Search results for " Alloys"

showing 10 items of 1469 documents

An efficient synthesis of new fluorinated uracil derivativesElectronic supplementary information (ESI) available: general procedures for the preparat…

2003

A series of potentially biologically active fluorinated uracil derivatives has been prepared in three steps from oxazolines and fluorinated nitriles with good chemical yields.

chemistry.chemical_compoundchemistryMaterials ChemistryMetals and AlloysCeramics and CompositesOrganic chemistryUracilGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical Communications
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Über Inhibitoren der Korrosion III. Nachweis und Eigenschaften einiger mit Inhibitoren in Salzsäure aufgebauter Schutzschichten auf Eisen

1964

Fur den Aufbau einer Schutzschicht durch den Inhibitor oder eines seiner Folgeprodukte sprechen folgende Befunde: 1 Erhaltung der Schutzwerte nach Ubertragung inhibierter Drahte in inhibitorfreie, frische Salzsaure. 2 Verfolgung des zeitlichen Aufbaus der Schutzschicht durch den gleichen Test. 3 Erhaltung oder Verringerung der Schutzwirkung der inhibierten Drahte (a) durch Behandlung mit verschiedenen Losungsmitteln und (b) durch Bestimmung der thermischen Stabilitat der Schutzschicht. 4 Der an Blei- bzw. Quecksilberkathoden beobachtete Abbau quaternarer Phosphonium- und Arsoniumsalze eroffnet moglicherweise einen Zugang zu den am Aufbau der Schutzschichten beteiligten Verbindungen. On corr…

chemistry.chemical_compoundchemistryMechanics of MaterialsMechanical EngineeringMaterials ChemistryMetals and AlloysEnvironmental ChemistryGeneral MedicinePhosphoniumMedicinal chemistrySurfaces Coatings and FilmsMaterials and Corrosion
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Uranium( iv ) cyclobutadienyl sandwich compounds: synthesis, structure and chemical bonding

2019

The 1 : 1 reactions of uranium(IV) tetrakis(borohydride) with the sodium and potassium salts of the cyclobutadienyl anion [C4(SiMe3)4]2− (Cb′′′′) produce the half-sandwich complexes [Na(12-crown-4)2][U(η4-Cb′′′′)(BH4)3] and [U(η4-Cb′′′′)(μ-BH4)3{K(THF)2}]2. In the 1 : 2 reaction of U(BH4)4 with Na2Cb′′′′, formation of [U(η4-Cb′′′′)(η3-C4H(SiMe3)3-κ-(CH2SiMe2)(BH4))]− reveals that a Cb′′′′ ligand undergoes an intramolecular deprotonation, resulting in an allyl/tuck-in bonding mode. A computational study reveals that the uranium–Cb′′′′ bonding has an appreciable covalent component with contributions from the uranium 5f and 6d orbitals. peerReviewed

chemistry.chemical_element010402 general chemistryBorohydride01 natural sciencesMedicinal chemistryCatalysisIonkemialliset sidoksetchemistry.chemical_compoundDeprotonationMaterials Chemistrykemiallinen synteesi010405 organic chemistryLigandChemistryMetals and AlloyskompleksiyhdisteetGeneral ChemistryUranium3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsuraaniChemical bondCovalent bondIntramolecular forceCeramics and CompositesChemical Communications
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Non-covalent graphene nanobuds from mono- and tripodal binding motifs.

2017

Graphene nanobuds were prepared via the non-covalent anchoring of C60-based molecules endowed with one or three pyrene units, respectively. TGA, FTIR, UV-Vis and TEM investigations confirmed the formation of nanohybrids. For the two molecular derivatives, striking differences were determined in their interaction with graphene or carbon surfaces by Raman, cyclic voltammetry and molecular mechanics calculations, revealing the important role of pyrene adsorption in modulating the electronic properties of the nanohybrids.

chemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesCatalysislaw.inventionsymbols.namesakechemistry.chemical_compoundAdsorptionlawMaterials ChemistryOrganic chemistryMoleculeFourier transform infrared spectroscopyGrapheneMetals and Alloystechnology industry and agricultureQuímica orgánicaGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistryCeramics and CompositessymbolsPyreneCyclic voltammetry0210 nano-technologyRaman spectroscopyCarbonChemical communications (Cambridge, England)
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Rhodium catalyzed oxidative coupling of salicylaldehydes with diazabicyclic olefins: a one pot strategy involving aldehyde C–H cleavage and π-allyl c…

2013

An efficient one pot strategy for the synthesis of cyclopentene fused chromanone derivatives through the direct oxidative coupling of salicylaldehydes with bicyclic olefins in the presence of a rhodium-copper catalyst system is described. This is the first report on the ring opening-ring closing of bicyclic hydrazines via metal catalyzed oxidative coupling reaction.

chemistry.chemical_elementAlkenesRing (chemistry)Medicinal chemistryAldehydeCatalysisCatalysisRhodiumchemistry.chemical_compoundMaterials ChemistryOrganic chemistryMoleculeCyclopenteneRhodiumta116chemistry.chemical_classificationAldehydesAza CompoundsMolecular StructureOxidative CouplingBicyclic moleculeMetals and AlloysGeneral ChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryChromonesCyclizationCeramics and CompositesOxidative coupling of methaneChemical Communications
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Influence of Mn site doping on electrical resistivity of polycrystalline La1-yAyMn1-xBxO3 (A=Ba, Sr; B=Cu, Cr, Co) Manganites

2008

We have the measured electrical resistivity of La1-yBayMn1-xCuxO3 (0.17?y?0.30; 0.04?x?0.10), La1-ySryMn1-xCrxO3 and La1-ySryMn1-xCoxO3 (0.270?y?0.294; 0.02?x?0.10) polycrystalline samples in the 25-325 K temperature range. The increase of Mn site doping concentration leads to an increase of the electrical resistivity of the samples and the appearance of a ?double-peak? structure in the electrical resistivity versus temperature graphs. The first peak represents the insulator-metal transition in vicinity of the paramagnetic-ferromagnetic transition (TC). We have found that the intensity of the second peak increases with an increase of concentration of Mn substituents, due to the hole scatter…

colossal magnetoresistanceMaterials scienceRandom potentialColossal magnetoresistanceCondensed matter physicsScatteringDopingAnalytical chemistryMetals and AlloysAtmospheric temperature rangelcsh:Chemical technologyCondensed Matter PhysicsImpurityElectrical resistivity and conductivityManganitesMaterials ChemistryCeramics and Compositeslcsh:TP1-1185Crystalliteelectrical resistivityScience of Sintering
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Reactivity of bis(cyclohexylammonium) 4-nitrophenylphosphate with SnMe3 Cl. X-ray structure of 4-NO2 C6 H4 PO4(SnMe3)2·H2 O

2014

The reaction of bis(cyclohexylammonium) 4-nitrophenylphosphate with Me3 SnCl (1:2) under reflux in ethanol yielded the title compound 4-NO2 C6 H4 PO4(SnMe3)2H2 O (1). The X-ray crystallographic analysis achieved on single crystals obtained by slow evaporation at room temperature revealed the formation of an unexpected supramolecular coordination network. The elementary building block can be viewed as two Me3 Sn moieties linked by a bridging 4-nitrophenylphosphate ligand. The two tin atoms are five-coordinated and describe a trans-Me3 SnO2 geometry in a trigonal bipyramidal arrangement. However, the Sn atoms are distinct, exhibiting two different environments. Thus, one is linked to two axia…

coordination-driven self-assemblyHydrogen bondChemistryStereochemistryIntermolecular forceMetals and AlloysSupramolecular chemistryX-raychemistry.chemical_elementGeneral Chemistryhydrogen bondingCondensed Matter PhysicsChemistryCrystallographyX-ray crystallographyAtomtrimethyltin(iv) 4-nitrophenylphosphatoMaterials ChemistryMoleculeTinQD1-999x-ray crystallographyMain Group Metal Chemistry
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An Overview on the Performance of 1,2,3-Triazole Derivatives as Corrosion Inhibitors for Metal Surfaces

2021

This review accounts for the most recent and significant research results from the literature on the design and synthesis of 1,2,3-triazole compounds and their usefulness as molecular well-defined corrosion inhibitors for steels, copper, iron, aluminum, and their alloys in several aggressive media. Of particular interest are the 1,4-disubstituted 1,2,3-triazole derivatives prepared in a regioselective manner under copper-catalyzed azide-alkyne cycloaddition (CuAAC) click reactions. They are easily and straightforwardly prepared compounds, non-toxic, environmentally friendly, and stable products to the hydrolysis under acidic conditions. Moreover, they have shown a good efficiency as corrosi…

corrosion inhibitorAzidesmetalQH301-705.5Surface PropertiesReviewCatalysisInorganic ChemistryPhysical and Theoretical ChemistryBiology (General)metal alloysMolecular BiologyQD1-999Spectroscopymechanism of inhibitionCycloaddition ReactionMolecular StructureOrganic ChemistryGeneral MedicineQuímicaTriazolesComputer Science ApplicationsCorrosionChemistryMetalsclick chemistry123-triazoleInternational Journal of Molecular Sciences
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Organotin(IV) selenate derivatives – Crystal structure of [{(Ph 3 Sn) 2 SeO 4 } ⋅ CH 3 OH] n

2021

Abstract Crystallization of [(Ph3Sn)2SeO4] ⋅ 1.5H2O in methanol leads to the formation of [{(Ph3Sn)2SeO4} ⋅ CH3OH] n (1) which constitutes a new specimen of organotin(IV) selenate derivatives. In the solid state, complex 1 is arranged in polymeric zig-zag chains, composed of alternating Ph3Sn and SeO4 groups. In addition, pendant Ph3Sn ⋅ CH3OH moieties are branched along chains according to a syndiotactic organization and via Sn-O-Se connections. From a supramolecular point of view, intermolecular hydrogen bonds established between the selenate groups (uncoordinated oxygen) and the hydroxyl functions (CH3OH) of the pendant groups link the chains together.

crystal structure010405 organic chemistryMetals and AlloysGeneral ChemistryCrystal structureorganotin(iv)010402 general chemistryCondensed Matter Physics01 natural sciencesSelenate3. Good health0104 chemical scienceschemistry.chemical_compoundCrystallographyChemistrychemistryMaterials Chemistryinorganic chain[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryseleniumsn-o-se moietyQD1-999
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Synthesis, spectroscopic study, and crystal structure of a new organotin(IV) selenate derivative

2018

Abstract The polymeric organotin(IV) selenate complex [(Me3Sn)3(SeO4)(OH)]n (1) has been isolated as single crystals from the reaction of [(Me2NH2)2SeO4] and Me3SnCl in methanol. In the solid state, compound 1 was characterized by X-ray diffraction analysis, Fourier transform-infrared spectroscopy, and elemental analysis. 1 crystallizes in the orthorhombic system space group Pbca with a=11.0231(2) Å, b=16.3461(3) Å, c=20.9945(4) Å, α=β=γ=90°, V=3782.89(12) Å3, and Z=8. Its structure can be described as a polymeric zigzag chain based on Me3Sn moieties linked by tridentate selenate anions. Pendant (Me3Sn)2OH groups are also connected to the chain, according to a syndiotactic organization, and…

crystal structurechemistry.chemical_elementCrystal structureorganotin(iv)010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesSelenateoxoanionschemistry.chemical_compoundComputational chemistryMaterials Chemistry[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryseleniumQD1-999ComputingMilieux_MISCELLANEOUSMetals and AlloysGeneral ChemistryCondensed Matter Physics0104 chemical sciencesChemistrychemistrysn-o-se moietySeleniumDerivative (chemistry)Main Group Metal Chemistry
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