Search results for "Lithium"

showing 10 items of 680 documents

CCDC 791091: Experimental Crystal Structure Determination

2011

Related Article: J.Konu, H.M.Tuononen, T.Chivers|2009|Inorg.Chem.|48|11788|doi:10.1021/ic901878h

(((Diisopropylphosphoroselenoyl)methylene)(diisopropyl)(selanyl)phosphoranato)-(NNN'N'-tetramethylethane-12-diamine)-lithiumSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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RBS and ERD cross-sections and optical model parameters for the analysis of lithium, boron and nickel

2000

Abstract Elastic scattering cross-sections for RBS analysis of nickel by 7 Li and 11 B ion backscattering near the Coulomb barrier have been determined. The lithium ion measurements were performed in the energy range of 8–15 MeV at the laboratory angles of 115° and 135°. For boron ions the energies between 14 and 24 MeV and scattering angles of 89°, 110° and 130° were used. For the analysis of lithium and boron by ERD the scattering cross-sections have been calculated by kinematically reversing the backscattering process. The calculated 58 Ni ion energies thus varied between 65 and 125 MeV for lithium and between 75 and 130 MeV for boron recoils. For the Li + Ni and B + Ni systems the thres…

010302 applied physicsElastic scatteringNuclear and High Energy PhysicsScatteringchemistry.chemical_elementCoulomb barrier02 engineering and technology021001 nanoscience & nanotechnology7. Clean energy01 natural sciencesIonNickelsymbols.namesakechemistry0103 physical sciencessymbolsLithiumRutherford scatteringAtomic physics0210 nano-technologyBoronInstrumentationNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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Anomalies of dielectric properties and conductivity in single domain LiNbO3:Zn crystals

2016

ABSTRACTA study of the temperature dependence of dielectric constant, conductivity, and piezoelectric modulus in the single-domain state of LiNbO3 crystals modified by Zn admixture at threshold concentration is reported. Unipolarity of the LiNbO3:Zn crystals is observed to increase after treatment of brand-new samples by high-temperature electro-diffusion annealing and by subsequent high-temperature annealing of short-circuited samples. The observed effects are explained as a result of meta-stable residual domains collapsing at high temperature the collapse being assisted by disintegration of charged clusters stabilizing domain walls. The rise of unipolarity is accompanied by anomalies on t…

010302 applied physicsMaterials scienceCondensed matter physicsAnnealing (metallurgy)Lithium niobateMineralogyModulus02 engineering and technologyDielectricConductivity021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesPiezoelectricityElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryControl and Systems Engineering0103 physical sciencesMaterials ChemistryCeramics and CompositesElectrical and Electronic EngineeringSingle domain0210 nano-technologyAfter treatmentIntegrated Ferroelectrics
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Atomic Layer Deposition of LiF Thin Films from Lithd, Mg(thd)2, and TiF4 Precursors

2013

Lithium fluoride is an interesting material because of its low refractive index and large band gap. Previously LiF thin films have been deposited mostly by physical methods. In this study a new way of depositing thin films of LiF using atomic layer deposition (ALD) is presented. Mg(thd)2, TiF4 and Lithd were used as precursors, and they produced crystalline LiF at a temperature range of 300–350 °C. The films were studied by UV–vis spectrometry, field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), atomic force microscopy (AFM), time-of-flight elastic recoil detection analysis (ToF-ERDA), and energy dispersive X-ray spectroscopy (EDX). In addition, film adhesion was t…

010302 applied physicsMaterials scienceta214ta114Band gapGeneral Chemical EngineeringAnalytical chemistryLithium fluoride02 engineering and technologyGeneral ChemistryAtmospheric temperature range021001 nanoscience & nanotechnology01 natural sciencesElastic recoil detectionchemistry.chemical_compoundAtomic layer depositionchemistryImpurity0103 physical sciencesMaterials ChemistryThin film0210 nano-technologySpectroscopyChemistry of Materials
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Development, Characterization, and Testing of a SiC-Based Material for Flow Channel Inserts in High-Temperature DCLL Blankets

2018

This work has been carried out within the framework of the EUROfusion Consortium. The views and opinions expressed herein do not necessarily reflect those of the European Commission.

010302 applied physicsNuclear and High Energy PhysicsMaterials scienceFabricationelectrical conductivityBlanketCondensed Matter Physics01 natural sciencesTemperature measurement010305 fluids & plasmasCorrosionchemistry.chemical_compoundThermal conductivitydual-coolant lead-lithium (DCLL) blanketFlexural strengthchemistryCorrosion by PbLi0103 physical sciencesThermalSilicon carbide:NATURAL SCIENCES:Physics [Research Subject Categories]flow channel insert (FCI)thermal conductivityComposite materialporous SiCIEEE Transactions on Plasma Science
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Photolysis of Tertiary Amines in the Presence of CO2: The Paths to Formic Acid, α-Amino Acids, and 1,2-Diamines

2017

The photolysis of triethylamine (1a) in the presence of carbon dioxide leads to the hydrogenation of CO2, the α-C-C coupling of triethylamine (1a), and the CO2-insertion into the α-C-H σ-bond of amine 1a. This reaction is proposed to proceed through the radical ion pair [R3N·+·CO2·-] generated by the photoionization of amine 1a and the electron capture by CO2. The presence of lithium tetrafluoroborate in the reaction medium promotes the efficient and stereoselective α-C-C coupling of 1a by enhancing the production of α-dialkylamino radicals and the isomerization of N,N,N',N'-tetraethylbutane-2,3-diamine (4a).

010405 organic chemistryFormic acidRadicalOrganic ChemistryPhotodissociationLithium tetrafluoroborate010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical scienceschemistry.chemical_compoundRadical ionchemistryAmine gas treatingAminoàcidsQuímica orgànicaIsomerizationTriethylamineThe Journal of Organic Chemistry
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Deprotonation of Benzoxazole and Oxazole Using Lithium Magnesates

2005

International audience; The first deprotonations of oxazole and benzoxazole using lithium magnesates are described. The reactions occurred in tetrahydrofuran at room temperature using 1/3 equiv of lithium tributylmagnesate. As 2-lithiooxazole and 2-lithiobenzoxazole, lithium tri(2-oxazolyl)magnesate and lithium tri(2-benzoxazolyl)magnesate very rapidly and completely isomerized to the more stable 2-(isocyano)enolate and 2-(isocyano)phenolate type structures, respectively, a result shown by NMR analysis. The isolation of 2-substituted oxazoles and benzoxazoles in medium to good yields after electrophilic trapping was interpreted in two ways:  (1) the equilibration between the open and closed…

010405 organic chemistryLithium bromide[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistrychemistry.chemical_element[CHIM.THER]Chemical Sciences/Medicinal Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry[CHIM.CATA]Chemical Sciences/CatalysisBenzoxazole[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryPhotochemistry01 natural sciencesMedicinal chemistry0104 chemical scienceschemistry.chemical_compoundDeprotonationchemistryIntramolecular forceElectrophile[CHIM]Chemical SciencesLithium[CHIM.RADIO]Chemical Sciences/RadiochemistryTetrahydrofuranOxazole
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Conformational Control of Metallocene Backbone by Cyclopentadienyl Ring Substitution: a New Concept in Polyphosphane Ligands Evidenced by “Through-Sp…

2009

The present study deals with the conformational control of the metallocene backbone within ferrocenyl polyphosphane ligands and their performance in the highly topical palladium-catalyzed heteroaromatics arylation by direct C−H activation. New substituted cyclopentadienyl rings were synthesized, which allowed the assembling of original tri- and diphosphanes. The bulky cyclopentadienyl lithium salts diphenylphosphino-3-(triphenyl)methylcyclopentadienyllithium (4) and 1,2-bis(diphenylphosphino)-4-(triphenyl)methylcyclopentadienyllithium (5) were prepared in excellent yield. The assembling of these new hindered cyclopentadienyl salts (Cp) with other Cp fragments was performed in order to prepa…

010405 organic chemistryStereochemistryOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistrychemistry.chemical_element[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistryRing (chemistry)01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic Chemistry[ CHIM.CATA ] Chemical Sciences/Catalysischemistry.chemical_compoundchemistryCyclopentadienyl complexYield (chemistry)Lithium[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistrySpin (physics)MetalloceneComputingMilieux_MISCELLANEOUS
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A reinvestigation of compound CpMo(PMe3)2(CH3)2: Alkylation by single electron transfer and radical addition?

2001

International audience; The synthesis of the half-sandwich molybdenum(III) diphosphine dimethyl complex CpMo(PMe3)2(CH3)2 has been reinvestigated. The compound was obtained from the corresponding dichloro complex CpMo(PMe3)2Cl2 and methyllithium at low temperatures and isolated as a crystalline product by conducting all operations at temperatures lower than −10 °C. The complex is thermally unstable at room temperature but has been fully characterised by EPR spectroscopy, cyclic voltammetry and X-ray diffraction. The formation reaction is retarded by excess phosphine. On the basis of this and other related observations, a mechanism involving phosphine pre-dissociation followed by single elec…

010405 organic chemistrychemistry.chemical_elementGeneral ChemistryAlkylation010402 general chemistryPhotochemistry01 natural sciences0104 chemical scienceslaw.inventionSingle electronchemistry.chemical_compoundchemistrylawMolybdenumPolymer chemistryMethyllithium[CHIM.COOR]Chemical Sciences/Coordination chemistryCyclic voltammetryElectron paramagnetic resonancePhosphine
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A comprehensive review of energy sources for unmanned aerial vehicles, their shortfalls and opportunities for improvements

2020

Unmanned Aerial Vehicles were first introduced almost 40 years ago and their applications have increased and diversified substantially since then, in both commercial and private use. One of the UAVs main issues when it comes to mobility is that the power sources available are inadequate, this highlights an area for improvement as the interest in drones is on the increase. There exist many different types of power supplies applied to UAVs, however each has their own limitations and strengths that pertain to weight contributions, charging and discharging times, size, payload capabilities, energy density and power density. The aim of this paper is to review the main power sources available for…

0301 basic medicineComputer scienceSuper-capacitor (SC)Review Article03 medical and health sciencesEnergy storage technology0302 clinical medicineElectric power transmissionLithium-polymer (Li-Po)lcsh:Social sciences (General)lcsh:Science (General)MultidisciplinaryEnergyPayloadHydrogen energyFuel cellFuel technology(FC)DroneVDP::Teknologi: 500030104 developmental biologyElectric power transmissionAerospace engineeringRisk analysis (engineering)Electrical engineeringEnergy densityUnmanned aerial vehicle (UAV)Fuel cellslcsh:H1-99Energy source030217 neurology & neurosurgerylcsh:Q1-390Heliyon
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