3,248 research outputs found

    Bi- and tri-dentate imino-based iron and cobalt pre-catalysts for ethylene oligo-/polymerization

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    Recent progress on the use of iron and cobalt complex pre-catalysts for ethylene reactivity is reviewed. The review is organized in terms of the denticity of the chelate ligands employed, with particular reference to the influence of the ligand frameworks and their substituents on the catalytic performance for ethylene oligomerization/polymerization catalysis. The majority of the systems bear tri-dentate ligation at the iron/cobalt centre, though it is clear that bi-dentate iron/cobalt complex pre-catalysts have also attracted significant attention. Such systems produce in most cases highly linear products ranging from oligomeric α-olefins to high molecular weight polyethylene, and as such are promising candidates for both academic and industrial considerations

    Low Cost Ferritic Stainless Steel in Dye Sensitized Solar Cells with Cobalt Complex Electrolyte

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    Cheap ferritic stainless steel is applied here as the counter electrode substrate in dye sensitized solar cells with cobalt complex electrolyte. A 5.0% efficiency was reached with these type of cells which is more than 2.5 times higher compared to previously reported devices with metal counter electrode and cobalt complex electrolyte. The electrochemical impedance spectra analysis showed that the best cells with the ferritic steel counter electrode had as low charge transfer resistance (3.6 Ωcm2) as the reference glass cells with the same electrolyte. While in previous studies many metals have corroded in the cobalt complex electrolyte, the stability analysis including scanning electron microscope imaging of the aged electrodes suggested that the ferritic stainless steel substrates did not corrode in the electrolyte. Hence ferritic stainless steel appears as a possible alternative counter electrode in dye solar cells with cobalt electrolyte in terms of cost, performance and stability.Peer reviewe

    Biphenyl-bridged 6-(1-aryliminoethyl)-2-iminopyridyl-cobalt complexes: synthesis, characterization and ethylene polymerization behavior

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    A series of biphenyl-bridged 6-(1-aryliminoethyl)-2-iminopyridine derivatives reacted with cobalt dichloride in dichloromethane/ethanol to afford the corresponding binuclear cobalt complexes. The cobalt complexes were characterized by FT-IR spectroscopy and elemental analysis, and the structure of a representative complex was confirmed by single-crystal X-ray diffraction. Upon activation with either MAO or MMAO, these cobalt complexes performed with high activities of up to 1.2 × 10⁷ g (mol of Co)⁻¹ h⁻¹ in ethylene polymerization, which represents one of the most active cobalt-based catalytic systems in ethylene reactivity. These biphenyl-bridged bis(imino)pyridylcobalt precatalysts exhibited higher activities than did their mononuclear bis(imino)pyridylcobalt precatalyst counterparts, and more importantly, the binuclear precatalysts revealed a better thermal stability and longer lifetimes. The polyethylenes obtained were characterized by GPC, DSC, and high-temperature NMR spectroscopy and mostly possessed unimodal and highly linear features

    Cobalt ion-containing epoxies

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    Varying concentrations of an organometallic cobalt complex were added to an epoxy system currently used by the aerospace industry as a composite matrix resin. Methods for combining cobalt (III) acetylacetonate with a tetraglycidyl 4,4 prime - diaminodiphenylmethane-based epoxy were investigated. The effects of increasing cobalt ion concentration on the epoxy cure were demonstrated by epoxy gel times and differential scanning calorimetry cure exotherms. Analysis on cured cobalt-containing epoxy castings included determination of glass transition temperatures by thermomechanical analysis, thermooxidative stabilities by thermogravimetric analysis, and densities in a density gradient column. Flexural strength and stiffness were also measured on the neat resin castings

    Process for improving mechanical properties of epoxy resins by addition of cobalt ions

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    A resin product useful as an adhesive, composite or casting resin is described as well as the process used in its preparation to improve its flexural strength mechanical property characteristics. Improved flexural strength is attained with little or no change in density, thermal stability or moisture resistance by chemically incorporating 1.2% to 10.6% by weight Co(3) ions in an epoxidized resin system

    A cobalt complex redox shuttle for dye-sensitized solar cells with high open-circuit potentials

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    Dye-sensitized solar cells are a promising alternative to traditional inorganic semiconductor-based solar cells. Here we report an open-circuit voltage of over 1,000 mV in mesoscopic dye-sensitized solar cells incorporating a molecularly engineered cobalt complex as redox mediator. Cobalt complexes have negligible absorption in the visible region of the solar spectrum, and their redox properties can be tuned in a controlled fashion by selecting suitable donor/acceptor substituents on the ligand. This approach offers an attractive alternate to the traditional I3−/I− redox shuttle used in dye-sensitized solar cells. A cobalt complex using tridendate ligands [Co(bpy-pz)2]3+/2+(PF6)3/2 as redox mediator in combination with a cyclopentadithiophene-bridged donor-acceptor dye (Y123), adsorbed on TiO2, yielded a power conversion efficiency of over 10% at 100 mW cm−2. This result indicates that the molecularly engineered cobalt redox shuttle is a legitimate alternative to the commonly used I3−/I− redox shuttle

    A cobalt complex of a microbial arene oxidation product

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    We report the first synthesis of a cobalt Cp diene complex wherein the diene is derived by microbial dearomatising dihydroxylation of an aromatic ring. The complex has been characterised crystallographically and its structure is compared to that of an uncomplexed diene precursor
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