Search results for "yield"

showing 10 items of 1338 documents

The upgraded ISOLDE yield database – A new tool to predict beam intensities

2020

At the CERN-ISOLDE facility a variety of radioactive ion beams are available to users of the facility. The number of extractable isotopes estimated from yield database data exceeds 1000 and is still increasing. Due to high demand and scarcity of available beam time, precise experiment planning is required. The yield database stores information about radioactive beam yields and the combination of target material and ion source needed to extract a certain beam along with their respective operating conditions. It allows to investigate the feasibility of an experiment and the estimation of required beamtime. With the increasing demand for ever more exotic beams, needs arise to extend the functi…

Radioactive ion beamsNuclear and High Energy PhysicsYieldsComputer sciencecomputer.software_genre114 Physical sciences01 natural sciencesISOLDEDatabaseFLUKACERN0103 physical sciencesddc:530Production Yield010306 general physicsInstrumentationLarge Hadron ColliderDatabase010308 nuclear & particles physicsIn-target productionYield predictionCross sectionsYield (chemistry)ABRABLAIONIZATIONRelease efficiencycomputerRadioactive beamBeam (structure)Radioactive beamsNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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A new method for radiochemical separation of arsenic from irradiated germanium oxide.

2005

Abstract Radioarsenic labelled radiopharmaceuticals could be a valuable asset to Positron Emission Tomography (PET). In particular, the long half-lives of 72 As ( T 1/2 =26 h) and 74 As ( T 1/2 =17.8 d) allow to investigate slow physiological or metabolical processes, like the enrichment and distribution of antibodies in tumor tissue. This work describes the direct production of no-carrier-added (nca) arsenic isotopes *As, with *=71, 72, 73, 74 or 77, the reaction to [*As]AsI 3 and its radiochemical separation from the irradiated solid germanium oxide via polystyrene-based solid-phase extraction. The germanium oxide target, irradiated at a cyclotron or a nuclear reactor, is dissolved in con…

RadioisotopesRadiationGermaniumExtraction (chemistry)RadiochemistryHalidechemistry.chemical_elementIodineArsenicchemistry.chemical_compoundHydrofluoric acidchemistryYield (chemistry)Positron-Emission TomographySolid phase extractionRadiopharmaceuticalsArsenicGermanium oxideNuclear chemistryHalf-LifeApplied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine
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Post-elution processing of 44Ti/44Sc generator-derived 44Sc for clinical application

2009

The (44)Ti/(44)Sc (T(1/2)(44)Ti=60a) generator provides cyclotron-independent access to positron-emitting (44)Sc (T(1/2)=3.97d) for PET imaging. This work aims to post-elution processing of initial (44)Sc generator eluates in order to reduce its volume, HCl concentration and remove the oxalate anions. The on-line adsorption of (44)Sc on cationic resin AG 50W-X8 (200-400 mesh, H(+)-form) is achieved with >98% efficacy. Subsequently, the purified (44)Sc is desorbed by using 3ml of 0.25M ammonium acetate (pH=4.0). The post-processing takes 10min. The overall yield of the post-processing reached 90%, which is referred to the (44)Sc obtained from the (44)Ti/(44)Sc generator. In addition to the c…

RadioisotopesTitaniumRadiationElutionIon chromatographyAnalytical chemistryCationic polymerizationchemistry.chemical_elementOxalatechemistry.chemical_compoundAdsorptionchemistryIsotope LabelingPositron-Emission TomographyYield (chemistry)ScandiumRadiopharmaceuticalsScandiumAmmonium acetateNuclear chemistryApplied Radiation and Isotopes
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Observation and analysis of Fano-like lineshapes in the Raman spectra of molecules adsorbed at metal interfaces

2015

Surface enhanced Raman spectra from molecules (bipyridyl ethylene) adsorbed on gold dumbells are observed to become increasingly asymmetric (Fano-like) at higher incident light intensity. The electronic temperature (inferred from the anti-Stokes (AS) electronic Raman signal increases at the same time while no vibrational AS scattering is seen. These observations are analyzed by assuming that the molecule-metal coupling contains an intensity dependent contribution (resulting from light-induced charge transfer transitions as well as renormalization of the molecule metal tunneling barrier). We find that interference between vibrational and electronic inelastic scattering routes is possible in …

Raman scatteringsurface-enhanced Raman scatteringbipyridyl ethyleneMaterials scienceFOS: Physical sciencesNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesMolecular physicsSpectral linesymbols.namesakeMesoscale and Nanoscale Physics (cond-mat.mes-hall)MoleculePhysics::Chemical Physicsta116ta114Condensed Matter - Mesoscale and Nanoscale PhysicsScatteringadsorbtion021001 nanoscience & nanotechnologyRay0104 chemical sciences3. Good healthX-ray Raman scatteringYield (chemistry)symbols0210 nano-technologyRaman spectroscopymetal surfacesRaman scatteringPhysical Review B
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Solvatochromism Unravels the Emission Mechanism of Carbon Nanodots

2016

High quantum yield, photoluminescence tunability, and sensitivity to the environment are hallmarks that make carbon nanodots interesting for fundamental research and applications. Yet, the underlying electronic transitions behind their bright photoluminescence are strongly debated. Despite carbon-dot interactions with their environment should provide valuable insight into the emitting transitions, they have hardly been studied. Here, we investigate these interactions in a wide range of solvents to elucidate the nature of the electronic transitions. We find remarkable and systematic dependence of the emission energy and kinetics on the characteristics of the solvent, with strong response of …

Range (particle radiation)PhotoluminescenceChemistrySettore FIS/01 - Fisica SperimentaleSolvatochromismQuantum yield02 engineering and technologyElectron010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistryCondensed Matter::Mesoscopic Systems and Quantum Hall Effect01 natural sciencesFluorescence0104 chemical sciencesCondensed Matter::Materials ScienceChemical physicsAtomic electron transitionGeneral Materials ScienceSpontaneous emissionCarbon dots photoluminescence nanomaterialsPhysical and Theoretical Chemistry0210 nano-technologyThe Journal of Physical Chemistry Letters
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Diastereoselective Synthesis of Spiro[pyrazolone-4,3′-tetrahydrothiophenes] via a Sulfa-Michael/Aldol Domino Reaction

2016

Synthesis : journal of synthetic organic chemistry 48(23), 4091-4098(2016). doi:10.1055/s-0035-1562473

Reaction conditions010405 organic chemistryChemistryOrganic ChemistryPyrazolone010402 general chemistry54001 natural sciencesCombinatorial chemistryCatalysisDomino0104 chemical scienceschemistry.chemical_compoundCascade reactionAldol reactionYield (chemistry)ddc:540medicineOrganic chemistryTetrahydrothiophenemedicine.drug
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ChemInform Abstract: Reactions of 3-Vinylindole Derivatives with Dienophiles.

2010

Reactions of 3-(1-cyclohexenyl)-1,2-dimethylindole (1a) and the 1,2-dihydrocarbazole 1b with some carbo- and heterodienophiles are described. Thus, compound 1a reacts to give ene, Michael-type, and Diels-Alder adducts, depending on the dienophile and reaction conditions. The 3-vinylindole 1b reacts with 4-phenyl-1,2,4-triazoline-3,5-dione or N-phenylmaleimide in a dehydrogenative reaction to yield the fully aromatized carbazole 8.

Reaction conditionsAddition reactionchemistry.chemical_compoundChemistryCarbazoleYield (chemistry)Organic chemistryGeneral MedicineEne reactionAdductChemInform
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First Fluorous Synthesis of Fluorinated Uracils

2006

This paper describes a novel fluorous synthesis of fluorinated uracils 4. In this new protocol, fluorous alcohols 1, which are used as fluorous tags, are acetylated to yield acetates 2, which in turn are treated with a base to form their enolates. These are then reacted with fluorinated nitriles to furnish tagged β-enamino esters 3. Although this condensation step had been performed easily in previous solution and solid-phase syntheses, it proved to be very elusive in the fluorous version. Meticulous control of the reaction conditions was thus essential in order to achieve satisfactory yields of β-enamino esters 3. The final treatment of compounds 3 with isocyanates or isothiocyanates effic…

Reaction conditionsChemistryYield (chemistry)Organic ChemistryDrug DiscoveryOrganic chemistryGeneral MedicineCombinatorial chemistryComputer Science ApplicationsQSAR & Combinatorial Science
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1,3-Oxazin-2-ones vs tetrahydrofurans by iodocyclisation of 2-alkoxycarbonylamino-3-alken-1-ols

2000

Abstract Iodocyclisation of primary homoallylic alcohols 2a – d , containing either a 2- t -butoxy- or a benzyloxycarbonylamino group, was studied, in order to establish the nucleophilic group involved in cyclofunctionalisation. In fact, the N - t -Boc derivative 2a gave the oxazinone 3 , exclusively, whereas starting from the N -Cbz derivative 2b a diastereomeric mixture of substituted tetrahydrofurans 4 and 5 resulted in ratios depending upon the reaction conditions. These results were rationalised by means of computational methods. On the contrary, migration of both the t -butyl or benzyl group to the hydroxy group was observed when both 2c and 2d underwent cyclisation to give the corres…

Reaction conditionsStereochemistryChemistryOrganic ChemistryHydroxy groupDiastereomerCatalysisInorganic Chemistrychemistry.chemical_compoundNucleophileYield (chemistry)Benzyl groupOrder (group theory)Physical and Theoretical ChemistryDerivative (chemistry)Tetrahedron: Asymmetry
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Three-Component Synthesis of α-Aminoperoxides Using Primary and Secondary Dialkylzinc Reagents with O2 and α-Amido Sulfones

2020

A straightforward strategy for the synthesis of unprecedented α-aminoperoxides bearing primary and secondary alkylperoxide substituents is described. Commercially available dialkylzinc reagents are oxidized with molecular oxygen and the consequent peroxide species react with stable (hetero)­aromatic and aliphatic α-amido sulfones in excellent yields (>90%). The now available α-aminoperoxides are of potential interest in medicinal chemistry, specifically for the synthesis of antimalarial compounds. Moreover, modification of the reaction conditions selectively leads to N,O-acetals in good yields.

Reaction conditionschemistry.chemical_compoundPrimary (chemistry)chemistryComponent (thermodynamics)Yield (chemistry)ReagentOrganic ChemistryMolecular oxygenPhysical and Theoretical ChemistryBiochemistryCombinatorial chemistryPeroxideOrganic Letters
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