Search results for "solution"

showing 10 items of 5638 documents

Atomic structure solution of the complex quasicrystal approximant Al77Rh15Ru8 from electron diffraction data

2014

The crystal structure of the novel Al77Rh15Ru8phase (which is an approximant of decagonal quasicrystals) was determined using modern direct methods (MDM) applied to automated electron diffraction tomography (ADT) data. The Al77Rh15Ru8E-phase is orthorhombic [Pbma,a= 23.40 (5),b= 16.20 (4) andc= 20.00 (5) Å] and has one of the most complicated intermetallic structures solved solely by electron diffraction methods. Its structural model consists of 78 unique atomic positions in the unit cell (19 Rh/Ru and 59 Al). Precession electron diffraction (PED) patterns and high-resolution electron microscopy (HRTEM) images were used for the validation of the proposed atomic model. The structure of the E…

ChemistryMetals and AlloysQuasicrystalCrystal structureelectron diffraction tomography; icosahedral and decagonal quasicrystals; modern direct methodsAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsCrystallographyElectron diffractionmodern direct methodsMaterials ChemistryAtomic modelicosahedral and decagonal quasicrystalsPrecession electron diffractionOrthorhombic crystal systemelectron diffraction tomographyHigh-resolution transmission electron microscopyElectron backscatter diffraction
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Solution Processed Micro- and Nano-Bioarrays for Multiplexed Biosensing

2012

This Feature article reports on solution dispensing methodologies which enable the realization of multiplexed arrays at the micro- and nanoscale for relevant biosensing applications such as drug screening or cellular chips.

ChemistryNanotechnologyBiosensing TechniquesElectrochemical TechniquesEquipment DesignHardware_PERFORMANCEANDRELIABILITYMicroarray AnalysisMultiplexingHigh-Throughput Screening AssaysAnalytical ChemistrySolution processedNano-Hardware_INTEGRATEDCIRCUITSAnimalsHumansNanotechnologyBiochipBiosensorAnalytical Chemistry
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Installation of Amine Moieties into a Polycyclic Anodic Product Derived from 2,4-Dimethylphenol

2011

When 2,4-dimethylphenol is anodically treated, a dehydrotetramer with four contiguous stereocentres is readily obtained on a multi-gram scale. The substitution of a 2,4-dimethyl-phenoxy fragment by several amines was demonstrated, and the best results were obtained with primary amines. Optically pure α-chiral aliphatic amines yield diastereomeric mixtures that can be separated in most cases. The basic amine causes a partial hemiketal-opening of the bisbenzofuran moiety leading to an equilibrium within an α,β-unsaturated cyclohexenone. This dynamic behaviour occurs on the time scale of NMR spectroscopy and is also found by X-ray analysis providing a consistent picture.

ChemistryOrganic ChemistryDiastereomerGeneral ChemistryNuclear magnetic resonance spectroscopyCatalysisChiral resolutionchemistry.chemical_compoundCyclohexenoneYield (chemistry)MoietyOrganic chemistryAmine gas treatingAminationChemistry - A European Journal
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Asymmetric Synthesis of Dihydropyranones with Three Contiguous Stereocenters by an NHC‐Catalyzed Kinetic Resolution

2021

An oxidative NHC-catalyzed kinetic resolution (KR) of racemic mixtures is presented. The developed reaction furnishes tricyclic dihydropyranones with three contiguous stereocenters in excellent dia- and enantioselectivity, with good-to-moderate yields. Mechanistic studies indicate that the rate-determining step of the reaction is the formation of the Breslow intermediate, while the selectivity determining step occurs later in the mechanism. The presented methodology enables rapid synthesis of complex structures in a single step.

ChemistryOrganocatalysisOrganic ChemistryEnantioselective synthesisSingle stepPhysical and Theoretical ChemistrySelectivityCombinatorial chemistryCatalysisKinetic resolutionStereocenterEuropean Journal of Organic Chemistry
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Graphical representation of polynuclear acid-base and complex equilibria.

1983

Abstract A calculation procedure for diagrams of log CM = ƒ(pL) at various values of the ratio of analytical concentrations, CL/CM, in polynuclear binary systems is described. The diagrams are useful in the resolution of analytical problems of practical interest involving acid-base equilibria (such as the preparation of buffer solutions) and complex equilibria. The presence of a solid phase is also considered.

ChemistryPhase (matter)Resolution (electron density)ThermodynamicsBinary numberRepresentation (mathematics)Base (topology)Analytical ChemistryTalanta
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Preparation and characterization of organofunctionalized bentonite clay bearing aminophosphonic groups in heavy metal uptake

2019

Abstract Bentonite (Bnt) with covalently immobilized N-propylaminodi(methylenephosphonic) groups (Bnt-ADPA) was obtained through a two-step synthesis including aminosilanization and phosphorylation of resulting aminobentonite through Moedritzer-Irani reaction. The grafting of an aminosilane layer in the interplanar space of the bentonite was investigated by XRD, and the presence of N and P-containing groups was confirmed by FTIR, 31P and 29Si MAS NMR. The immobilization of the organic functional groups increased the interplanar distance in bentonite matrix at 52% that essentially improved filtration properties compared to raw bentonite. The number of surface acid groups was evaluated to 0.8…

ChemistryProcess Chemistry and TechnologyMetal ions in aqueous solution02 engineering and technology010501 environmental sciences021001 nanoscience & nanotechnologyGrafting01 natural sciencesPollutionMatrix (chemical analysis)MetalAdsorptionCovalent bondvisual_artBentonitevisual_art.visual_art_mediumChemical Engineering (miscellaneous)Fourier transform infrared spectroscopy0210 nano-technologyWaste Management and Disposal0105 earth and related environmental sciencesNuclear chemistryJournal of Environmental Chemical Engineering
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Surface characterisation of metal ions loaded TiO2 photocatalysts: structure–activity relationship

2004

Abstract Transition metal loaded TiO 2 powders were characterised and tested for the photodegradation of some organic acids. Both Lewis and Bronsted surface acid sites were present in the samples containing large amounts of Mo, V and W. The Bronsted sites are associated to the presence of the transition metals as they do not exist in the unloaded support, and in particular to the presence of these metals in high oxidation states. The trend of the pzc values of the various powders matches rather well both with the surface acidity of the samples experimentally determined by NH 3 adsorption and with a scale of acidity/basicity for bulk binary oxides. XPS investigation indicates that only the p…

ChemistryProcess Chemistry and TechnologyMetal ions in aqueous solutionInorganic chemistryCatalysischemistry.chemical_compoundAdsorptionTransition metalPhotocatalysisReactivity (chemistry)Point of zero chargePhotodegradationGeneral Environmental ScienceBenzoic acidApplied Catalysis B: Environmental
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High-resolution photoacoustic Raman spectroscopy of gases

1992

A high-resolution photoacoustic Raman spectroscopy experiment is described. The resolution achieved by using two single-mode pulsed lasers is about 0.0054 cm −1 (full width at half maximum intensity). The experiment was tested first on the v 1 /2v 2 bands of CO 2 and gave an increase of at least about one order of magnitude in the signal-to-noise ratio with respect to stimulated Raman spectroscopy at low pressure (ca. 10 Torr ≃ 1.3 kPa). The sensitivity is also demonstrated by the study of the weak hot band v 1 +v 2 −v 2 of CO 2 . In both cases, the experimental line shape is well reproduced by taking into account Doppler and collisional effects. A comparison with CARS spectra was also made

ChemistryResolution (electron density)Analytical chemistryLaserHot bandSpectral linelaw.inventionsymbols.namesakeFull width at half maximumlawsymbolsGeneral Materials ScienceRaman spectroscopySpectroscopyDoppler effectSpectroscopyJournal of Raman Spectroscopy
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Analysis of Active-Site Distribution in ZSM-5 Crystals by Infrared Microscopy

1993

Abstract The acid Site distribution over large ZSM-5 crystals was analyzed using FTIR microscopy. Results of the analysis of the OH-stretching vibrations and of vibrations of pyridine adsorbed on Bronsted and Lewis acid sites were found to be in good agreement. The resolution which can be obtained using this novel technique is about 10-20 μm. This limits the application to large crystals as analyzed in this study. Comparison of the results of IR microscopy with aluminum distributions obtained by electron microprobe analysis revealed that IR microscopy cannot resolve inhomogeneities on a scale smaller than the above-stated limits. The results of both methods on a larger scale, however. are i…

ChemistryResolution (electron density)MicroscopyAnalytical chemistryInfrared spectroscopyElectron microprobePhysical and Theoretical ChemistryFourier transform infrared spectroscopyZSM-5Infrared microscopySingle crystalCatalysisJournal of Catalysis
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Rietveld Refinement of Tetragonal V4+–ZrO2 Solid Solutions Obtained from Gels by X-ray Powder Diffraction

2002

Abstract The crystal structure of three tetragonal V x Zr 1− x O 2 solid solutions, with x =0.025, 0.05, and 0.075, prepared by heating dried gel precursors at 450°C in air atmosphere, have been determined by Rietveld refinement on the basis of powder X-ray powder diffractometer data. They contain V 4+ cations surrounded by eight oxygens, four at a distance between 2.079 and 2.093 A and another four at longer distances between 2.369 and 2.348 A. The estimation of the crystal average oxygen position from the X-ray lattice parameter of V x Zr 1− x O 2 conform with the relationship proposed by Howard et al. ( J. Am. Ceram. Soc. 81, 241 (1998)).

ChemistryRietveld refinementCrystal structureCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsInorganic ChemistryCrystalTetragonal crystal systemCrystallographyLattice constantPowder DiffractometerMaterials ChemistryCeramics and CompositesPhysical and Theoretical ChemistryPowder diffractionSolid solutionJournal of Solid State Chemistry
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