Search results for "Titani"
showing 10 items of 931 documents
Linked Benzylamido-Cyclopentadienyl Ligands: Synthesis and Characterization of Alkyl Titanium Complexes
1997
Titanium complexes of the general type Ti(η5:η1-C5H4Si-Me2NCH2C6H3X2-2,5)Cl2 (XH, F), containing a linked benzylamido-cyclopentadienyl ligand, were prepared by reaction of Ti(η5-C5H4SiMe2Cl)Cl3 with lithium amide Li(NHCH2C6H3X2-2,5). A single-crystal X-ray structural analysis of Ti(η5: η1-C5H4SiME2NCH2C6H3F2-2,5)Cl2 revealed a conformation in the solid state in which the aryl ring is turned away from the metal center. Ti(η5:η1-C5H4SiMe2NCH2C6H5)Cl2 can be alkylated with a variety of reagents to form extremely sensitive complexes of the type Ti(η5-C5H4SiMe,2NCH2C6H5)R2 (RMe, CH2 C6H5, CH2SiME3, CH2CMe2C6H5). Reaction of Li2[C5Me4SiMe2NCH2C6H5] with TiCl3(THF)3 gave Ti(η5: η1-C5Me4SiMe2NCH2C6…
Biologizing titanium alloy implant material with morphogenetically active polyphosphate
2015
As a further step towards a new generation of bone implant materials, we developed a procedure for biological functionalization of titanium alloy surfaces with inorganic calcium polyphosphate (Ca-polyP). This polymer has been demonstrated to exhibit morphogenetic activity. The coating of titanium oxidized Ti-6Al-4V scaffolds with biologically active amorphous Ca-polyP microparticles is formed by Ca2+ ion bridges to the silane coupling agent APTMS. This surface is durable and stable as an almost homogeneous Ca-polyP layer onto the metal. The homogenously coated Ca-polyP titanium scaffold was found to be biologically active and supported the growth and functional activity of bone cell-related…
Superhydrophobic TiO2/Fluorinated Polysiloxane Hybrid Coatings with Controlled Morphology for Solar Photocatalysis
2021
Abstract Technological applications of polysiloxane coatings have been influenced by their intrinsic low surface energy, which increases their water repellence. Accurate control of composition and interfacial properties through the introduction of perfluorinated moieties further lowers the polysiloxane surface energy, while mixing with metal oxide nanoparticles enhances roughness, resulting in a great potential in the development of superhydrophobic materials for photocatalysis. Herein, a series of hydrophobic and superhydrophobic hybrid coatings were prepared by dehydrocoupling and hydrosilylation reactions of polymethylhydrosiloxane with 1H,1H,2H,2H‐perfluorooctyltriethoxysilane and 1,3-d…
Production of titanium ion beams in an ECR ion source
2002
Abstract Intensive highly charged Ti ion beams were successfully produced in the 14 GHz ECR ion source at the Accelerator Laboratory, University of Jyvaskyla (JYFL). The Ti beams were produced using the MIVOC technique, i.e. by allowing the vapor of an organic compound containing titanium to diffuse into the ion source at room temperature. After optimizing the source parameters the intensity of the 48 Ti 11+ ion beam reached a value of 45 μA.
Synthesis of all-syn Functionalized Triphenylene Ketals
2011
The stereoselective synthesis of triphenylene ketals offers access to unique scaffolds. For a good performance in supramolecular applications an all-syn orientation of the functional groups is essential. The oxidative trimerization of catechol ketals by molybdenum pentachloride or mixtures with titanium tetrachloride leads to a template-directed formation. Several heterocyclic moieties are suitable for this transformation. A template-directed isomerization of anti,anti,syn isomers to the desired C 3 -symmetric derivative was demonstrated in two cases.
Photoelectrocatalytic selective oxidation of 4-methoxybenzyl alcohol in water by TiO2 supported on titanium anodes
2013
The photoelectrocatalytic partial oxidation of 4-methoxybenzyl alcohol in aqueous solution irradiated by near-UV light was carried out in a three-electrode batch reactor. TiO2 films were either deposited by dip-coating of a TiO2 sol onto a Ti foil and subsequent calcination or generated on Ti plates by thermal oxidation in air at 400-700 degrees C. The effects of the anode preparation method and bias potential values on conversion and selectivity to the corresponding aldehyde were investigated. The photoelectrocatalytic results were compared with the photocatalytic and electrocatalytic ones. The results indicated that no reaction occurred during the electrocatalytic experiments, whereas the…
Photocatalytic Selective Oxidation of 4-Methoxybenzyl Alcohol to Aldehyde in Aqueous Suspension of Home-Prepared Titanium Dioxide Catalyst
2007
WOS: 000246040000026
Heterogeneous oxidation of pyrimidine and alkyl thioethers in ionic liquids over mesoporous Ti or Ti/Ge catalysts.
2004
Heterogeneous catalytic oxidation of a series of thioethers (2-thiomethylpyrimidine, 2-thiomethyl-4,6-dimethyl-pyrimidine, 2-thiobenzylpyrimidine, 2-thiobenzyl-4,6-dimethylpyrimidine, thioanisole, and n-heptyl methyl sulfide) was performed in ionic liquids by using MCM-41 and UVM-type mesoporous catalysts containing Ti, or Ti and Ge. A range of triflate, tetrafluoroborate, trifluoroacetate, lactate and bis(trifluoromethanesulfonyl)-imide-based ionic liquids were used. The oxidations were carried out by using anhydrous hydrogen peroxide or the urea-hydrogen peroxide adduct and showed that ionic liquids are very effective solvents, achieving greater reactivity and selectivity than reactions p…
Photoreactivity of Iron-Doped Titanium Dioxide Powders for Dinitrogen Reduction to Ammonia
1989
The production of NH3 from N2 and H2O on Fe/TiO2 has been studied in a continuous photoreactor under UV radiation. An ESR study of the catalysts shows that Fe3+ ions are better electron traps than Ti4+ ions. This trapping can be irreversible if the corresponding holes originate stable species adsorbed on the catalyst surface. The charge separation, thus favoured by the Fe3+ ions, helps the N2 adsorption by its reaction with surface species activated by holes. The best activity is found when no excess Fe is segregated at the surface; overall turnover for N2 reduction as high as 6 e−/Fe atom can be reached before catalyst deactivation.
Influence of hydrogen peroxide on the kinetics of phenol photodegradation in aqueous titanium dioxide dispersion
1990
Abstract The influence of hydrogen peroxide on the phenol photodegradation rate under near UV radiation was investigated in homogeneous and heterogeneous systems: the heterogeneous systems were aqueous dispersions of titanium dioxide (anatase). The hydrogen peroxide photodecomposition reaction was also investigated for all the systems used. The highest rate of phenol photodegradation was observed in the heterogeneous system for the contemporary presence of hydrogen peroxide and oxygen. The rate equations for phenol photodegradation and hydrogen peroxide photodecomposition for both systems were obtained. A mechanistic model able to explain the main experimental results is also proposed.