Vibrational Spectra of Platinum Superoxo Complexes

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. 1388-1393

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 C_3i symmetry of the Pt(OH)₆^2- group. The Raman spectra of the decomposition products of the solid superoxo complex (ν_O-O = 1080 cm^-1 for O₂^-) show the bands that arise from a platinum peroxo complex (ν_O-O = 829 cm^-1 for O₂^2-).

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Possibilities of cryogenic autoradiography

Possibilities of cryogenic autoradiography. Pankratov D.A., Korobkov V.I. //Journal of Analytical Chemistry. 2014. V. 69. Is. 7. P. 632–637

Photographic properties of the nuclear photographic detector BioMax MR Film from KODAK are studied at the temperature of liquid nitrogen. The characteristic curves obtained at room and cryogenic temperatures indicate that the detector retains its physical and photographic properties, and its possibilities can be expanded to studies of deeply frozen samples. The data obtained point to an increase in the sensitivity of the photographic material frozen to cryogenic temperatures at short exposures.

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Electron paramagnetic resonance spectra near the spin-glass transition in iron oxide nanoparticles

Electron paramagnetic resonance spectra near the spin-glass transition in iron oxide nanoparticles. Koksharov Yu.A., Gubin S.P., Kosobudsky I.D., Yurkov G.Yu., Pankratov D.A., Ponomarenko L.A., Mikheev M.G., Beltran M., Khodorkovsky Y., Tishin A.M. //Physical Review B: Condensed Matter and Materials Physics. 2001. V. 63. № 1. P. 124071-124074

Electron paramagnetic resonance (EPR) in iron-oxide nanoparticles (∼ 2.5 nm) embedded in a polyethylene matrix reveals the sharp line broadening and the resonance field shift on sample cooling below T_F ≈ 40 K. At the same temperature a distinct anomaly in the field-cooled magnetization is detected. The temperature dependences of EPR parameters below T_F are definitely different than those found for various nanoparticles in the superparamagnetic regime. In contrast to canonical bulk spin glasses, a linear fall-off of the EPR linewidth is observed. Such behavior can be explained in terms of the random-field model of exchange anisotropy.

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Potassium hexahydroperoxostannate: synthesis and structure

Potassium hexahydroperoxostannate: synthesis and structure. Ippolitov E.G., Tripol'skaya T.A., Prikhodchenko P.V., Pankratov D.A. //Russian Journal of Inorganic Chemistry. 2001. V.46. №6. P.851-857

Polycrystalline potassium hexahydroperoxostannate was prepared by replacement of hydroxo groups in potassium hexahydroxostannate upon its dissolution in hydrogen peroxide. A comparative study of the product and the starting hydroxostannate by powder X-ray diffraction analysis, thermogravimetry, and IR, ²H, ³⁹K, and ¹¹⁹Sn NMR, and Mössbauer spectroscopy was carried out. The peroxo compound K₂Sn(OOH)₆ crystallizes in the hexagonal system with a = 7.264(7) Å, c = 10.168(4) Å. IR, NMR, and Mössbauer spectroscopy data show that the tin coordination polyhedron in the peroxo compound is an octahedron formed by the coordinated hydroperoxo groups.

Previously, sodium hexahydroperoxostannate was prepared and characterized by powder X-ray diffraction analysis, thermogravimetry, IR, ¹H NMR, and Mossbauer spectroscopy, and by thermodynamic and kinetic method. The tin atom in this compound were found to occur in the octahedral environment of hydroperoxo group. It appeared pertinent to confirm the possibility of formation of this type of tin compound by preparing a new hydroperoxo complex. To this end, we performed the first synthesis of potassium hexahydroperoxostannate. Comparative study of potassium hexahydrosstannate (1) and hexahydroperoxosstannate (2) and their deuterated analogue (1a and 2a, respectively) was carried out by powder X-ray diffraction analysis, thermogravimetry, and IR, NMR (²H, ³⁹K and ¹¹⁹Sn), and Mossbauer spectroscopy.

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