Search results for "Composites"

showing 10 items of 1905 documents

Synthetic Pathways for New Tubular Transition Metal Hydroxo- and Fluoro-Selenites: Crystal Structures ofM12(X)2(SeO3)8(OH)6(M=Co2+,Ni2+;X= OH−)

1996

The dumortierite-family structuresM12X2(SeO3)8(OH)6(M= Co2+and Ni2+;X= OH−and F−) have been synthesized. The crystal structures of the hydroxo-derivatives have been refined from X?ray powder diffraction data in the space groupP63mc(Z= 1) witha= 12.887(3) A andc= 4.981(4) A (M= Co2+,X= OH−or F−) anda= 12.704(5) A andc= 4.925(6) A (M= Ni2+,X= OH−or F−). Application of the Partial Charge Transference Model allows the understanding of the selenite derivatives crystal chemistry.

Crystal chemistryInorganic chemistrychemistry.chemical_elementCrystal structureCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsInorganic ChemistryPartial chargeCrystallographychemistryTransition metalMaterials ChemistryCeramics and CompositesChemical preparationPhysical and Theoretical ChemistrySeleniumPowder diffractionJournal of Solid State Chemistry
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Asymmetric [N–I–N]+ halonium complexes

2020

The first asymmetric halogen-bonded iodonium complexes [I(py)(4-DMAP)]PF6 (2c) and [I(py)(4-Etpy)]PF6 (2e) were prepared via [N–Ag–N]+ → [N–I–N]+ cation exchange of their analogous 2-coordinate silver complexes. The complexes were characterised by 1H and 1H–15N HMBC NMR spectroscopy, and single crystal X-ray crystallography.

CrystallographyChemistryMaterials ChemistryMetals and AlloysCeramics and CompositesHalonium ionGeneral ChemistryNuclear magnetic resonance spectroscopySingle crystalCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical Communications
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Acyclic imidoselenium(ii) dihalides: synthesis and X-ray structures of ClSe[N(But)Se]nCl (n = 1, 2)

2000

The reaction of SeCl2 with tert-butylamine in THF yields the acyclic imidoselenium(II) dichlorides ClSeN(But)NSeCl and ClSeN(But)SeN(But)SeCl, in addition to the six-membered ring Se3(NBut)3.

CrystallographyChemistryStereochemistryMaterials ChemistryMetals and AlloysCeramics and CompositesX-rayGeneral ChemistryRing (chemistry)CatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical Communications
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Crystal Structure of the Microwave Dielectric Resonator Ba2Ti9O20

1983

A single-crystal X-ray study of dibarium nonatitanate, Ba2Ti9O20, yielded the triclinic space group P 1 with a=0.7471(1), b= 1.4081(2), c= 1.4344(2) nm, α=89.94(2)°, β= 79.43(2)°, γ= 84.45(2)°, V = 1.476 nm3 Z = 4, and Dx= 4.61 Mg/m3. A refinement of atomic coordinates and isotropic thermal parameters led to a residual of 0.03. The structure consists of hexagonally closest-packed layers of Ba and O atoms in the sequence (hch)3. All Ti atoms reside in octahedral interstices of this closest packing. The various Ti coordination octahedra share only edges and corners with each other. One-half of the Ba atoms is twelve-coordinated by oxygen atoms, the other half is eleven-coordinated.

CrystallographyMaterials scienceOctahedronGroup (periodic table)IsotropyMaterials ChemistryCeramics and CompositesCrystal structureDielectric resonatorAtomic coordinatesTriclinic crystal systemMicrowaveJournal of the American Ceramic Society
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Epoxidation of stilbene using supported gold nanoparticles: cumyl peroxyl radical activation at the gold nanoparticle surface.

2014

The catalytic epoxidation of cis-stilbene using cumene as a solvent in the presence of supported gold nanoparticles (AuNP) yields a mixture of cis and trans-stilbene oxides. EPR and product distribution studies support a new mechanistic proposal where oxygen centred radicals activate the AuNP surface and form active surface oxygen species responsible for the epoxidation products.

CumeneChemistryRadicalMetals and AlloysNanoparticleGeneral ChemistryPhotochemistryCatalysisProduct distribution3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionCatalysisSolventchemistry.chemical_compoundlawColloidal goldMaterials ChemistryCeramics and CompositesElectron paramagnetic resonanceChemical communications (Cambridge, England)
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Cyanide-bridged Fe(III)–Co(II) bis double zigzag chains with a slow relaxation of the magnetisation

2003

Reaction of [FeIII(bipy)(CN)4]¯ with fully solvated MII cations [M = Co (1) and Mn (2)] produces the isostructural bis double zigzag chains [[FeIII(bipy)(CN)4]2MII(H2O)]·MeCN·1/2H2O; 1 exhibits intrachain ferromagnetic and interchain antiferromagnetic couplings, slow magnetic relaxation and hysteresis effects. Luminita Marilena, Toma, Luminita.Toma@uv.es ; Lescouezec, Alain Francois Rodri, Alain.Lescouezec@uv.es ; Lloret Pastor, Francisco, Francisco.Lloret@uv.es ; Julve Olcina, Miguel, Miguel.Julve@uv.es

Cyanide-bridged Fe(III)–Co(II)CyanideUNESCO::QUÍMICA:QUÍMICA [UNESCO]Catalysischemistry.chemical_compoundMagnetizationMaterials ChemistryAntiferromagnetismIsostructuralHysteresis effectsCondensed matter physicsUNESCO::QUÍMICA::Química inorgánicaRelaxation (NMR)Metals and AlloysGeneral ChemistryCyanide-bridged Fe(III)–Co(II) ; Slow relaxation ; Ferromagnetic ; Antiferromagnetic ; Hysteresis effectsAntiferromagnetic:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyHysteresischemistryZigzagFerromagnetismFerromagneticCeramics and CompositesSlow relaxation
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Photoinduced HS state in the first spin-crossover chain containing a cyanocarbanion as bridging ligand

2009

A new polymeric approach, based on cyanocarbanion ligands, for the design of spin crossover (SCO) compounds led us to the compound [Fe(abpt)2(tcpd)] (1) (tcpd^2 = (C[C(CN)2|3)^2 , abpt = 4-amino-3,5-bis(pyridin-2-yl)-1,2,4-triazole) which has been characterised as the first SCO molecular chain involving a cyanocarbanion as bridging ligand. Gomez Garcia, Carlos Jose, Carlos.Gomez@uv.es

Cyanocarbanion ligandsChemistryStereochemistryUNESCO::QUÍMICAPolimeryc approachMetals and AlloysBridging ligandBridging ligandGeneral ChemistryState (functional analysis)UNESCO::QUÍMICA::Química macromolecular:QUÍMICA [UNESCO]CatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChain (algebraic topology)Polimeryc approach ; Cyanocarbanion ligands ; Photoinduction ; Bridging ligandSpin crossoverPhotoinductionMaterials ChemistryCeramics and Composites:QUÍMICA::Química macromolecular [UNESCO]
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Fluorescent Sensing of Maleate versus Fumarate by a Neutral Cyclohexane Based Thiourea Receptor.

2006

A new cyclohexyl based fluorescent anion receptor, is able to recognize maleate versus fumarate both as their TMA salts. Costero Nieto, Ana Maria, Ana.Costero@uv.es ; Colera Llavata, Manuel, Manuel.Colera@uv.es ; Gaviña Costero, Pablo, Pablo.Gavina@uv.es ; Gil Grau, Salvador, Salvador.Gil@uv.es

CyclohexaneUNESCO::QUÍMICAurologic and male genital diseases:QUÍMICA [UNESCO]Medicinal chemistryCatalysischemistry.chemical_compoundhemic and lymphatic diseasesNeutral cyclohexaneMaterials ChemistryFluorescentOrganic chemistryUNESCO::QUÍMICA::Química orgánicaReceptorneoplasmsAnion receptorThiourea receptorFumarateMaleate:QUÍMICA::Química orgánica [UNESCO]Metals and AlloysGeneral ChemistryGeneral MedicineFluorescenceSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsFluorescent ; Neutral cyclohexane ; Thiourea receptor ; Maleate ; FumarateThioureachemistryCeramics and CompositesChemInform
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Asymmetric synthesis of cyclopentanes bearing four contiguous stereocenters via an NHC-catalyzed Michael/Michael/esterification domino reaction.

2016

An NHC-catalyzed Michael/Michael/esterification domino reaction via homoenolate/enolate intermediates for the asymmetric synthesis of tetrasubstituted cyclopentanes is described.

CyclopentanesStereochemistry010402 general chemistry01 natural sciencesCatalysisDominoCatalysisStereocenterCascade reactiondomino reactionMaterials Chemistryta116cyclopentane motifs010405 organic chemistryChemistryMetals and AlloysEnantioselective synthesisGeneral Chemistry5400104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemistryddc:540Ceramics and CompositesChemical communications (Cambridge, England)
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Enantiocontrol in the intermolecular cyclopropanation reaction catalyzed by dirhodium(II) complexes with ortho-metalated aryl phosphine ligands

2001

(P) and (M) dirhodium(II) complexes with ortho-metalated aryl phosphines are assessed as chiral catalysts in the enantioselective cyclopropanation of styrenes by ethyl diazoacetate; enantioselectivities up to 91% and up to 87%, respectively, for cis- and trans-2-arylcyclopropanecarboxylates are observed. Barberis, Mario, Mario.Barberis@uv.es ; Lahuerta Peña, Pascual, Pascual.lahuerta@uv.es ; Perez Prieto, Julia, Julia.Perez@uv.es ; Sanau Torrecilla, Mercedes, Mercedes.Sanau@uv.es

CyclopropanationUNESCO::QUÍMICAMedicinal chemistry:QUÍMICA [UNESCO]CatalysisCatalysischemistry.chemical_compoundEthyl diazoacetateMaterials ChemistryOrganic chemistryPhosphine ligandsEnantiocontrol ; Intermolecular cyclopropanation ; Catalyst ; Phosphine ligandsArylIntermolecular forceMetals and AlloysEnantioselective synthesisGeneral ChemistryUNESCO::QUÍMICA::Química macromolecularSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsEnantiocontrolchemistryCeramics and Composites:QUÍMICA::Química macromolecular [UNESCO]CatalystIntermolecular cyclopropanationPhosphine
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