Search results for "Mono"

showing 10 items of 6843 documents

Marginal and internal fit evaluation of conventional metal-ceramic versus zirconia CAD/CAM crowns

2019

Background The purpose of this in vivo study was to compare the marginal and internal gap widths of monolithic zirconia crowns fabricated by CAD/CAM technique and metal-ceramic crowns fabricated by conventional technique. Material and methods 10 participants needing a single restoration were selected. Zirconia crowns using CAD/CAM technology (Group A) (n=10) and metal-ceramic crowns (Group B) (n=10) using lost wax casting technique were fabricated for each selected tooth. The marginal and internal gaps of crowns were recorded using a replica technique with light body silicone material stabilized with a regular set putty. Each replica was sectioned buccolingually and mesiodistally and then e…

010302 applied physicsOrthodonticsProsthetic DentistryMaterials scienceResearchMonolithic zirconiaCAD02 engineering and technology:CIENCIAS MÉDICAS [UNESCO]021001 nanoscience & nanotechnology01 natural sciencesMetal ceramicPaired samplesUNESCO::CIENCIAS MÉDICAS0103 physical sciencesStereo microscopeCubic zirconia0210 nano-technologyGeneral DentistryConventional techniqueJournal of Clinical and Experimental Dentistry
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Correlation between in situ structural and optical characterization of the semiconductor-to-metal phase transition of VO2 thin films on sapphire

2020

A detailed structural investigation of the semiconductor-to-metal transition (SMT) in vanadium dioxide thin films deposited on sapphire substrates by pulsed laser deposition was performed by in situ temperature-dependent X-ray diffraction (XRD) measurements. The structural results are correlated with those of infrared radiometry measurements in the SWIR (2.5-5 μm) and LWIR (8-10.6 μm) spectral ranges. The main results indicate a good agreement between XRD and optical analysis, therefore demonstrating that the structural transition from monoclinic to tetragonal phases is the dominating mechanism for controlling the global properties of the SMT transition. The picture that emerges is a SMT tr…

010302 applied physicsPhase transitionMaterials scienceTransition temperatureAnalytical chemistryPulsed laser depositionphase change material; VO202 engineering and technologyVO2 thin films021001 nanoscience & nanotechnology01 natural sciencesSettore ING-INF/01 - ElettronicaPulsed laser depositionTetragonal crystal systemVO20103 physical sciencesSapphireThermal hysteresisGeneral Materials ScienceCrystalliteThin film0210 nano-technologyphase change materialMonoclinic crystal systemSemiconductor-to-metal (SMT) transition
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Very Long Term Stabilization of a 2D Magnet down to the Monolayer for Device Integration

2020

2D materials have recently demonstrated a strong potential for spintronic applications. This has been further reinforced by the discovery of ferromagnetic 2D layers. Nevertheless, the fragility of ...

010302 applied physics[PHYS]Physics [physics]Materials scienceSpintronicsNanotechnology02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesElectronic Optical and Magnetic MaterialsTerm (time)FragilityFerromagnetismMagnet0103 physical sciencesMonolayerMaterials ChemistryElectrochemistry[PHYS.COND]Physics [physics]/Condensed Matter [cond-mat]0210 nano-technologyComputingMilieux_MISCELLANEOUS
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Electrochemical deposition of aniline derivatives for conductometric gas sensors

2019

International audience; Polymer film of poly(2,3,5,6-tetrafluoroaniline) (PTFA) were electroplated on ITO substrate from acidic medium by chronoamperometry. Electrochemical and morphological characterizations were performed and compared to polyaniline properties similarly coated. It seemed that PTFA film had an irreversible redox response with poor conductivity due to the absence of acid-base doping. This film were then incorporated in a patented device called MSDI heterojunction to perform ammonia sensing in humid atmosphere.

010302 applied physicschemistry.chemical_classificationMaterials scienceheterojunctionHeterojunction02 engineering and technologyPolymerConductivityChronoamperometry021001 nanoscience & nanotechnologyElectrochemistryammonia01 natural sciencespolyanilineconductometric sensorschemistry.chemical_compound[CHIM.POLY]Chemical Sciences/PolymersAnilineMonomerchemistryChemical engineering0103 physical sciencesPolyaniline[CHIM.OTHE]Chemical Sciences/Other0210 nano-technologyMaterials Today: Proceedings
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Unexpected Substituent Effects in the Iso-Heterocyclic Boulton-Katritzky Rearrangement of 3-Aroylamino-5-methyl-1,2,4-oxadiazoles: A Mechanistic Stud…

2019

The kinetics of the iso-heterocyclic mononuclear rearrangement of some 3-aroylamino-5-methyl-1,2,4-ozadiazoles was carefully examined under largely variable acidic or alkaline conditions. This reaction may proceed via two different mechanistic pathways (an uncatalyzed and a base-catalyzed one), as accounted for also by the evaluation of the relevant activation parameters. Substituent effects, as quantified by means of the Hammett’s equation, appear relatively modest; however, they reveal some interesting anomalies, which enabled us to draw a very precise picture of the intimate reaction course.

010304 chemical physicsChemistryKineticsSubstituent124-oxadiazoleSettore CHIM/06 - Chimica OrganicaMononuclear Heterocyclic Rearrangement010402 general chemistry01 natural sciences0104 chemical sciencesKineticschemistry.chemical_compoundSubstituent effectComputational chemistry0103 physical sciencesPhysical and Theoretical ChemistryReaction mechanismThe journal of physical chemistry. A
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Towards Atomically Precise Supported Catalysts from Monolayer‐Protected Clusters: The Critical Role of the Support

2020

Abstract Controlling the size and uniformity of metal clusters with atomic precision is essential for fine‐tuning their catalytic properties, however for clusters deposited on supports, such control is challenging. Here, by combining X‐ray absorption spectroscopy and density functional theory calculations, it is shown that supports play a crucial role in the evolution of monolayer‐protected clusters into catalysts. Based on the acidic nature of the support, cluster‐support interactions lead either to fragmentation of the cluster into isolated Au–ligand species or ligand‐free metallic Au0 clusters. On Lewis acidic supports that bind metals strongly, the latter transformation occurs while pre…

010402 general chemistry01 natural sciencesgold clustersNanomaterials | Hot PaperCatalysiskultaCatalysisNanomaterialsmonolayer-protected clustersMetalklusteritnoncovalent interactionskatalyytitMonolayerCluster (physics)Non-covalent interactionschemistry.chemical_classificationX-ray absorption spectroscopyFull Paper010405 organic chemistryOrganic ChemistryX-ray absorption spectroscopyGeneral ChemistryFull Papersgold0104 chemical sciencesX-Ray Absorption SpectroscopychemistryChemical physicsvisual_artdensity functional calculationsvisual_art.visual_art_mediumDensity functional theorynanohiukkasetcluster-support interactionChemistry (Weinheim an Der Bergstrasse, Germany)
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Kinetic control in the temperature-dependent sequential growth of surface-confined supramolecular copolymers

2017

We report the sequential growth of supramolecular copolymers on gold surfaces, using oppositely charged dendritic peptide amphiphiles. By including water-solubilising thermoresponsive chains in the monomer design, we observed non-linear effects in the temperature-dependent sequential growth. The step-wise copolymerisation process is characterised using temperature dependent SPR and QCM-D measurements. At higher temperatures, dehydration of peripheral oligoethylene glycol chains supports copolymer growth due to more favourable comonomer interactions. Both monomers incorporate methionine amino acids but remarkably, desorption of the copolymers via competing sulphur gold interactions with the …

010405 organic chemistryChemistryComonomerSupramolecular chemistryQuartz crystal microbalance010402 general chemistry01 natural sciences0104 chemical sciencesMetalchemistry.chemical_compoundMonomerChemical engineeringDesorptionvisual_artAmphiphilePolymer chemistryCopolymervisual_art.visual_art_mediumPhysical and Theoretical ChemistryFaraday Discussions
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Ethene/norbornene copolymerization with (isodicyclopentadienyl)titanium complex-MAO catalyst

2007

Norbornene (NB) homopolymerization and ethene/NB copolymerizations with a silylene-bridged (isodicyclopentadienyl)(tert-butylamido)titanium dichloride-methylalumoxane (MAO) catalyst system were investigated. This catalytic system shows no efficiency towards NB homopolymerization but produces poly(ethene-co-norbornene)s. An increase in the initial NB feed content leads to a loss of copolymerization activity as well as NB copolymer incorporation. The structure of the isodicyclopentadienyl fragment (IsodiCp) has a strong limiting effect on comonomer incorporation possibilities.

010405 organic chemistryChemistryComonomeriso(dicyclopentadienyl)titaniumchemistry.chemical_elementGeneral ChemistryLimitingethene/norbornene copolymerization010402 general chemistry01 natural sciencescatalysts0104 chemical sciencesCatalysis[ CHIM.POLY ] Chemical Sciences/Polymerschemistry.chemical_compound[CHIM.POLY]Chemical Sciences/PolymersPolymer chemistryCopolymeraluminoxanesComputingMilieux_MISCELLANEOUSTitaniumNorbornene
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A Ferroelectric Iron(II) Spin Crossover Material

2017

A dual-function material in which ferroelectricity and spin crossover coexist in the same temperature range has been obtained. Our synthetic strategy allows the construction of acentric crystal structures in a predictable way and is based on the high directionality of hydrogen bonds. The well-known iron(II) spin crossover complex [Fe(bpp)₂]²+ (bpp = 2,6-bis(pyrazol-3-yl)pyridine), a four-fold noncentrosymmetric H-bond donor, was combined with a disymmetric H-bond acceptor such as the isonicotinate (isonic) anion to afford [Fe(bpp)₂](isonic)₂·2H₂O. This low-spin iron(II) compound crystallises in the acentric nonpolar I-4 space group and shows piezoelectricity and SHG properties. Upon dehydra…

010405 organic chemistryChemistryHydrogen bondInorganic chemistryGeneral MedicineGeneral ChemistryCrystal structure010402 general chemistry01 natural sciencesAcceptorFerroelectricityCatalysis0104 chemical sciencesCrystallographySpin crossoverPhase (matter)Acentric factorMonoclinic crystal systemAngewandte Chemie International Edition
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Self-assembly of the tetrachlorido(oxalato)rhenate( iv ) anion with protonated organic cations: X-ray structures and magnetic properties

2016

Two novel ReIV compounds of formulae [H2bpy][ReIVCl4(ox)] (1) and [H3biim]2[ReIVCl4(ox)] (2) [H2bpy2+ = 4,4′-bipyridinium dication, H3biim+ = 2,2′-biimidazolium monocation, and ox2− = oxalate dianion] have been synthesised and magneto-structurally characterised. 1 crystallises in the monoclinic system with space group C2/c, and 2 crystallises in the triclinic system with space group P[1 with combining macron]. The ReIV ion in 1 and 2 is six-coordinate, bonded to four chloride ions and two oxalate-oxygen atoms in a distorted octahedral geometry. Short intermolecular ReIV–Cl⋯Cl–ReIV contacts, Cl⋯π type interactions and hydrogen bonds are present in the crystal lattice of both compounds, gener…

010405 organic chemistryChemistryInorganic chemistrySupramolecular chemistryGeneral ChemistryCrystal structureTriclinic crystal system010402 general chemistryCondensed Matter Physics01 natural sciencesMagnetic susceptibilityOxalate0104 chemical sciencesDicationchemistry.chemical_compoundCrystallographyOctahedral molecular geometryGeneral Materials ScienceMonoclinic crystal system
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