Search results for " Chemistry"

showing 10 items of 41321 documents

Structural Motifs of Alkali Metal Superbases in Non‐coordinating Solvents

2020

Abstract Lochmann–Schlosser superbases (LSB) are a standard reagent in synthetic chemistry to achieve an exchange of a proton on an organic framework with an alkali metal cation, which in turn can be replaced by a wide range of electrophilic groups. In standard examples, the deprotonating reagent consists of an equimolar mixture of n‐butyllithium and potassium t‐butoxide. However, the nature of the reactive species could not be pinned down either for this composition or for similar mixtures with comparable high reactivity. Despite the poor solubility and the fierce reactivity, some insights into this mixture were achieved by some indirect results, comparison with chemically related systems,…

superbasealkali metalschemistry.chemical_element010402 general chemistry01 natural sciencesChemical synthesisCatalysisReactivity (chemistry)Solubility010405 organic chemistrypotassiumOrganic ChemistrySuperbaseaggregationMinireviewsGeneral ChemistryAlkali metalCombinatorial chemistry0104 chemical scienceschemistrylithiumReagentElectrophileLithiumMinireviewOrganometallic Chemistry | Reviews ShowcaseChemistry – A European Journal
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CO(2)-water supercritical mixtures: Test of a potential model against neutron diffraction data

2007

Abstract A neutron diffraction experiment on supercritical mixtures of water and CO 2 at two concentrations is presented. Data are analyzed within the EPSR framework and the water–water and water–CO 2 radial distribution functions are compared with those calculated by a Molecular Dynamics simulation performed by using the TIPS2 and EPM-M potential models for water and CO 2 respectively. It is found that the Molecular Dynamics simulation reproduces the overall shape of the site–site radial distribution functions, although missing a few subtle changes brought along when the CO 2 concentration is increased.

supercritical fluidChemistryNeutron diffractionAnalytical chemistryThermodynamicsRadial distributionCondensed Matter PhysicsAtomic and Molecular Physics and OpticsSupercritical fluidElectronic Optical and Magnetic MaterialsMolecular dynamicsneutron diffractionMaterials ChemistryAstrophysics::Earth and Planetary AstrophysicsPhysical and Theoretical ChemistryPhysics::Atmospheric and Oceanic PhysicsSpectroscopy
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On the adsorption and reactivity of element 114, flerovium

2022

Flerovium (Fl, element 114) is the heaviest element chemically studied so far. To date, its interaction with gold was investigated in two gas-solid chromatography experiments, which reported two different types of interaction, however, each based on the level of a few registered atoms only. Whereas noble-gas-like properties were suggested from the first experiment, the second one pointed at a volatile-metal-like character. Here, we present further experimental data on adsorption studies of Fl on silicon oxide and gold surfaces, accounting for the inhomogeneous nature of the surface, as it was used in the experiment and analyzed as part of the reported studies. We confirm that Fl is highly v…

superheavy elementsatomitatomifysiikkaadsorptionradiokemiaalkuaineetradiochemistrynuclear chemistryadsorptiorecoil separatorselement 114kemialliset ominaisuudet
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Catalytic applications of TiO2

2021

Abstract The use of TiO2 as heterogeneous catalyst and/or active support for metals or other oxides is here reported. Many reactions of industrial relevance involve, in fact, titania-based catalysts, among them, NOx abatement, Fischer–Tropsch and water–gas shift, Deacon and Claus processes, hydrodesulfurizations and hydrogenations, selective reductions and selective oxidations. This chapter aims to discuss the main applications of TiO2, in its different forms, as effective support or catalyst for thermocatalytic and photo-thermocatalytic reactions, focusing on the role of its structural and physicochemical properties on the catalytic performance (activity, selectivity, stability).

supported metalsTitaniaChemistryselective catalytic reductionHeterogeneous catalysisCombinatorial chemistryCatalysisCatalysisstrong metal and support interactionMetal oxidesSettore CHIM/07 - Fondamenti Chimici Delle TecnologieSelectivityActive supportNOx
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Determination of glyphosate and its metabolite aminomethylphosphonic acid in fruit juices using supported-liquid membrane preconcentration method wit…

2005

Abstract The application of supported-liquid membrane (SLM) technique for effective extraction of N -(phosphonomethyl)glycine (glyphosate) and its primary metabolite aminomethylphosphonic acid (AMPA) from juices (orange, grapefruit, apple and blackcurrant) in combination with HPLC-UV detection after derivatization with p -toluenesulphonyl chloride (TsCl) is presented. The influence of various parameters such as the composition of acceptor phase, flow-rate, concentration of analytes, on the performance of extraction procedure, was studied. It was shown that by appropriate manipulation of SLM parameters the level of detection could be significantly improved. The influence of SLM conditions on…

supported-liquid membrane extractionMetaboliteGlycineOrganophosphonatesTetrazolesaminomethylphosphonic acidfruit juiceBiochemistryHigh-performance liquid chromatographyChlorideAnalytical ChemistryBeveragesTosyl Compoundschemistry.chemical_compoundglyphosatemedicineSample preparationAminomethylphosphonic acidDerivatizationChromatography High Pressure LiquidChromatographyOrganic ChemistryPrimary metaboliteMembranes ArtificialIsoxazolespesticidesGeneral MedicinechemistryFruitGlyphosateCalibrationSpectrophotometry UltravioletHPLCmedicine.drugJournal of Chromatography A
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Superconducting Triplet Rim Currents in a Spin-Textured Ferromagnetic Disk

2022

Since the discovery of the long-range superconducting proximity effect, the interaction between spin-Triplet Cooper pairs and magnetic structures such as domain walls and vortices has been the subject of intense theoretical discussions, while the relevant experiments remain scarce. We have developed nanostructured Josephson junctions with highly controllable spin texture, based on a disk-shaped Nb/Co bilayer. Here, the vortex magnetization of Co and the Cooper pairs of Nb conspire to induce long-range triplet (LRT) superconductivity in the ferromagnet. Surprisingly, the LRT correlations emerge in highly localized (sub-80 nm) channels at the rim of the ferromagnet, despite its trivial band s…

suprajohtavuusCondensed Matter - SuperconductivityMechanical EngineeringFOS: Physical sciencesnanotekniikkaBioengineeringGeneral ChemistryCondensed Matter Physics114 Physical sciencessuprajohteetSuperconductivity (cond-mat.supr-con)General Materials SciencemagnetismifysiikkaNano Letters
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6-Methyluracil: a redetermination of polymorph (II)

2019

6-Methyluracil, C5H6N2O2, exists in two crystalline phases: form (I), monoclinic, space group P21/c [Reck et al. (1988). Acta Cryst. A44, 417–421] and form (II), monoclinic, space group C2/c [Leonidov et al. (1993). Russ. J. Phys. Chem. 67, 2220–2223]. The structure of polymorph (II) has been redetermined providing a significant increase in the precision of the derived geometric parameters. In the crystal, molecules form ribbons approximately running parallel to the c-axis direction through N—H...O hydrogen bonds. The radical differences observed between the crystal packing of the two polymorphs may be responsible in form (II) for an increase in the contribution of the polar canonical forms…

supramolecular chemistry; crystal engineering; nucleobasecrystal structure010405 organic chemistryChemistryHydrogen bondUracilCrystal structurenucleobases010402 general chemistry01 natural sciencessupramolecular chemistry0104 chemical sciencesNucleobaseCrystalchemistry.chemical_compoundCrystallographycrystal engineeringGroup (periodic table)lcsh:QD901-999Canonical formlcsh:CrystallographynucleobaseMonoclinic crystal systemIUCrData
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The Hexameric Resorcinarene Capsule as a Brønsted Acid Catalyst for the Synthesis of Bis(heteroaryl)methanes in a Nanoconfined Space

2019

Herein, we show that the hexameric resorcinarene capsule C is able to catalyze the formation of bis(heteroaryl)methanes by reaction between pyrroles or indoles and carbonyl compounds (α-ketoesters or aldehydes) in excellent yields and selectivity. Our results suggest that the capsule can play a double catalytic role as a H-bond catalyst, for the initial activation of the carbonyl substrate, and as a Bronsted acid catalyst, for the dehydration of the intermediate alcohol.

supramolecular organocatalysisAlcohol02 engineering and technology010402 general chemistry01 natural sciencesCatalysislcsh:Chemistrychemistry.chemical_compoundPolymer chemistryBrønsted acid catalystOriginal ResearchChemistrySubstrate (chemistry)CapsuleH-bond catalystGeneral Chemistryself-assemblyResorcinareneSupramolecular organocatalysis; Resorcinarene hexameric capsule; Bis(heteroaryl)methanes; Self-assembly; H-bond catalyst; Brønsted acid catalyst021001 nanoscience & nanotechnology0104 chemical sciencesChemistrylcsh:QD1-999Self-assembly0210 nano-technologyBrønsted–Lowry acid–base theorySelectivityresorcinarene hexameric capsulebis(heteroaryl)methanesFrontiers in Chemistry
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Supramolecular Organocatalysis in Water Mediated by Macrocyclic Compounds

2018

In the last decades many efforts have been devoted to design supramolecular organocatalysts able to work in water as the reaction medium. The use of water as solvent provides promising benefits with respect to environmental impact. In this context, macrocyclic compounds played a role of primary importance thanks to their ease of synthesis and their molecular recognition abilities toward the reactants. The aim of this review is to give an overview of the recent advances in the field of supramolecular organocatalysis in water, focusing the attention on calixarene and cyclodextrins derivatives. Calixarenes and cyclodextrins, thanks to their hydrophobic cavities, are able to host selectively th…

supramolecular organocatalysisSupramolecular chemistryContext (language use)Review010402 general chemistry01 natural scienceslcsh:ChemistryHydrophobic effectMolecular recognitionCalixareneHydrophobic effectsupramolecular organocatalysis Water Hydrophobic effect molecular recognition Calixarenes CyclodextrinsCyclodextrins010405 organic chemistryChemistryRegioselectivityWaterGeneral ChemistryCombinatorial chemistry0104 chemical sciencesChemistrylcsh:QD1-999Organic reactionOrganocatalysismolecular recognitionCalixarenes
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Influencing the self‐sorting behavior of [2.2]paracyclophane based ligands by introducing isostructural binding motifs

2020

Two isostructural ligands with either nitrile ( L nit ) or isonitrile ( L iso ) moieties directly connected to a [2.2]paracyclophane backbone with pseudo‐meta substitution pattern have been synthesized. The ligand itself ( L nit ) or its precursors ( L iso ) were resolved via HPLC on a chiral stationary phase and the absolute configuration of the isolated enantiomers was assigned by XRD analysis and/or by comparison of quantum‐chemical simulated and experimental ECD‐spectra. Surprisingly, the resulting metallosupramolecular aggregates formed in solution upon coordination of [(dppp)Pd(OTf) 2 ] differ in their composition: whereas L nit forms dinuclear complexes L iso exclusively forms trinuc…

supramolekulaarinen kemianitrile ligandsself-assemblyliganditsupramolecular chemistryisonitrile ligandsself-sorting
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