EPR Spectroscopy Of Transformations Of Iridium(III) And Iridium(IV) Hydroxo Complexes In Alkaline Media

Schematics of transformation of iridium compounds in alkaline solutions (where the area of each block is proportional to the number of moles of a reagent involved in reaction)EPR spectroscopy of transformations of iridium(III) and iridium(IV) hydroxo complexes in alkaline media. Pankratov D.A., Komozin P.N., Kiselev Yu.M. //Russian Journal of Inorganic Chemistry. 2011. V.56. №11. P.1794-1799.Search the full text below. Ищи полный текст ниже.

Processes that occur in strong alkaline solutions of iridium(III) and iridium(IV) hydroxo complexes have been studied by EPR and electronic absorption spectroscopy. It has been demonstrated that dissolution of iridium compounds in alkaline solutions should be accompanied by a series of complicated transformations involving oxygen, which lead to the formation of several binuclear iridium(III, III), (III, IV), and (IV, IV) dioxygen complexes.

Most research into the chemistry of platinum metals has focused on their complexes. However, the chemistry of their hydroxo complexes is still one of the least studied fields. There are both objective (experimental complexity of operation in alkaline and strong alkaline media, tendency to polymerization of many hydroxo compounds, and others) and subjective reasons for this situation. In particular, it is believed that the chemistry of platinum metal hydroxo complexes is insufficiently diverse. Nevertheless, we previously showed the possibility of the existence of platinum(IV) hydroxo complexes as mono- and binuclear as mono- (superoxo-) and bi- (hydroxo- and superoxo-) bridging superoxo complexes of different composition forming under oxidative conditions in strong alkaline media.

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Mössbauer study of oxo derivatives of iron in the Fe2O3-Na2O2 system

Possible models for describing of sum Mössbauer spectra at different temperaturesMössbauer study of oxo derivatives of iron in the Fe2O3-Na2O2 system. Pankratov D.A. //Inorganic Materials. 2014. V. 50. № 1. P. 82-89Search the full text below. Ищи полный текст ниже.

Various compositions of oxo derivatives of iron reacting with sodium peroxide have been studied by Mössbauer spectroscopy. We have examined several mathematical models of the measured spectra. The results obtained are inconsistent with hypotheses made previously that such conditions may lead to the formation of compounds of iron in oxidation states above (+6). We demonstrate that a large excess of an alkali peroxide leads, most likely, to the formation of at least two iron(V) derivatives in tetrahedral coordination. In their Mössbauer spectra, they have isomer shifts of −0.45 and −0.51 mm/s and unusually large quadrupole splittings: 1.32 and 1.94 mm/s (at room temperature).

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A Mössbauer study of pentavalent iron in a vanadium(V) oxide matrix

Mossbauer absorption spectra of iron-doped V2O5.

A Mössbauer study of pentavalent iron in a vanadium(V) oxide matrix. Dedushenko S.K., Perfiliev Y.D., Tcheboukov D.E., Pankratov D.A., Kiselev Y.M. //Mendeleev Communications. 1999. V. 9. № 5. P. 211-212Search the full text below. Ищи полный текст ниже.

The formation of iron in the 5+ oxidation state was observed in iron-doped vanadium(V) oxide; this state is characterised by a singlet with the isomer shift δ = -0.56 ± 0.01 mm·s-1 relative to α-iron in the Mössbauer spectrum at room temperature.

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