Search results for " surface"

showing 10 items of 2838 documents

Structural characterization of frozen n-heptane solutions of metal-containing reverse micelles

2007

The microstructure of temperature-quenched solutions of reverse micelles formed by sodium, cobalt, ytterbium, and cobalt/ytterbium bis(2-ethylhexyl)sulfosuccinate in n-heptane has been investigated by SAXS and EXAFS. Some changes in the X-ray absorption spectra with respect to the same systems at room temperature have been observed. The analysis of the SAXS spectra leads to the hypothesis that at 77 K the closed spherical structure of reverse micelles is retained and that during the temperature quench they undergo a clustering process involving the transition from a quite random dispersion to the formation of more or less large clusters of strongly packed reverse micelles. This behavior is …

chemistry.chemical_classificationHeptaneAbsorption spectroscopyExtended X-ray absorption fine structureSmall-angle X-ray scatteringAnalytical chemistrychemistry.chemical_elementSurfaces and InterfacesCondensed Matter PhysicsMicellechemistry.chemical_compoundColloid and Surface ChemistrychemistryElectrochemistryGeneral Materials ScienceCounterionPhysical and Theoretical ChemistryDispersion (chemistry)CobaltSpectroscopy
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Isolation of a stable, acyclic, two-coordinate silylene.

2012

The synthesis and characterization of a stable, acyclic two-coordinate silylene, Si(SAr(Me(6)))(2) [Ar(Me(6)) = C(6)H(3)-2,6(C(6)H(2)-2,4,6-Me(3))(2)], by reduction of Br(2)Si(SAr(Me(6)))(2) with a magnesium(I) reductant is described. It features a V-shaped silicon coordination with a S-Si-S angle of 90.52(2)° and an average Si-S distance of 2.158(3) A. Although it reacts readily with an alkyl halide, it does not react with hydrogen under ambient conditions, probably as a result of the ca. 4.3 eV energy difference between the frontier silicon lone pair and 3p orbitals.

chemistry.chemical_classificationHydrogenSiliconMagnesiumSilyleneHalidechemistry.chemical_elementGeneral ChemistryPhotochemistryBiochemistryCatalysischemistry.chemical_compoundCrystallographyColloid and Surface ChemistryAtomic orbitalchemistryLone pairta116AlkylJournal of the American Chemical Society
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Distance Matters: Biasing Mechanism, Transfer of Asymmetry, and Stereomutation in N-Annulated Perylene Bisimide Supramolecular Polymers

2021

International audience; The synthesis of two series of N-annulated perylene bisimides (PBIs), compounds 1 and 2, is reported, and their self-assembling features are thoroughly investigated by a complete set of spectroscopic measurements and theoretical calculations. The study corroborates the enormous influence that the distance between the PBI core and the peripheral groups exerts on the chiroptical properties and the supramolecular polymerization mechanism. Compounds 1, with the peripheral groups separated from the central PBI core by two methylenes and an ester group, form J-type supramolecular polymers in a cooperative manner but exhibit negligible chiroptical properties. The lack of cl…

chemistry.chemical_classificationIsodesmic reactionQuenching (fluorescence)010405 organic chemistrySupramolecular chemistryQuímica orgánicaGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryArticleCatalysis0104 chemical sciencesSupramolecular polymersSolventchemistry.chemical_compoundCrystallographyColloid and Surface ChemistrychemistryPolymerization[CHIM]Chemical SciencesMethylcyclohexanePerylene
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Polymer Films in the Normal-Liquid and Supercooled State: A Review of Recent Monte Carlo Simulation Results

2000

This paper reviews recent Monte Carlo simulation studies of the glassy behavior in thin polymer films. The simulations employ a version of the bond-fluctuation lattice model, in which the glass transition is driven by the competition between a stiffening of the polymers and their dense packing in the melt. The melt is geometrically confined between two impenetrable walls separated by distances ranging from once to about fifteen times the bulk radius of gyration. The confinement influences static and dynamic properties of the films: Chains close to the wall preferentially orient parallel to it. This orientation tendency propagates through the film and leads to a layer structure at low temper…

chemistry.chemical_classificationLattice model (finance)Materials scienceCondensed matter physicsMonte Carlo methodRelaxation (NMR)FOS: Physical sciencesGyration tensorSurfaces and InterfacesPolymerDisordered Systems and Neural Networks (cond-mat.dis-nn)Condensed Matter - Soft Condensed MatterCondensed Matter - Disordered Systems and Neural NetworksCondensed Matter::Soft Condensed MatterColloid and Surface ChemistrychemistryRadius of gyrationSoft Condensed Matter (cond-mat.soft)Physical and Theoretical ChemistryGlass transitionSupercooling
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Metal ion affinity-based biomolecular recognition and conjugation inside synthetic polymer nanopores modified with iron-terpyridine complexes.

2011

Here we demonstrate a novel biosensing platform for the detection of lactoferrin (LFN) via metal-organic frameworks, in which the metal ions have accessible free coordination sites for binding, inside the single conical nanopores fabricated in polymeric membrane. First, monolayer of amine-terminated terpyridine (metal-chelating ligand) is covalently immobilized on the inner walls of the nanopore via carbodiimide coupling chemistry. Second, iron-terpyridine (iron-terPy) complexes are obtained by treating the terpyridine modified-nanopores with ferrous sulfate solution. The immobilized iron-terPy complexes can be used as recognition elements to fabricate biosensing nanodevice. The working pri…

chemistry.chemical_classificationLigandPolymersPyridinesSurface PropertiesMetal ions in aqueous solutionIronInorganic chemistrytechnology industry and agricultureGeneral ChemistryBiosensing TechniquesBiochemistryCombinatorial chemistryCatalysisNanoporechemistry.chemical_compoundLactoferrinNanoporesColloid and Surface ChemistrychemistryMonolayerNon-covalent interactionsTerpyridineNanodeviceBiosensorJournal of the American Chemical Society
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Semiconductor Nanocrystals with Multifunctional Polymer Ligands

2002

In this letter, we describe the preparation of a versatile polymer ligand, which can be attached to CdSe/ZnS semiconductor nanocrystals via a phase transfer reaction. The ligand is based on a chain of reactive esters, which can, in principle, be substituted by any compound containing amino-functionalities. The polymer/nanocrystal complexes are characterized in terms of structure and photostability.

chemistry.chemical_classificationLigandfungiInorganic chemistryfood and beveragesQuantum yieldGeneral ChemistryPolymerBiochemistryCombinatorial chemistryCatalysisFluorescence spectroscopyColloid and Surface ChemistryNanocrystalchemistryPhase (matter)Surface modificationSemiconductor nanocrystalsJournal of the American Chemical Society
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Kinetics of Molecule Transfer between Lipid Vesicles and β-Cyclodextrins

1996

Abstract We propose a calorimetric method based on the van't Hoff model of depression of the freezing temperature to investigate slow kinetics involving lipid vesicles (liposomes) and drug–β-cyclodextrin (Cyd) complexes. Some nonsteroidal antiinflammatory drugs (NSAIDs) were examined and standard phospholipid liposomes were used in our experiments. Three different kinetic processes were investigated: (a)9Transfer of drugs from water-soluble Cyd-complexes to void liposomes. (b)9Uptake of drugs from the surface of liposomes by free Cyd dissolved in the aqueous phase. (c)9Exchange of drugs from loaded to void vesicles, and the effect of free Cyd in enhancing such a transfer. Most experiments w…

chemistry.chemical_classificationLiposomeChromatographyCyclodextrinChemistryVesicleBilayerKineticsPhospholipidSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsInclusion compoundBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryDifferential scanning calorimetryBiophysicsJournal of Colloid and Interface Science
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Butene Isomerization and Double-Bond Migration on the H-ZSM-5 Outer Surface: A Density Functional Theory Study

2011

Isomerization of trans-but-2-ene to cis-but-2-ene and double bond migration of trans-but-2-ene to but-1-ene have been investigated by means of density functional theory calculations on a suitable model of H-ZSM-5 surface. The study has been afforded on outer surface sites by considering the hydroxyl group of either a SiO2(OH)2 or a AlO2H(OH)2 moiety. On these outer surface sites, one alkoxide species occurs as a stable intermediate both along the isomerization and double bond migration pathways. The latter process could also occur via a single-step mechanism, which involves a six-center transition state. The energy barriers of the outer surface processes above do not take any advantage by t…

chemistry.chemical_classificationMFI zeolite outer surface DFTDouble bondHydrogenchemistry.chemical_elementPhotochemistryButeneSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral EnergychemistryAlkoxideMoietyDensity functional theoryPhysical and Theoretical ChemistryZSM-5IsomerizationThe Journal of Physical Chemistry C
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Langmuir–Blodgett films based on inorganic molecular complexes with magnetic or optical properties

2005

Langmuir and Langmuir–Blodgett (LB) films of a great variety of molecular metal complexes with interesting magnetic or optical properties have been prepared in the last few years. Some of the results obtained by our group and others are summarized in this article. (i) LB films of polyoxometalates (POM) were first prepared taking advantage of the adsorption properties of these cluster anions along a positively charged monolayer of an organic surfactant spread in water. A correct choice of the POM allowed the preparation of LB films with magnetic, electrochromic, or luminescent properties. Besides this semiamphiphilic method, two new methods to prepare LB films of POMs have been developed by …

chemistry.chemical_classificationManganeseOptics and PhotonicsLangmuirChemical PhenomenaChemistry PhysicalSurface PropertiesChemistryMembranes ArtificialSurfaces and InterfacesLangmuir–Blodgett filmMagneticsMagnetizationchemistry.chemical_compoundCrystallographyColloid and Surface ChemistryElectrochromismFerritinsMonolayerOrganometallic CompoundsOrganic chemistryBehenic acidPhysical and Theoretical ChemistryAlkylSuperparamagnetismAdvances in Colloid and Interface Science
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A novel approach to polymer-template mesoporous molecular sieves

2000

A novel synthesis route was developed to produce spherical silica particles. The synthesis is based on a modified Stoeber method and the room-temperature synthesis of MCM 41S-materials applying tetraethoxysilane, alcohol, water, ammonia and homopolymers as template. The specific surface area, the specific pore volume and the average pore diameter were varied in the following ranges: 5 – 1,000 m2/g; 0.1 – 1.0 cm3/g and 2-50 nm. With respect to catalytic applications hetero-atoms e.g. Al were incorporated into the silica framework.

chemistry.chemical_classificationMaterials scienceAlcoholPolymerMolecular sieveCatalysisAmmoniachemistry.chemical_compoundVolume (thermodynamics)chemistryChemical engineeringSpecific surface areaOrganic chemistryMesoporous material
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