Search results for "Single"

showing 10 items of 4920 documents

Risk Disclosure in the European Banking Industry: Qualitative and Quantitative Content Analysis Methodologies

2022

This book aims to shed light on the advantages and disadvantages of both qualitative and quantitative content analysis methodologies by examining risk disclosure practices in the European banking industry. Content analysis methodologies allow to assess the level of transparency of financial and non-financial reports by focusing on the information disclosed to the public with reference to their risk exposure and management. There is an ongoing debate in the literature to understand whether qualitative or quantitative content analysis methodologies are more effective and useful to analyse disclosure practices. Some authors contend that qualitative methodologies may be more appropriate because…

Content AnalysisBanking UnionDerivative DisclosureSingle Supervisory MechanismSettore SECS-P/11 - Economia Degli Intermediari FinanziariDisclosureBankingEuropean BankBanking Supervision
researchProduct

Model of a CNC Feed Drive for On-Site Tuning of the Controllers for Single Axis Motion

2016

The accuracy of CNC machine-tools is heavily influenced by the correct tuning of the feed drives controllers. While an initial tuning is performed by the machine-tool manufactures, in time the values have to be changed by the user in order to preserve positioning and contouring accuracy of the machine. This paper presents a model of a CNC feed drive, for a particular CNC machine-tool, but with a high degree of generality. The objective is to provide the user the necessary knowledge, together with a simple, yet accurate simulation tool, in order to assist him in the process of tuning the controllers.

ContouringEngineeringbusiness.industryControl theorySingle axisFeed driveProcess (computing)PID controllerControl engineeringGeneral MedicineMotion controlbusinessMotion (physics)Applied Mechanics and Materials
researchProduct

Analysis of the dopant segregation effects at the floating zone growth of large silicon crystals

1997

Abstract A computer simulation is carried out to study the dopant concentration fields in the molten zone and in the growing crystal for the floating zone (FZ) growth of large (> 100mm) Si crystals with the needle-eye technique and with feed/crystal rotation. The mathematical model developed in the previous work is used to calculate the shape of the molten zone and the velocity field in the melt. The influence of melt convection on the dopant concentration field is considered. The significance of the rotation scheme of the feed rod and crystal on the dopant distribution is investigated. The calculated dopant concentration directly at the growth interface is used to determine the normalized …

ConvectionSiliconDopantCondensed matter physicschemistry.chemical_elementMineralogyCondensed Matter PhysicsRotationInorganic ChemistryCrystalchemistryElectrical resistivity and conductivityHeat transferMaterials ChemistrySingle crystalJournal of Crystal Growth
researchProduct

Convective phenomena in large melts including magnetic fields

2007

The set of characteristic parameters which describe modern large industrial CZ silicon single crystal growth systems is introduced. The main melt flow driving mechanisms are considered, and the characteristic density values of various in the melt acting forces are estimated. The analysis is illustrated with examples of numerical simulation and comparisons with experiments.

ConvectionSingle crystal growthComputer simulationSiliconChemistrychemistry.chemical_elementMineralogyCrystal growthMechanicsCondensed Matter PhysicsMagnetic fieldInorganic ChemistryMaterials ChemistryFluid dynamicsMelt flow indexJournal of Crystal Growth
researchProduct

Syntheses, Structures, Magnetic Properties, and Density Functional Theory Magneto-Structural Correlations of Bis(μ-phenoxo) and Bis(μ-phenoxo)-μ-acet…

2013

The bis(mu-phenoxo) (FeNiIII)-Ni-II compound [Fe-III(N-3)(2)LNiII(H2O)(CH3CN)](ClO4) (1) and the bis(mu-phenoxo)-mu-acetate/bis(mu-phenoxo)-bis(mu-acetate) (FeNiII)-Ni-III compound {[Fe-III(OAc)LNiII(H2O)(mu-OAc)](0.6)center dot[(FeLNiII)-L-III(mu-OAc)(2)](0.4)}(ClO4)center dot 1.1H(2)O (2) have been synthesized from the Robson type tetraiminodiphenol macrocyclic ligand H2L, which is the [2 + 2] condensation product of 4-methyl-2,6-diformylphenol and 2,2'-dimethy1-1,3-diaminopropane. Single-crystal X-ray structures of both compounds have been determined. The cationic part of the dinuclear compound 2 is a cocrystal of the two species [Fe-III(OAc)LNiII(H2O)(mu-OAc)](+) (2A) and [(FeLNiII)-L-I…

Coordination ClustersCopper(Ii) ComplexesSingle-Molecule MagnetTransition-Metal-ComplexesChemistryStereochemistryTheoretical ExplorationExchange InteractionsCationic polymerizationCocrystalAnisotropy BarrierInorganic ChemistryCrystallographyFerromagnetismAntiferromagnetismLanthanide ComplexesDensity functional theoryMacrocyclic ligandPhysical and Theoretical ChemistrySpin Ground-StateGaussian-Basis SetsInorganic Chemistry
researchProduct

A Copper(II)-Cytidine Complex as a Building Unit for the Construction of an Unusual Three-Dimensional Coordination Polymer

2010

The chiral [Cu(cyd) 4 ] 6- anion acts as a multiarmed complex-ligand toward auxiliary copper(II) centers leading to the first example of cytidinate-bridged three-dimensional (3D) coordination polymer of formula [Cu 6 (H 2 O) 7 (ClO 4 ) 3 Cu(cyd) 4 ]-(ClO 4 ) 3 (1). Single crystal X-ray analysis of 1 shows a unique 3D covalent network supported by the exclusive hypercoordination of the cytidinate ligand that bridges four crystallographically independent copper(II) ions via the N3, O2, O2', O3', and O5' set of atoms. Magnetic susceptibility measurements in the temperature range 1.9-295 K reveal the coexistence of ferro- and antiferromagnetic interactions within the hexacopper(II) core of 1, t…

Coordination polymerStereochemistryLigandchemistry.chemical_elementGeneral ChemistryAtmospheric temperature rangeCondensed Matter PhysicsCopperMagnetic susceptibilitychemistry.chemical_compoundCrystallographychemistryNetwork covalent bondingAntiferromagnetismGeneral Materials ScienceSingle crystalCrystal Growth & Design
researchProduct

Structural, magnetic and electrical properties of one-dimensional tetraamidatodiruthenium compounds

2013

The first bromo and iodo tetraamidatodiruthenium compounds of the type [Ru2X(μ-NHOCC6H4-R)4]n [X = Br, R = o-Me (1), m-Me (2), p-Me (3); X = I, R = o-Me (4), m-Me (5), p-Me (6)] have been prepared using solvothermal or microwave activation procedures. In these reactions ethanol or methanol as solvents have been used to make the synthesis procedures more environment-friendly. Solvothermal synthesis has allowed us to isolate single crystals of these extremely insoluble compounds and the crystal structures of all of them have been determined using single crystal X-ray diffraction. The change of the bridging halide ligand permits us to discuss the properties of these complexes on the basis of t…

Coordination polymerStereochemistrySolvothermal synthesischemistry.chemical_elementCrystal structureAtmospheric temperature rangeMagnetic susceptibilityRutheniumInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryBromideSingle crystalDalton Trans.
researchProduct

Synthesis and characterization of vanadyl(IV) complexes of Schiff bases derived from anthranilic acid and salicylaldehyde (or its derivatives) or ace…

1997

Anhydrous, dimeric vanadyl(IV) complexes of Schiff bases derived from [1+1] condensation of salicylaldehyde (or its derivatives) and anthranilic acid, have been synthesized from CH3CN and were characterized by elemental analysis, FTIR, EPR, absorption, TGA, cyclic voltammetry and room temperature magnetic susceptibility measurements. These complexes were found to be oxidized by air in polar solvents like MeOH and DMF to V-V products. The E(1/2) values were found to be around 660 mV indicating that the carboxylate group favours vanadyl(IV) binding when compared to the alkoxo-bound vanadium complexes. Oxidative instability of these complexes are dependent on the substituent on the salicylalde…

Coordination sphereAcetylacetoneDimeric Vanadyl(Iv)Inorganic chemistryDecavanadateVanadiumchemistry.chemical_elementRedoxSingle Crystal X-RayInorganic Chemistrychemistry.chemical_compoundOxidationPyridinePolymer chemistryMaterials ChemistryAnthranilic acidPhysical and Theoretical ChemistrySchiff BasesSchiff baseReactivityVanadiumBindingMononuclear Octahedral Vo3+chemistrySalicylaldehydeDecavanadatesPyridiniumOxidative InstabilityOxovanadium(Iv)Polyhedron
researchProduct

A Two-State Computational Investigation of Methane C-H and Ethane C-C Oxidative Addition to [CpM(PH3)]n+ (M=Co, Rh, Ir;n=0, 1)

2006

Reductive elimination of methane from methyl hydride half-sandwich phosphane complexes of the Group 9 metals has been investigated by DFT calculations on the model system [CpM(PH(3))(CH(3))(H)] (M = Co, Rh, Ir). For each metal, the unsaturated product has a triplet ground state; thus, spin crossover occurs during the reaction. All relevant stationary points on the two potential energy surfaces (PES) and the minimum energy crossing point (MECP) were optimized. Spin crossover occurs very near the sigma-CH(4) complex local minimum for the Co system, whereas the heavier Rh and Ir systems remain in the singlet state until the CH(4) molecule is almost completely expelled from the metal coordinati…

Coordination sphereC-C activation010402 general chemistryPhotochemistry7. Clean energy01 natural sciencesCatalysisReductive eliminationMetalSpin crossover[CHIM.COOR]Chemical Sciences/Coordination chemistrySinglet stateC-H activation010405 organic chemistryHydrideChemistryOrganic ChemistryGeneral ChemistrySpin crossoverOxidative addition0104 chemical sciencesliminationDensity functional calculations13. Climate actionvisual_artvisual_art.visual_art_mediumPhysical chemistryGround state
researchProduct

Exceptionally long-lived light-emitting electrochemical cells: multiple intra-cation π-stacking interactions in [Ir(C^N)2(N^N)][PF6] emitters

2015

A series of cyclometalated iridium(iii) complexes [Ir(C^N)2(N^N)][PF6] (N^N = 2,2′-bipyridine (1), 6-phenyl-2,2′-bipyridine (2), 4,4′-di-tert-butyl-2,2′-bipyridine (3), 4,4′-di-tert-butyl-6-phenyl-2,2′-bipyridine (4); HC^N = 2-(3-phenyl)phenylpyridine (HPhppy) or 2-(3,5-diphenyl)phenylpyridine (HPh2ppy)) are reported. They have been synthesized using solvento precursors so as to avoid the use of chlorido-dimer intermediates, chloride ion contaminant being detrimental to the performance of [Ir(C^N)2(N^N)][PF6] emitters in light-electrochemical cell (LEC) devices. Single crystal structure determinations and variable temperature solution 1H NMR spectroscopic data confirm that the pendant pheny…

Coordination sphereF300ChemistryF100F200StackingAnalytical chemistrychemistry.chemical_elementGeneral ChemistryIonElectrochemical cellCrystallographyProton NMRIridiumLuminescenceSingle crystal
researchProduct