Search results for "Reaction products"

showing 8 items of 8 documents

Dialkyl(butadiene)cyclopentadienylmolybdenum(III) Complexes. Synthesis, Characterization, and Reactivity

2000

International audience; Treatment of CpMo(η4-diene)Cl2 (diene = 1,3-butadiene, C4H6, 1‘; isoprene, C5H8, 1‘ ‘; 2,3-dimethyl-1,3-butadiene, C6H10, 1‘ ‘) in diethyl ether at low temperature with 2 equiv of alkylmagnesium RMgX reagents affords the corresponding dialkyl complexes CpMo(η4-1,3-diene)R2 (2, 2‘, 2‘ ‘, R = CH3, a; CH2Ph, b; CH2SiMe3, c). These species are isolable in moderate yields and have been fully characterized by EPR, elemental analyses, and cyclic voltammetry. They all show a reversible reduction process at relatively low potentials and an irreversible oxidation. The structure of 2‘ ‘a was confirmed by single-crystal X-ray diffraction. The mixed complex CpMo(η4-C4H6)Cl(CH3), …

DieneStereochemistryReaction productsLigands010402 general chemistry01 natural sciencesMedicinal chemistryInorganic Chemistrychemistry.chemical_compound[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM.COOR]Chemical Sciences/Coordination chemistryRedistribution (chemistry)Redox reactionsPhysical and Theoretical ChemistryIsoprene010405 organic chemistryLigandArylOrganic ChemistryAlkyls0104 chemical scienceschemistryReagentCyclic voltammetryDiethyl etherElectron paramagnetic resonance spectroscopyOrganometallics
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Deoxygenative Divergent Synthesis : En Route to Quinic Acid Chirons

2020

The installation of vicinal mesylate and silyl ether groups in a quinic acid derivative generates a system prone for stereoselective borane-catalyzed hydrosilylation through a siloxonium intermediate. The diversification of the reaction conditions allowed the construction of different defunctionalized fragments foreseen as useful synthetic fragments. The selectivity of the hydrosilylation was rationalized on the basis of deuteration experiments and computational studies. peerReviewed

Hydrosilylation010402 general chemistry01 natural sciencesBiochemistrySilyl etherchemistry.chemical_compoundredox reactionsPhysical and Theoretical Chemistryhapetus-pelkistysreaktioorgaaniset yhdisteeteetteritkemiallinen synteesi010405 organic chemistryreaction productsOrganic ChemistryhydrosilylationQuinic acidCombinatorial chemistry0104 chemical sciencesbond cleavageetherschemistryStereoselectivitySelectivityDivergent synthesisDerivative (chemistry)Vicinal
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Intra- vs Intermolecular Aurophilic Contacts in Dinuclear Gold(I) Compounds: Impact on the Population of the Triplet Excited State.

2022

Two series of dinuclear gold(I) complexes that contain two Au–chromophore units (chromophore = dibenzofurane or dimethylfluorene) connected through a diphosphane bridge that differs in the flexibility and length (diphosphane = dppb for 1,4-bis(diphenylphosphino)butane, DPEphos for bis[(2-diphenylphosphino)phenyl]ether, xanthphos for 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene, and BiPheP for 2,2′-bis(diphenylphosphino)-1,1′-biphenyl) have been synthesized and structurally characterized. Their photophysical properties have been carefully investigated, paying attention to the role of the presence, or absence, of aurophilic contacts and their nature (intra- or intermolecular character). Th…

Inorganic Chemistryabsorptiocrystal structurereaction productsX-raysröntgensäteilymolekyylitPhysical and Theoretical Chemistrykidetiedeabsorptionmolecular interactionsInorganic chemistry
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Reaction pathways for atomic layer deposition with lithium hexamethyl disilazide, trimethyl phosphate, and oxygen plasma

2020

Atomic layer deposition (ALD) of lithium-containing films is of interest for the development of next-generation energy storage devices. Lithium hexamethyl disilazide (LiHMDS) is an established precursor to grow these types of films. The LiHMDS molecule can either be used as a single-source precursor molecule for lithium or as a dual-source precursor molecule for lithium and silicon. Single-source behavior of LiHMDS is observed in the deposition process with trimethylphosphate (TMP) resulting in the deposition of crystalline lithium phosphate (Li3PO4). In contrast, LiHMDS exhibits dual-source behavior when combined with O2 plasma, resulting in a lithium silicate. Both processes were characte…

Materials scienceInorganic chemistryReaction productschemistry.chemical_elementEnergy storageCoatings and FilmsPlasmaAtomic layer depositionchemistry.chemical_compoundElectronicOptical and Magnetic MaterialsPhysical and Theoretical ChemistryOXIDESPrecursorsALUMINUM PHOSPHATEMoleculesatomikerroskasvatusSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsTrimethyl phosphateSurfacesChemistryGeneral EnergylitiumchemistryOxygen plasmaLithiumAdsorptionohutkalvotALUMINUM PHOSPHATE
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Population of neutron-rich nuclei around 48ca with deep inelastic collisions

2009

The deep inelastic reaction 48Ca+64Ni at 6 MeV/A has been studied using the CLARA–PRISMA setup. Angular distributions for pure elastic scattering and total cross-sections of the most relevant transfer channels have been measured. The experimental results are compared with predictions from a semiclassical model, showing good agreement for the presently analyzed few neutrons transfer channels. The decay of the most intense reaction products has also been studied, giving indications of the population of states with very short lifetimes. Gadea Raga, Andrés, Gadea.Andres@ific.uv.es

Neutron-rich nucleiReacción InelásticaUNESCO::FÍSICAUNESCO::FÍSICA::Nucleónica::Física de partículasInelastic collision Neutron-rich nuclei Reaction products Semiclassical model Transfer channel; Angular distribution; CalciumReaction productsCanales de transmisiónSemiclassical modelCLARA–PRISMAReacción Inelástica ; CLARA–PRISMA ; Distribuciones angulares ; Secciones cruzadas ; Modelo semiclásico ; Canales de transmisión ; Muy corta vidaInelastic collisionDistribuciones angularesdeep inelastic reaction; semiclassical model; closed shell nuceli:FÍSICA [UNESCO]:FÍSICA::Nucleónica::Física de partículas [UNESCO]Muy corta vidaTransfer channelSecciones cruzadasCalciumAngular distributionModelo semiclásico
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The performance of the cryogenic buffer-gas stopping cell of SHIPTRAP

2018

Direct high-precision mass spectrometry of the heaviest elements with SHIPTRAP, at GSI in Darmstadt, Germany, requires high efficiency to deal with the low production rates of such exotic nuclides. A second-generation gas stopping cell, operating at cryogenic temperatures, was developed and recently integrated into the relocated system to boost the overall efficiency. Offline measurements using 223Ra and 225Ac recoil-ion sources placed inside the gas volume were performed to characterize the gas stopping cell with respect to purity and extraction efficiency. In addition, a first online test using the fusion-evaporation residue 254No was performed, resulting in a combined stopping and extrac…

Speichertechnik - Abteilung BlaumNuclear and High Energy PhysicsMaterials scienceDIRECT MASS MEASUREMENTSProtonBuffer gaschemistry.chemical_elementPenning trapsMass spectrometry7. Clean energy01 natural sciencesFusion-evaporation reaction productsNuclear physicsIonization0103 physical sciencesCalibrationStopping and extraction efficiencyNuclide010306 general physicsInstrumentationCALIBRATION[PHYS]Physics [physics]nobeliumSPECTROSCOPYMass spectrometry010308 nuclear & particles physicsTransfermium elementsCryogenic gas stopping cellExtraction timeHEAVIEST ELEMENTSchemistryIONIZATIONNobeliumOrder of magnitude
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Role of Alkyl Substituent and Solvent on the Structural, Thermal, and Magnetic Properties of Binary Radical Salts of 1,2,3,5-Dithia- or Diselenadiazo…

2022

The synthesis, structural, thermal, and magnetic properties of a series of simple binary organic salts based on the radical anion of 7,7,8,8-tetracyanoquinodimethane (TCNQ) and 4-(N-alkylpyridinium-3-yl)-1,2,3,5-dithiadiazolyl (DTDA), 1R (R = Et, Pr, Bu), radical cations and their heavier selenium analogues (DSDA), 2R, are described. Single-crystal X-ray structural analyses reveal that short alkyl substituents on the pyridinium moiety of DTDA/DSDA cations lead to crystallization of isostructural acetonitrile (MeCN) solvates 1Et·MeCN, 1Pr·MeCN, 2Et·MeCN, and 2Pr·MeCN with trans-cofacial DTDA radical cation and eclipsed-cofacial TCNQ radical anion dimers. A slight increase in the substituent …

anionitsuolatreaction productssaltskationitGeneral Materials ScienceGeneral ChemistryoligomersCondensed Matter PhysicsanionscationsCrystal Growth & Design
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5-Carbonyl-1,3-oxazine-2,4-diones from N-Cyanosulfoximines and Meldrum’s Acid Derivatives

2020

At elevated temperatures, N-cyanosulfoximines react with Meldrum’s acid derivatives to give sulfoximines with N-bound 5-carbonyl-1,3-oxazine-2,4-dione groups. A representative product was characterized by single-crystal X-ray structure analysis. The product formation involves an unexpected molecular reorientation requiring several sequential bond-forming and -cleaving processes. peerReviewed

crystal structurekemiallinen synteesicyclizationaddition reactionskemialliset reaktiotreaction productsrikkiyhdisteetchemical reactionstyppiyhdisteetorgaaniset yhdisteet
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