Search results for "A.S.I."

showing 10 items of 16703 documents

On-line commissioning of SHIPTRAP

2006

Abstract The on-line commissioning of the Penning-trap mass spectrometer SHIPTRAP was successfully completed with a mass measurement of holmium and erbium radionuclides produced at SHIP. A large fraction of contaminant ions created in the stopping cell was identified to originate from the buffer-gas supply system. Using a liquid nitrogen cold trap they were reduced to a tolerable amount and mass measurements of Er 147 , Er 148 , and Ho 147 with relative uncertainties of about 1 × 1 0 − 6 were performed.

010308 nuclear & particles physicsAnalytical chemistrychemistry.chemical_elementLiquid nitrogen[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]Condensed Matter PhysicsMass spectrometryPenning trap01 natural sciencesAtomic massIonMasschemistry07.75.+h; 21.10.Dr0103 physical sciencesPhysical and Theoretical Chemistry010306 general physicsHolmiumInstrumentationSpectroscopyCold trap
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Gold/Isophorone Interaction Driven by Keto/Enol Tautomerization

2016

The binding behavior of isophorone (C9H14O) to Au adatoms and clusters deposited on MgO/Ag(001) thin films is investigated by scanning tunneling microscopy (STM) and density functional theory (DFT). The STM data reveal the formation of various metal/organic complexes, ranging from Au1/isophorone pairs to larger Au aggregates with molecules bound to their perimeter. DFT calculations find the energetically preferred keto-isophorone to be unreactive toward gold, while the enol-tautomer readily binds to Au monomers and clusters. The interaction is governed by electrostatic forces between the hydroxyl group of the enol and negative excess charges residing on the ad-gold. The activation barrier b…

010402 general chemistryPhotochemistry01 natural sciencesChemical reactionlaw.inventionchemistry.chemical_compoundlawketo-enol tautomerismgold compoundsMoleculePhysical and Theoretical Chemistryta116Isophoroneta114010405 organic chemistryKeto–enol tautomerismEnolTautomer0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsisophoroneGeneral EnergychemistryDensity functional theoryScanning tunneling microscopeJournal of Physical Chemistry C
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Photoswitching of the antiferromagnetic coupling in an oxamato-based dicopper(ii) anthracenophane

2011

Thermally reversible photomagnetic (ON/OFF) switching behavior has been observed in a dinuclear oxamatocopper(ii) anthracenophane upon UV light irradiation and heating; the two CuII ions (SCu = 1/2) that are antiferromagnetically coupled in the dicopper(ii) metallacyclic precursor (ON state) become uncoupled in the corresponding [4+4] photocycloaddition product (OFF state), as substantiated from both experimental and theoretical studies. © 2011 The Royal Society of Chemistry.

010405 organic chemistryChemistryMetals and AlloysLight irradiation[CHIM.MATE]Chemical Sciences/Material chemistryGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysisAntiferromagnetic coupling0104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonCrystallographyMaterials ChemistryCeramics and CompositesChemical Communications
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Planar Benzo[1,2-b:4,5-b′]dithiophene Derivatives Decorated with Nitronyl and Imino Nitroxides

2018

Four weakly antiferromagnetic interacting biradicals of benzo[1,2- b:4,5- b']dithiophene (BDT) and BDT extended with two thiophenes (BDTTh2) linked with nitronyl and imino nitroxides (NN and IN) as BDT-NN, BDT-IN, BDTTh2-NN, and BDTTh2-IN were designed, synthesized, and characterized. Short intermolecular π-π distances were found (3.42 A) for BDT-NN, whereas larger ones were found for BDT-IN (3.54 A) and BDTTh2-NN (3.67 A), respectively. Intramolecular magnetic interaction ( Jintra,exp/ kB) of BDT-NN (-26 K) is much larger than for BDT-IN (-5.3 K), while it is reduced for the dithiophene-extended molecule BDTTh2-NN (-2.3 K). Intermolecular interactions ( zJinter,exp/ kB) of BDT-NN (-6.5 K) …

010405 organic chemistryChemistryOrganic ChemistryCrystalline materialsIntermolecular force010402 general chemistry01 natural sciences0104 chemical sciencesCrystallographyPlanarIntramolecular forceAntiferromagnetismMoleculeMagnetic interactionSpin (physics)The Journal of Organic Chemistry
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Mechanism and cis/trans Selectivity of Vinylogous Nazarov-type [6π] Photocyclizations

2017

Vinylogous Nazarov-type cyclizations yield seven-membered rings from butadienyl vinyl ketones via a photochemical [6π] photocyclization followed by subsequent isomerization steps. The mechanism of this recently developed method was investigated using unrestricted DFT, SF-TDDFT, and CASSCF/NEVPT2 calculations, suggesting three different pathways that lead either to pure trans, pure cis, or mixed cis/trans configured products. Singlet biradicals or zwitterions occur as intermediates. The computational results are supported by deuterium-labeling experiments.

010405 organic chemistryChemistryStereochemistryYield (chemistry)Organic ChemistrySinglet state010402 general chemistrySelectivity01 natural sciencesIsomerizationCis–trans isomerism0104 chemical sciencesThe Journal of Organic Chemistry
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Cis- and trans molybdenum oxo complexes of a prochiral tetradentate aminophenolate ligand : Synthesis, characterization and oxotransfer activity

2020

Abstract Reaction of [MoO2Cl2(dmso)2] with the tetradentate O2N2 donor ligand papy [H2papy = N-(2-hydroxybenzyl)-N-(2-picolyl)glycine] leads to formation of the dioxomolybdenum(VI) complex [MoO2(papy)] (1) as a mixture of cis and trans isomers. Recrystallization from methanol furnishes solid cis-1, whereas the use of a dichloromethane-hexane mixture allows for the isolation of the trans-1 isomer. Both isomers have been structurally characterized by X-ray crystallography and the energy difference between the isomeric pair has been investigated by electronic structure calculations. Optimization of two configurational isomers in the gas phase predicts the trans isomer to lie 2.5 kcal/mol lower…

010405 organic chemistryChemistrycomputational modellingStereoisomerism010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesCatalysisInorganic ChemistrySolventvariable temperature NMRTripodal ligandepoxidationMaterials ChemistryTheoretical chemistryProton NMRtripodal ligandPhysical and Theoretical ChemistryIsomerizationOxo Atom TransferCis–trans isomerism
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The separation of cis- and trans-1,3-cyclohexanediol isomers by copper complexation. Crystal structures of cis-1,3-cyclohexanediol and copper(II) chl…

2002

Abstract A 1:1 complex between copper(II) chloride and cis-1,3-cyclohexanediol has been synthesized and its crystal structure determined. The structure is composed of two different dinuclear [CuCl2(c-13chd)]2 units in which the copper(II) ions are surrounded by the two oxygen atoms of the diol and the two halide ions in a distorted cis-square planar arrangement in both cases. A fifth coordination site is occupied by a halide ion in one dinuclear unit for both copper ions and an O atom belonging to the adjacent CuCl2(c-13chd) moiety in the other dinuclear unit for both copper ions, thus forming a distorted square pyramidal geometry for the metals in all cases. The ability of CuCl2 to prefere…

010405 organic chemistryInorganic chemistryHalidechemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciencesChlorideCopperSquare pyramidal molecular geometry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMaterials ChemistrymedicineCopper(II) chlorideMoietyPhysical and Theoretical ChemistryCis–trans isomerismmedicine.drugPolyhedron
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Macrocyclic complexes based on [N⋯I⋯N]+ halogen bonds

2021

New 1–2 nm macrocyclic iodine(I) complexes prepared VIA a simple ligand exchange reaction manifest rigid 0.5–1 nm cavities that bind the hexafluorophosphate anion in the gas phase. The size of the cavities and the electrostatic interactions with the iodine(I) cations influence the anion binding properties of these macrocyclic complexes.

010405 organic chemistryLigandMetals and Alloyschemistry.chemical_elementGeneral Chemistry010402 general chemistryElectrostaticsIodine01 natural sciencesCatalysis0104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonGas phasechemistry.chemical_compoundchemistryHexafluorophosphatePolymer chemistryHalogenMaterials ChemistryCeramics and CompositesAnion bindingChemical Communications
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Budyko’s Based Method for Annual Runoff Characterization across Different Climatic Areas: an Application to United States

2018

Runoff data knowledge is of fundamental importance for a wide range of hydrological, ecological, and socioeconomic applications. The reconstruction of annual runoff is a fundamental task for several activities related to water resources management, especially for ungauged basins. At catchment scales, the Budyko's framework provides an extremely useful and, in some cases, accurate estimation of the long-term partitioning of precipitation into evapotranspiration and runoff as a function of the prevailing climatic conditions. Recently the same long-term partitioning rules have been successfully used to describe water partitioning also at the annual scale and calculate the annual runoff distrib…

010504 meteorology & atmospheric sciences0208 environmental biotechnologyDrainage basin02 engineering and technologyStructural basinWater resources assessment01 natural sciencesBudyko's curveEvapotranspirationRange (statistics)Precipitation0105 earth and related environmental sciencesWater Science and TechnologyCivil and Structural EngineeringSubdivisionHydrologygeographygeography.geographical_feature_categorybusiness.industrySettore ICAR/02 - Costruzioni Idrauliche E Marittime E IdrologiaMOPEX data020801 environmental engineeringWater resourcesEnvironmental scienceAnnual water balanceAnnual runoff distributionSurface runoffbusiness
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Assessment of the Potential Evapotranspiration MODIS Product Using Ground Measurements in the Pampas

2018

Evapotranspiration is the hydrological variable of greatest relevance in the Argentina Pampas Region (APR). The estimation of potential evapotranspiration (PET) in this area becomes essential since primary productivity is directly linked to water availability. In order to evaluate the MOD16_A2 product of evapotranspiration (ET), a comparison with in situ measurements was conducted. We used ET data provided by the Oficina de Riesgo Agropecuario, corresponding to 24 stations placed in the region covering all seasons for the years 2012 to 2014. Results show an overestimation of 86% and 52% in Autumn-Winter and Spring-Summer, respectively. Mean Absolut Error (MAE) range between ±0.9 and ±2.1 mm…

010504 meteorology & atmospheric sciences0211 other engineering and technologies02 engineering and technologyLongwave radiationAtmospheric sciences01 natural sciencesTerm (time)EvapotranspirationProduct (mathematics)Range (statistics)Environmental sciencePrimary productivity021101 geological & geomatics engineering0105 earth and related environmental sciences2018 IEEE Biennial Congress of Argentina (ARGENCON)
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