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Mössbauer Spectroscopic Study Of An Iron(III) Complex With Crown Porphyrin

Plots of the relative areas (A refers to the left scale) and intensities (B refers to the right scale) of (1) the doublet and (2) the extended absorption vs. the temperature

Mössbauer Spectroscopic Study Of An Iron(III) Complex With Crown Porphyrin. Pankratov D.A., Stukan R.A., Al'Ansari Ya.-F., Savinkina E.V., Kiselev Yu.M. //Russian Journal of Inorganic Chemistry. 2011. V. 56. № 10. P. 1603-1608

A complex of 57Fe with 5-{4-[((4′-hydroxybenzo-15-crown-5)-5′-yl)diazo]phenyl}-10,15,20-triphenylporphyrin was studied by Mössbauer spectroscopy. The presence of signals of two types in the spectra (a doublet and an extended absorption band over a wide velocity range) suggests that the Fe atoms occupy two structurally different positions in this complex. The dependences of the doublet asymmetry on temperature and the angle between the normal to the sample plane and the γ-ray beam were studied. The isomer shift δ of the doublet in the temperature range from 360 to 5 K changes from 0.25 to 0.41 mm/s, while the quadrupole splitting remains virtually unchanged (Δ ≈ 0.65 mm/s). The relaxation-type absorption over a wide velocity range, the relative area of which strongly varies with temperature, can be described by a broad singlet with the following parameters: δ = 0.30–0.44 mm/s and Γ = 2.8–3.38 mm/s. According to the δ values, both signals are due to Fe(III) derivatives.

The structures and properties of metalloporphyrins (MPs), such as hemoglobin, chlorophyll, and vitamin В12, involved in vital processes depend on the complexing metal and the peripheral substituents. A great number of MPs are chemically inert and thermally stable, have high molar absorption coefficients in the UV-Vis and near-IR ranges, and show reversible redox transitions. This accounts for the interest in comprehensive study of the corresponding properties using a variety of physicochemical techniques.

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Ab Initio Calculations Of Hydroxoplatinum Compounds: I. Hexahydroxoplatinum(IV), (V), And (VI) Complexes

Equilibrium structure of the hexahydroxoplatinum cluster Pt(OH)6 with symmetry CiAb Initio Calculations Of Hydroxoplatinum Compounds: I. Hexahydroxoplatinum(IV), (V), And (VI) Complexes. Pankratov D.A., Dement'ev A.I., Kiselev Yu.M. //Russian Journal of Inorganic Chemistry. 2008. V.53. №2. P.242-246.Search the full text below. Ищи полный текст ниже.

The structural and spectral data on Pt(OH)6n clusters (n = -2, -1, 0) obtained by ab initio methods have been considered. The data for n = -2 are in good agreement with the published data for hexahydroxoplatinates (IV).

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Ab Initio Calculations Of Hydroxoplatinum Compounds: II. Binuclear Platinum(IV) Superoxo Complexes

Equilibrium structure of the binuclear monobridged platinum superoxo complexes [(OH)5Pt(μ-O2)Pt(OH)5]3–Ab Initio Calculations Of Hydroxoplatinum Compounds: II. Binuclear Platinum(IV) Superoxo Complexes. Pankratov D.A., Dement'ev A.I., Kiselev Yu.M. //Russian Journal of Inorganic Chemistry. 2008. V.53. №2. P.247-253.Search the full text below. Ищи полный текст ниже.

The structural and spectral data have been obtained by ab initio methods for the [(OH)4Pt(μ-O2)(μ-OH)Pt(OH)4]2-, [(OH)4Pt(μ-O2)(μ-OH)Pt(OH)4(OH)]3-, [(OH)5Pt(μ-O2)Pt(OH)5]3-, and [(H2O)(OH)4Pt(μ-O2)Pt(OH)4•(H2O)]- clusters, corresponding to binuclear platinum (IV) superoxo complexes with one and two bridges. The data obtained are in good agreement with experimental data and make it possible to judge the structure of available complexes.

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Possibilities of cryogenic autoradiography

Characteristic curves obtained under different conditions: 1, at room temperature; 2, at the temperature of liquid nitrogen (experimental data, approximating straight lines of the regions of normal exposures, regions of photographic latitude, and inertia points are shown).

Possibilities of cryogenic autoradiography. Pankratov D.A., Korobkov V.I. //Journal of Analytical Chemistry. 2014. V. 69. Is. 7. P. 632–637Search the full text below. Ищи полный текст ниже.

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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Constrained growth of anisotropic magnetic δ-FeOOH nanoparticles in the presence of humic substances

Function distribution magnetic splitting the mossbauer spectrum for different temperatures of the composite d-FeOOH-HSConstrained growth of anisotropic magnetic δ-FeOOH nanoparticles in the presence of humic substances. Polyakov A.Yu., Goldt A.E., Sorkina T.A., Perminova I.V., Pankratov D.A., Goodilin E.A., Tretyakov Y.D. //CrystEngComm. 2012. V.14. №23. P.8097-8102.Search the full text below. Ищи полный текст ниже.

Natural polyelectrolytes, humic substances, are suggested to control in situ growth of feroxyhyte nanoparticles of a highly reduced mean size and with enhanced colloidal stability in salt solutions. The feroxyhyte is formed as 2-5 nm thick and 20 × 20 nm wide nanoflakes due to the blocking of developing facets of feroxyhyte and constraints caused by diffusion limitations of ionic constituents across partially charged branches of humic substances.

Superparamagnetic iron oxide nanoparticles (SPIONs) are known as effective biocompatible agents for various biomedical applications like drug delivery, in vivo magnetic resonance imaging, cell and protein separation, hyperthermia and transfection. At present, synthesis and application of rods, disks, fibers, tubes, sheets, ellipsoids, dumbbell-shaped, acorn-shaped and other anisotropic nanoparticles attract growing attention because of their unique properties. Aggregation is a serious problem in the preparation and storage of such magnetic nanoparticles limiting considerably their practical applications. This problem can be solved by a surface modification of nanoparticles with organic macromolecules, their preparation in the presence of surfactants, application of hydrophilic, surface-active ligands improving biocompatibility and resulting in multifunctional nanoparticles for medical diagnostics.

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