Search results for "Colloid"

showing 10 items of 1288 documents

Ex Vivo Tracking of Endogenous CO with a Ruthenium(II) Complex.

2017

[EN] A two-photon fluorescent probe based on a ruthenium(II) vinyl complex is capable of selectively detecting carbon monoxide in cells and ex vivo using mice with a subcutaneous air pouch as a model for inflammation. This probe combines highly selective and sensitive ex vivo detection of endogenous CO in a realistic model with facile, inexpensive synthesis, and displays many advantages over the widely used palladium-based systems.

StereochemistryChemistry MultidisciplinaryFLUORESCENT-PROBEFluorescent-Probechemistry.chemical_elementCarbonylationEndogeny010402 general chemistryFluorogenic probes01 natural sciencesBiochemistryCatalysischemistry.chemical_compoundQUIMICA ORGANICAColloid and Surface ChemistrySelective detectionQUIMICA ANALITICACarbon-MonoxideLIVING CELLSCARBON-MONOXIDEScience & Technology010405 organic chemistryAirSELECTIVE DETECTIONFLUOROGENIC PROBESAIRQUIMICA INORGANICACARBONYLATIONLiving cellsGeneral ChemistryFluorescence0104 chemical sciencesRutheniumChemistrychemistryPhysical SciencesBiophysicsSubcutaneous airHEME OXYGENASE-103 Chemical SciencesCarbonylationHeme Oxygenase-1Ex vivoCarbon monoxidePalladiumJournal of the American Chemical Society
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Increased dynamic effects in a catalytically compromised variant of Escherichia coli dihydrofolate reductase

2013

Isotopic substitution (15N, 13C, 2H) of a catalytically compromised variant of Escherichia coli dihydrofolate reductase, EcDHFR-N23PP/S148A, has been used to investigate the effect of these mutations on catalysis. The reduction of the rate constant of the chemical step in the EcDHFR-N23PP/S148A catalyzed reaction is essentially a consequence of an increase of the quasi-classical free energy barrier and to a minor extent of an increased number of recrossing trajectories on the transition state dividing surface. Since the variant enzyme is less well set up to catalyze the reaction, a higher degree of active site reorganization is needed to reach the TS. Although millisecond active site motion…

StereochemistryCoupled motionsKnockoutHydride transferProtein dynamicsChemical stepmedicine.disease_causeTemperature-dependenceBiochemistryCatalysisArticleCatalysisEnzyme catalysisColloid and Surface ChemistryReaction rate constantDihydrofolate reductasemedicineEscherichia coliQDEscherichia colichemistry.chemical_classificationbiologyChemistryProtein dynamicsActive siteEnzyme catalysisGeneral ChemistryTetrahydrofolate DehydrogenaseEnzymeDehydrogenasebiology.proteinBiocatalysisConformational motions
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Rotational Isomerism in Acetic Acid: The First Experimental Observation of the High-Energy Conformer

2003

The high-energy conformer of acetic acid (cis-AA) is produced in an Ar matrix by vibrational excitation of the OH stretching overtone of the ground conformational state (trans-AA). IR-absorption spectroscopy provides a clear identification of the reaction product. cis-AA converts back to trans-AA in a time scale of minutes at 8 K by tunneling. http://dx.doi.org/10.1021/ja038341a

StereochemistryOvertoneMolecular ConformationInfrared spectroscopy010402 general chemistry01 natural sciencesBiochemistryCatalysisAcetic acidchemistry.chemical_compoundColloid and Surface ChemistryIsomerismAb initio quantum chemistry methods0103 physical sciencesSpectroscopy Fourier Transform InfraredSpectroscopyConformational isomerismAcetic Acid010304 chemical physicsChemistryMatrix isolationGeneral Chemistry3. Good health0104 chemical sciencesKineticsModels ChemicalPhysical chemistryExcitation
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Potassium Triggers a Reversible Specific Stiffness Transition of Polyethylene Glycol

2017

We use plasmon rulers made from two connected gold nanoparticles to monitor the conformation and stiffness of single PEG molecules and their response to cations. By observing equilibrium fluctuations of the interparticle distance, we obtain the spring constants or stiffness of the connecting single-molecule tether with pico-Newton sensitivity. We observe a transition of the PEG molecules’ extension and stiffness above about 1.2 mM K+ ion concentration which is specific to potassium ions. Molecular dynamics simulations reveal the formation of crown-like structures as the most likely molecular mechanism responsible for this specific effect.

StereochemistryPotassiumchemistry.chemical_elementmacromolecular substances02 engineering and technologyPolyethylene glycol010402 general chemistry01 natural sciencesIonchemistry.chemical_compoundMolecular dynamicsmedicineMoleculePhysical and Theoretical ChemistrySpecific modulustechnology industry and agricultureStiffness021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergychemistryColloidal goldChemical physicsmedicine.symptom0210 nano-technologyThe Journal of Physical Chemistry C
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Detection of Single Oxygen Molecules with Fluorescence-Labeled Hemocyanins

2005

This study introduces a method to detect individual oxygen molecules by fluorescence microscopy of single hemocyanins. These respiratory proteins from a tarantula bind oxygen with high affinity. A spectrometric signature of the oxygenated protein is transferred to an attached fluorescence label, which can be detected at the single-molecule level. This technique opens new perspectives for the development of small and sensitive oxygen sensors as well as for the investigation of cooperative oxygen binding in respiratory proteins.

Stereochemistrymedicine.medical_treatmentchemistry.chemical_elementBiochemistryOxygenCatalysisColloid and Surface ChemistrySpecies SpecificityChemical affinitymedicineFluorescence microscopeAnimalsMoleculeFluorescent DyesChemistrySpidersHemocyaninGeneral ChemistryFluorescenceOxygenSpectrometry FluorescenceHemocyaninsBiophysicsOxygen sensorCopperOxygen bindingJournal of the American Chemical Society
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Bulky Surface Ligands Promote Surface Reactivities of [Ag141X12(S-Adm)40]3+ (X = Cl, Br, I) Nanoclusters: Models for Multiple-Twinned Nanoparticles

2017

Surface ligands play important roles in controlling the size and shape of metal nanoparticles and their surface properties. In this work, we demonstrate that the use of bulky thiolate ligands, along with halides, as the surface capping agent promotes the formation of plasmonic multiple-twinned Ag nanoparticles with high surface reactivities. The title nanocluster [Ag141X12(S-Adm)40]3+ (where X = Cl, Br, I; S-Adm = 1-adamantanethiolate) has a multiple-shell structure with an Ag71 core protected by a shell of Ag70X12(S-Adm)40. The Ag71 core can be considered as 20 frequency-two Ag10 tetrahedra fused together with a dislocation that resembles multiple-twinning in nanoparticles. The nanocluster…

StereochemistrynanoclustersShell (structure)HalideNanoparticle02 engineering and technology010402 general chemistry01 natural sciencesBiochemistryCatalysisNanoclusterschemistry.chemical_compoundColloid and Surface ChemistryCluster (physics)ta116Plasmonta114ChemistryGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesCrystallographysurface ligandsPhenylacetyleneAbsorption bandnanoparticles0210 nano-technologyJournal of the American Chemical Society
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Peptide Metal–Organic Frameworks for Enantioselective Separation of Chiral Drugs

2017

We report the ability of a chiral Cu(II) 3D MOF based on the tripeptide Gly-L-His-Gly (GHG) for the enantioselective separation of metamphetamine and ephedrine. Monte Carlo simulations suggest that chiral recognition is linked to preferential binding of one of the enantiomers as result of either stronger or additional H-bonds with the framework that lead to energetically more stable diastereomeric adducts. Solid phase extraction (SPE) of a racemic mixture by using Cu(GHG) as extractive phase permits isolating more than 50% of the (+)-ephedrine enantiomer as target compound in only four minutes. To the best of our knowledge, this represents the first example of a MOF capable of separating ch…

StereoisomerismTripeptideMolecular Dynamics Simulation010402 general chemistry01 natural sciencesBiochemistryCatalysisMethamphetamineColloid and Surface ChemistryOrganic chemistryMoleculeMetal-Organic FrameworksEphedrineMolecular Structure010405 organic chemistryChemistryDiastereomerEnantioselective synthesisStereoisomerismQuímicaGeneral ChemistryCombinatorial chemistry0104 chemical sciences13. Climate actionRacemic mixtureMetal-organic frameworkPèptidsEnantiomerPeptidesMonte Carlo MethodCopperJournal of the American Chemical Society
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Exploration of the Solid-State Sorption Properties of Shape-Persistent Macrocyclic Nanocarbons as Bulk Materials and Small Aggregates.

2020

Porous molecular materials combine benefits such as convenient processability and the possibility for atom-precise structural fine-tuning which makes them remarkable candidates for specialty applications in the areas of gas separation, catalysis, and sensing. In order to realize the full potential of these materials and guide future molecular design, knowledge of the transition from molecular properties into materials behavior is essential. In this work, the class of compounds termed cycloparaphenylenes (CPPs)-shape-persistent macrocycles with built-in cavities and radially oriented π-systems-was selected as a conceptually simple class of intrinsically porous nanocarbons to serve as a platf…

Steric effectsAnalyteChemistryHeteroatomSolid-stateSorptionNanotechnologyGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesCatalysisColloid and Surface ChemistryGas separationPorosityJournal of the American Chemical Society
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An unprecedented, bridged dihydrogen complex of a cofacial metallodiporphyrin and its relevance to the bimolecular reductive elimination of hydrogen

1990

Recently, the authors characterized the first metalloporphyrin dihydrogen complex, Os(OEP)(H{sub 2}), and proposed that a similar ruthenium porphyrin dihydrogen complex, Ru(OEP)(H{sub 2}), is involved as an intermediate in the catalytic H/D isotopic exchange between water and hydrogen. They now report that treatment of a metal-metal-bonded cofacial ruthenium porphyrin dimer with a sterically bulky ligand in the presence of hydrogen gas has yielded the first known complex containing a dihydrogen ligand bound between two metals. Such a bridged dihydrogen complex is proposed as an intermediate in the bimolecular elimination of dihydrogen from two metalloporphyrin hydrides.

Steric effectsLigandDimerchemistry.chemical_elementGeneral ChemistryReaction intermediateBiochemistryPorphyrinMedicinal chemistryCatalysisReductive eliminationRutheniumchemistry.chemical_compoundColloid and Surface ChemistrychemistryDihydrogen complexJournal of the American Chemical Society
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Two dimensional self-assembly of bis-acylureas having various functional end groups.

2011

We present the synthesis and morphology study of thirteen bis-acylurea molecules with various functional end groups. The bis-acylureas have two acylurea groups, -NH-CO-NH-CO-, divided by a pentamethylene spacer, -(CH(2))(5)-, and two symmetric functional end groups, such as, aliphatic, benzyl, mono- and bi-thiophenyl, sulfur-containing, and propargyl (HC[triple bond]CCH(2)-) moieties. The bis-acylureas were synthesized by the coupling reactions of ureas with pimeloyl chloride or pimelic acid. Upon cooling from hot isotropic solutions, the bis-acylureas spontaneously form supermolecules. In the cases of aliphatic, benzyl, mono- and bi-thiophenyl functional groups, two dimensional supramolecu…

Steric effectsModels MolecularStereochemistrySupramolecular chemistryHydrogen BondingCrystal structureSupermoleculeCrystallography X-RaySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundCrystallographyEnd-groupColloid and Surface ChemistrychemistryPropargylFunctional groupMoleculeUreaJournal of colloid and interface science
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