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Каталог книг и продолжающихся изданий
Сводный каталог иностранных периодических изданий, имеющихся в библиотеках УрО РАН
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Каталог диссертаций и авторефератов диссертаций УрО РАН
Каталог препринтов УрО РАН (1975 г. - )
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Изобретения уральских ученых
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Нанотехнологии
Демидовские премии
Гибель династии Романовых
История Урала
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Труды Института высокотемпературной электрохимии УрО РАН
Труды Института истории и археологии УрО РАН
Труды сотрудников Института горного дела УрО РАН
Труды сотрудников Института органического синтеза УрО РАН
Труды сотрудников Института теплофизики УрО РАН
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Труды сотрудников ЦНБ УрО РАН
Публикации Черешнева В.А.
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Каталог библиотеки ИЭРиЖ УрО РАН
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1.
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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2.
Инвентарный номер: нет.
   

   
    3-(2-Arylhydrazono)-1,1,1-trifluro-3-(phenylsulfonyl)propan-2-ones as selective carboxylesterase inhibitors / E. V. Shchegolkov, Y. V. Burgart, N. A. Elkina [et al.] // Russian chemical bulletin. - 2022. - Vol. 71, № 1. - P158-164
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: We improved the synthetic procedure for 3-(2-arylhydrazono)-1,1,1-trifluro-3-(phenylsulfonyl)propan-2-ones and established their structure. The study of their esterase profile showed the absence of cholinesterase inhibition and the selectivity against carboxylesterase with micromolar activity exceeding the anticarboxylesterase activity of the diketone analog. Carboxylesterase inhibition data are consistent with molecular docking results. 3-(2-Arylhydrazono)-1,1,1-trifluro-3-(phenylsulfonyl)propan-2-ones exhibit a high radical-scavenging effect in the ABTS test exceeding that of Trolox.

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3.
Инвентарный номер: нет.
   

   
    Acylative kinetic resolution of racemic methyl-substituted cyclic alkylamines with 2,5-dioxopyrrolidin-1-yl (R)-2-phenoxypropanoate / D. A. Gruzdev, S. A. Vakarov, M. A. Korolyova [et al.] // Organic & biomolecular chemistry. - 2022. - Vol. 20, № 4. - P862-869
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The diastereoselective acylation of a number of racemic methyl-substituted cyclic alkylamines with active esters of 2-phenoxypropanoic acid was studied in detail. The ester of (R)-2-phenoxypropanoic acid and N-hydroxysuccinimide was found to be the most selective agent. The highest stereoselectivity was observed in the kinetic resolution of racemic 2-methylpiperidine in toluene at −40 °C (selectivity factor s = 73) with the predominant formation of (R,R)-amide (93.7% de). To explain the observed stereoselectivity, DFT modelling of the transition states in the reactions of the title acylating agent with 2-methylpiperidine and 2-methylpyrrolidine was performed. The calculated values were in good agreement with experimental data. It has been demonstrated that the acylation proceeds via a concerted mechanism, in which the addition of an amine occurs simultaneously with the elimination of the hydroxysuccinimide fragment. The high stereoselectivity of the (R,R)-amide formation is largely ensured by the lower steric hindrances in the transition states as compared to the formation of (R,S)-amide.

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4.
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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5.
Инвентарный номер: нет.
   
   C 55

   
    Choice of optimal conditions for the dynamic concentration of silver(I) ions from complex solutions with sulfoethylated polyaminostyrenes / L. M. Alifkhanova, Y. S. Petrova, S. N. Bosenko [и др.] // Russian Journal of Inorganic Chemistry. - 2021. - Т. 66, № 4. - С. 578-585
ББК Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: This work was intended to study the selectivity of silver(I) ion adsorption with sulfoethylated polyaminostyrenes under dynamic conditions. The greatest selectivity of the extraction of silver(I) ions in the presence of copper(II) ions is at pH 6.0 and a solution flow rate of 2 mL/min. The breakthrough curves of metal adsorption were obtained in the joint presence of sorbates from ammonium acetate buffer solution. The dynamic capacities of adsorbents, rate constants of reactions, and 50% sorbate breakthrough times were determined. The silver(I) adsorption selectivity increases with an increase in degree of substitution of polyaminostyrenes. The breakthrough curves were fitted with the Thomas, Adams–Bohardt, and Yoon–Nelson models. For the quantitative desorption of silver(I) ions from the adsorbents, 20.0 mL of 1 M nitric acid is most appropriate.

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6.
Инвентарный номер: нет.
   

   
    Design of fluorescent sensors based on azaheterocyclic push-pull systems towards nitroaromatic explosives and related compounds: a review / E. V. Verbitskiy, G. L. Rusinov, O. N. Chupakhin, V. N. Charushin // Dyes and pigments. - 2020. - Vol. 180. - P108414
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
NITROAROMATIC EXPLOSIVES -- FLUORESCENCE QUENCHING -- PYRIDINES -- PYRAZINE -- PYRIMIDINES -- TRIAZINES
Аннотация: Highly sensitive and selective detection of nitro containing high energy organic compounds such as picric acid (PA), 2,4,6-trinitrotoluene (TNT) and 2,4-dinitrotoluene (DNT) has become a challenging task due to concerns over national security, criminal investigations and environment protections. Among various known detection methods, fluorescence sensors have gained special attention in recent time. The family of fluorescent sensors based on push-pull systems that incorporate nitrogen heterocycles as an electron-withdrawing group have a growing interest due to their high sensitivity, selectivity and easy tuning. The fluorescent sensors discussed in this review are classified and organized according to used azaheterocyclic scaffold, their functionality and their ability to detect of nitroaromatics by fluorescence quenching.

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7.
Инвентарный номер: нет.
   

   
    Effect of complex-former ion concentration on the selectivity of metal ion sorption on cross-linked N-2-sulfoethylchitosan / Y. S. Petrova, L. K. Neudachina, M. Y. Oseeva, A. V. Pestov // Russian journal of inorganic chemistry. - 2018. - Т. 63, № 3. - P400-405
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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8.
Инвентарный номер: нет.
   

   
    Effect of the degree of sulfoethylation of polyethylenimine on the selectivity of sorption of palladium(II) from binary solutions / E. I. Kapitanova, A. R. Sinelshchikova, Yu. S. Petrova [et al.] // Russian chemical bulletin. - 2021. - Vol. 70, № 6. - P1161-1166
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
POLYETHYLENIMINE -- SULFOETHYLATION -- SORPTION -- PLATINUM(IV) -- PALLADIUM(II) -- GOLD(III)

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9.
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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10.
Инвентарный номер: нет.
   
   F 33

   
    Features of sorption preconcentration of noble metal ions with sulfoethylated amino polymers / L. M. Alifkhanova, K. Y. Lopunova, A. A. Marchuk [и др.] // Russian journal of inorganic chemistry. - 2021. - Vol. 66, № 6. - С. 909-915
ББК Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Dependencies for the sorption of palladium(II), gold(III), and platinum(IV) chloro complexes from individual and binary solutions with sorbents based on sulfoethylated polyallylamine and poly(aminostyrene) have been obtained. It has been found that predominant sorption mechanism is complexation with functional groups of the sorbents for gold(III) and palladium(II) and ion exchange for platinum(IV). It has been shown that increase in the sulfoethylation degree of aminopolymer matrix leads to decrease of platinum(IV) sorption and therefore, to increase in palladium(II) sorption selectivity relative to this ion. This effect is the largest for the sorbents based on polyallylamine. The conditions of quantitative desorption of the studied metals from sorbent surface have been determined. The sorption of gold(III) by the sorbent based on polyallylamine has been shown to be complicated by gold(III) reduction in sorbent phase.

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11.
Инвентарный номер: нет.
   
   I-60

   
    Influence of the structure of the aminoalkyl group in polysiloxane on the selectivity of its interaction with metal ions / A. S. Kholmogorova, E. A. Fedoseeva, L. K. Neudachina [et al.] // Russian Journal of Applied Chemistry. - 2021. - Vol. 94, № 4. - P478-485
ББК Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Polysiloxanes containing nonchelating 3-aminopropyl and chelating N-(2-aminoethyl)-3-aminopropyl groups with the degree of functionalization of 28 and 24%, respectively, were prepared by sol–gel synthesis. The polysiloxanes obtained showed comparable activity in sorption of Pd(II), Pt(IV), Fe(III), Cd(II), Zn(II), Co(II), Ni(II), Cu(II), Mn(II), Pb(II), Ca(II), and Mg(II) ions from model multicomponent solutions. At pH 3,3-aminopropylpolysiloxane selectively takes up platinoid ions. The chelating structure of N-(2-aminoethyl)-3-aminopropyl groups leads to a decrease in the selectivity of the interaction with Pd(II) ions but increases the affinity for Fe(III), Ni(II), and Cu(II). Preconcentration in the dynamic mode allows quantitative sorption of Pd(II) and Pt(IV), followed by virtually quantitative elution of the metal ions from the sorbent surface.

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12.
Инвентарный номер: нет.
   

   
    Investigation of hydrogen transfer from coal tar pitch and petroleum pitches using a-methylstyrene as hydrogen acceptor / E. I. Andreikov, A. P. Krasikova, M. G. Pervova, A. S. Kabak // Chemistry for sustainable development. - 2022. - Vol. 30, № 5. - P446-454
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
A-METHYLSTYRENE -- COAL TAR PITCH -- PETROLEUM PITCHES
Аннотация: The reaction of hydrogen transfer from coal tar pitch and petroleum pitches to Α-methylstyrene with the formation of cumene was investigated in glass ampoules within the temperature range of 200-360 °C and reaction time of 15-60 min and when passing Α-methylstyrene through a layer of coal tar pitch. It is shown that the formation of non-chromatographable products of Α-methylstyrene condensation with polycyclic aromatic compounds of pitches occurs simultaneously. The dependences of Α-methylstyrene conversion, the selectivity for cumene and condensation products on the temperature and reaction time, the ratio of pitch/Α-methylstyrene are determined. The amount of hydrogen transferred from pitches to Α-methylstyrene was determined, and the results obtained were compared with the literature data on the transfer of hydrogen from pitches obtained using anthracene as a hydrogen acceptor.

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13.
Инвентарный номер: нет.
   
   K 46

   
    Kinetic resolution of racemic 6-substituted 1,2,3,4-tetrahydroquinaldines with chiral acyl chlorides. Experiment and quantum chemical simulation / E. N. Chulakov, M. A. Korolyova, L. S. Sadretdinova [et al.] // Russian chemical bulletin. - 2021. - Vol. 70, № 5. - P890-899
ББК Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A comparative study of the kinetic resolution (KR) of racemic 6-substituted 2-methyl-1,2,3,4-tetrahydroquinolines with acyl chlorides of (S)-naproxen, N-phthaloyl-(S)-leucine, and (R)-O-phenyllactic acid was carried out. The selectivity factors in the KR of racemic amines with acyl chlorides of (S)-naproxen and (R)-O-phenyllactic acid were shown to be approximately the same and higher than those for the KR of N-phthaloyl-(S)-leucyl chloride. The reasons for the stereodifferentiation in the KR of racemic tetrahydroquinaldines containing groups of different electronic properties by acyl chlorides of three different chiral acids were explained using the DFT method. The conditions for stabilizing π—π interactions of aromatic fragments of the reagents, which do not occur in the same form in the transition state and lead to the minor diastereoisomeric product, are created in the transition state of the faster acylation reaction with (S)-naproxen and (R)-O-phenyllactic acyl chlorides. In the case of the KR of 2-methyl-1,2,3,4-tetrahydroquinoline and 2-methyl-6-methoxy-1,2,3,4-tetrahydroquinoline with N-phthaloyl-(S)-leucyl chloride, the acylation diastereoselectivity is determined, most likely, by conformational factors. The individual (S)-enantiomer of 2-methyl-6-methoxy-1,2,3,4-tetrahydroquinoline of high optical purity was synthesized using the KR of the racemate with (S)-naproxen acyl chloride.

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14.
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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15.
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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16.
Инвентарный номер: нет.
   
   N 52

   
    New modified 2-aminobenzimidazole nucleosides: Synthesis and evaluation of their activity against herpes simplex virus type 1 / M. I. Kharitonova, A. O. Denisova, A. L. Kayushin, I. D. Konstantinova, A. I. Miroshnikov, S. K. Kotovskaya, V. N. Charushin, V. L. Andronova, G. A. Galegov // Bioorganic and Medicinal Chemistry Letters. - 2017. - Vol. 27, № 11. - P2484-2487
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ANTIVIRAL ACTIVITY -- BENZIMIDAZOLES -- FLUORINATED COMPOUNDS -- NUCLEOSIDE PHOSPHORYLASES -- NUCLEOSIDES -- TRANSGLYCOSYLATION REACTION
Аннотация: Using the enzymatic transglycosylation reaction β-d-ribo- and 2′-deoxyribofuranosides of 2-amino-5,6-difluorobenzimidazole nucleosides have been synthesized. 2-Amino-5,6-difluoro-benzimidazole riboside proved to exhibit a selective antiviral activity (selectivity index >32) against a wild strain of the herpes simplex virus type 1, as well as towards virus strains that are resistant to acyclovir, cidofovir, and foscarnet. We believe that this compound might be used for treatment of herpes infections in those cases, when acyclovir is not efficient.

\\\\Expert2\\NBO\\Bioorganic and Medicinal Chemistry Letters\\2017 v.27 p.2484-2487.pdf
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17.
Инвентарный номер: нет.
   
   O-97

   
    Oxidation of terpenoid diols with chlorine dioxide. Easy preparation of α-hydroxyketones [Electronic resource] / L. L. Frolova, A. V. Popov, L. V. Bezuglaya, P. A. Slepukhin, A. V. Kuchin // Russian Journal of General Chemistry. - 2014. - Vol.84, №5. - С. 853-859. - Bibliogr. : p. 859 (16 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CHLORINE DIOXIDE -- OXIDATION -- SELECTIVITY
Аннотация: Oxidative dehydrogenation of vicinal diols of bornane and pinane type with chlorine dioxide in dimethylformamide has yielded α-hydroxyketones with high selectivity. 3α-Hydroxy-10β-pinane-4-one has been prepared for the first time with yield of 63-65%; the product structure has been confirmed by X-ray diffraction studies

\\\\expert2\\nbo\\Russian Journal of General Chemistry\\2014, V. 84, N 5, p. 853–859.pdf
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18.
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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19.
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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20.
Инвентарный номер: нет.
   
   S 61

   
    Simple synthesis and chelation capacity of N-(2-sulfoethyl)chitosan, a taurine derivative [Electronic resource] / Yu. S. Petrova, L. K. Neudachina, A. Mechaev, A. V. Pestov // Carbohydrate Polymers. - 2014. - Vol.112. - С. 462-468. - Bibliogr. : p. 467-468 (60 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CHITOSAN -- SELECTIVITY -- SORPTION
Аннотация: This study presents a simple and effective synthesis method of N-(2-sulfoethyl)chitosan (NSE-chitosan) via a reaction between sodium 2-bromoethanesulfonate and chitosan that allows polymer transformation without using additional reagents and organic solvents. The chemical structure of the obtained NSE-chitosan was characterized by FT-IR and 1H NMR spectroscopies. Thermogravimetric study of NSE-chitosan coupled with FT-IR analysis has shown stability of the polymer up to 200 °C, which almost does not change with the increase of degree of substitution (DS). The sorption of transition and alkaline earth metal ions from multicomponent solutions on NSE-chitosan was investigated. The synthesized sorbents showed the selective recovery of silver(I) and copper(II) ions from ammonium acetate buffer solution. The increase of DS enhanced the selectivity to silver(I) ions sorption in comparison with copper(II) ions. Selectivity coefficients KAg/Cu increase from 1.3 to 10.9 with DS increasing up to 0.7 (ammonium acetate buffer solution, pH 6.5). Sorption isotherms of transition metal ions on NSE-chitosan with DS = 0.5 have been fitted using Langmuir, Freundlich, and Redlich-Peterson models. The maximum sorption capacities of sorbent in ammonium acetate buffer solution at pH 6.0 were 1.72 mmol/g for Cu(II), 1.23 mmol/g for Ag(I) and below 0.5 mmol/g for Co(II), Zn(II), Cd(II), Pb(II), Mn(II) and Ni(II) ions

\\\\expert2\\nbo\\Carbohydrate Polymers\\2014, v. 112, p. 462.pdf
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