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1.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis and antiviral activity of nonannulated tetrazolylpyrimidines / V. A. Ostrovskii, G. G. Danagulyan, O. M. Nesterova [et al.] // Chemistry of Heterocyclic Compounds. - 2021. - Vol. 57, № 4. - P448–454
УДК
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PYRIMIDINES -- TETRAZOLES -- BIOLOGICAL ACTIVITY -- LINKERS
Аннотация: Nonannulated tetrazolylpyrimidines in the structure of which the heterocyclic fragments are separated by hydrazinocarbonylmethyl, methylpyrazolyl groups or a sulfur atom were synthesized. Some of these compounds showed moderate in vitro activity against H1N1 subtype of influenza A virus. The selectivity index of the anti-influenza action of {5-[(4,6-dimethylpyrimidin-2-yl)sulfanyl]-1H-tetrazol1-yl}acetic acid, which has very low cytotoxicity, was twice as high as the selectivity index of the reference drug rimantadine.

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2.
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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3.
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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4.
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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5.
Инвентарный номер: нет.
   
   T 44


   
    The portable detector of nitro-explosives in vapor phase with new sensing elements on a base of pyrimidine scaffold / A. A. Baranova, K. O. Khokhlov, R. D. Chuvashov, E. V. Verbitskiy, E. M. Cheprakova, G. L. Rusinov, V. N. Charushin // Journal of Physics: Conference Series. - 2017. - Vol. 830. - P012159[1-6]
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PORTABLE DETECTOR -- NITROEXPLOSIVE -- VAPOR PHASE -- SENSING ELEMENT -- PYRIMIDINE SCAFFOLD -- C(5) MONO(HETEROARYL) -- C(4) MONO(HETEROARYL) -- DI(HETEROARYL) SUBSTITUTED -- PYRIMIDINES -- PYRIMIDINE RING -- VOLATILE INTERFERENT -- NITROSCAN -- TEMPERATURE 293 K TO 298 K
Аннотация: In this paper, the new sensors based on the C(4) or/and C(5) mono(heteroaryl) and di(heteroaryl) substituted pyrimidines are described. The effect of different substituents in pyrimidine ring on the detection limits and selectivity for prepared sensors are explained. The results of detection towards various nitro-explosives and volatile interferents at room temperature with use of the portable detector “Nitroscan” are shown.

\\\\Expert2\\NBO\\Journal of Physics Conference series\\2017 v.830 p.012159.pdf
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6.
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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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.
   
   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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9.
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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10.
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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11.
Инвентарный номер: нет.
   


   
    Sorption selectivity of palladium(II) by poly(N-2-sulfoethylallylamine) under static and dynamic conditions / L. M. Alifkhanova, Yu. S. Petrova, K. Ya. Kuznetsova [et al.] // Russian Journal of Applied Chemistry. - 2022. - Vol. 95, № 3. - P451-459
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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12.
Инвентарный номер: нет.
   


   
    Synthesis of δ-Valerolactone Using Stable Hydrogen Peroxide Derivatives / Y. V. Solovyova, A. V. Pestov, I. S. Puzyrev [et al.] // Russian Journal of Organic Chemistry. - 2022. - Vol. 58, № 4. - P480-483
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The efficiencies of hydrogen peroxide derivatives in the Baeyer–Villiger oxidation of cyclopen­tanone to δ-valerolactone have been compared. The oxidants used were hydrogen peroxide in acetic, formic, or trifluoroacetic acid, magnesium and sodium monoperoxyphthalates, cumene hydroperoxide, and tert-butyl hydroperoxide. The oxidation was carried out in water, aqueous methanol, and water–ethyl acetate. Sodium and magnesium monoperoxyphthalates turned out to provide high conversion and selectivity under mild conditions.

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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.
   


   
    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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15.
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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16.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of 2-Aryl-1,2,3-triazoles by Oxidative Cyclization of 2-(Arylazo)ethene-1,1-diamines: A One-Pot Approach [Electronic resource] / K. D Gavlik, S. G. Lesogorova, E. S. Sukhorukova, J. O. Subbotina, P. A. Slepukhin, E. Benassi, N. P. Belskaia // European Journal of Organic Chemistry. - 2016. - № 15. - С. 2700-2710
ББК 54
Рубрики: ХИМИЧЕСКАЯ ТЕХНОЛОГИЯ
Кл.слова (ненормированные):
SYNTHETIC METHODS -- nUCLEOPHILIC ADDITION -- OXIDATIVE DEQUATERNIZATION
Аннотация: A one-pot approach for the synthesis of 2-aryl-5-amino-1,2,3-triazoles is reported. This approach involves a tandem nucleophilic addition of alkylamines to hydrazonoyl cyanides and in situ oxidative cyclization of the resulting 2-(aryl-azo)ethene-1,1-diamines in the presence of copper(II) acetate and air. The described one-pot procedure is characterized by good yields, excellent selectivity, methodical simplicity, and uses readily available chemicals. This method was applied to the gram-scale synthesis of 2-aryl-1,2,3-triazoles.

\\\\expert2\\NBO\\European Journal of Organic Chemistry\\2016, v. 15, p. 2700.pdf
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17.
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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18.
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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19.
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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20.
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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