Search results for "Inorganic & Nuclear"

showing 10 items of 143 documents

Synthesis, Structure, and Reactivity of (Dihydrogen)(hydrido)iron(II) Complexes Bearing Chiral Diphos­phanes

2015

The heterolytic cleavage of molecular hydrogen by [Fe(H2O)6][BF4]2 and the chiral phosphane (+)-1,2-bis[(2R,5R)-2,5-dimethylphospholano]benzene [(R,R)-Me-DuPhos] or its enantiomer [(S,S)-Me-DuPhos] yields the (dihydrogen)(hydrido)iron complexes [FeH(2-H2){(R,R)-Me-DuPhos}2]BF4 ([R,R-1]BF4) and [FeH(2-H2){(S,S)-Me-DuPhos}2]BF4 ([S,S-1]BF4), respectively. These complexes are fluxional in solution at room temperature, and the trans isomers are observed at 200 K. The ()-cis-[R,R-1]BF4 complex was identified crystallographically as the only stereoisomer at room temperature. The energetic and structural differences between the cis ( and ) and trans isomers were analyzed from a computational (DFT)…

PhanesStereochemistryHydrogen molecule010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesMedicinal chemistryHeterolysis0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryReactivity (chemistry)EnantiomerDuPhosBenzeneCis–trans isomerismEuropean Journal of Inorganic Chemistry
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Crystal polymorphism of (μ4–O)-body centered adamantanoid Cu(II) complexes

2016

Abstract Two novel polymorphs of [Cu4(μ4–O)(μ–Cl)6(DASO)4], (DASO = diallyl sulfoxide; C6H10OS), rhombic (C) and triclinic (D), were obtained and examined by single crystal X-ray diffraction analysis at two temperatures, 295(2) and 100(1) K. This study, in addition to our recent work on the tetragonal (A) and trigonal (B) forms of the title compound, allowed determining the nature of polymorphism and temperature-induced phase transitions. It is stated that both the packing arrangement and the displacive transformation integrate these structures, forming the symmetrically and thermodynamically related series: A,B → C → D. The C3h → C4 distortion of Cu(II) trigonal bipyramidal coordination ge…

Phase transitionO-body centered adamantanoid cageChemistryOrganic ChemistryTriclinic crystal system010403 inorganic & nuclear chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryInorganic ChemistryTrigonal bipyramidal molecular geometryCrystallographyTetragonal crystal systemCu(II) coordination sphere distortionPolymorphism (materials science)Diffusionless transformation0103 physical sciences010306 general physicsSingle crystalSpectroscopyPacking and displacive polymorphismCoordination geometryorder–disorder transformationJournal of Molecular Structure
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Quasifission in heavy and superheavy element formation reactions

2016

Superheavy elements are created in the laboratory by the fusion of two heavy nuclei. The large Coulomb repulsion that makes superheavy elements decay also makes the fusion process that forms them very unlikely. Instead, after sticking together for a short time, the two nuclei usually come apart, in a process called quasifission. Mass-angle distributions give the most direct information on the characteristics and time scales of quasifission. A systematic study of carefully chosen mass-angle distributions has provided information on the global trends of quasifission. Large deviations from these systematics reveal the major role played by the nuclear structure of the two colliding nuclei in de…

Physics010308 nuclear & particles physicsPhysicsQC1-999Nuclear TheoryNuclear structureSuperheavy Elements01 natural sciencesCoulomb repulsionNuclear physicsChemistryInorganic & Nuclear0103 physical sciencesNaturvetenskapNuclear010306 general physicsNatural SciencesNuclear ExperimentEPJ Web of Conferences
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Measurements of charge state distributions of 0.74 and 1.4  MeV/u heavy ions passing through dilute gases

2017

In many modern heavy-ion accelerator facilities, gas strippers are used to increase the projectile charge state for improving the acceleration efficiency of ion beams to higher energies. For this application, the knowledge on the behavior of charge state distributions of heavy-ions after passing through dilute gases is of special interest. Charge state distributions of uranium ($^{238}\mathrm{U}$), bismuth ($^{209}\mathrm{Bi}$), titanium ($^{50}\mathrm{Ti}$), and argon ($^{40}\mathrm{Ar}$) ion beams with energies of $0.74\text{ }\mathrm{MeV}/\mathrm{u}$ and $1.4\text{ }\mathrm{MeV}/\mathrm{u}$ after passing through hydrogen (${\mathrm{H}}_{2}$), helium (He), carbon dioxide (${\mathrm{CO}}_{…

PhysicsNuclear and High Energy PhysicsArgonPhysics and Astronomy (miscellaneous)Hydrogen010308 nuclear & particles physicschemistry.chemical_elementCharge (physics)Surfaces and Interfaces010403 inorganic & nuclear chemistry01 natural sciences0104 chemical sciencesBismuthIonNeonchemistry0103 physical sciencesPhysics::Accelerator PhysicsProduction (computer science)Atomic physicsHeliumPhysical Review Accelerators and Beams
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First ionization potential of the heaviest actinide lawrencium, element 103

2016

The first ionization potential (IP1 ) of element 103, lawrencium (Lr), has been successfully determined for the first time by using a newly developed method based on a surface ionization process. The measured IP 1 value is 4.9630.08 0.07 eV. This value is the smallest among those of actinide elements and is in excellent agreement with the value of 4.963(15) eV predicted by state-of-the-art relativistic calculations also performed in this work. Our results strongly support that the Lr atom has an electronic configuration of [Rn]7s 2 5f 14 7p 1 1/2 , which is influenced by strong relativistic effects. The present work provides a reliable benchmark for theoretical calculations and also opens t…

PhysicsPhysicsQC1-99905 social sciences050301 educationThermal ionizationchemistry.chemical_elementActinide010403 inorganic & nuclear chemistry01 natural sciences0104 chemical scienceschemistryNuclear Physics - TheoryAtomNuclear Physics - Experimentddc:530Atomic numberElectron configurationAtomic physicsIonization energyRelativistic quantum chemistry0503 educationLawrencium
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Complex chemistry with complex compounds

2016

In recent years gas-phase chemical studies assisted by physical pre-separation allowed for the investigation of fragile single molecular species by gas-phase chromatography. The latest success with the heaviest group 6 transactinide seaborgium is highlighted. The formation of a very volatile hexacarbonyl compound Sg(CO)6 was observed similarly to its lighter homologues molybdenum and tungsten. The interactions of these gaseous carbonyl complex compounds with quartz surfaces were investigated by thermochromatography. Second-generation experiments are under way to investigate the intramolecular bond between the central metal atom of the complexes and the ligands addressing the influence of re…

PhysicsQC1-999Transactinide elementchemistry.chemical_elementTungsten010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciences0104 chemical sciencesMetalchemistryGroup (periodic table)Computational chemistryMolybdenumChemical physicsvisual_artIntramolecular forceSeaborgium540 ChemistryAtomvisual_art.visual_art_medium570 Life sciences; biologyEPJ Web of Conferences
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Impact of prompt gamma emission of 44Sc on quantification in preclinical and clinical PET systems

2021

Abstract 44Sc is an increasingly investigated positron emitter for use in positron emission tomography (PET) imaging. However, 44Sc is a non-pure positron emitter, since prompt photons are co-emitted during the decay process. This study investigates coincidence energy spectra of 44Sc and its impact on PET quantification on a preclinical and clinical PET system in comparison with 18F. The raw data of the coincidence events revealed characteristic differences comparing the photon energy distribution of 44Sc and 18F. Due to prompt gamma emission of 44Sc, activity recovery is underestimated on PET systems. However, clinical PET imaging of 44Sc with acceptable quantitative accuracy appears feasi…

RadiationMaterials sciencemedicine.diagnostic_testAstrophysics::High Energy Astrophysical PhenomenaPhysics::Medical PhysicsPositron emittersGamma rayPet imagingPhoton energy010403 inorganic & nuclear chemistry01 natural sciencesQuantitative accuracyCoincidence030218 nuclear medicine & medical imaging0104 chemical sciences03 medical and health sciences0302 clinical medicineNuclear magnetic resonancePositron emission tomographymedicinePhysics::Accelerator PhysicsPet quantificationApplied Radiation and Isotopes
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Resonant laser–SNMS for spatially resolved and element selective ultra-trace analysis of radionuclides

2018

The newly developed resonant laser–SNMS system at the IRS Hannover combines the high spatial and decent mass resolution of a TOF-SIMS instrument with the element-selective process of resonant laser ionization. This setup was characterized by use of synthetic uranium, plutonium and technetium samples to prepare and demonstrate the performance for measurements on environmental samples. The laser–SNMS system will be applied for the detection, visualization and ultra-trace analysis of radionuclide containing nanoparticles in environmental samples with strongly reduced or even completely omitted chemical preparation. The necessary suppression of isobaric contamination was demonstrated as well as…

RadionuclideMaterials science010401 analytical chemistryAnalytical chemistrychemistry.chemical_elementNanoparticleUranium010403 inorganic & nuclear chemistryLaser01 natural sciences0104 chemical sciencesAnalytical ChemistryPlutoniumlaw.inventionSecondary ion mass spectrometrychemistrylawIonizationIsobaric processSpectroscopyJournal of Analytical Atomic Spectrometry
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2017

In the context of radiopharmacy and molecular imaging, the concept of theranostics entails a therapy-accompanying diagnosis with the aim of a patient-specific treatment. Using the adequate diagnostic radiopharmaceutical, the disease and the state of the disease are verified for an individual patient. The other way around, it verifies that the radiopharmaceutical in hand represents a target-specific and selective molecule: the “best one” for that individual patient. Transforming diagnostic imaging into quantitative dosimetric information, the optimum radioactivity (expressed in maximum radiation dose to the target tissue and tolerable dose to healthy organs) of the adequate radiotherapeutica…

Radionuclidemedicine.diagnostic_testbusiness.industrymedicine.medical_treatmentPharmaceutical ScienceNuclear dataContext (language use)010403 inorganic & nuclear chemistry01 natural sciences030218 nuclear medicine & medical imaging0104 chemical sciencesRadiation therapy03 medical and health sciences0302 clinical medicinePositron emission tomographyDrug DiscoverymedicineMedical imagingMolecular MedicineDosimetryMolecular imagingNuclear medicinebusinessPharmaceuticals
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Disordered sodium alkoxides from powder data: crystal structures of sodium ethoxide, propoxide, butoxide and pentoxide, and some of their solvates

2021

The crystal structures of NaOEt, NaOPr, NaOBu and NaOAm (Am = amyl = pentyl) were determined from powder data. These compounds crystallize in an anti-PbO structure in the space groups P 21 m and P4/nmm. Additionally, solvates with the composition NaOEt·2EtOH, NaOPr·2PrOH, NaOiPr·5iPrOH and NaOtAm·tAmOH were synthesized, and their structures were determined from single crystals. They form interesting chain structures of different compositions and topologies.

Recrystallization (geology)Sodiumchemistry.chemical_elementAlcoholCrystal structure010402 general chemistry010403 inorganic & nuclear chemistry01 natural scienceschemistry.chemical_compoundsolvateBärnighausen treeMaterials Chemistryddc:530Alkylchemistry.chemical_classificationSodium ethoxideChemistryMetals and AlloysResearch PapersAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsisopropanolCrystallographysodium alkoxide548PXRDddc:540Alkoxidepowder dataPowder diffraction
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