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1.
Инвентарный номер: нет.
   
   L 79

   
    Liquid-phase oxidation of anthracene by hydrogen-peroxide in the presence of vanadium-oxide bronzes CuXV2O5 [Text] / S. Y. Men'shikov, A. V. Vurasko, L. A. Petrov, V. L. Volkov, A. A. Novoselova // Pet-Chem Equipment Corp. - 1992. - Vol. 32, N 2. - P128-130
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Vanadium oxide bronzes of the general formula CuXV2O5, where 0x1, catalyse the liquid-phase oxidation of anthracene H2O2. The anthracene conversion and the selectivity with respect to anthraquinone are maximum withing the region of beta- and xi-phases respectively close to the compositions CuO. 6V2O5 and CuO.95V2O5.

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2.
Инвентарный номер: нет.
   
   K 80

    Kozhevnikov, D. N.
    Sigma-adducts of 1,2,4-triazine 4-oxides with Nucleophiles. I.Site Selectivity for the Addition Reaction Controlled by Strength of Acids [Text] : доклад, тезисы доклада / D. N. Kozhevnikov, O. N. Chupakhin, V. L. Rusinov // International Memorial I.Postovsky Conference on Organic Chemisty, Ekaterinburg, March 17-20, 1998 : program and abstracts. - Ekaterinburg, 1998. - P79
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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3.
Инвентарный номер: нет.
   
   N 52

   
    New hybrid chelating sorbents with grafted 3-aminopropionate groups based on mixed silicon, aluminum, titanium, or zirconium oxides [Electronic resource] / Yu. G. Yatluk, N. A. Zhuravlev, O. V. Koryakova, L. K. Neudachina, Yu. A. Skorik // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2005. - Vol. 54, № 8. - P1836-1841
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A series of new hybrid organo-inorganic sorbents with the 3-aminopropionate chelating group was synthesized. The synthesis includes the copolycondensation (sol—gel method) of tetraethoxysilane, 3-aminopropyltriethoxysilane, and several modifiers (MeSi(OEt)3, EtSi(OEt)3, Ti(OEt)4, AlONO3, ZrOCl2) followed by carboxyethylation with acrylic acid. The obtained chelating sorbents were characterized by elemental analysis, FT-IR and 1H NMR spectroscopy, and thermogravimetry. The N-carboxylated sorbents have a higher sorption capacity with respect to metal ions (0.5–0.9 mmol g?1, pH 6.3, NH4OAc, 20 °C) than the starting sorbents with the primary amino group (0.05–0.2 mmol g?1) and manifest high selectivity for copper(II) ion extraction

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2005, 54 (8), 1836.pdf
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4.
Инвентарный номер: нет.
   
   S 98

   
    Synthesis and sorption properties of new hybrid chelating sorbents with ?-alanine functional groups [Electronic resource] / Yu. G. Yatluk, D. V. Eremin, L. K. Neudachina, Yu. A. Skorik // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2004. - Vol. 53, № 12. - P2730-2735
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A series of gamma-aminopropylsilylated sorbents was obtained from different oxide supports (silica gels, silica fillers, macroporous glasses, alumina) and by the direct synthesis (hydrolytic polycondensation of tetraalkoxysilanes with gamma-aminopropyltriethoxysilane). The highest degree of immobilization was achieved for silicas, while the most convenient solvent was methanol. Sorbents with beta-alanine functional groups were obtained by the subsequent reaction with acrylic acid. The degree of beta-carboxyethylation was 1.3–1.9, and the highest content of functional groups (vCOOH = 3.23 mmol g–1) was achieved for carboxyethylated xero gel synthesized by the copolycondensation of tetraethoxysilane with -aminopropyltriethoxysilane. The sorbents containing beta-alanine possess a higher selectivity of Cu2+ ion sorption than the initial gamma-aminopropylsilylated sorbents

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2004, 53 (12), 2730.pdf
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5.
Инвентарный номер: нет.
   

   
    3,3,3-Trifluoro-N-(3-trifluoromethylphenyl)-1,2-propanediamine and its N-mono-and N,N-dicarboxyethyl derivatives: synthesis, protolytic and complexation properties [Electronic resource] / V. Yu. Korotaev, Yu. A. Skorik, A. Yu. Barkov, M. I. Kodess, A. Ya. Zapevalov // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2005. - Vol. 54, № 11. - P2545-2549
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: 3,3,3-Trifluoro-N-(3-trifluoromethylphenyl)-1,2-propanediamine (5) was synthesized by the reaction of 2-diazo-1,1,1-trifluoro-3-nitropropane or 3,3,3-trifluoro-1-nitropropene with 3-aminobenzotrifluoride followed by the reduction of the nitro group. The Michael 1,4-addition of diamine 5 to acrylic acid occurs only at the N(1) atom and affords N-mono-or N,N-dicarboxyethyl derivatives 6 and 7, depending on the reactant ratio. Protolytic equilibria 5–7 in aqueous solutions were studied by pH-potentiometry and UV spectroscopy. Only the aliphatic amino group can be protonated in an aqueous solution, while the aromatic amino group remains unprotonated even in 12 M HCl. The stability constants of transition metal (Cu2+, Ni2+, Zn2+) complexes with ligands 5–7 were determined by pH-potentiometric titration. The stability of the complexes and selectivity of the ligands toward Cu2+ ions increase with an increase in the number of N-carboxyethyl groups

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2005, 54 (11), 2545.pdf
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6.
Инвентарный номер: нет.
   
   S 66

    Skorik, Yu. A.
    Evaluation of various chitin-glucan derivatives from Aspergillus niger as transition metal adsorbents [Text] / Yu. A. Skorik, A. V. Pestov, Yu. G. Yatluk // Bioresource Technology . - 2010. - Vol. 101, № 6. - P1769-1775
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A number of chelating resins were prepared by chemical derivatization of the chitin-glucan (CG) complex isolated from Aspergillus niger biomass, namely chitosan-glucan (CsG), O-carboxymethyl-chitin-glucan (CM-CG), O-(2-sulfoethyl)chitin-glucan (SE-CG), and N-(2-carboxyethyl)chitosan-glucan (CE-CsG). The chemical modification was confirmed by FT-IR and elemental analysis. Nanosecond electron beam irradiation was used to produce insoluble resins and to preserve the reactive functional groups. Batch experiments were carried out to evaluate the adsorption selectivity and capacity of the resins toward transition metal ions (Cu2+, Ni2+, Co2+, Zn2+). The resins showed good adsorption capability with the following selectivity series: Co2+ Ni2+ Cu2+ Zn2+. The total metal adsorption capacities of CG, CsG, CM-CG, SE-CG, and CE-CsG resins at pH 6.5 (ammonium acetate buffer) were found to be 0.205, 0.382, 1.752, 0.319, and 0.350 mmol g?1, respectively. Our results suggest that, depending on the type of chemical modification, the chitin-glucan complexes can be used either for selective Cu2+ removal (CsG) or for total transition metal adsorption (CM-CG) from aqueous effluents

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7.
Инвентарный номер: нет.
   
   C 31

   
    Catalytic effect of nanosized metal oxides on the Hantzsch reaction [Text] / O. V. Fedorova, O. V. Koryakova, M. S. Valova, I. G. Ovchinnikova, Yu. A. Titova, G. L. Rusinov, V. N. Charushin // Kinetics and Catalysis. - 2010. - Vol. 51, № 4. - P566-572
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
METAL OXIDES -- HANTZSCH REACTION -- ALUMINUM OXIDES
Аннотация: The effect of nanosized copper and aluminum oxides, which have a higher sorption capacity than that of bulk samples, on the Hantzsch reaction was studied. The adsorption of starting benzaldehydes and ethyl acetoacetate on the surface of copper and aluminum nanooxides resulted in the activation of these molecules and accelerated the Hantzsch reaction. In addition, considerable activation of ammonia and intermediates (chalcone and enamine) on the surface of aluminum nanooxide facilitated an increase in the rate and selectivity of the process. The experimental results were used to develop a one-pot method for the preparation of nifedipine and nitrendipine

\\\\Expert2\\nbo\\Kinetics and Catalysis\\2010, v. 51, N 4, p. 566-572.pdf
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8.
Инвентарный номер: нет.
   
   T 45

   
    Thiocarbamoyl chitosan as a novel sorbent with high sorption capacity and selectivity for the ions of gold(III), platinum(IV), and palladium [Electronic resource] / A. V. Pestov, S. Yu. Bratskaya, A. Slobodyuk, V. A. Avramenko, Yu. G. Yatluk // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2010. - Vol. 59, № 7. - P1303-1306
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CHITOSAN -- THIOCARBAMOYL CHITOSAN -- IONS OF GOLD(III)
Аннотация: Thiocarbamoyl chitosan (TCC) was synthesized by grafting thiourea on chitosan backbone in eutectic composition of ammonium thiocyanate—thiourea. Insoluble products with the amno group functionalization degree of 0.3–1.1 can be prepared by varying the conditions of polymer-analogous (synthesis in a gel) transformation. Structure of the synthesized chitosan derivatives was characterized by elemental analysis, diffuse reflectance infrared spectroscopy, and the solid state 13C NMR. Study of sorption properties of TCC shows high sorption capacity and selectivity for the ions of gold(III), platinum(IV), and palladium(II) as evidenced by results obtained at pH 2 in the presence of 100–1000-fold excess of iron(III), copper(II), zinc(II), and nickel(II). Sorption capacity of TCC for all ions increases with the increase in the degree of substitution and changes in the series: AuIII > PdII > PtIV

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2010, 59 (7), 1303-1306.pdf
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9.
Инвентарный номер: нет.
   
   S 45

   
    Selective mоnо-N-2-carboxyethylation of chitosan in the presence of magnesium halides [Text] / A. V. Pestov, M. I. Kodess, E. G. Matochkina, Yu. G. Yatluk // Carbohydrate Polymers. - 2011. - Vol. 86, № 2. - P783-788. - Bibliogr. : p. 787-788 (19 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The solubility of chitosan in aqueous solutions of lithium and magnesium halides varies in the order: LiCl LiBr LiI; MgCl2 MgBr2 MgI2. A method for selective production of mono-N-(2-carboxyethyl)chitosan (NCE-chitosan) was developed by synthesis in gel (concentration of chitosan 4-20%) of the magnesium halides solution (1.1-3.5 M) using acrylic acid. Using for reaction of MgI2 or MgBr2 provides relative greater amount of the monosubstituted amino groups (73-87%) in comparison with their absence (50-70%) at the high degree of substitution (DS) more than 0.7. DS of the prepared NCE-chitosan and the ratios mono-: disubstitution of amino groups was determined by 1H NMR spectroscopy. The chemical structure of the obtained NCE-chitosan was characterized by FT-IR and 13C NMR spectroscopies

\\\\Expert2\\nbo\\Carbohydrate Polymers\\2011, v. 86, p.783.pdf
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10.
Инвентарный номер: нет.
   
   S 98

   
    Synthesis of chelating polymer sorbents by using the S-N(H) methodology / A. V. Pestov, P. A. Slepukhin, Yu. G. Yatluk, V. N. Charushin, O. N. Chupakhin // Journal of Applied Polymer Science . - 2012. - Vol.125, №3. - С. 1970-1978
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
FUNCTIONALIZATION OF POLYMERS -- PHENOL -- X-RAY ANALYSIS
Аннотация: The article describes a new synthetic approach to modify the structure of phenol-formaldehyde and resorcinol-formaldehyde resins, which enables one to functionalize a polymer matrix by using the S?NH (nucleophilic aromatic substitution of hydrogen) methodology. Direct heteroarylation of phenol (resorcinol) fragments in polymer chains with 1,2,4-triazine derivatives illustrates a new synthetic method in the polymer chemistry. The feature of this methodology is that it provides an opportunity to accomplish direct one-pot polymer transformations by incorporating of rather complicated chelating groups through the displacement of hydrogen in phenol moieties. It has been shown that in order to obtain chemically modified polymers on the basis of phenol-formaldehyde and resorcinol-formaldehyde resins with a high degree of substitution with chelating units, a polymer matrix has to react with 3-(pyridin-2'-yl)-1,2,4-triazin-5(2H)-one. Also, it has been found that polymer sorbents with a high selectivity can be obtained by using the template method. Targeted synthesis of model compounds, as structural units of the chelating polymers, and elucidation of the structure of their complexes with copper (II) ions have shown that the most plausible type of coordination is formation of the bridge 1 : 1 complexes of the a,a'-bipyridinyl type.

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