Search results for "Colloid"

showing 10 items of 1288 documents

Nonlinear hairy layer theory of electrophoretic fingerprinting applied to consecutive layer by layer polyelectrolyte adsorption onto charged polystyr…

1997

The consecutive layer-by-layer adsorption of poly(allylamine hydrochloride) (PAH) and poly(styrenesulfonate) (PSS) on colloidal charged latex particles is investigated by measuring the electrophoretic mobility as a function of pH and ionic strength over a broad range (electrophoretic fingerprinting). Meaningful interpretation of the data required the development of a nonlinear approach to hairy particle electrophoresis including dissociation, adsorption, and association. Steric and electrostatic exclusion of mobile ions from the hairy layer has been considered. Also, the surface conductivity correction is extended to the case of charged hairy layer particles. We deposited up to three polyel…

ChemistryLayer by layerSurfaces and InterfacesCondensed Matter PhysicsPolyelectrolyteSurface conductivityColloidElectrophoresisAdsorptionPolyelectrolyte adsorptionChemical engineeringIonic strengthPolymer chemistryElectrochemistryGeneral Materials ScienceSpectroscopy
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Ancillary Ligand Effect on Single-Site Styrene Polymerization:  Isospecificity of Group 4 Metal Bis(phenolate) Catalysts

2003

Styrene is polymerized isospecifically by group 4 metal complexes that contain a C2-symmetrically coordinated 1,4-dithiabutane-linked bis(phenolato) ligand activated by methylaluminoxane.

ChemistryLigandMethylaluminoxaneGeneral ChemistryBiochemistryCatalysisStyreneCatalysisMetalchemistry.chemical_compoundColloid and Surface ChemistryPolymerizationSingle siteGroup (periodic table)visual_artPolymer chemistryvisual_art.visual_art_mediumJournal of the American Chemical Society
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Mechanistic Study of Stepwise Methylisocyanide Coupling and C-H Activation Mediated by a Low-Valent Main Group Molecule

2013

An experimental and DFT investigation of the mechanism of the coupling of methylisocyanide and C-H activation mediated by the germylene (germanediyl) Ge(Ar(Me6))2 (Ar(Me6) = C6H3-2,6(C6H2-2,4,6-Me3)2) showed that it proceeded by initial MeNC adduct formation followed by an isomerization involving the migratory insertion of the MeNC carbon into the Ge-C ligand bond. Addition of excess MeNC led to sequential insertions of two further MeNC molecules into the Ge-C bond. The insertion of the third MeNC leads to methylisocyanide methyl group C-H activation to afford an azagermacyclopentadienyl species. The X-ray crystal structures of the 1:1 (Ar(Me6))2GeCNMe adduct, the first and final insertion …

ChemistryLigandStereochemistryIsocyanideMigratory insertionGeneral ChemistryCrystal structureBiochemistryCatalysisAdductchemistry.chemical_compoundColloid and Surface ChemistryMoleculeIsomerizationta116Methyl groupJournal of American Chemical Society
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Intramolecular pi-stacking in a phenylpyrazole-based iridium complex and its use in light-emitting electrochemical cells.

2010

A novel iridium(III) complex, [Ir(dmppz)(2)pbpy][PF(6)] (Hdmppz = 3,5-dimethyl-1-phenylpyrazole and pbpy = 6-phenyl-(2,2'-bipyridine)), is reported. The complex shows an intramolecular face-to-face pi-stacking between the phenyl ring of the dmppz ligand and the pendant phenyl of the pbpy ligand. This interaction provides a supramolecular cage formation that holds also in the excited states. Light-emitting electrochemical cells (LECs) using the novel complex show extraordinary lifetimes of approximately 2000 h. The high stability is favored by the presence of pendant methyl groups on the dmppz ligands that hinder the entrance of water molecules rendering the degradation of the complex more d…

ChemistryLigandStereochemistryStackingSupramolecular chemistrychemistry.chemical_elementGeneral ChemistryRing (chemistry)BiochemistryCatalysisCrystallographyColloid and Surface ChemistryIntramolecular forceExcited stateMoleculeIridiumJournal of the American Chemical Society
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Chemical modification of porous calcium hydroxyapatite surfaces by grafting phenylphosphonic and phenylphosphite acids

2006

Abstract It is well known that the incorporation of organic molecules can provide an effective route to modify the surface properties of apatite ceramics. The present study shows that phosphonates can react with calcium ions to control the formation of the hydroxyapatite structures. The grafting of C6H5PO(OH)2 (PPOH) and C6H5PO(OH)H (PPH) was used to increase the specific surface area as well as the porosity of hydroxyapatite materials. The higher specific surface area for HAp treated by PPOH is around 267 m2/g compared to the pure HAp (140 m2/g). The phenyl (C6H5) groups are removed by thermal treatment around 500 °C. After treatment at 800 °C, organoapatites (PP-HAp) are converted to stoi…

ChemistryMineralogychemistry.chemical_elementChemical modification02 engineering and technologyThermal treatmentCalcium010402 general chemistry021001 nanoscience & nanotechnologyGrafting01 natural sciencesApatite0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryColloid and Surface Chemistryvisual_artSpecific surface area[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryvisual_art.visual_art_mediumHydroxyapatites0210 nano-technologyPorosityComputingMilieux_MISCELLANEOUSNuclear chemistry
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Scalable heterogeneous synthesis of metallic nanoparticles and aggregates with polyvinyl alcohol

2009

Here we report on a new route to synthesize colloidal silver and gold nanoparticles, potentially scalable for massive nanoparticle-production. This method is based on the microwave-assisted heterogeneous reduction of the metal salts with polyvinylalcohol. The reaction is carried out in alcohols, which are non-solvents for polyvinylalcohol. Nanoparticles can be very easily separated by filtration. The reaction kinetics are extremely fast. Size-controlled formation of nanoparticle agglomerates is accomplished with a seed-mediated synthesis of nanoparticles upon MW exposure.

ChemistryNanoparticleNanotechnologyColloidal silverGeneral ChemistryPolyvinyl alcoholCatalysislaw.inventionChemical kineticschemistry.chemical_compoundlawColloidal goldAgglomerateMaterials ChemistryMetal nanoparticlesFiltrationNew Journal of Chemistry
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Understanding the microscopic origin of gold nanoparticle anisotropic growth from molecular dynamics simulations.

2013

We use molecular dynamics simulations in order to understand the microscopic origin of the asymmetric growth mechanism in gold nanorods. We provide the first atomistic model of different surfaces on gold nanoparticles in a growing electrolyte solution, and we describe the interaction of the metal with the surfactants, namely, cetyltrimethylammonium bromide (CTAB) and the ions. An innovative aspect is the inclusion of the role of the surfactants, which are explicitly modeled. We find that on all the investigated surfaces, namely, (111), (110), and (100), CTAB forms a layer of distorted cylindrical micelles where channels among micelles provide direct ion access to the surface. In particular,…

ChemistryNanoparticleSurfaces and InterfacesElectrolyteCondensed Matter PhysicsMicelleIonMetalCrystallographyMolecular dynamicsChemical physicsColloidal goldvisual_artElectrochemistryvisual_art.visual_art_mediumGeneral Materials ScienceNanorodSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Photoinduced phenomena in corona poled polar organic films.

2005

Abstract Organic materials have received considerable attention because of their large dipole moments and optical nonlinearities. The optically induced switching of material properties is important for studying the optoelectronic effects including second harmonic generation. Organic materials for photonic applications contain chromophore dipole which consist of acceptor and donor groups bridged by a delocalized π-electron system. Both theoretical and experimental data show a reversible highly dipolar photoinduced intra molecular charge transfer in betaine type molecules accompanied by change of the sign and the value of the dipole moment. The arrangement of polar molecules in films is studi…

ChemistryPhotochemistryPolymersSurface PropertiesChemical polarityAnalytical chemistrySecond-harmonic generationMembranes ArtificialSurfaces and InterfacesChromophoreMicroscopy Atomic ForceAcceptorSensitivity and SpecificityCondensed Matter::Materials ScienceDelocalized electronDipoleColloid and Surface ChemistryChemical physicsMonolayerMoleculePhysical and Theoretical ChemistryParticle SizeAdvances in colloid and interface science
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Isolation of Free Phenylide-like Carbanions with N-Heterocyclic Carbene Frameworks

2009

A series of 1,3-bis(2,6-diisopropylphenyl)-5-methyl-1,3-diaza-4,6-diborabenzenes with methyl, phenyl, and dimethylamino substituents on the ring boron atoms were prepared using the cyclocondensation reaction between N,N'-bis(2,6-diisopropylphenyl)trimethylsilylformamidine and the appropriately substituted 1,1-bis(organochloroboryl)ethane, followed by deprotonation of the cationic ring intermediate. The planar, heterocyclic benzene analogues could be further deprotonated at the other ring carbon using an additional equivalent of potassium hexamethyldisilazide to yield organometallic derivatives akin to the potassium phenylide. The potassium cations could be efficiently sequestered in both so…

ChemistryPotassiumCationic polymerizationchemistry.chemical_elementGeneral ChemistryRing (chemistry)PhotochemistryBiochemistryMedicinal chemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistryDeprotonationYield (chemistry)BenzeneCarbeneCarbanionJournal of the American Chemical Society
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Effect of Ti(IV) loading on CO oxidation activity of gold on TiO2 doped amorphous silica

2006

Abstract Amorphous SiO 2 , doped with various amount of TiO 2 , was used as support for gold nanoparticles. Gold was deposited through the controlled sol formation technique. The effect of the TiO 2 loading on the structural and surface properties was investigated by transmission electron microscopy, X-ray diffraction, Raman and X-ray photoelectron spectroscopy. The catalytic behavior was tested in the oxidation of CO. A significant enhancement in the activity was observed for the gold supported on mixed oxide with low TiO 2 loading. On the basis of characterization data, the positive effect is assigned to the electronic modification of the Ti(IV) of the newly formed Ti O Si bonds.

ChemistryProcess Chemistry and TechnologyInorganic chemistrytechnology industry and agricultureNanoparticleCatalysisAmorphous solidsymbols.namesakeTransition metalX-ray photoelectron spectroscopyTransmission electron microscopyColloidal goldsymbolsMixed oxideRaman spectroscopyApplied Catalysis A: General
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