Search results for "Interfaces."

showing 10 items of 1252 documents

Homocoupling of terminal alkynes on calcite (10.4)

2018

Abstract On-surface synthesis has been identified as highly versatile strategy to prepare molecular structures on surfaces with single-atom precision. Inspired by the classical Glaser coupling, homocoupling of terminal alkynes has attracted great attention for on-surface synthesis. This coupling is known for providing a rigid and linear linkage, which is highly interesting for the synthesis of molecular wires. For molecular wire formation, non-conductive substrates are needed for electronic decoupling. So far, however, coupling of terminal alkynes has not been performed on a bulk insulator surface. Here, we present an atomic force microscopy study, indicating that 4,4″-diethynyl-[1,1′:4′,1″…

chemistry.chemical_classificationMaterials scienceAnnealing (metallurgy)AlkyneMolecular electronics02 engineering and technologySurfaces and Interfaces010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences5300104 chemical sciencesSurfaces Coatings and FilmsElectron transferMolecular wirechemistry.chemical_compoundCrystallographyMonomerchemistryMaterials ChemistryMoietyGlaser coupling0210 nano-technology
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Micropatterning of neurons using organic substrates in culture

1997

Abstract In this study, we have used spatially defined surfaces of organic thin films to micropattern the outgrowth of central nervous system neurons in culture. Glass substrates were first chemically modified with synthetic peptides derived from an extra-cellular matrix protein laminin to couple a functionality that promotes a neuron-substrate interaction. The modification procedure was verified using X-ray photoelectron spectroscopy. The functionality of the modified glass surfaces was examined by growing neurons dissociated from mammalian central nervous tissues in culture. Spatially defined surfaces of the peptide were then fabricated by selectively attaching the peptide to coplanar sur…

chemistry.chemical_classificationMaterials scienceAtomic force microscopyMetals and AlloysNanotechnologyPeptideSurfaces and InterfacesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsX-ray photoelectron spectroscopychemistryMonolayerMaterials ChemistryUv laserBiophysicsThin filmLithographyMicropatterningThin Solid Films
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Self-organization of amphiphilic N-acylated linear polyethyleneimines: investigation of a reversible monolayer collapse

1996

Abstract Poly-N-4-decyloxybenzoylethyleneimine, highly crystalline in bulk, forms a stable monolayer at the air-water interface which undergoes a reversible collapse into a probable bilayer structure at higher surface pressures. We achieved transfer both from the monolayer and “bilayer” region of the polymer film at the water surface onto hydrophilic and hydrophobized quartz supports. Based on X-ray investigations on the deposited Langmuir-Blodgett films, a possible mechanism for the reversible collapse is proposed.

chemistry.chemical_classificationMaterials scienceBilayerMetals and AlloysCollapse (topology)Surfaces and InterfacesPolymerSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistryMonolayerAmphiphileMaterials ChemistryQuartzThin Solid Films
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Photocleavable microcapsules built from photoreactive nanospheres.

2005

We show how photo-cross-linking of nanoparticles within the micrometer-sized thin oil shell of water-oil-water emulsion droplets leads to a new species of optically addressable microcontainers. The inner water droplet of these emulsions may contain drugs, dyes, or other water-soluble components, leading to filled containers. The thickness, mechanical stability, and light resistance of the container walls can be controlled in a simple way by the amount and adjustable photoreactivity of the nanoparticles. Importantly, the chemical bonds between the nanoparticles constituting the microcapsule shell can be cleaved photochemically by irradiation with UV light. This optically controlled destructi…

chemistry.chemical_classificationMaterials scienceCyclodextrinShell (structure)NanoparticleNanotechnologySurfaces and InterfacesCondensed Matter PhysicsControlled releaseMicrometrechemistryChemical bondElectrochemistryMoleculeGeneral Materials ScienceIrradiationSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Affinity Distributions of a Molecularly Imprinted Polymer Calculated Numerically by the Expectation-Maximization Method

2003

Affinity distributions are calculated from adsorption isotherm data obtained for the enantiomers of L- and D-phenylalanine anilide (PA) on native and thermally annealed polymers molecularly imprinted with L-PA. The calculation is obtained with an iterative algorithm called expectation-maximization that does not require prior fit of the data to an isotherm model before inversion and thus yields a distribution indicative of the data only. The results show bimodal distributions, suggestive of a two-site model describing relatively selective and nonselective adsorption modes of the L-enantiomer and a corresponding unimodal/nonselective adsorption mode for the D-enantiomer. The nonselective adso…

chemistry.chemical_classificationMaterials scienceGaussianAnalytical chemistryMolecularly imprinted polymerSurfaces and InterfacesPolymerCondensed Matter Physicssymbols.namesakeAdsorptionDistribution (mathematics)chemistrySelective adsorptionExpectation–maximization algorithmElectrochemistrysymbolsGeneral Materials ScienceEnantiomerSpectroscopyLangmuir
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Covalently attached polymer mono- and multilayers on silanized glass substrates

1996

Abstract Applying grazing incidence FTIR and ellipsometry, the reaction of poly [(1-methyl-vinyl isocyanate)-alt-(maleic anhydride)](IAP) with amino-silanized glass and silicon oxide surfaces has been investigated. A reactive surface containing isocyanate and anhydride groups was formed after the adsorption of the polymer. The layer could be further functionalized using 2-aminoethanol. Multilayers could be built up by adsorbing a second layer of IAP onto an already reacted first layer of IAP.

chemistry.chemical_classificationMaterials scienceMetals and AlloysMaleic anhydrideSurfaces and InterfacesPolymerIsocyanateSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundAdsorptionchemistrySilanizationPolymer chemistryMaterials ChemistryFourier transform infrared spectroscopySilicon oxideLayer (electronics)Thin Solid Films
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Structured Nanoparticles from the Self-Assembly of Polymer Blends through Rapid Solvent Exchange

2017

Molecular dynamics simulations were performed to study systematically the rapid mixing of a polymer blend in solution with a miscible nonsolvent. In agreement with experiments, we observe that polymers self-assemble into complex nanoparticles, such as Janus and core-shell particles, when the good solvent is displaced by the poor solvent. The emerging structures can be predicted on the basis of the surface tensions between the polymers as well as between the polymers and the surrounding liquid. Furthermore, the size of the nanoparticles can be independently tuned through the mixing rate and the polymer concentration in the feed stream; meanwhile, the composition of the nanoparticles can be c…

chemistry.chemical_classificationMaterials scienceMixing (process engineering)Nanoparticle02 engineering and technologySurfaces and InterfacesPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesSolventMolecular dynamicsChemical engineeringchemistryPolymer chemistryElectrochemistryGeneral Materials ScienceParticle sizePolymer blendJanus0210 nano-technologySpectroscopyLangmuir
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On the Stability of Polymeric Nanoparticles Fabricated through Rapid Solvent Mixing.

2018

We study the stability of polymeric nanoparticles fabricated through the rapid mixing of polymers in a good solvent with a poor solvent that is miscible with the good solvent. In previous experiments where water was used as the poor solvent, a negative surface charge was measured on the precipitated nanoparticles, which led to the long-time stability of the dispersion. It was argued that these charges originate presumably from either water or hydroxide adsorption at the hydrophobic nanoparticle surface or from impurities in the feed streams that preferentially adsorb on the precipitated nanoparticles. To elucidate the origin of this stabilization mechanism, we performed experiments wherein …

chemistry.chemical_classificationMaterials scienceMixing (process engineering)Nanoparticle02 engineering and technologySurfaces and InterfacesPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesSolventchemistry.chemical_compoundAdsorptionChemical engineeringchemistryElectrochemistryHydroxideGeneral Materials ScienceSurface charge0210 nano-technologyDispersion (chemistry)SpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Interfacial Tensions from Drop Retraction versus Pendant Drop Data and Polydispersity Effects

2004

Interfacial tensions sigma were measured by means of both methods for the following polymer pair: polyisobutylene (PIB 3) plus poly(dimethylsiloxane) (PDMS 152) and poly(dimethyl-co-methylphenylsiloxane) (CoP26*) plus PDMS 48. The numbers after the abbreviation state the molar masses in kilograms; the homopolymers exhibit polydispersities on the order of 2. The reliability of the method of drop retraction is backed up by systematic measurements, which demonstrate that it is possible to study the time evolution of sigma. Because of the free choice of the phases (drop or matrix) and the possibility to vary the overall composition of the system in a wide range, drop retraction yields more info…

chemistry.chemical_classificationMaterials scienceMolar massDrop (liquid)DispersityTime evolutionThermodynamicsSurfaces and InterfacesPolymerCondensed Matter PhysicsDrop methodSurface tensionchemistryPolymer chemistryElectrochemistryGeneral Materials ScienceSpectroscopyLangmuir
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Magnetic molecular nanostructures: Design of magnetic molecular materials as monolayers, multilayers and thin films

2007

In this paper we summarize the importance and versatility of the molecular approach in the design and development of novel magnetic molecular materials. These materials processing, in order to obtain controlled molecular structures at the nanoscale, will also be remarked.

chemistry.chemical_classificationMaterials scienceNanostructureGeneral Physics and AstronomyNanotechnologySurfaces and InterfacesGeneral ChemistryCondensed Matter PhysicsSurfaces Coatings and FilmsCoordination complexNanolithographychemistryMonolayerMoleculeSelf-assemblyThin filmNanoscopic scaleApplied Surface Science
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