Search results for "Colloid"

showing 8 items of 1288 documents

Total Structure and Electronic Structure Analysis of Doped Thiolated Silver [MAg24(SR)18]2– (M = Pd, Pt) Clusters

2015

With the incorporation of Pd or Pt atoms, thiolated Ag-rich 25-metal-atom nanoclusters were successfully prepared and structurally characterized for the first time. With a composition of [PdAg24(SR)18](2-) or [PtAg24(SR)18](2-), the obtained 25-metal-atom nanoclusters have a metal framework structure similar to that of widely investigated Au25(SR)18. In both clusters, a M@Ag12 (M = Pd, Pt) core is capped by six distorted dimeric -RS-Ag-SR-Ag-SR- units. However, the silver-thiolate overlayer gives rise to a geometric chirality at variance to Au25(SR)18. The effect of doping on the electronic structure was studied through measured optical absorption spectra and ab initio analysis. This work d…

ta114ChemistryStereochemistryDopingAb initioGeneral ChemistryElectronic structureengineering.materialpalladiumBiochemistryCatalysissilver nanoclustersNanoclustersCatalysisOverlayerCrystallographyColloid and Surface ChemistryengineeringNoble metalplatinumChirality (chemistry)ta116thiolsJournal of the American Chemical Society
researchProduct

Structural Evolution of Atomically Precise Thiolated Bimetallic [Au12+nCu32(SR)30+n]4– (n = 0, 2, 4, 6) Nanoclusters

2014

A series of all-thiol stabilized bimetallic Au-Cu nanoclusters, [Au(12+n)Cu32(SR)(30+n)](4-) (n = 0, 2, 4, 6 and SR = SPhCF3), are successfully synthesized and characterized by X-ray single-crystal analysis and density functional theory (DFT) calculations. Each cluster consists of a Keplerate two-shell Au12@Cu20 core protected by (6 - n) units of Cu2(SR)5 and n units of Cu2Au(SR)6 (n = 0, 2, 4, 6) motifs on its surface. The size and structural evolution of the clusters is atomically controlled by the Au precursors and countercations used in the syntheses. The clusters exhibit similar optical absorption properties that are not dependent on the number of surface Cu2Au(SR)6 units. Although DFT…

ta114ChemistrySuperatomGeneral ChemistryCrystal structureElectronic structureBiochemistryCatalysisNanoclustersCrystallographyColloid and Surface ChemistryNanocrystalCluster (physics)Density functional theoryta116Bimetallic stripJournal of the American Chemical Society
researchProduct

Biodegradable Ultrasmall-in-Nano Gold Architectures: Mid-Period In Vivo Distribution and Excretion Assessment

2018

theranosticsPeriod (periodic table)Chemistry02 engineering and technologyGeneral ChemistryBiodegradationgold010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesbiodegradation0104 chemical sciencesExcretionIn vivoColloidal goldsilicaEnvironmental chemistryDistribution (pharmacology)General Materials Scienceexcretion0210 nano-technologybiodegradation; excretion; gold; silica; theranostics
researchProduct

Oxidation-responsive and "clickable" poly(ethylene glycol) via copolymerization of 2-(methylthio)ethyl glycidyl ether

2016

Poly(ethylene glycol) (PEG) is a widely used biocompatible polymer. We describe a novel epoxide monomer with methyl-thioether moiety, 2-(methylthio)ethyl glycidyl ether (MTEGE), which enables the synthesis of well-defined thioether-functional poly(ethylene glycol). Random and block mPEG-b-PMTEGE copolymers (Mw/Mn = 1.05-1.17) were obtained via anionic ring opening polymerization (AROP) with molecular weights ranging from 5 600 to 12 000 g·mol-1. The statistical copolymerization of MTEGE with ethylene oxide results in a random microstructure (rEO = 0.92 ± 0.02 and rMTEG E = 1.06 ± 0.02), which was confirmed by in situ 1H NMR kinetic studies. The random copolymers are thermorespon…

thioether-functional PEGoxidation-responsiveEpoxide02 engineering and technology010402 general chemistry01 natural sciencesBiochemistryRing-opening polymerizationMicelleCatalysischemistry.chemical_compoundColloid and Surface ChemistryPolymer chemistryCopolymerMoiety2-(methylthio)ethyl glycidyl etherEthylene oxidepoly(ethylene glycol)sulfoniumGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesmulti-functional PEGMonomerchemistryPEOpolyetherthermoresponsive0210 nano-technologyEthylene glycol
researchProduct

Calcium mediated polyelectrolyte adsorption on like-charged surfaces.

2011

International audience; Monte Carlo simulations within the primitive model of calcium-mediated adsorption of linear and comb polyelectrolytes onto like-charged surfaces are described, focusing on the effect of calcium and polyion concentrations as well as on the ion pairing between polymers and calcium ions. We use a combination of Monte Carlo simulations and experimental data from titration and calcium binding to quantify the ion pairing. The polymer adsorption is shown to occur as a result of surface overcharging by Ca2+ and ion pairing between charged monomers and Ca2+. In agreement with experimental observations, the simulations predict that the polymer adsorption isotherm goes through …

titrationInorganic chemistrychemistry.chemical_element02 engineering and technologyCalcium010402 general chemistry01 natural sciencesIonQuantitative Biology::Cell BehaviorQuantitative Biology::Subcellular ProcessesinterfacesAdsorptionElectrochemistryGeneral Materials ScienceSpectroscopypolyelectrolytechemistry.chemical_classificationQuantitative Biology::BiomoleculesQuantitative Biology::Neurons and CognitionSurface Chemistry and ColloidsSurfaces and InterfacesPolymerPolymer adsorption021001 nanoscience & nanotechnologyCondensed Matter PhysicsPolyelectrolyte0104 chemical sciencesCondensed Matter::Soft Condensed Matter[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]chemistryPolyelectrolyte adsorptionChemical physicsadsorptionMonte Carlo SimulationsTitration[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technologyLangmuir : the ACS journal of surfaces and colloids
researchProduct

Kinetic evidence for the incorporation of the [(pentamethylcyclopentadienyl) (2,2′-bipyridyl)(aquo)rhodium(III)] complex into DPPC vesicles

2008

Abstract The binding of the [(pentamethylcyclopentadienyl) (2,2′-bipyridyl)(aquo)rhodium(III)] complex [Cp*RhIII(bpy)H2O]2+, to l -α-dipalmitoylphosphatidyl choline (DPPC) vesicles has been estimated by studying the kinetics of the electron transfer reaction between the rhodium(III) complex and formiate ions. Kinetic measurements carried out under anaerobic conditions in absence and presence of DPPC show that the total reaction is composed of two steps. The rate of the first reaction increases with the phospholipid concentration, while that of the second process is independent of the concentration of DPPC. This is consistent with a reaction, where the two reacting species are partitioned be…

vesicles L-alfa-dipalmitoylphosphatidyl choline (DPPC) rate constant bindingAqueous solutionLiaisonStereochemistryVesicleKineticstechnology industry and agriculturePhospholipidchemistry.chemical_elementBinding constantRhodiumchemistry.chemical_compoundCrystallographyElectron transferColloid and Surface Chemistrychemistrylipids (amino acids peptides and proteins)Colloids and Surfaces A: Physicochemical and Engineering Aspects
researchProduct

Effet colloide-protecteur d'extraits de parois de levures sur la stabilité tartrique d'une solution hydro-alcoolique modèle

1993

<p style="text-align: justify;">L'effet colloïde-protecteur d'extraits mannoprotéiques de parois de levures vis-à-vis de la précipitation tartrique a été étudié en solution hydroalcoolique, en utilisant un IST mètre (Indice de Stabilité Tartrique).</p><p style="text-align: justify;">Nous avons montré que les deux extraits levuriens inhibaient la cristallisation du bitartrate de potassium au même titre que l'acide métatartrique et la carboxyméthylcellulose, mais à un niveau plus faible. Le niveau de stabilité retenu (ISTC-75) est assuré avec des concentrations par litre de 7,5 mg d'acide métatartrique et de 18 mg de carboxyméthylcellulose. Des concentrations en extraits man…

yeast wallslcsh:Agriculturehydroalcoholic solutionMannoproteins extractslcsh:Botanycolloid-protective effectlcsh:Startaric precipitationHorticulturelcsh:QK1-989Food ScienceOENO One
researchProduct

Neorganisko jonu ietekme uz jonu apmaiņas ekstrahentu adsorbciju uz fāžu robežvirsmām starp ūdens un organiskiem šķīdumiem

2000

Šķīdumi (Ķīmija):NATURAL SCIENCES::Chemistry::Physical chemistry [Research Subject Categories]Virsmu ķīmijaAdsorbcijaFāžu robežvirsmasFizikālā ķīmijaLiquidsColloidsAdsorptionSolution chemistrySurface chemistry
researchProduct