Search results for "visual_art"

showing 10 items of 2987 documents

Experimental Investigations and Numerical Analysis for Improving Knowledge of Incremental Sheet Forming Process for Sheet Metal Parts

2009

The paper is related to the analysis of shape distortions and springback effects arising in Single Point Incremental Forming. An experimental set up has been designed and manufactured to carry single point incremental forming on small size sheet metal parts. The experimental set up is mounted on 3-axes CNC milling machine tool and the forming tool is attached and move with the spindle. Experiments have been carried out on sheet metal parts to obtain tronconical shapes. The forming strategy associated to the movement of the forming tool has been also investigated. The experiments indicate that shape distortions arising in the corners of the tronconical shape are clearly related to forming st…

business.product_categoryMaterials sciencebusiness.industryMechanical EngineeringNumerical analysisDesign toolProcess (computing)Structural engineeringCondensed Matter PhysicsFinite element methodMachine toolMechanics of Materialsvisual_artvisual_art.visual_art_mediumGeneral Materials ScienceBoundary value problembusinessSheet metalIncremental sheet formingMaterials Science Forum
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Helical Shift Mechanics of Rubber V-Belt Variators

2011

A very common configuration of V-belt variators for motorcycles considers the correction of the belt tensioning depending on the resistant torque by means of suitable helical-shaped tracks allowing the driven half-pulleys to close/open. The theoretical model for belt-pulley coupling is rather complex for this configuration, where one half-pulley may run in advance and the other one behind with respect to the belt, and requires the repeated numerical solution of a strongly nonlinear differential system by a sort of shooting technique, until all the operating conditions are fulfilled (angular contact extent, torque, and axial force). After solving the full equations, the present study develop…

business.product_categoryNumerical solutionThrustResistant torqueStrongly nonlinearPulleyAxial thrustNatural rubberTorqueBoundary value problemAxial forceTheoretical modelTension levelCouplingPhysicsOperating conditionTension (physics)Mechanical EngineeringMechanicsComputer Graphics and Computer-Aided DesignSettore ING-IND/13 - Meccanica Applicata Alle MacchineComputer Science ApplicationsClosed form approximationVariatorsClosure (computer programming)Mechanics of Materialsvisual_artShooting techniquevisual_art.visual_art_mediumAstrophysics::Earth and Planetary Astrophysicsbusiness
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Dynamic Stabilization of the Ligand-Metal Interface in Atomically Precise Gold Nanoclusters Au68 and Au144 Protected by meta-Mercaptobenzoic Acid

2017

Ligand-stabilized, atomically precise gold nanoclusters with a metal core of a uniform size of just 1–3 nm constitute an interesting class of nanomaterials with versatile possibilities for applications due to their size-dependent properties and modifiable ligand layers. The key to extending the usability of the clusters in applications is to understand the chemical bonding in the ligand layer as a function of cluster size and ligand structure. Previously, it has been shown that monodispersed gold nanoclusters, stabilized by meta-mercaptobenzoic acid (m-MBA or 3-MBA) ligands and with sizes of 68–144 gold atoms, show ambient stability. Here we show that a combination of nuclear magnetic reson…

carboxylic acidsspectroscopyGeneral Physics and AstronomyInfrared spectroscopyNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesNanoclustersNanomaterialsMetalMolecular dynamicsNMR spectroscopyGeneral Materials Scienceclustersta116thiolsta114LigandChemistryGeneral Engineeringgold021001 nanoscience & nanotechnologymolecular dynamicsvibrational spectroscopy0104 chemical sciencesCrystallographyChemical bondgold nanoclustervisual_artvisual_art.visual_art_mediumDensity functional theory0210 nano-technologyACS Nano
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Effect of Pre-Reduction on the Properties and the Catalytic Activity of Pd/Carbon Catalysts: A Comparison with Pd/Al2O3

2013

The effect of pre-reduction in solution with chemical reagents on the catalytic performance and catalyst properties of Pd/carbon catalysts was systematically investigated with a multitechnique approach. The results are critically discussed in comparison to those recently obtained on analogous Pd/alumina catalysts. It was proved that the Pd phase on the carbon surface is characterized by a high mobility, opposite to what occurs on alumina. As a result, the Pd particles on carbon aggregate together during pre-reduction, with a consequent decrease in available metal surface. Pd particles remain aggregated also in reaction conditions; the decreased Pd dispersion negatively affects the catalyst …

characterization techniqueCO chemisorptionInorganic chemistryPd-based catalystchemistry.chemical_elementTPRHeterogeneous catalysisPd/CarbonCatalysisCatalysisMetalCharacterization techniquesCatalyst pre-reductionTemperature-programmed reductionX-ray absorption spectroscopymetal nanoparticlein situPd-based catalystsPd/aluminaSAXSGeneral ChemistryXANESSmall Angle X-ray ScatteringX-ray Absorption SpectroscopyPd/Carbon; Pd/alumina; metal nanoparticle; catalysis; Catalyst pre-reduction; in situ; SAXS; XANES; Pd-based catalysts; heterogeneous catalysis; Characterization techniques; Temperature-programmed reduction; TPR; CO chemisorption; TEM; X-ray absorption spectroscopy; Small Angle X-ray Scatteringheterogeneous catalysischemistryReagentvisual_arttemperature-programmed reductionvisual_art.visual_art_mediumTEMheterogeneous catalysiSmall Angle X-ray SpectroscopyDispersion (chemistry)Carbon
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Sequential Reactions of Alkynes on an Iridium(III) Single Site

2017

Sequential insertion of terminal alkynes on IrIII cyclometalated complexes allow the formation of novel metallapolycycles in a controlled and efficient manner. ortho-Methylarylethynyl derivatives led to an unprecedented cascade combination of three fundamental processes (C−C bond formation, C(sp3)−H activation, and reductive coupling) on a single IrIII center, in a process compatible with functionalized biomolecules and photoactive substrates. The reaction with tert-butylacetylene led to a [6,5,4]-polycycle that incorporates an iridacyclobutenylidene in its structure. The sequence is a multicomponent reaction in which the metal not only promotes the different steps but also determines their…

chemistry.chemical_classification010405 organic chemistryBiomoleculeOrganic Chemistrychemistry.chemical_elementSequence (biology)General Chemistry010402 general chemistryPhotochemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesMetalchemistry.chemical_compoundchemistrySingle sitevisual_artvisual_art.visual_art_mediumStereoselectivityIridiumBODIPYSelectivityChemistry - A European Journal
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2017

Eight coordination compounds of formulae [FeII(L˙)2][ReIVCl6] (1a), [FeII(L˙)2][ReIVBr6] (1b), [CoII(L˙)2][ReIVCl6]·CH3CN (2a), [CoII(L˙)2][ReIVBr6] (2b), [NiII(L˙)(CH3CN)3][ReIVCl6]·CH3CN (3a), [NiII(L˙)(CH3CN)3][ReIVBr6]·3CH3CN (3b), [CuII(L˙)2][ReIVCl6] (4a) and [CuII(L˙)2][ReIVBr6] (4b), where L˙ is the aminoxyl radical chelating ligand, 4,4′-dimethyl-2,2′-di(2-pyridyl)oxazolidine-N-oxide, have been synthesised. Structural and magnetic studies reveal metal–radical intramolecular antiferromagnetic interactions in the [MII(L˙)2]2+ cations in the iron, cobalt and copper based compounds (1a, 1b, 2a, 2b, 4a and 4b) with the central metal ion low-spin in the case of iron (1a and 1b) and a gra…

chemistry.chemical_classification010405 organic chemistryChemistryInorganic chemistryInfrared spectroscopychemistry.chemical_element010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesCoordination complexInorganic ChemistryMetalCrystallographyMagnetizationchemistry.chemical_compoundvisual_artvisual_art.visual_art_mediumAntiferromagnetismAcetonitrileCobaltDalton Transactions
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Strongly Coupled Cyclometalated Ruthenium Triarylamine Chromophores as Sensitizers for DSSCs

2016

A series of anchor-functionalized cyclometalated bis(tridentate) ruthenium(II) triarylamine hybrids [Ru(dbp-X)(tctpy)](2-) [2 a](2-) -[2 c](2-) (H3 tctpy=2,2';6',2''-terpyridine-4,4',4''-tricarboxylic acid; dpbH=1,3-dipyridylbenzene; X=N(4-C6 H4 OMe)2 ([2 a](2-) ), NPh2 ([2 b](2-) ), N-carbazolyl [2 c](2-) ) was synthesized and characterized. All complexes show broad absorption bands in the range 300-700 nm with a maximum at about 545 nm. Methyl esters [Ru(Me3 tctpy)(dpb-X)](+) [1 a](+) -[1 c](+) are oxidized to the strongly coupled mixed-valent species [1 a](2+) -[1 c](2+) and the Ru(III) (aminium) complexes [1 a](3+) -[1 c](3+) at comparably low oxidation potentials. Theoretical calculati…

chemistry.chemical_classification010405 organic chemistryChemistryOrganic ChemistryCenter (category theory)chemistry.chemical_elementGeneral ChemistryTricarboxylic acidChromophore010402 general chemistryPhotochemistry01 natural sciencesMedicinal chemistryCatalysis0104 chemical sciencesRutheniumMetalBipyridinechemistry.chemical_compoundDye-sensitized solar cellvisual_artvisual_art.visual_art_mediumCobaltChemistry - A European Journal
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Structural diversity of copper(II) amino alcoholate complexes

2017

Abstract Amino alcohols which carry both amino and hydroxyl groups in the same molecule are good chelating and bridging ligands. They have been broadly used for the preparation of copper(II) amino alcoholate complexes through the self-assembly process, which generally leads to the formation of diverse structures from mononuclear to polynuclear copper(II) clusters. There are three main factors to control the nuclearity of these clusters: (i) the molar ratio of Cu(II) to amino alcohol, (ii) the choice of the counter anions and (iii) the nature of the amino alcohol. These structures can be used as model systems in magnetic studies, allowing a better understanding about the magnetic interaction…

chemistry.chemical_classification010405 organic chemistryChemistryStereochemistrychemistry.chemical_elementAlcoholPolymer010402 general chemistry01 natural sciencesCopper0104 chemical sciencesInorganic ChemistryHydroxylationMetalchemistry.chemical_compoundvisual_artPolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumMoleculeChelationPhysical and Theoretical ChemistryLiterature surveyCoordination Chemistry Reviews
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New Route to Polynuclear Ni(II) and Cu(II) Complexes with Bridging Oxime Groups That Are Inaccessible by Conventional Preparations

2019

A series of new polynuclear complexes of divalent Ni and Cu with 2-cyano-2-oximino-acetic acid (later AACO2-) were obtained as the result of the ligand modification reaction in the process of complexation, using 2-cyano-2-oximino-acetates such as methyl- (later as MeCO), and ethyl- (as ECO later on). Synthesized compounds were characterized by spectroscopic methods, thermal analysis, magnetochemistry, and X-ray crystallography. Crystal data revealed the formation of the dimeric [Ni(AACO)(H2O)3]2·H2O (1), trimeric K2[Ni3(AACO)4(H2O)4]·4H2O (2), and K2[Cu3(AACO)4(H2O)4]·4H2O (3) complexes, with bridging NO-groups cyanoxime dianions. In the latter two compounds, the AACO2– anions adopt cis-arr…

chemistry.chemical_classification010405 organic chemistryGeneral Chemistry010402 general chemistryCondensed Matter PhysicsOxime01 natural sciencesAntiferromagnetic coupling0104 chemical sciencesDivalentMetalchemistry.chemical_compoundCrystallographychemistryMagnetochemistryvisual_artCrystal datavisual_art.visual_art_mediumGeneral Materials ScienceThermal analysisCrystal Growth & Design
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Reductions of M{N(SiMe3)2}3 (M = V, Cr, Fe): Terminal and Bridging Low-Valent First-Row Transition Metal Hydrido Complexes and “Metallo-Transaminatio…

2021

The reaction of the vanadium(III) tris(silylamide) V{N(SiMe3)2}3 with LiAlH4 in diethyl ether gives the highly unstable mixed-metal polyhydride [V(μ2-H)6[Al{N(SiMe3)2}2]3][Li(OEt2)3] (1), which was structurally characterized. Alternatively, performing the same reaction in the presence of 12-crown-4 affords a rare example of a structurally verified vanadium terminal hydride complex, [VH{N(SiMe3)2}3][Li(12-crown-4)2] (2). The corresponding deuteride 2D was also prepared using LiAlD4. In contrast, no hydride complexes were isolated by reaction of M{N(SiMe3)2}3 (M = Cr, Fe) with LiAlH4 and 12-crown-4. Instead, these reactions afforded the anionic metal(II) complexes [M{N(SiMe3)2}3][Li(12-crown-…

chemistry.chemical_classification010405 organic chemistryHydrideVanadiumchemistry.chemical_elementTrimethylamine010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryTransition metalvisual_artvisual_art.visual_art_mediumLithiumPhysical and Theoretical ChemistryDiethyl etherCrown etherInorganic Chemistry
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