Центральная Научная Библиотека УрО РАН

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   С 71


    Спектральные проявления активных центров на поверхности наноразмерного оксида меди = Ftir study of the active centers on surface of ultrafine copper oxide [] / В. Г. Харчук, О. В. Корякова, Е. Ф. Хмара, М. А. Уймин // Аналитика и контроль. - 2005. - Т. 9, № 4. - С. 423-427. - Библиогр.: с. 427 (10 назв.)

ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Приводятся результаты ИК спектроскопического изучения активных центров нанокристаллических оксидов меди, основанного на выделении специфических взаимодействий молекул-зондов: H2O, CO2, NH3

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   H 99


    Hydrophilic nature and sorption—diffusion properties [Electronic resource] / A. I. Suvorova, A. L. Suvorov, I. S. Tyukova, N. N. Malysheva, A. V. Okhokhonin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2013. - Vol. 61, №3. - С. 555-562. - Bibliogr. : p. 562 (34 ref.)

ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
POLYSULFONE -- SILICA -- SOL—GEL PROCESS
Аннотация: Hybrid nanocomposite films containing silica (11.4 wt.%) or titania (18.8 wt.%) in the polymer matrix were prepared by the sol—gel method using the hydrolytic polycondensation of tetraethoxysilane and tetrabutoxysilane in a THF solution of aromatic polymer, polysulfone (PSF). The influence of the oxide nature and the film composition on the structure, the interaction of the polymer with oxides, hydrophilicity, and sorption—diffusion properties of the hybrid films were studied by FTIR spectroscopy, atomic force microscopy, dynamic light scattering, and a complex of other physicochemical methods. The absence of chemical or intermolecular hydrogen bonds between the polymer and oxide particles in the PSF films was shown. The average size of the oxides (SiO2, 20 nm; TiO2, ~90 nm) in the films and roughness of their surface (~0.2—0.8 nm) were determined. The introduction of oxides into the polymer matrix increases the hydrophilic properties and the ability of the PSF films to swell in water; the diffusion coefficients of water and permeability of water vapor in the PSF films also increase. Titania also induces a more considerable change in the structure of the polymer matrix and more strongly affects the sorption—diffusion properties of the hybrid films in aqueous solutions of THF. All prepared nanocomposite films PSF/SiO2 and PSF/TiO2 are capable of extracting an organic component from aqueous solutions and can be used as sorbents and membrane films for the removal of organic substances from the aqueous medium

\\\\expert2\\NBO\\Russian Chemical Bulletin\\2012, 61 (3), 555-562.pdf
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   C 31


    Catalysts for enantioselective Biginelli reaction based on the composite silica-zirconia xerogels prepared using different zirconium sources [Electronic resource] / I. V. Krivtsov, Yu. A. Titova, M. V. Ilkaeva, V. V. Avdin, O. V. Fedorova, S. A. Khainakov, J. R. Garcia, G. L. Rusinov, V. N. Charushin // Journal of Sol-Gel Science and Technology . - 2014. - Vol.69, №2. - С. 448-452. - Bibliogr. : p. 452 (17 ref.)

ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
SOL-GEL METHOD -- ZIRCONIUM OXYCHLORIDE -- SILICA-ZIRCONIA XEROGELS
Аннотация: The composite silica-zirconia xerogels have been prepared via sol-gel method using zirconium oxychloride, oxynitrate, acetate and sodium silicate as the precursors. The prepared materials have been characterized using FTIR, TG/DTA, EDX and surface area analyses. It has been established that surface area of silica-zirconia xerogels significantly depends on the zirconium source, but phase transitions and structural features of the xerogels seem to be unaffected by the choice of the zirconia precursor. Prepared xerogels increase the activity of chiral inductor in the asymmetric Biginelli reaction. The anion of the zirconium salt adsorbed on the surface of the synthesized material and the presence of Si-O-Zr heterolinkages determines the reaction yield. The highest chemo- and enantioselectivity towards formation of ee isomer have been provided by the catalyst prepared from zirconium oxychloride.

\\\\expert2\\nbo\\Journal of Sol-Gel Science and Technology\\2014, v.69, N 2, p.448-452.pdf
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   I-55


    Immobilization of pmida on Fe3O4 magnetic nanoparticles surface: mechanism of bonding / A. M. Demin, A. V. Mekhaev, V. P. Krasnov, A. A. Esin, D. K. Kuznetsov, P. S. Zelenovskiy, Y. Y. Shur // Applied surface science. - 2018. - V 440. - С. 1196-1203

ББК 24
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
FTIR -- MAGNETIC NANOPARTICLES -- MECHANISM OF IMMOBILIZATION -- PMIDA -- TGA -- XPS
Аннотация: The mechanism of N-phosphonomethyl iminodiacetic acid (PMIDA) binding with the Fe3O4 magnetic nanoparticle (MNPs) surface by Fourier transformed infrared spectroscopy, X-ray photoelectron spectroscopy and thermogravimetry was comprehensive studied. To study of microstructure, size and core structure of synthesized nanoparticles the scanning electron microscopy, X-ray diffraction analysis and Raman spectroscopy were carried out. A new scheme for the tridentate bonding of the phosphonomethyl derivative with surface Fe atoms involving unequal P–O–Fe bonds was proposed. The mechanism of thermal decomposition of PMIDA molecules on the MNP surface was studied using a thermogravimetric analyzer combined with infrared spectrometer. It was shown for the first time that during the thermal treatment of phosphonomethyl-modified MNPs, PMIDA molecules are not desorbed from the surface of MNPs but gradually decompose. We believe that obtained in this work data will be useful for a deeper understanding of the mechanisms of phosphonic acid derivatives interaction with MNPs, as well as in the design of new biomedical materials, in which the conjugation of biomolecules with carboxyl groups of PMIDA-modified MNPs is assumed.

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    Development of the method of polystyrene chloromethylation using the synthesis in gel approach / D. V. Nesterov, A. P. Rodionova, A. V. Mekhaev [et al.] // Russian chemical bulletin. - 2021. - Vol. 70, № 6. - P1149-1153
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
POLYSTYRENE -- CHLOROMETHYLATION -- SYNTHESIS IN GEL
Аннотация: A new method for the preparation of poly(chloromethylstyrene) by synthesis in a gel via treating of linear polystyrene with cyclic formals in thionyl chloride has been developed. The method allows to obtain a polymer with a high degree of functionalization. The degree of chloromethylation depends on the molar ratio of the reagents and the catalyst used. The reactivity of the formals increases in the series 1,3-dioxolane < trioxane < paraform. The composition and structure of polymer products were characterized by elemental analysis, FTIR spectroscopy, and thermogravimetry. It is established that carrying out of chloromethylation in gel allows, in comparison with the known methods, to achieve a greater degree of functionalization faster and with lower consumption of reagents and solvents.

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    Functionalization of halloysite with N-(2-aminoethyl)-3-aminopropyl-trimethoxysilane / V. A. Osipova, A. V. Pestov, A. V. Mekhaev [et al.] // Russian chemical bulletin. - 2021. - Vol. 70, № 6. - P1180-1184
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
HALLOYSITE -- N-(2-AMINOETHYL)-3-AMINOPROPYLTRIMETHOXYSILANE -- SORPTION OF cU(II)
Аннотация: In order to increase the affinity of the halloysite mineral to 3d-metal ions, its surface was functionalized with N-(2-aminoethyl)-3-aminopropyltrimethoxysilane. A significant influence of the nature of the solvent and silane concentration on the degree of functionalization of halloysite was revealed. According to the data of elemental analysis, FTIR spectroscopy, and thermogravimetry, it was found that the most efficient solvents were tetrahydrofuran and acetonitrile at an equimolar silane to halloysite ratio. The functionalization of halloysite with N-(2-aminoethyl)-3-aminopropylsilyl groups significantly increases the sorption capacity of the material in comparison with both unmodified halloysite and halloysite functionalized with non-chelating 3-aminopropylsilyl groups.

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    Design, synthesis, biological evaluation and molecular docking studies of 1,4-disubstituted 1,2,3-triazoles: peg-400:h2o mediated click reaction of fluorescent organic probes under ultrasonic irradiation / C. K. R. Reddivari, S. R. Devineni, R. R. Yellalavenkata [et al.] // Polycyclic aromatic compounds. - 2021. - Vol. 42, № 7. - P3953-3974
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ULTRASONICATION -- 123-TRIAZOLE -- ANTIOXIDANT ACTIVITY
Аннотация: The perpetual demand of medicinally significant scaffolds has prompted the synthetic chemists to identify simple and efficient routes for flawless synthesis. A PEG-400:H2O mediated highly versatile, efficacious and selective “Click reaction” of fluorescent organic Probes under ultrasonic irradiation is reported. 1,2,3-Triazole ring has also been revealed to play a crucial role in bioorthogonal methodologies, fragment-based drug design, and biomolecular mimetics. This methodology provides a rapid and efficient approach for the synthesis of 1,4-Disubstituted 1,2,3-triazoles under Copper (I)-Catalyzed Azide-Alkyne [3 + 2] Cycloaddition (CuAAC) conditions in good to excellent yields in less time. This synthetic protocol has been proven to endorse easy work-up under benign reaction conditions. The green solvent system employed has been efficaciously reused several times without any loss of its activity in an aqueous medium. All the title compounds were characterized by using elemental analysis, 1HNMR, 13CNMR, FTIR, and mass spectral data. The newly synthesized compounds were biologically evaluated for their antioxidant activity. The antioxidant activity results demonstrate that all compounds showed good to excellent antioxidant activity, particularly the compounds 5d, 8 b, 8c and 8d exhibited promising radical scavenging activity. Further, photophysical properties of the compounds were accomplished using spectrofluorimeter. By this method, compounds 5c, 5e, 5f, 8a, 8 b, 8c and 8d exhibited fluorescence in the visible region. Molecular docking studies suggested the antioxidant activity of synthesized compounds due to the inhibition of neuronal nitric oxide synthase (HnNOS).

https://doi.org/10.1080/10406638.2021.1878246
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    Synthesis and properties of azines functionalized graphene with extremely high adsorptive ability to Eu3+ ions / O. N. Chupakhin, A. A Musikhina, I. A. Utepova [et al.] // Flatchem. - 2022. - Vol. 33. - P100348
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: In this work, a versatile synthetic protocol for obtaining of new promising carbon materials based on the C–C coupling of graphenide lithium species with azaaromatic compounds (1,10-phenanthroline, phenyl-1,2,5-oxadiazolo[3,4-b]pyrazine) has been suggested. It was shown that more electrophilic oxadiazolopyrazine gave the product with high degree of graphene functionalization and demonstrated non-isomorphic properties. At the same time, phenanthrolinyl graphene has less functionalization degree due to a lower electrophilicity of azine. However, the large size of pores between organic residues in phenanthrolinyl graphene allows adsorbing almost 10% of Eu3+. The mesurment of adsorption isotherm showed an extremely high affinity of phenanthrolinylgraphene to Eu (III) ions in netural or alkaline conditions, and the obtained hybrid material could work at least 5 sorption/desorption cycles. The structures of azine-graphene dyads were verified by complex of modern physicochemical analyses methods (the Raman spectroscopy, FTIR, XPS, SEM, EDS and TGA analyses).

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