Carotid Artery-Derived Cells as an Optimized Supportive Cell Layer in 2-D Capillary Network Assays

2014

PLoS one 9(3), e91664 (2014). doi:10.1371/journal.pone.0091664

Vascular Endothelial Growth Factor APathologyCellBecaplerminlcsh:MedicineCardiovascularUmbilical veinUmbilical CordDrug DiscoveryMolecular Cell BiologyBiological Systems EngineeringMyocyteCardiovascular Imaginglcsh:ScienceMultidisciplinaryProto-Oncogene Proteins c-sisAnimal ModelsFlow CytometryEndothelial stem cellBevacizumabmedicine.anatomical_structureCarotid ArteriesMonoclonalMedicineImmunohistochemical AnalysisResearch ArticleBiotechnologymedicine.medical_specialtyCell typeDrugs and DevicesDrug Research and DevelopmentMyocytes Smooth MuscleImmunologyBiomedical EngineeringBioengineeringBiologyAntibodies Monoclonal HumanizedCell LineModel OrganismsVascular Biologymedicine.arterymedicineAnimalsHumansBiologySheeplcsh:REndothelial CellsFeeder CellsUmbilical arteryMolecular biologyVascular Endothelial Growth Factor Receptor-2Coculture TechniquesCapillariesCell cultureImmunologic Techniqueslcsh:QCytometry
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Ferromagnetic kinetic exchange interaction in magnetic insulators

2020

The superexchange theory predicts dominant antiferromagnetic kinetic interaction when the orbitals accommodating magnetic electrons are covalently bonded through diamagnetic bridging atoms/groups. Here we show that explicit consideration of magnetic and (leading) bridging orbitals, together with the electron transfer between the former, reveals a strong ferromagnetic kinetic exchange contribution. First principle calculations show that it is comparable in strength with antiferromagnetic superexchange in a number of magnetic materials with diamagnetic metal bridges. In particular, it is responsible for a very large ferromagnetic coupling ($-10$ meV) between the iron ions in a Fe$^{3+}$-Co$^{…

Work (thermodynamics)magneettiset ominaisuudetMaterials scienceelectronic-structurePhysics MultidisciplinaryFOS: Physical sciencesmagnetic couplingelektronitmagneettikentätKinetic energyteoriatORBITAL PHYSICSCondensed Matter - Strongly Correlated ElectronsCondensed Matter::Materials ScienceANTIFERROMAGNETISMHUBBARD-MODELPhysics - Chemical PhysicsSUPEREXCHANGE INTERACTIONSdensity functional theoryChemical Physics (physics.chem-ph)Condensed Matter - Materials SciencecomplexesScience & TechnologyStrongly Correlated Electrons (cond-mat.str-el)Condensed matter physicsCRYSTALmagnetic insulatorsPhysicsSUPERCONDUCTIVITYExchange interactionMaterials Science (cond-mat.mtrl-sci)transitionORDERhubbard-modelsuperexchange interactionsWannier function methodsELECTRONIC-STRUCTUREFerromagnetismPhysical SciencesCondensed Matter::Strongly Correlated ElectronsCOMPLEXESTRANSITION
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Impact of small organic molecules on the nucleation of calcium silicate hydrate

2021

Superplasticizers are nowadays commonly employed in concrete to improve its workability and mechanical performance. They generally have the side effect of retarding the hydration of Portland cement which results from two simultaneous reactions: the dissolution of cement grains and the precipitation of cement hydrates. The mechanisms responsible for this retardation and thus delay the setting time of cement remain however largely unexplained. The present work intended to tackle this puzzle from the perspective of cement hydrate formation and employing four small organic molecules as model for superplasticizers. In particular, the impact of these organics on the homogeneous nucleation of calc…

[CHIM.OTHE] Chemical Sciences/OtherNucleationAdditivesAdditifsC-S-H
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Isotope Shifts of Radium Monofluoride Molecules

2021

Isotope shifts of $^{223-226,228}$Ra$^{19}$F were measured for different vibrational levels in the electronic transition $A^{2}{}{\Pi}_{1/2}\leftarrow X^{2}{}{\Sigma}^{+}$. The observed isotope shifts demonstrate the particularly high sensitivity of radium monofluoride to nuclear size effects, offering a stringent test of models describing the electronic density within the radium nucleus. Ab initio quantum chemical calculations are in excellent agreement with experimental observations. These results highlight some of the unique opportunities that short-lived molecules could offer in nuclear structure and in fundamental symmetry studies.

[PHYS.NUCL] Physics [physics]/Nuclear Theory [nucl-th]FIELD SHIFTNuclear TheoryAtomic Physics (physics.atom-ph)Ab initioGeneral Physics and AstronomyNUCLEAR-STRUCTUREnucl-ex01 natural sciencesPhysics - Atomic Physics010305 fluids & plasmasENERGYchemistry.chemical_compoundatomifysiikkaMOMENTSPhysics::Atomic PhysicsNuclear Experiment (nucl-ex)Nuclear ExperimentNuclear ExperimentPhysicsIsotopePhysicsNuclear structureradiumNuclear Physics - TheoryPhysical SciencesAtomic physicsydinfysiikkanucl-th[PHYS.NUCL]Physics [physics]/Nuclear Theory [nucl-th]Monofluoride[PHYS.NEXP] Physics [physics]/Nuclear Experiment [nucl-ex][PHYS.PHYS.PHYS-GEN-PH] Physics [physics]/Physics [physics]/General Physics [physics.gen-ph]Physics MultidisciplinaryOther Fields of PhysicsFOS: Physical sciences[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]physics.atom-phMolecular electronic transitionELECTRONIC-STRUCTURE CALCULATIONSNuclear Theory (nucl-th)ATOMS0103 physical sciencesMoleculeSPECTRANuclear Physics - ExperimentSensitivity (control systems)010306 general physicsisotoopitScience & Technology[PHYS.PHYS.PHYS-GEN-PH]Physics [physics]/Physics [physics]/General Physics [physics.gen-ph]chemistryMECHANICSMASS DEPENDENCELASERElectronic density
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Copper Dynamics and Impact on Microbial Communities in Soils of Variable Organic Status

2008

International audience; The effect of soil organic status on copper impact was investigated by means of a microcosm study carried out on a vineyard soil that had been amended with varying types of organic matter during a previous long-term field experiment. Soil microcosms were contaminated at 250 mg Cu kg−1 and incubated for 35 days. Copper distribution and dynamics were assessed in the solid matrix by a sequential extraction procedure and in the soil solution by measuring total and free exchangeable copper concentrations. Copper bioavailability was also measured with a whole-cell biosensor. Modifications of microbial communities were assessed by means of biomass-C measurements and charact…

[SDE] Environmental SciencesSEQUENTIAL EXTRACTIONRELATION SOL MICROORGANISME[SDV]Life Sciences [q-bio]010501 environmental sciences01 natural sciencesTOXICITY[ SDE ] Environmental SciencesSoilRNA Ribosomal 16SSoil PollutantsAGRICULTURAL SOILSDNA FungalSoil MicrobiologyTriticumComputingMilieux_MISCELLANEOUS2. Zero hungerchemistry.chemical_classificationCopper toxicity04 agricultural and veterinary sciencesCONTAMINATED SOILS6. Clean waterEnvironmental chemistryVINEYARD SOILS[SDE]Environmental SciencesBACTERIAL COMMUNITIESMicrocosmSoil microbiologyDNA BacterialSEWAGE-SLUDGEAmendmentchemistry.chemical_elementGENETIC-STRUCTUREcomplex mixturesmedicineEnvironmental ChemistryOrganic matter0105 earth and related environmental sciencesSTRUCTURE DU GENOMESPACER ANALYSIS FINGERPRINTSGeneral Chemistrymedicine.diseaseCopperBioavailabilitychemistryDENSITYSoil water040103 agronomy & agriculture0401 agriculture forestry and fisheriesCopper
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Lettre de rémission accordée par Charles V à Guiot le Beau...

1989

M. Le Moël; International audience

[SHS.HIST] Humanities and Social Sciences/HistoryPaléographie[SHS.HIST]Humanities and Social Sciences/HistoryActeFac-similé
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Study of parameters endogeneous and exogeneous to ordinary Portland ciment influencing hydration of its main phase : tricalcium silicate

2012

This work devoted to study various parameters influencing hydration of silicate phase main Ordinary Portland Cement (OPC) was performed at the Laboratoire Interdisciplinaire Carnot de Bourgogne (ICB). This study is part of the project "Crystal Growth Control" initiated by BASF in order to monitor and provide the best as possible the hydration of Ordinary Portland Cement. The dissolution of alite, like the pure C3S one, is fast in pure water. Speed decreases with deviation from equilibrium and the concentration of aluminates ions in solution. There is also an adsorption on the surface of the aluminum which is into the alite and released by dissolution. Germination and growth of C-S-H has bee…

[SPI.OTHER]Engineering Sciences [physics]/OtherInorganic saltsOrdinary Portland cement[ SPI.OTHER ] Engineering Sciences [physics]/OtherSilicate tricalcique[SPI.OTHER] Engineering Sciences [physics]/OtherHydratationTricalcium silicateHydrationCiment Portland OrdinaireCinétiqueKineticsSels inorganiquesAlite[CHIM.OTHE] Chemical Sciences/Other[ CHIM.OTHE ] Chemical Sciences/OtherCroissance C-S-HC-S-H GrowthAluminium[CHIM.OTHE]Chemical Sciences/OtherDissolution
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Etude expérimentale et modélisation thermodynamique du système CaO-SiO2-(Al2O3)-H2O

2012

The aim of this work is to build a thermodynamic model at 25°C to describe the main hydrates of ordinary Portland cement with or without supplementary cementitious materials (SCM) : calcium hydrosilicates. With high aluminium content, SCM in blended cements modify the nature and the composition of the hydrates of cement paste.The simplified model system CaO-SiO2-H2O was studied by synthesising of C-S-H with identical protocol and analysis. We distinguished, hydration solutions undersaturated and supersaturated from Portlandite.This last system has been extended to CaO-Al2O3-SiO2-H2O system. Then, we determined the most suitable protocol to synthesize pure C-A-S-H.The nanoparticular nature a…

[SPI.OTHER]Engineering Sciences [physics]/OtherSolubilité[ SPI.OTHER ] Engineering Sciences [physics]/Other[SPI.OTHER] Engineering Sciences [physics]/OtherC-A-S-HStructureNo english keywordCimentThermodynamiqueC-S-HSCM[CHIM.OTHE] Chemical Sciences/OtherModélisation[ CHIM.OTHE ] Chemical Sciences/OtherAluminium[CHIM.OTHE]Chemical Sciences/Other
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Electrochemistry of Bis(pyridine)cobalt (Nitrophenyl)corroles in Nonaqueous Media

2018

International audience; A series of bis(pyridine)cobalt corroles with one or three nitrophenyl groups on the meso positions of the corrole macrocycle were synthesized and characterized as to their electrochemical and spectroscopic properties in dichloromethane, benzonitrile, and pyridine. The potentials for each electrode reaction were measured by cyclic voltammetry and the electron-transfer mechanisms evaluated by analysis of the electrochemical data combined with UV-visible spectra of the neutral, electroreduced, and electroxidized forms of the corroles. The proposed electronic configurations of the initial compounds and the prevailing redox reactions involving the electroactive central c…

[SPI.OTHER]Engineering Sciences [physics]/Otherelectronic-structuremanganese corroleschemistry.chemical_element[CHIM.INOR]Chemical Sciences/Inorganic chemistryConjugated system010402 general chemistryElectrochemistry01 natural sciencesInorganic Chemistryporphyrin-corrole dyadschemistry.chemical_compoundcopper corroleswater-oxidationPyridinePolymer chemistryacid-media[CHIM]Chemical Sciencesaryl-substituted corrolesredox potentialsPhysical and Theoretical ChemistryCorrole010405 organic chemistry0104 chemical sciencesSolventBenzonitrilechemistrystructural-characterizationefficient synthesisCyclic voltammetryCobaltInorganic Chemistry
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Palladium-catalyzed heteroaryl thioethers synthesis overcoming palladium dithiolate resting states inertness: Practical road to sulfones and NH-sulfo…

2018

International audience; We provide efficient synthetic access to heteroaryl sulfones in two-steps using a simple palladium-1,1'-bis [(diphenyl)phosphanyl]ferrocene catalyst to form in high yields variously functionalized heteroaromatic thioethers. Pyridinyl-containing substrates can be subsequently selectively oxidized into sulfones and NH-sulfoximines by using very mild oxidation conditions with a high functional group tolerance. In the palladium catalyzed C-S coupling of heteroaromatic thiols, reactivity limitation is attached with electron-deficient thiols. We show that this limitation can be resolved by the successful use of 2-bromoheteroarenes in the C-S coupling. We established herein…

bond formationarenessulfideschemistry.chemical_element010402 general chemistry01 natural sciencesCatalysisefficientCatalysischemistry.chemical_compounds-arylation[CHIM]Chemical SciencesReactivity (chemistry)SulfonesResting statethiols[PHYS]Physics [physics]010405 organic chemistryProcess Chemistry and TechnologyGeneral Chemistryindolesacid saltsCombinatorial chemistry0104 chemical sciencesThiolatesC-S couplingchemistryFerroceneNH-sulfoximinesReagentElectrophileFunctional groupH functionalizationdirecting groupPalladiumStoichiometryPalladiumCatalysis Communications
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