Search results for "Rut"

showing 10 items of 2295 documents

Ab initiosimulations on rutile-based titania nanowires

2012

The rod symmetry groups for monoperiodic (1D) nanostructures have been applied for construction of models for bulk-like TiO2 nanowires (NWs) cut from a rutile-based 3D crystal along the chosen [001] and [110] directions of crystallographic axes. In this study, we have considered nanowires described by both the Ti-atom centered rotation axes as well as the hollow site centered axes passing through the interstitial positions between the Ti and O atoms closest to the axes. The most stable [001]-oriented TiO2 NWs with rhombic cross sections are found to display the energetically preferable {110} facets only while the nanowires with quasi-square sections across the [110] axis are formed by the a…

CrystallographyNanostructureLinear combination of atomic orbitalsRutileChemistryAb initioNanowireDensity functional theorySymmetry groupEnergy minimizationMolecular physicsIOP Conference Series: Materials Science and Engineering
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XAFS STUDIES OF OCTAHEDRAL AMORPHOUS OXIDES

1993

The relationships between the structures of octahedral and tetrahedral amorphous oxides, studied by XAFS spectroscopy, are considered. It was found that a-WO3, a-MoO3, a-V2O5 thin films and glasses have strongly distorted, but well defined, oxygen octahedra, which are joined by vertices (a-WO3, a-MoO3) or by vertices and edges (a-V2O5), and form a random network. At the same time, a-IrO2 and a-NiO have less distorted oxygen octahedra, which form the rutile type and rock salt type nanocrystalline structures. The variation of the structure with the change of the metal valence is considered and the possibility of small radius polaron detection by XAFS is discussed.

CrystallographyValence (chemistry)Materials scienceOctahedronRutileGeneral EngineeringGeneral Physics and AstronomyPolaronSpectroscopyNanocrystalline materialAmorphous solidX-ray absorption fine structure
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Fluorido Complex Formation of Element 104, Rutherfordium (Rf)

2011

We have investigated the cation-exchange behavior of element 104, rutherfordium (Rf), together with its lighter group-4 homologs Zr and Hf, and the tetravalent pseudo-homolog Th in HF/HNO3 mixed so...

CrystallographychemistryComplex formationRutherfordiumchemistry.chemical_elementGeneral ChemistryBulletin of the Chemical Society of Japan
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Catacomba di Villagrazia di Carini. Il cubicolo X20. Ricerche 2008-2013

2014

Il X20 è una camera funeraria quadrangolare preceduta da un dromos che deriva da un preesistente arcosolio bisomo. Al suo interno accoglie 29 sepolture: dodici arcosoli per adulti e per bambini, una tomba a nicchia, due tombe a cassa e quattordici fosse pavimentali. Si è potuto accertare che l’aspetto attuale del cubicolo è il risultato di quattro fasi costruttive. Alla prima fase appartiene la decorazione ad affresco con temi floreali e vegetali, che riveste la parete settentrionale. In un momento successivo l’estensione della camera viene raddoppiata e di fonte all’ingresso si crea una scenografica sistemazione di arcosoli e tombe a cassa; nelle due ultime fasi il pavimento viene interame…

Cubicolo X20 Catacomba Villagrazia Carini scavo analisi strutturale materialiSettore L-ANT/08 - Archeologia Cristiana E Medievale
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Science and art from a transevolutionary perspective

2018

From its origins, the human species has manipulated not only the real world but also the figurative one. While that manipulative action of the human species over both worlds was critical for the survival of the species in the beginning of its evolution -now transevolution-, it is also true that in the subsequent culture those worlds have been approached by two trades with highly different conceptual bases, science and art. In this paper I hold the thesis that both trades are necessary to know how to be in the world as well as how to transform it in an appropriate way.

Cultural StudiesCienciaSociology and Political SciencetruthSurvival of the fittestSciencerevealingtransevoluciónLiteral and figurative languageGeneral WorkstransformacióntransevolutionarteAmanipulaciónartdesocultamientoGeneral Arts and HumanitiesPhilosophytransformationAction (philosophy)manipulationverdadHuman speciesHumanitiesKnow-howArbor: Ciencia, Pensamiento y Cultura
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Synthesis, characterization and crystal structure of the bimetallic cyano-bridged [(η5-C5H5)(PPh3)2Ru(μ-CN)Ru(PPh3)2(η5-C5H5)][PF6]

2005

Abstract The bimetallic cyano-bridged [(η 5 -C 5 H 5 )(PPh 3 ) 2 Ru(μ-CN)Ru(PPh 3 ) 2 (η 5 -C 5 H 5 )][PF 6 ] ( 1 ) was prepared by reaction of [(η 5 -C 5 H 5 )(PPh 3 ) 2 RuCl] with N , N ′-bis(cyanomethyl)ethylenediamine. The single crystal structure determined by X-ray diffraction showed crystallization on the triclinic P1 space group with a perfect alignment of the cyanide bridges. This accentric crystallization was explored having in view the NLO properties at the macroscopic level, determined by the Kurtz Powder technique. Besides the very low efficiency values for the second harmonic generation, the value obtained for the bimetallic complex 1 showed to be higher than one of the parent…

Cyanidechemistry.chemical_elementEthylenediamineCrystal structureTriclinic crystal systemlaw.inventionRutheniumInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrylawMaterials ChemistryPhysical and Theoretical ChemistryCrystallizationBimetallic stripSingle crystalInorganica Chimica Acta
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CCDC 229367: Experimental Crystal Structure Determination

2005

Related Article: C.Ornelas, C.Gandum, J.Mesquita, J.Rodrigues, M.H.Garcia, N.Lopes, M.P.Robalo, K.Nattinen, K.Rissanen|2005|Inorg.Chim.Acta|358|2482|doi:10.1016/j.ica.2005.02.002

Cyano-(eta^5^-cyclopentadienyl)-bis(triphenylphosphine)-ruthenium methanol solvate hydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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The Preparation of Tetramethyl 1,1′,3,3′-Ruthenocenetetra­carboxylate and Tetramethyl 1,1′,3,3′-Osmocenetetracarboxylate, and a Simplified Synthesis …

2018

Substituted metallocenes with more than two substituents have to be synthesized using doubly substituted cyclopentadiene rings in a reaction with a metal compound or by the introduction of additional functional groups to an already di-substituted metallocene. The direct formation of tetra-substituted metallocenes often suffers due to insufficient reactivity of the reagents or the resulting product mixtures, which are hard to separate. In this work, a protocol, which was successful in a tetra-substitution of ferrocene by a tetra-metalation followed by a reaction with carbon dioxide, is used to perform the tetra-substitution of ruthenocene and osmocene. In addition, a simplified protocol for …

Cyclopentadiene010405 organic chemistryOrganic ChemistrySuperbase010402 general chemistryOsmocene01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundchemistryFerrocenePolymer chemistryRuthenoceneReactivity (chemistry)CarboxylateMetalloceneSynthesis
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Cyclopentadienyl derivatives of octahedral carbonylcarbide hexaruthenium clusters: synthesis, NMR, IR and X-ray characterization

1996

Abstract The reaction of hexanuclear carbonylcarbide cluster Ru6C(CO)17 (1) with pentamethylcyclopentadiene by reflux in heptane leads to a new chelate cluster Ru6C(μ-η1-η5-CH2C5Me4)(CO)14 (2). The compound 2 contains a CH2 group α-bonded to one of the Ru atoms in the Ru6 cluster and a C5Me4-ligand η5-coordinated by the adjacent Ru atom of the Ru6 cluster. Reflux of 1 in hexane with two molecular equivalents of nickelocene, Ni(C5H5)2  NiCp2, used as a source of cyclopentadiene yields the Ru6C(CO)12Cp2 (3) cluster. The compounds 2 and 3 have been characterized by NMR and IR spectroscopy and their crystal structures determined by X-ray diffraction studies.

CyclopentadieneOrganic ChemistryNickeloceneInorganic chemistryPentamethylcyclopentadieneInfrared spectroscopychemistry.chemical_elementCrystal structureBiochemistryRutheniumInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryCyclopentadienyl complexMaterials ChemistryCluster (physics)Physical and Theoretical ChemistryJournal of Organometallic Chemistry
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Ruthenium titanocene and ruthenium titanium half-sandwich bimetallic complexes in catalytic cyclopropanation

2005

Abstract The reaction of the phosphine functionalised titanium half-sandwich complexes 7, 9 and 10 with the binuclear complex [(p-cymene)RuCl2]2 allowed the access to three new early-late bimetallic complexes (p-cymene)[(μ-η5:η1-C5H4(CH2)nPR2)TiX3]RuCl2 (11–13). The structure of 11 (n = 0, X = Cl) has been confirmed by X-ray diffraction. The ruthenium titanium half-sandwich bimetallic complexes so formed and the ruthenium titanocene analogues 4–6 catalyse the addition of ethyl diazoacetate to styrene with high selectivity toward cyclopropanation versus metathesis contrary to the monometallic complexes (p-cymene)RuCl2PR3.

CyclopropanationOrganic Chemistrychemistry.chemical_elementMetathesisBiochemistryCatalysisRutheniumInorganic Chemistrychemistry.chemical_compoundchemistryEthyl diazoacetatePolymer chemistryMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryBimetallic stripPhosphineTitaniumJournal of Organometallic Chemistry
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