Search results for "solu"

showing 10 items of 7577 documents

Thermodynamic properties and cloud droplet activation of a series of oxo-acids

2010

Abstract. We have investigated the thermodynamic properties of four aliphatic oxo-dicarboyxlic acids identified or thought to be present in atmospheric particulate matter: oxosuccinic acid, 2-oxoglutaric acid, 3-oxoglutaric acid, and 4-oxopimelic acid. The compounds were characterized in terms of their cloud condensation nuclei (CCN) activity, vapor pressure, density, and tendency to decarboxylate in aqueous solution. We deployed a variety of experimental techniques and instruments: a CCN counter, a Tandem Differential Mobililty Analyzer (TDMA) coupled with a laminar flow-tube, and liquid chromatography/mass spectrometry (LC/MS). The presence of the oxo functional group in the α-position ca…

chemistry.chemical_classificationAtmospheric ScienceAqueous solutionTandemVapor pressureInorganic chemistryParticulatesMass spectrometrylcsh:QC1-999lcsh:Chemistrychemistry.chemical_compoundDicarboxylic acidchemistrylcsh:QD1-999Functional groupOrganic chemistryCloud condensation nucleilcsh:PhysicsAtmospheric Chemistry and Physics
researchProduct

Selective Surface Modification of SiO2−TiO2 Supports with Phosphonic Acids

2004

The selective surface modification by phosphonic acids of SiO2−TiO2 supports at the micrometer and molecular scale was investigated. Under aqueous conditions, phosphonic acids bind to TiO2 and not to SiO2 surfaces. A micropatterned support was prepared by electron beam microlithography and selectivity, of the surface modification was evidenced using scanning Auger electron spectroscopy (SAES). The second support was a mesoporous SiO2−TiO2 mixed oxide (10 mol % Ti) epoxidation catalyst prepared by sol−gel processing. Selectivity was deduced from the decrease of the catalytic activity upon modification and from chemical analysis; bonding modes to the surface were investigated using solid-stat…

chemistry.chemical_classificationAuger electron spectroscopyAqueous solutionGeneral Chemical EngineeringInorganic chemistryGeneral ChemistryPolymerCatalysischemistryMaterials ChemistrySurface modificationMixed oxideSelectivityMesoporous materialChemistry of Materials
researchProduct

Complexes of Azelaic and Diethylenetrioxydiacetic Acids with Na+, Mg2+, and Ca2+ in NaCl Aqueous Solutions, at 25 °C

1999

Formation constants of Na + , Mg 2+ , and Ca 2+ complexes of azelaic and diethylenetrioxydiacetic acids have been determined by potentiometry (H + -glass electrode) at different ionic strengths (0 ≤ I ≤ 1 mol dm -3 ), at t = 25 °C. For all the systems the species ML and MHL have been found. The relative formation constants are reported together with the parameters for the dependence on ionic strength. Results are discussed in comparison with those for other carboxylic ligands. Speciation problems are considered also.

chemistry.chemical_classificationAzelaic acidAqueous solutionGeneral Chemical EngineeringCarboxylic acidInorganic chemistryGeneral ChemistryGlass electrodelaw.inventionchemistryStability constants of complexeslawIonic strengthmedicineQualitative inorganic analysisMagnesium ionmedicine.drugJournal of Chemical & Engineering Data
researchProduct

Temperature and light sensitive copolymers containing azobenzene moieties prepared via a polymer analogous reaction

2009

Abstract Four different series of polyacrylamides containing different amounts of azobenzene moieties have been synthesized via a polymer analogous reaction of poly(pentafluorophenylacrylate) (PPFPA). All copolymers were designed to exhibit a lower critical solution temperature (LCST) in aqueous solution, which was dependent on (i) the amount of incorporated chromophoric azobenzene groups and (ii) the isomerization state of the respective azobenzene group. Higher LCST values were measured for UV-irradiated solutions of the copolymers in comparison to the non-irradiated copolymer solutions. A maximum difference in the LCST of up to 7 °C was found for the copolymer poly(N,N-dimethylacrylamide…

chemistry.chemical_classificationAzo compoundPolymers and PlasticsPhotoisomerizationOrganic ChemistryPolymerLower critical solution temperatureCis trans isomerizationchemistry.chemical_compoundchemistryAzobenzenePolymer chemistryMaterials ChemistryCopolymerIsomerizationPolymer
researchProduct

High resolution electron microscopy of liquid crystalline polymers

1990

Les images de microscopie electronique a haute resolution des polymeres cristaux liquides calamitiques [CO−CH(R)−CO 2 −(CH 2 ) 6 −OPh−N:N−PhO−(CH 2 ) 6 −O] n (R=CH 2 −CH=CH 2 , (CH 2 ) 6 −O−Ph N=N−Ph−CN) et discotique poly (hexadecanedioate de triphenylene) sont simulees sur ordinateur et comparees avec les structures obtenues a partir des resultats experimentaux de diffraction electronique. Une theorie est developpee pour expliquer le bon accord observe

chemistry.chemical_classificationAzo polymerChemistryLiquid crystallineDiscotic liquid crystalHigh resolutionPolymerlaw.inventionHigh resolution electron microscopylawLiquid crystalPolymer chemistryPhysical chemistryElectron microscopeJournal de Physique
researchProduct

Molecular Recognition-Induced Function and Competitive Replacement by Hydrogen-Bonding Interactions:  Amphiphilic Barbituric Acid Derivatives, 2,4,6-…

1998

The phenomenon of molecular recognition inducing further function is common in nature. However, there are few synthetic systems which achieve this cascade type mechanism, and those are generally ca...

chemistry.chemical_classificationBarbituric acidAqueous solutionDouble bondHydrogen bondStereochemistrySurfaces and InterfacesCrystal structureCondensed Matter PhysicsCombinatorial chemistrychemistry.chemical_compoundMolecular recognitionchemistryCarbon–carbon bondAmphiphileElectrochemistryGeneral Materials ScienceSpectroscopyLangmuir
researchProduct

Structure and fluxional behaviour of heptaleneirontricarbonyl and heptalenebis (Irontricarbonyl)

1987

Abstract The synthesis of heptaleneirontricarbonyl ( 4 ) is described. The structures of 4 and of the closely related heptalenebis(irontricarbonyl) ( 3 ) are elucidated by NMR spectroscopy ( 1H and 13C) and by X-ray crystallography. Compounds 3 and 4 are shown by dynamic NMR to undergo an isodynamic 1 ,2-migration of the Fe(CO3)-groups as well as a carbonyl scrambling. The relevant kinetic data allow for a mechanistic discussion of the dynamics and a comparison with other irontricarbonyl complexes.

chemistry.chemical_classificationBicyclic moleculeStereochemistryOrganic ChemistryCrystal structureNuclear magnetic resonance spectroscopyBiochemistrychemistry.chemical_compoundchemistryComputational chemistryDrug DiscoveryX-ray crystallographyHeptaleneChemical solutionMoleculeInorganic compoundTetrahedron
researchProduct

Synthesis, characterization, and complexation of tetraarylborates with aromatic cations and their use in chemical sensors.

2005

Five aromatic borate anions, namely tetrakis(4-phenoxyphenyl)borate (1), tetrakis(biphenyl)borate (2), tetrakis(2-naphthyl)borate (3), tetrakis(4-phenylphenol)borate (4), and tetrakis(4-phenoxy)borate (5), have been prepared and tested as ion-recognition sites in chemical sensors for certain aromatic cations and metal ions. To gain further insight into the complexation of the cations, some complexes have been prepared and structurally characterized. The complexation behavior of 1 and 2 towards N-methylpyridinium (6), 1-ethyl-4-(methoxycarbonyl)pyridinium (7), tropylium (8), imidazolium (9), and 1-methylimidazolium (10) cations has been studied, and the stability constants of the complexes o…

chemistry.chemical_classificationBiphenylModels MolecularTetraphenylborateMolecular StructureMetal ions in aqueous solutionOrganic ChemistryInorganic chemistrychemistry.chemical_elementGeneral ChemistryCrystal structureCrystallography X-RayMedicinal chemistryHydrocarbons AromaticCatalysisIon selective electrodechemistry.chemical_compoundchemistryCationsBoratesNon-covalent interactionsPyridiniumBoronElectrodesChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

Boehmite Supported Pyrene Polyamine Systems as Probes for Iodide Recognition

2013

New organic–inorganic fluorescent probes made by attaching the tripodal polyamine (tris(2-aminoethyl))amine (tren), propylamine, or diethylenetriamine functionalized with pyrene as a fluorophore to an γ-aluminum oxohydroxide matrix have been prepared and studied both in solution and supported on the surface of boehmite nanoparticles. Both kinds of systems have been revealed as sensitive and selective fluorescence turn-off chemosensors for iodide in aqueous solution with an estimated detection limit that reaches 36 ppb. The recognition characteristics and photophysical properties of these molecules are essentially preserved when they are grafted to the surface of the particles. Since the nan…

chemistry.chemical_classificationBoehmiteAqueous solutionFluorophoreChemistryInorganic chemistryIodideNanoparticlePropylamineSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral EnergyDiethylenetriaminePyrenePhysical and Theoretical ChemistryThe Journal of Physical Chemistry C
researchProduct

Effects of organic matter complexation on partitioning of transition metals into calcite: Cave-analogue crystal growth experiments

2022

We highlight the potential for first row transition metals to carry paleohydrological signals in speleothems, and argue that these metals constitute valuable proxies for climate reconstructions. Metal availability to speleothems is hypothesised to be restricted by organic complexation, which strongly limits the free ion activity of transition metals (Co2+, Ni2+ and Cu2+) in dripwater, thereby creating a kinetic overprint on metal concentrations and isotope ratios in speleothem calcite. This study presents the results of the first cave-analogue experiments of transition metal partitioning into calcite in the absence and presence of organic ligands. The Geological Microclimate (GeoMic) system…

chemistry.chemical_classificationCalcitegeographyAqueous solutiongeography.geographical_feature_categoryInorganic chemistryNitrilotriacetic acidSpeleothemF800Metalchemistry.chemical_compoundchemistryTransition metalGeochemistry and Petrologyvisual_artvisual_art.visual_art_mediumOrganic matterChelation
researchProduct