Search results for "ROM"

showing 10 items of 37506 documents

Direct mass measurements and ionization potential measurements of the actinides

2019

Abstract The precise determination of atomic and nuclear properties such as masses, differential charge radii, nuclear spins, electromagnetic moments and the ionization potential of the actinides has been extended to the late actinides in recent years. In particular, laser spectroscopy and mass spectrometry have reached the region of heavy actinides that can only be produced only at accelerator facilities. The new results provide deeper insight into the impact of relativistic effects on the atomic structure and the evolution of nuclear shell effects around the deformed neutron shell closure at N = 152. All these experimental activities have also opened the door to extend such measurements t…

010308 nuclear & particles physicsChemistryNuclear TheoryTransactinide elementActinideSuperheavy ElementsMass spectrometry01 natural sciences0103 physical sciencesAtomic numberPhysical and Theoretical ChemistryIonization energyAtomic physicsNuclear Experiment010306 general physicsSpectroscopyTransuranium elementRadiochimica Acta
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Antineutrino monitoring of spent nuclear fuel

2016

Military and civilian applications of nuclear energy have left a significant amount of spent nuclear fuel over the past 70 years. Currently, in many countries world wide, the use of nuclear energy is on the rise. Therefore, the management of highly radioactive nuclear waste is a pressing issue. In this letter, we explore antineutrino detectors as a tool for monitoring and safeguarding nuclear waste material. We compute the flux and spectrum of antineutrinos emitted by spent nuclear fuel elements as a function of time, and we illustrate the usefulness of antineutrino detectors in several benchmark scenarios. In particular, we demonstrate how a measurement of the antineutrino flux can help to…

010308 nuclear & particles physicsNuclear engineeringDetectorGeneral Physics and AstronomyFluxRadioactive wasteFOS: Physical sciences01 natural sciencesSpent nuclear fuel3. Good healthHigh Energy Physics - ExperimentOverburdenHigh Energy Physics - Experiment (hep-ex)High Energy Physics - PhenomenologyHigh Energy Physics - Phenomenology (hep-ph)0103 physical sciencesElectromagnetic shieldingEnvironmental scienceNeutrinoNuclear Experiment (nucl-ex)010306 general physicsNuclear ExperimentLeakage (electronics)
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Measurement of the laser resonance ionization efficiency for lutetium

2019

Abstract The development of a highly efficient resonance ionization scheme for lutetium is presented. A laser ion source, based on the all-solid-state Titanium:sapphire laser system, was used at the 30 keV RISIKO off-line mass separator to characterize different possible optical excitation schemes in respect to their ionization efficiency. The developed laser resonance ionization scheme can be directly applied to the use at radioactive ion beam facilities, e. g. at the CERN-MEDICIS facility, for large-scale production of medical radioisotopes.

010308 nuclear & particles physicschemistry.chemical_elementMass spectrometry01 natural sciencesLutetiumIsotope separationlaw.inventionchemistrylawIonization0103 physical sciencesSapphireLaser resonancePhysics::Atomic PhysicsPhysical and Theoretical ChemistryAtomic physics010306 general physicsSpectroscopyRadiochimica Acta
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Sensitive Assays by Nucleophile-Induced Rearrangement of Photoactivated Diarylethenes.

2018

Upon light-induced isomerization, diarylethenes (DAEs) equipped with reactive aldehyde moieties rearrange selectively in the presence of amines, accompanied by decoloration. In a comprehensive study, the probe structure was optimized with regard to its inherent reactivity in the nucleophile-triggered rearrangement reaction. Detailed structure−reactivity relationships could be derived, in particular with regard to the type of integrated (het)aryl moieties as well as the location of the formyl residue, and the probes’ intrinsic reactivity with primary and secondary amines was optimized. Utilizing an ancillary base, the initially formed rearrangement product can engage in a subsequent catalyti…

010402 general chemistry01 natural sciencesBiochemistryAldehydeCatalysischemistry.chemical_compoundPhotochromismColloid and Surface ChemistryNucleophile541 Physikalische ChemieReactivity (chemistry)Rearrangement reactionsensingchemistry.chemical_classification010405 organic chemistryArylGeneral ChemistryphotochromismCombinatorial chemistry0104 chemical sciences540 Chemie und zugeordnete WissenschaftenaminechemistryCatalytic cycleddc:540diaryletheneddc:541547 Organische ChemieIsomerizationddc:547Journal of the American Chemical Society
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2,4,5-Triaryl imidazole probes for the selective chromo-fluorogenic detection of Cu(II). Prospective use of the Cu(II) complexes for the optical reco…

2019

The sensing behaviour toward metal cations and biothiols of two 2,4,5-triarylimidazole probes (3a and 3b) is tested in acetonitrile and in acetonitrile-water. In acetonitrile the two probes present charge-transfer absorption bands in the 320-350 nm interval. Among all cations tested only Cu(11) is able to induce bathochromic shifts of the absorption band in the two probes, which is reflected in marked colour changes. Colour modulations are ascribed to the formation of 1:1 Cu(II)-probe complexes in which the cation interacts with the imidazole acceptor heterocycle. Besides, the two probes present intense emission bands (at 404 and 437 nm for 3a and 3b respectively) in acetonitrile that are q…

010402 general chemistryPhotochemistryCu(II) detection01 natural sciencesCu(II) imagingInorganic ChemistryMetalchemistry.chemical_compoundBathochromic shiftMaterials ChemistryImidazolePhysical and Theoretical ChemistryAcetonitrileImidazole-based probesAqueous solutionScience & Technology010405 organic chemistryGSH imagingAcceptor0104 chemical sciences3. Good healthchemistryAbsorption bandvisual_artvisual_art.visual_art_mediumHypsochromic shiftBiothiols recognition
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The substituent effect of π-electron delocalization in N-methylamino-nitropyridine derivatives: crystal structure and DFT calculations

2020

AbstractThe crystal and molecular structures of 3-(N-methylamino)-2-nitropyridine, 5-(N-methylamino)-2-nitropyridine and 2-(N-methylamino)-5-nitropyridine have been characterized by X-ray diffraction. To perform conformational analysis, the geometries of the compounds as well as their conformers and rotamers were optimized at the B3LYP/6-311++G(3df,3pd) level. The resulting data were used to analyze the π-electron delocalization effect in relation to the methylamino group rotation in ortho-, meta- and para-substitution positions. Quantitative aromaticity indices were calculated based on which we estimated the electronic structures of the analyzed compounds. The substituent effect of the met…

010405 organic chemistryAromaticityCrystal structureSubstituentAromaticityCrystal structure010402 general chemistryCondensed Matter PhysicsRing (chemistry)DFT calculations01 natural sciences0104 chemical sciencesCrystallographychemistry.chemical_compoundDelocalized electronSubstituent effectchemistryCharge of the substituent active regionIntramolecular forcePyridineSubstituent effect stabilization energyPhysical and Theoretical ChemistryConformational isomerismStructural Chemistry
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Tuning the Electronic Properties of Nonplanar exTTF-Based Push–Pull Chromophores by Aryl Substitution

2012

International audience; A new family ofπ-extended tetrathiafulvalene (exTTF) donor−acceptorchromophores has been synthesized by [2 + 2] cycloaddition of TCNE with exTTF-substituted alkynes and subsequent cycloreversion. X-ray data and theoretical calculations,performed at the B3LYP/6-31G**level, show that the new chromophores exhibit highlydistorted nonplanar molecular structures with largely twisted 1,1,4,4-tetracyanobuta-1,3-diene (TCBD) units. The electronic and optical properties, investigated by UV/visspectroscopy and electrochemical measurements, are significantly modified when theTCBD acceptor unit is substituted with a donor phenyl group, which increases the twistingof the TCBD unit…

010405 organic chemistryBand gap[CHIM.ORGA]Chemical Sciences/Organic chemistryArylOrganic ChemistryChromophore010402 general chemistryPhotochemistry01 natural sciencesAcceptorCycloaddition0104 chemical scienceschemistry.chemical_compoundchemistry[ CHIM.ORGA ] Chemical Sciences/Organic chemistryPhenyl groupSpectroscopyTetrathiafulvaleneComputingMilieux_MISCELLANEOUS
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A novel MALDI-MS approach for the analysis of neutral metallosupramolecular architectures

2011

Matrix assisted laser desorption/ionisation mass spectrometry (MALDI-MS) methods have been developed for the characterisation of neutral [2×2] metallogrids derived fromdiimine, dihydrazone and diacylhydrazone ligands. Such grids may be protonated in solution to give cationic species but in most cases these are labile, so that rather delicate conditions are required for observation of the intact metallogrids as monoprotonated derivatives in the gas phase. As a MALDI matrix, 2,4,6-trihydroxyacetophenone (THAP) is sufficiently acidic to enable monoprotonation of the grids unaccompanied by dissociation, and if the grid sample is initially deposited by a layering technique to avoid any prelimina…

010405 organic chemistryChemistryAnalytical chemistrySupramolecular chemistryCrystal structure010402 general chemistryMass spectrometryGrid01 natural sciencesDissociation (chemistry)0104 chemical sciencesInorganic ChemistryCluster (physics)Mass spectrum[CHIM]Chemical Sciencesta116StoichiometryComputingMilieux_MISCELLANEOUS
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Two bimetallic layered materials with “Cu4Fe3” defective cubane units: syntheses, structures and magnetic properties of {[CuII(tn)]2[FeII(CN)6]}3·[Na…

2005

Abstract Reactions of the [Fe III (CN) 6 ] 3− anion with the [Cu II (tn)] 2+ ion (tn = 1,3-diaminopropane) afford the compounds {[Cu II (tn)] 2 [Fe II (CN) 6 ]}3·[Na 3 Fe III (CN) 6 ]·12H 2 O (1) and {[Cu n (tn)] 2 [Fe II (CN) 6 ]}·KCl·5H 2 O (2). Despite the differences concerning their asymmetric units, both structures present strong similar features: in both structures, the Cu(II) ion presents a square-base pyramidal CuN 5 environment and each [Fe II (CN) 6 ] 4− anion is linked to six Cu(II) ions through its six N atoms leading to infinite [Cu II (tn)] 2 [Fe II (CN) 6 ] layers which can be viewed as 2-D layered arrangement generated by the defective cubane units Cu 4 Fe 3 involving Fe-CN…

010405 organic chemistryChemistryCoordination polymerMechanical EngineeringInorganic chemistryMetals and AlloysCrystal structure010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciencesElectronic Optical and Magnetic MaterialsParamagnetismchemistry.chemical_compoundCrystallographyTransition metalMechanics of MaterialsCubaneMaterials ChemistryMoleculeAntiferromagnetismBimetallic stripSynthetic Metals
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Exploring the Chemoselectivity towards Cysteine Arylation by Cyclometallated Au III Compounds: New Mechanistic Insights

2020

To gain more insight into the factors controlling the efficient cysteine arylation by cyclometalated Au(III) complexes, the reaction between selected gold compounds and different peptides was investigated by high‐resolution liquid chromatography electrospray ionization mass spectrometry (HR‐LC‐ESI‐MS). The deducted mechanisms of C–S cross‐coupling, also supported by density functional theory (DFT) and quantum mechanics/molecular mechanics (QM/MM) calculations, evidenced the key role of secondary peptidic gold binding sites in favouring the process of reductive elimination.

010405 organic chemistryChemistryElectrospray ionizationOrganic Chemistrycyclometallated gold complexes010402 general chemistryMass spectrometry01 natural sciencesBiochemistryCombinatorial chemistryMolecular mechanicsReductive elimination0104 chemical sciencesddc:cysteine arylationGold CompoundschemoselectivitySettore CHIM/03 - Chimica Generale E InorganicapeptidesMolecular MedicineDensity functional theoryChemoselectivityMolecular BiologyCysteinemass spectrometry
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