Search results for "colloid"

showing 10 items of 1288 documents

Reversed Enantioselectivity of Diisopropyl Fluorophosphatase against Organophosphorus Nerve Agents by Rational Design

2009

Diisopropyl fluorophosphatase (DFPase) from Loligo vulgaris is an efficient and robust biocatalyst for the hydrolysis of a range of highly toxic organophosphorus compounds including the nerve agents sarin, soman, and cyclosarin. In contrast to the substrate diisopropyl fluorophosphate (DFP) the nerve agents possess an asymmetric phosphorus atom, which leads to pairs of enantiomers that display markedly different toxicities. Wild-type DFPase prefers the less toxic stereoisomers of the substrates which leads to slower detoxification despite rapid hydrolysis. Enzyme engineering efforts based on rational design yielded two quadruple enzyme mutants with reversed enantioselectivity and overall en…

Models MolecularSarinStereochemistryRational designCyclosarinStereoisomerismGeneral ChemistryNervous SystemBiochemistryCatalysisKineticschemistry.chemical_compoundOrganophosphorus CompoundsPhosphoric Triester HydrolasesColloid and Surface ChemistrychemistrySomanHydrolasemedicineDiisopropyl fluorophosphateChemical Warfare AgentsCrystallizationDiisopropyl-fluorophosphatasemedicine.drugNerve agentJournal of the American Chemical Society
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Langevin dynamics simulations of a two-dimensional colloidal crystal under confinement and shear

2012

Langevin dynamics simulations are used to study the effect of shear on a two-dimensional colloidal crystal (with implicit solvent) confined by structured parallel walls. When walls are sheared very slowly, only two or three crystalline layers next to the walls move along with them, while the inner layers of the crystal are only slightly tilted. At higher shear velocities, this inner part of the crystal breaks into several pieces with different orientations. The velocity profile across the slit is reminiscent of shear banding in flowing soft materials, where liquid and solid regions coexist; the difference, however, is that in the latter case the solid regions are glassy while here they are …

Models MolecularShearing (physics)Materials scienceCondensed matter physicsbusiness.industryCrystal structureColloidal crystalCondensed Matter::Soft Condensed MatterPhysics::Fluid DynamicsCrystalColloidOpticsModels ChemicalShear (geology)Computer SimulationColloidsSolitonCrystallizationRheologyShear StrengthbusinessLangevin dynamicsPhysical Review E
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An Intermetallic Au24Ag20 Superatom Nanocluster Stabilized by Labile Ligands

2015

An intermetallic nanocluster containing 44 metal atoms, Au24Ag20(2-SPy)4(PhC≡C)20Cl2, was successfully synthesized and structurally characterized by single-crystal analysis and density funtional theory computations. The 44 metal atoms in the cluster are arranged as a concentric three-shell Au12@Ag20@Au12 Keplerate structure having a high symmetry. For the first time, the co-presence of three different types of anionic ligands (i.e., phenylalkynyl, 2-pyridylthiolate, and chloride) was revealed on the surface of metal nanoclusters. Similar to thiolates, alkynyls bind linearly to surface Au atoms using their σ-bonds, leading to the formation of two types of surface staple units (PhC≡C-Au-L, L …

Models MolecularSilversynthesisInorganic chemistryIntermetallicMolecular ConformationCrystal structureLigandsBiochemistryCatalysisSilver nanoparticleNanoclustersMetalColloid and Surface ChemistryCluster (physics)ta116intermetallic nanoclustersta114LabilityChemistrySuperatomGeneral ChemistryNanostructuresCrystallographysurface ligandsvisual_artvisual_art.visual_art_mediumGoldJournal of the American Chemical Society
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Magnesium Exchanged Zirconium Metal−Organic Frameworks with Improved Detoxification Properties of Nerve Agents

2019

UiO-66, MOF-808 and NU-1000 metal-organic frameworks exhibit a differentiated reactivity toward [Mg(OMe)2(MeOH)2]4 related to their pore accessibility. Microporous UiO-66 remains unchanged while mesoporous MOF-808 and hierarchical micro/mesoporous NU-1000 materials yield doped systems containing exposed MgZr5O2(OH)6 clusters in the mesoporous cavities. This modification is responsible for a remarkable enhancement of the catalytic activity toward the hydrolytic degradation of P-F and P-S bonds of toxic nerve agents, at room temperature, in unbuffered aqueous solutions.

Models MolecularSurface PropertiesQuímica organometàl·licachemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryCatalysisCatalysisColloid and Surface ChemistryPolymer chemistryReactivity (chemistry)MagnesiumParticle SizeMaterialsMetal-Organic FrameworksZirconiumAqueous solutionMagnesiumHydrolysisTemperatureGeneral ChemistryMicroporous material0104 chemical scienceschemistryMetal-organic frameworkZirconiumMesoporous materialNerve AgentsOxidation-ReductionPorosity
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Characterization of Iron−Carbonyl-Protected Gold Clusters

2009

Ligand-stabilized nanometer-sized gold particles are interesting building blocks for molecular electronics, precursors for catalysts, optical labels for biomolecules and diagnosis, and potential nontoxic carriers for therapeutics. In this work we characterize for the first time, by means of near-infrared and Raman spectroscopy and time-dependent density functional calculations, gold clusters protected with iron-carbonyl ligands, such as {Au(22)[Fe(CO)(4)](12)}(6-) shown in the figure. Surprisingly, our results show that these novel compounds bear many analogues to another, well-studied, class of gold clusters, namely those of thiolate-monolayer-protected gold clusters. Our work adds a new d…

Models MolecularTime FactorsSpectrophotometry InfraredPhosphinesInfraredIronMolecular ConformationElectronsNanotechnologySpectrum Analysis RamanBiochemistryCatalysisCatalysissymbols.namesakeColloid and Surface ChemistryNano-chemistry.chemical_classificationAldehydesChemistryBiomoleculeMolecular electronicsGeneral ChemistryCombinatorial chemistryCharacterization (materials science)Gold particlesLinear ModelssymbolsQuantum TheoryGoldRaman spectroscopyJournal of the American Chemical Society
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Pentameric Circular Iron(II) Double Helicates and a Molecular Pentafoil Knot

2012

We report on the synthesis of 11 pentameric cyclic helicates formed by imine condensation of alkyl monoamines with a common bis(formylpyridine)bipyridyl-derived building block and iron(II) and chloride ions. The cyclic double-stranded helicates were characterized by NMR spectroscopy, mass spectrometry, and in the case of a 2,4-dimethoxybenzylamine-derived pentameric cyclic helicate, X-ray crystallography. The factors influencing the assembly process (reactant stoichiometry, concentration, solvent, nature and amount of anion) were studied in detail: the role of chloride in the assembly process appears not to be limited to that of a simple template, and larger circular helicates observed with…

Models Molecularchemistry.chemical_classificationCircular dichroismMolecular StructureStereochemistryImineGeneral ChemistryNuclear magnetic resonance spectroscopyCrystallography X-RayBiochemistryCatalysisCrystallographychemistry.chemical_compoundBipyridineColloid and Surface ChemistrychemistryDiamineHelixFerrous CompoundsIminesAminesta116AlkylStoichiometryJournal of the American Chemical Society
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Chelate Cooperativity and Spacer Length Effects on the Assembly Thermodynamics and Kinetics of Divalent Pseudorotaxanes

2011

Homo- and heterodivalent crown-ammonium pseudorotaxanes with different spacers connecting the two axle ammonium binding sites have been synthesized and characterized by NMR spectroscopy and ESI mass spectrometry. The homodivalent pseudorotaxanes are investigated with respect to the thermodynamics of divalent binding and to chelate cooperativity. The shortest spacer exhibits a chelate cooperativity much stronger than that of the longer spacers. On the basis of crystal structure, this can be explained by a noninnocent spacer, which contributes to the binding strength in addition to the two binding sites. Already very subtle changes in the spacer length, i.e., the introduction of an additional…

Models Molecularchemistry.chemical_classificationSpectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyRotaxanesCooperative bindingThermodynamicsCooperativityGeneral ChemistryCrystal structureNuclear magnetic resonance spectroscopyBiochemistryCatalysisDivalentQuaternary Ammonium CompoundsKineticschemistry.chemical_compoundColloid and Surface ChemistrychemistryIntramolecular forceEffective molarityThermodynamicsMethyleneta116Chelating AgentsJournal of the American Chemical Society
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Structural and Theoretical Basis for Ligand Exchange on Thiolate Monolayer Protected Gold Nanoclusters

2012

Ligand exchange reactions are widely used for imparting new functionality on or integrating nanoparticles into devices. Thiolate-for-thiolate ligand exchange in monolayer protected gold nanoclusters has been used for over a decade; however, a firm structural basis of this reaction has been lacking. Herein, we present the first single-crystal X-ray structure of a partially exchanged Au(102)(p-MBA)(40)(p-BBT)(4) (p-MBA = para-mercaptobenzoic acid, p-BBT = para-bromobenzene thiol) with p-BBT as the incoming ligand. The crystal structure shows that 2 of the 22 symmetry-unique p-MBA ligand sites are partially exchanged to p-BBT under the initial fast kinetics in a 5 min timescale exchange reacti…

Models Molecularchemistry.chemical_classificationta114LigandMetal NanoparticlesBridging ligandGeneral ChemistryAssociative substitutionCrystal structureCrystallography X-RayLigandsBiochemistryArticleCatalysisNanoclustersCrystallographyColloid and Surface ChemistrychemistryMonolayerSolventsThiolThermodynamicsDensity functional theoryGoldJournal of the American Chemical Society
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The Low Barrier Hydrogen Bond in the Photoactive Yellow Protein: A Vacuum Artifact Absent in the Crystal and Solution

2016

Journal of the American Chemical Society 138(51), 16620 - 16631 (2016). doi:10.1021/jacs.6b05609

Models Molecularphotoactive yellow proteinlow-barrier hydrogen bondVacuumHydrogenProtein ConformationLow-barrier hydrogen bondNeutron diffractionchemistry.chemical_elementProtonationCrystallography X-RayPhotoreceptors Microbial010402 general chemistry01 natural sciencesBiochemistryCatalysisColloid and Surface ChemistryProtein structureBacterial Proteins0103 physical sciencesta116Photoactive yellow proteinvetysidokset010304 chemical physicsHydrogen bondChemistryHydrogen BondingGeneral Chemistry5400104 chemical sciencesSolutionsCrystallographyhydrogen bondsddc:540Proton NMRArtifactsJournal of the American Chemical Society
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Thermodynamic Studies of Sodium Dodecyl Sulfate–Sodium Dodecanoate Mixtures in Water

1996

Abstract Conductivity, density, heat capacity, enthalpy of dilution, and osmotic coefficient measurements of water–sodium dodecyl sulfate (NaDS)–sodium dodecanoate systems were carried out as functions of the surfactants total molality ( m t ) at different mole fractions ( X NaDS ). From conductivity data, the critical micelle concentration (cmc) and the degree of ionization of the micelles (β) were calculated. The cmc vs X NaDS profile deviates negatively from that predicted on the basis of the Clint approach, while the β vs X NaDS profile deviates positively from the line correlating the values for pure surfactants. At a given mole fraction, the profiles of all the investigated properties…

MolalitySodiumEnthalpyInorganic chemistryAnalytical chemistrychemistry.chemical_elementMole fractionMicelleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistrychemistryCritical micelle concentrationOsmotic coefficientSodium dodecyl sulfateJournal of Colloid and Interface Science
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