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  • articleNo Access

    Diiron N-bridged species bearing phthalocyanine ligand catalyzes oxidation of methane, propane and benzene under mild conditions

    Transformation of methane, the most abundant and the least reactive compound of natural gas to valuable products is one of the most difficult chemical problems of great practical importance. In Nature, methane monooxygenase enzymes transform methane to methanol in water under physiological conditions. However, chemical analogs for such a transformation are unknown. Here, we show the mild and efficient aqueous oxidation of methane by hydrogen peroxide, an ecologically and biologically relevant oxidant catalyzed by supported μ-nitrido diiron phthalocyanine dimer, (FePctBu4)2N. This bio-inspired complex containing a stable Fe–N–Fe motif catalyzes the oxidation of methane to methanol which is further transformed to formaldehyde and formic acid as is demonstrated using 13CH4 and 18O labelling. (FePctBu4)2N-H2O2 system shows a high activity in the oxidation of benzene to phenol which occurs via formation of benzene oxide and exhibits NIH shift typically accociated with biological oxidation. Mechanistic features of oxidation of methane and benzene as well as detected intermediate hydroperoxo- and high valent oxo diiron complexes support an O-atom transfer reaction mechanism relevant to bio-oxidation.

  • articleNo Access

    THE PREPARATION OF ULTRAFINE TUNGSTEN CARBIDE NANOPARTICLES BY DC ARC DISCHARGE PLASMA PROCESS

    Tungsten carbide nanoparticles were synthesized successfully by DC arc discharge plasma process with 23 A discharge current at atmospheric pressure, in which tungsten positive electrode reacted with carbon black produced from the benzene cracking. The XRD results indicate that the samples consist of carbon black, WC and W2 C. The TEM micrographs show that the tungsten carbide particles range from 3 to 7 nm in size, and are composed of WC and W2C.

  • articleNo Access

    SMALL MOLECULES ADSORBED ON SILICON SURFACES: TWO CASES THROUGH TIME

    The adsorption of small organic molecules on silicon surfaces has been long a subject of investigations, as it provides the fundamental basis of silicon-based technologies in many fields. Several approaches were used, both theoretical and experimental, on many types of adsorbate-substrate systems aiming at determining preferential sites and geometries of adsorption, stable configurations, transition barriers, adsorption mechanisms, electronic structures among others. The research efforts, though, did not always bring to conclusive arguments and on some systems investigations are still going on following the evolution of the experimental techniques and computational methods. In this review, two case studies are reported: benzene and methanol on Si(100)2×1, i.e. examples of a molecular and a dissociative adsorption. The adsorption of benzene on Si(100)2×1 is still an open case, as it may adsorb in di-σ or tetra-σ bonded configurations, but contrasting evidences have been reported so far, on which of the two is the most stable one and the debate is still open. The adsorption of methanol is less controversial and it is widely accepted it is dissociative with breakage of the O–H at low coverages. But also in this case, investigations are going on to elucidate the adsorption mechanism.