Search results for "Osmocene"

showing 2 items of 2 documents

Atomic Layer Deposition of Osmium

2011

Growth of osmium thin films and nanoparticles by atomic layer deposition is described. The Os thin films were successfully grown between 325 and 375 °C using osmocene and molecular oxygen as precursors. The films consisted of only Os metal as osmium oxides were not detected in X-ray diffraction measurements. Also the impurity contents of oxygen, carbon, and hydrogen were less than 1 at % each at all deposition temperatures. The long nucleation delay of the Os process facilitates either Os nanoparticle or thin film deposition. However, after the nucleation delay of about 350 cycles the film growth proceeded linearly with increasing number of deposition cycles. Also conformal growth of Os thi…

010302 applied physicsMaterials scienceta114General Chemical EngineeringInorganic chemistryAnalytical chemistryNucleationchemistry.chemical_element02 engineering and technologyGeneral ChemistryChemical vapor deposition021001 nanoscience & nanotechnologyOsmocene01 natural scienceschemistry.chemical_compoundAtomic layer depositionCarbon filmchemistry0103 physical sciencesMaterials ChemistryDeposition (phase transition)OsmiumThin film0210 nano-technologyta116Chemistry of Materials
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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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