Search results for "Surfaces"

showing 10 items of 2837 documents

Manganese carbonyl terpyridyl complexes: their synthesis, characterization and potential application as CO-release molecules

2014

MnI carbonyl terpyridyl complexes have been synthesized and characterized. The tricarbonyl derivative exhibits interesting behaviors for controlled CO-release by both thermal and photosynthetic pathways.

Carbon MonoxideManganeseLightMetals and Alloyschemistry.chemical_elementGeneral ChemistryManganesePhotosynthesisPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCharacterization (materials science)chemistry.chemical_compoundchemistryCoordination ComplexesMaterials ChemistryCeramics and CompositesMolecule[CHIM]Chemical SciencesCo releaseta116Derivative (chemistry)ComputingMilieux_MISCELLANEOUSChemical Communications
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Reversible switching of the electronic ground state in a pentacoordinated Cu(ii) complex.

2013

International audience; An easy reversible switching of the electronic ground state in a pentacoordinated copper(ii) complex is reported for the first time. The simple protonation of a carboxylic group in a Cu(ii) complex with a {dx(2)-y(2)}(1) electronic configuration leads to a flip of the ground electronic configuration from {dx(2)-y(2)}(1) to {dz(2)}(1) in the metal ion.

Carboxylic groupMolecular Conformationchemistry.chemical_elementInorganic compoundsElectronsProtonationCrystallography X-Ray010402 general chemistry01 natural sciencesCatalysisMetalCoordination ComplexesComputational chemistryElectronic ground stateMaterials Chemistry010405 organic chemistryChemistryMetals and AlloysGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistryCopper3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsReversible switchingvisual_artCeramics and Compositesvisual_art.visual_art_mediumQuantum TheoryPhysical chemistryElectron configurationGround stateCopper
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Stereoselective construction of the tetracyclic scalarane skeleton from carvone

1999

The tetracyclic scalarane skeleton 22 has been constructed from (S)-(+)-carvone using two intramolecular Diels–Alder reactions as key synthetic steps. Abad Somovilla, Antonio, Antonio.Abad@uv.es ; Agullo Blanes, M Consuelo, Consuelo.Agullo@uv.es ; Cuñat Romero, Ana Carmen, Ana.Cunat@uv.es ; Llosa Blasco, Maria Carmen, Carmen.Llosa@uv.es

CarvoneSynthetic stepsStereochemistryChemistryUNESCO::QUÍMICA:QUÍMICA::Química orgánica [UNESCO]Metals and AlloysGeneral ChemistrySkeleton (category theory)Carvone:QUÍMICA [UNESCO]CatalysisStereoselective TetracyclicStereoselective Tetracyclic ; Carvone ; Diels-Alder reactiones ; Synthetic stepsSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundIntramolecular forceDiels-Alder reactionesMaterials ChemistryCeramics and CompositesOrganic chemistryStereoselectivityUNESCO::QUÍMICA::Química orgánica
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Mixed Ligand Shell Formation upon Catechol Ligand Adsorption on Hydrophobic TiO2 Nanoparticles

2019

Modifying the surfaces of metal oxide nanoparticles (NPs) with monolayers of ligands provides a simple and direct method to generate multifunctional coatings by altering their surface properties. T...

CatecholChemistryLigandTio2 nanoparticlesShell (structure)02 engineering and technologySurfaces and InterfacesMetal oxide nanoparticlesMixed ligand010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical scienceschemistry.chemical_compoundAdsorptionChemical engineeringMonolayerElectrochemistryGeneral Materials Science0210 nano-technologySpectroscopyLangmuir
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Linking Electrostatic Effects and Protein Motions in Enzymatic Catalysis. A Theoretical Analysis of Catechol O-Methyltransferase

2014

The role of protein motions in enzymatic catalysis is the subject of a hot scientific debate. We here propose the use of an explicit solvent coordinate to analyze the impact of environmental motions during the reaction process. The example analyzed here is the reaction catalyzed by catechol O-methyltransferase, a methyl transfer reaction from S-adenosylmethionine (SAM) to the nucleophilic oxygen atom of catecholate. This reaction proceeds from a charged reactant to a neutral product, and then a large electrostatic coupling with the environment could be expected. By means of a two-dimensional free energy surface, we show that a large fraction of the environmental motions needed to attain the…

CatecholSubstrate (chemistry)ProteinsElectrostatic couplingCatalysisSurfaces Coatings and FilmsEnzyme catalysisCatalysisEnzymesSolventchemistry.chemical_compoundElectrostatic effectNucleophilechemistryComputational chemistryScientific methodMaterials ChemistryPhysical chemistryTransmission coefficientPhysical and Theoretical ChemistryProteïnesFisicoquímica
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Discovery of new G-quadruplex binding chemotypes

2013

We report here on the discovery and preliminary evaluation of a novel non-macrocyclic low molecular weight quadruplex-stabilizing chemotype. The lead compounds, based on a furan core, show high G-quadruplex stabilisation and selectivity as well as potent in vitro anti-proliferative activity.

Cell SurvivalAntineoplastic Agents010402 general chemistryG-quadruplex01 natural sciencesArticleCatalysis03 medical and health scienceschemistry.chemical_compoundCell Line TumorFuranMaterials ChemistryHumansheterocyclic compoundsFuransCell survival030304 developmental biologyG quadruplex binding0303 health sciencesG-quadruplexChemotypeChemistryCircular DichroismMetals and AlloysGeneral ChemistryCombinatorial chemistryIn vitro3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsG-QuadruplexesCeramics and CompositesSelectivityChem. Commun.
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Nanoscale Mapping of the Physical Surface Properties of Human Buccal Cells and Changes Induced by Saliva

2019

International audience; The mucosal pellicle, also called salivary pellicle, is a thin biological layer made of salivary and epithelial constituents, lining oral mucosae. It contributes to their protection against microbiological, chemical, or mechanical insults. Pellicle formation depends on the cells’ surface properties, and in turn the pellicle deeply modifies such properties. It has been reported that the expression of the transmembrane mucin MUC1 in oral epithelial cells improves the formation of the mucosal pellicle. Here, we describe an approach combining classical and functionalized tip atomic force microscopy and scanning microwave microscopy to characterize how MUC1 induces change…

Cell typeSalivaSurface Properties[SDV]Life Sciences [q-bio]Cellhuman buccal cells02 engineering and technology010402 general chemistry01 natural sciences[SPI]Engineering Sciences [physics]MicroscopyElectrochemistrymedicineElectric ImpedanceHumansNanotechnologyGeneral Materials ScienceSpectroscopyMUC1hydrophobicity[PHYS]Physics [physics]MouthsalivaChemistryMucinSurfaces and Interfaces021001 nanoscience & nanotechnologyCondensed Matter PhysicsTransmembrane protein0104 chemical sciencesScanning Microwave Microscopy SMMmedicine.anatomical_structureChemical force microscopydielectric propertiesBiophysicsChemical Force Microscopyfuntionalization0210 nano-technologyHydrophobic and Hydrophilic Interactions
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Design of enzyme-mediated controlled release systems based on silica mesoporous supports capped with ester-glycol groups

2012

[EN] An ethylene glycol-capped hybrid material for the controlled release of molecules in the presence of esterase enzyme has been prepared. The final organic-inorganic hybrid solid S1 was synthesized by a two-step procedure. In the first step, the pores of an inorganic MCM-41 support (in the form of nanoparticles) were loaded with [Ru(bipy) 3]Cl 2 complex, and then, in the second step, the pore outlets were functionalized with ester glycol moieties that acted as molecular caps. In the absence of an enzyme, release of the complex from aqueous suspensions of S1 at pH 8.0 is inhibited due to the steric hindrance imposed by the bulky ester glycol moieties. Upon addition of esterase enzyme, del…

Cell viabilityINGENIERIA DE LA CONSTRUCCIONEthyleneRuthenium complexesMCM-41 supportsCytotoxicityGlycol derivativesEsteraseFunctionalizedOrganic-inorganic hybrid solidsGlycolschemistry.chemical_compoundQUIMICA ORGANICATumor Cells CulturedElectrochemistryControlled release systemsOrganic chemistryControlled releaseGeneral Materials ScienceSteric hindrancesMCF-7 cellsSpectroscopyHydrolysisEsterasesSilicaEstersSurfaces and InterfacesSilicon DioxideCondensed Matter PhysicsControlled releaseChlorine compoundsEster bondsBody fluidsHybrid materialsHybrid materialPorosityCell deathCell SurvivalSurface PropertiesCytotoxic drugsRutheniumHydrolysisEnzymatic hydrolysisEsterase enzymesPolymer chemistryHumansCamptothecin (CPT)Molecular capSize reductionsTherapeutic ApplicationEthylene glycolTwo-step procedureEsterificationSuspensions (fluids)Ruthenium compoundsQUIMICA INORGANICAMesoporous supportOligo(ethylene glycol)Cell internalizationMolecular gatesConfocal microscopychemistryEnzymatic hydrolysisEnzyme-mediated hydrolysisNanoparticlesCamptothecinCell cultureMesoporous materialAqueous suspensionsEthylene glycolHeLa Cells
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Electrokinetic Properties which Control the Coagulation of Silicate Cement Suspensions during Early Age Hydration

1998

The coagulation of cement particles during early age hydration has been previously identified as the first step of the setting and hardening of cement pastes. By hydrating Ca3SiO5and a silicate-rich clinker under controlled conditions, a correlation between the coagulation of the suspensions and the electrokinetic properties of particles is established. The zeta potential, and hence the surface charge, of particles in suspension depends on the calcium content of the medium. At low concentrations of Ca2+, the zeta potential of Ca3SiO5particles, calcium silicate hydrate (C–S–H), and clinker is negative (<−30 mV) and the suspensions are well dispersed. A strong coagulation occurs at intermedia…

CementChemistryMineralogySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundElectrokinetic phenomenaColloid and Surface ChemistryChemical engineeringParticle-size distributionHardening (metallurgy)Zeta potentialSilicate CementSurface chargeCalcium silicate hydrateJournal of Colloid and Interface Science
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Surface Relaxivity of Cement Hydrates

2014

Numerous aspects of the physical chemistry of colloidal systems are conditioned by the solid–liquid interface, and this is also the case for hydrated cement systems. Estimating the surface area is thus essential for studying the kinetics of cement hydration and admixture adsorption. Proton nuclear magnetic resonance (NMR) relaxation techniques have already proven useful for this objective, but, for hydrating cements at early ages, it is necessary to know the surface relaxivities of all of the individual phases present to correctly interpret the relaxation data. This paper reports the results of a comparison of NMR relaxometry and Brunauer–Emmett–Teller gas adsorption measurements on various…

CementEttringiteRelaxometryMaterials scienceRelaxation (NMR)Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsColloidchemistry.chemical_compoundParamagnetismGeneral EnergyAdsorptionChemical engineeringchemistryProton NMRPhysical and Theoretical ChemistryThe Journal of Physical Chemistry C
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