New Platinum Superoxo Complex

    Evolution of the VIS-spectra of the pink solutions in time

    New Platinum Superoxo Complex. Kiselev Yu.M., Pankratov D.A., Shundrin L.A., Kiseleva I.N. //Russian Journal of Inorganic Chemistry. 1996. V. 41. № 12. P. 1963-1966Search the full text below. Ищи полный текст ниже.

    Products of oxidation of Pt(IV) hexahydroxo complexes with ozone in alkali media have been studied with physicochemical methods (electron spectroscopy, EPR, and cyclic voltammetry). The oxidation product is pink at alkali concentration in solution higher than 5 mol/l. The pink complex represents previously undescribed platinum superoxo complex with a bridging O2- group.

    Our previous study concerned the possibility of preparing platinum compounds in unusually high oxidation states from alka1ine solutions under the action of ozone. In that study, we detected a blue platinum superoxo complex of binuclear structure with the O2- bridging group. The bridge structure of this complex was supported by ESR, and the complex was show to form only at rather low alkalinity. At higher alkali concentrations (cOH- > 5 mol/l), a similar reaction results in a pale pink complex containing oxidizer.

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    Platinum(IV) Superoxo Complexes

    Evolution of the VIS-spectra of the blue solutions in time

    Platinum(IV) Superoxo Complexes. Kiselev Yu.M., Pankratov D.A., Ezerskaya N.A., Kiseleva I.N., Shundrin L.A., Popovich M.P. //Russian Journal of Inorganic Chemistry. 1994. V.39. №8. P. 1278-1283Search the full text below. Ищи полный текст ниже.

    The products of reaction of platinum(IV) hydroxo complexes with ozone in alkaline solutions were studied using various physicochemical methods: electronic spectroscopy, electron spin resonance, and cyclic voltammetry. The arguments presented suggest that the blue solutions obtained contain superoxo Pt(IV) complexes.

    One of the most efficient ways to stabilize higher oxidation states in the transition elements is complex formation in aqueous-alkaline media. In this case, hydroxyl ions offer advantages over other ligands and produce a stronger decrease in E° of a redox system than other, rather weakly polarizable ligands, which form complex ions in acid and neutral media. This circum stance is the one favoring stabilization of the highest oxidation states in neptunium, plutonium, americium(VII), and iron(VIII).

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    Vibrational Spectra of Platinum Superoxo Complexes

    Raman spectra of solutions of hexahydroxoplatinate(IV) and а syperoxo platinum(IV) соmрlех in 3 М КОН

    Vibrational spectra of platinum superoxo complexes. Pankratov D.A., Kiselev Yu.M., Sokolov V.B. //Russian Journal of Inorganic Chemistry. 2000. V. 45. № 9. P. 1388-1393Search the full text below. Ищи полный текст ниже.

    Aqueous alkaline (KOH, KOD) solutions of hexahydroxoplatinate and "blue" superoxohydroxo-platinate complexes were studied by Raman spectroscopy. The spectra of superoxo complexes shows the bands at 1020 and 1060 cm-1 that arise from the O2- moiety. Solid samples of platinum hydroxide and the precipitates isolated from "blue" solutions were studied by IR and Raman spectroscopy. The spectra of hexahydroxoplatinate(IV) were assigned assuming the C3i symmetry of the Pt(OH)62- group. The Raman spectra of the decomposition products of the solid superoxo complex (νO-O = 1080 cm-1 for O2-) show the bands that arise from a platinum peroxo complex (νO-O = 829 cm-1 for O22-).

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    EPR Spectra Of Solutions Of Platinum Superoxo Hydroxo Complexes

    EPR Spectra Of Solutions Of Blue Platinum Superoxo Hydroxo Complexes EPR Spectra Of Solutions Of Pink Platinum Superoxo Hydroxo Complexes

    EPR Spectra Of Solutions Of Platinum Superoxo Hydroxo Complexes. Komozin P.N., Pankratov D.A., Kiselev Yu.M. //Russian Journal of Inorganic Chemistry. 1999. V. 44. № 12. P. 1945-1951Search the full text below. Ищи полный текст ниже.

    EPR spectra of platinum superoxo hydroxo complexes in alkaline solutions were studied at various alkali concentrations. The EPR parameters for new platinum complexes were determined; the g-factors and hyperfine coupling constants were interpreted in terms of the ligand field theory. The structure of the platinum coordination sphere in the superoxo hydroxo complexes is discussed based on the EPR data.

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    Chlorination As A Means For Changing The Composition Of Iron-Containing Nanoparticles In A Polyethylene Matrix

    Mössbauer spectra of chlorine-treated nanocomposites synthesized from (a) iron(III) formate, (b) iron(III) acetate, and (c) iron(III) chloride

    Chlorination As A Means For Changing The Composition Of Iron-Containing Nanoparticles In A Polyethylene Matrix, Pankratov D.A., Yurkov G.Yu., Astaf'ev D.A., Gubin S.P. //Russian Journal of Inorganic Chemistry. 2008. Т. 53. № 6. С. 933-942

    Mössbauer spectroscopy, X-ray powder diffraction, and transmission electron microscopy were used to study the reactions of Fe3O4 or FeCl2·4H2O nanoparticles stabilized in a polyethylene (HPPE) matrix with gaseous chlorine and hydrogen chloride. These reactions produce FeCl2·2H2O nanoparticles, which retain the particle size and distribution over the HPPE matrix intrinsic to precursor nanoparticles. We propose chemical modification of iron-containing nanomaterials as a means for manufacturing iron(II) chloride nanoparticles.

    The synthesis and study of various nanomaterials and their properties have recently become a focus of research due to their unique electronic, optical, magnetic, and other physical and chemical properties. The physical and chemical properties of nanomaterials are primarily determined by their chemical composition. Therefore, preparing materials containing nanoparticles of the desired chemical composition is a problem faced by researchers. A considerable number of processes are known to yield metal-containing nanoparticles: chemical, electrochemical, pyrolytic, spark, micellar, and mechanochemical [10]. 

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