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Труды сотрудников Института органического синтеза УрО РАН - результаты поиска

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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. - )
Имидж-каталог отечественных книг (до 2010 г.)
Имидж-каталог иностранных книг (до 2010 г.)
Алфавитно-предметный указатель (АПУ) ЦНБ УрО РАН
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Изобретения уральских ученых
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Нанотехнологии
Демидовские премии
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История Урала
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Книжная коллекция Шубиных
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.
Публикации Чарушина В.Н.
Каталог библиотеки ИЭРиЖ УрО РАН
Электронная энциклопедия «Дискурсология»
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1.
Инвентарный номер: нет.
   
   A 10

   
    A Convenient Approach to CF3-Containing N-Heterocycles Based on 2-Methoxy-2-methyl-5-(trifluoromethyl)furan-3(2H)-one [Electronic resource] / D. N. Bazhin, Yu. S. Kudyakova, G. -V. Roeschenthaler, Ya. V. Burgart, P. A. Slepukhin, M. L. Isenov, V. I. Saloutin, V. N. Charushin // European Journal of Organic Chemistry. - 2015. - № 23. - С. 5236-5245. - Bibliogr. : p. 5245 (23 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
NITROGEN HETEROCYCLES -- FLUORINE -- OXYGEN HETEROCYCLES
Аннотация: New synthetic routes to trifluoromethylated N-heterocycles based on condensations of 2-methoxy-2-methyl-5-(trifluoromethyl)furan-3(2H)-one with bifunctional N-nucleophiles are described. For the first time, trifluoromethyl-containing pyrazoles, pyrazolines and isoxazolines bearing hydrazone or oxime groups could be obtained by a one-pot strategy based on reactions of 5-(trifluoromethyl)furan-3(2H)-one with two equivalents of the corresponding hydrazines or hydroxylamine in the presence of an acid. The interaction of furan-3(2H)-one with ureas proceeded under mild conditions to furnish 1H-furo[2,3-d]imidazol-2(3H)-one derivatives in good yield. Further, a trifluoromethyl-containing quinoxaline derivative was obtained by condensation of furan-3(2H)-one with ortho-phenylenediamine.

\\\\expert2\\nbo\\European Journal of Organic Chemistry\\2015, №23. p.5236-5245.pdf
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2.
Инвентарный номер: нет.
   
   A 10

   
    A simple one pot synthesis of condensed 1,2,4-triazines by using the tandem AN-SNipso and SNH-SNipso reactions [Text] / O. N. Chupakhin, G. L. Rusinov, D. G. Beresnev, V. N. Charushin, H. Neunhoeffer // Journal of Heterocyclic Chemistry. - 2001. - Т. 38, № 4. - P901-907
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A new synthetic approach to condensed 1,2,4-triazines based on using the tandem AN-SNipso and SNH-SNipso reactions has been developed. 5-Methoxy-3-penyl-l,2,4 1,2,4-triazine and its N1-methyl quaternary salt were found to react with C,N-, C,O- and N,N?-bifunctional nucleophiles (m-phenylenediamine, resorcinol, semicarbazide and ureas) into triazacarbazoles, benzofuro[2,3-e][1,2,4]-triazines, and 6-azapurine derivatives. In all cases nucleophiles attack first the unsubstituted C-6 carbon of the triazine ring, while the final stage is replacement of the methoxy group affording cyclization products.

\\\\Cserver\\dist\\НБО\\Электронная библиотека_Библиогр1\\Journal of Heterocyclic Chemistry\\2001.v.38.p.901.Chupachin.pdf
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3.
Инвентарный номер: нет.
   
   A 18

   
    Acid-base properties and prototropic tautomerism of isomeric 1,2,4-triazin-3- and -5-ones [Electronic resource] / I. V. Khabibulina, R. E. Trifonov, A.P. Volovodenko, M. S. Eremenkova, O. N. Chupakhin, V. L. Rusinov, G. V. Zyryanov, V. A. Ostrovskii // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2004. - Vol. 40, № 3. - P426-430. - Bibliogr. : p. 430 (40 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ACID -- BASE -- TRIAZINE DERIVATIVE -- AQUEOUS SOLUTION
Аннотация: The acidity and basicity constants of isomeric phenyl(aryl)-1,2,4-triazin- 3- and -5-ones in aqueous solution were determined by spectrophotometry: pK a = 7.3-6.2; pKBH+ = 0.1 to -2.2. 1,2,4-Triazin-3-ones are weaker bases than the corresponding 1,2,4-triazin-5-ones. According to the AM1 calculations, the most thermodynamically favorable tautomer in the gas phase is the oxo form: namely, 2H-tautomers of the neutral bases and 2,4-H,H +-tautomers of the conjugate acids.

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2004, 40 (3), 426.pdf
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4.
Инвентарный номер: нет.
   
   A 18

   
    Acidic hydrolysis of N-acyl-1-substituted 3-amino-1,2-dicarba-closo-dodecaboranes [Electronic resource] / G. L. Levit, A. M. Demin, M. I. Kodess, M. A. Ezhikova, L. Sh. Sadretdinova, V. A. Ol'shevskaya, V. N. Kalinin, V. P. Krasnov, V. N. Charushin // Journal of Organometallic Chemistry. - 2005. - Vol. 690, № 11. - P2783-2786
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Acidic hydrolysis of N-acyl 1-methyl- and 1-phenyl-3-amino-1,2-dicarba-closo-dodecaboranes has been studied. It has been shown that acidic hydrolysis of diastereomeric amides of 1-methyl-3-amino-1,2-dicarba-closo-dodecaborane results in the partial racemization of the target 3-amino-1-methylcarborane. Under the similar conditions, the hydrolysis of N-acyl-3-amino-1-phenyl-1,2-dicarba-closo-dodecaboranes resulted in amide bond cleavage accompanied by simultaneous deboronation with the removal of boron atom at position 6 of carborane cage and formation of 7,8-dicarba-nido-undecaborane derivative according to 11B and 1H NMR spectroscopy.

\\\\Expert2\\nbo\\Journal of Organometallic Chemistry\\2005, v. 690, p.2783.pdf
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5.
Инвентарный номер: нет.
   

   
    Activation effect of β-alanine and chitosan derivative on A. glycyphyllos and A. membranaceus seed germination and seedling growth and development / L. A. Khamidullina, A. V. Pestov, P. D. Tobysheva [et al.] // Agronomy research. - 2021. - Vol. 19, № 2. - P484-495
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Agricultural cultivation of astragalus is fraught with a number of difficulties caused by both certain requirements for climatic conditions and individual characteristics of plants of this genus. In this study, carboxyalkylated derivative of chitosan was first proposed to use for improvement of astragalus propagation. Effects of N-(2-carboxyethyl)chitosan on in vitro A. glycyphyllos and A. membranaceus seed germination and seedling growth and development in comparing with β-alanine and chitosan acetate were detected. Carboxyethylation of chitosan leads to an increase in hydrophilic properties of the molecule, which enhances a penetration of nutrients inside the plant owing to improved solvating effect and bioadhesive activity. Seed germination assay were performed on Murashige-Skoog growth medium with or without tested compounds. N-2-Carboxyethylated derivative of chitosan was found to demonstrate active stimulating effect on the plant growth and development, contrary to the effect of acetate chitosan, but not to cause an activating effect on seed germination, while β-alanine does.

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6.
Инвентарный номер: нет.
   
   A 20

   
    Adamantylation of 3-nitro- and 3-ethoxycarbonyl-1,2,4-triazolo[5,1-c]-1,2,4-triazin-4-ones [Electronic resource] / E. N. Ulomskii, S. L. Deev, A. V. Tkachev, I. K. Moiseev, V. L. Rusinov // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2002. - Vol. 38, № 2. - P272-280. - Bibliogr. : p. 280 (15 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ADAMANTANE DERIVATIVE -- SULFURIC ACID -- TRIAZINE DERIVATIVE -- UNCLASSIFIED DRUG
Аннотация: Reaction of 3-nitro- and 3-ethoxycarbonyl-1,2,4-triazolo[5,1-c]-1,2,4-triazin-4-ones with 1-adamantanol (or 1-adamantyl nitrate) in concentrated sulfuric acid or with 1-bromoadamantane in sulfolane affords N-adamantyl derivatives. The adamantylation of 3-nitro-1,4-dihydro-7H-1,2,4-triazolo[5,1-c]-1,2,4-triazin-4-one yields a mixture of N8- and N1-isomers that undergo interconversion in concentrated sulfuric acid along intermolecular mechanism.

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2002, 38 (2), 272.pdf
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7.
Инвентарный номер: нет.
   
   A 48

   
    Aminomethylation of chlorophyll a derivatives using bis(N,N-dimethylamino) methane [Text] / D. V. Belykh, I. S. Tarabukina, D. A. Gruzdev, M. I. Kodess, A. V. Kutchin // Journal of Porphyrins and Phthalocyanines. - 2009. - Vol. 13, № 7-8. - P949-956
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Bis(N,N-dimethylamino)methane has been shown to be a convenient reagent for the aminomethylation of chlorophyll a derivatives. Methylpheophorbide a (in enol form) and chlorin e6 13-amides were aminomethylated with bis(N,N-dimethylamino)methane. Reactivity of methylpheophorbide a exo-ring and chlorin e6 13-amides vinyl group were shown to be different. Selective methylpheophorbide a exo-ring aminomethylation was realized and isomerization of the exo-ring aminomethylation product with rhodochlorin 15-acrylic derivative formation was studied. The action of bis(N,N- dimethylamino)-methane in the presence of weak acid has been shown to be a simple and effective synthetic procedure to obtain a new chlorin e6 derivative with two N,N-dimethylaminomethyl substituents in the vinyl group. The aminomethylation products' high yields, the simplicity of the procedure, the use of metal-free chlorines and the possible synthesis of new compounds, were found to be the main advantages of using bis(N,N-dimethylamino)methane as an aminomethylation reagent in chlorophyll a derivatives' chemistry

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8.
Инвентарный номер: нет.
   
   A 62

   
    Anti-HIV activity of complex isoborneol ethers [Электронный ресурс] / A. G. Pokrovskii, O. I. Kiselev, O. N. Chupakhin, V. N. Charushin, M. G. Ponizovskii // Doklady Akademii Nauk . - 1992. - Vol.326, №2. - P376-379
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ANTIVIRUS AGENT -- ENCYCLAN -- QUINOXALINE DERIVATIVE

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9.
Инвентарный номер: нет.
   

   
    Assembly of annulated 1,3-diazapyrenes by consecutive cross-coupling and cyclodehydrogenation of (het)arene moieties / E. V. Verbitskiy, E. M. Dinastiya, O. S. Eltsov [et al.] // Mendeleev communications. - 2020. - Vol. 30, № 2. - P142-144
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Di(het)areno[e,l][1,3]diazapyrene core was constructed by FeCl3-mediated intramolecular oxidative cyclodehydrogenation of 5-[2,6-di(het)arylphenyl]pyrimidine precursors, which in turn were obtained by the Suzuki cross-coupling of 5-(2,6-dibromophenyl)pyrimidine derivative with the corresponding (het)arylboronic acids. Molecular orbital calculations as well as redox and photophysical measurements show that the fused products are promising for organic electronic application.

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10.
Инвентарный номер: нет.
   
   C 52

   
    Chiroptical properties and new derivatives of cyclopalladated 6-ferrocenyl-2,2-bipyridine. Molecular structure of a tert-butyl isocyanide derivative [Electronic resource] / L. A. Bulygina, Z. A. Starikova, K. K. Babievskii, I. A. Utepova, V. L. Rusinov, O. N. Chupakhin, V. I. Sokolov // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2008. - Vol. 57, № 10. - P2214-2216
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Optically active cyclopalladated 6-ferrocenyl-2,2?-bipyridine has been studied by circular dichroism and luminescent spectroscopy; a replacement of the chloride ion at palladium with the rhodanide ion and tert-butyl isocyanide molecule has been carried out; molecular structure of the product in the latter case has been determined by X-ray diffraction analysis

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2008, 57 (10), 2214-2216.pdf
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11.
Инвентарный номер: нет.
   

   
    Combined in silico, ex vivo, and in vivo assessment of L-17, a thiadiazine derivative with putative neuro-and cardioprotective and antidepressant effects / A. Sarapultsev, P. M. Vassiliev, D. M. Grinchii [et al.] // International journal of molecular sciences. - 2021. - Vol. 22, № 24. - P13626
Рубрики: ЗДРАВООХРАНЕНИЕ. МЕДИЦИНСКИЕ НАУКИ
Кл.слова (ненормированные):
TREATMENT-RESISTANT DEPRESSION -- POST-STROKE DEPRESSION -- C-FOS IMMUNOHISTOCHEMISTRY -- BINDING AFFINITY
Аннотация: Depression associated with poor general medical condition, such as post-stroke (PSD) or post-myocardial infarction (PMID) depression, is characterized by resistance to classical antidepressants. Special treatment strategies should thus be developed for these conditions. Our study aims to investigate the mechanism of action of 2-morpholino-5-phenyl-6H-1,3,4-thiadiazine, hydrobromide (L-17), a recently designed thiadiazine derivative with putative neuro- and cardioprotective and antidepressant-like effects, using combined in silico (for prediction of the molecular binding mechanisms), ex vivo (for assessment of the neural excitability using c-Fos immunocytochemistry), and in vivo (for direct examination of the neuronal excitability) methodological approaches. We found that the predicted binding affinities of L-17 to serotonin (5-HT) transporter (SERT) and 5-HT3 and 5-HT1A receptors are compatible with selective 5-HT serotonin reuptake inhibitors (SSRIs) and antagonists of 5-HT3 and 5-HT1A receptors, respectively. L-17 robustly increased c-Fos immunoreactivity in the amygdala and decreased it in the hippocampus. L-17 dose-dependently inhibited 5-HT neurons of the dorsal raphe nucleus; this inhibition was partially reversed by the 5-HT1A antagonist WAY100135. We suggest that L-17 is a potent 5-HT reuptake inhibitor and partial antagonist of 5-HT3 and 5-HT1A receptors; the effects of L-17 on amygdaloid and hippocampal excitability might be mediated via 5-HT, and putatively mediate the antidepressant-like effects of this drug. Since L-17 also possesses neuro- and cardioprotective properties, it can be beneficial in PSD and PMID. Combined in silico predictions with ex vivo neurochemical and in vivo electrophysiological assessments might be a useful strategy for early assessment of the efficacy and neural mechanism of action of novel CNS drugs.

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12.
Инвентарный номер: нет.
   
   D 46

   
    Design of fused systems based on sigma(H)-adducts of 6-nitro-1,2,4-triazolo[1,5-a]pyrimidine with pi-excessive heteroaromatic compounds [Electronic resource] / E. B. Gorbunov, G. L. Rusinov, O. N. Chupakhin, V. N. Charushin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2009. - Vol. 58, № 6. - P1309-1314
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A new method was developed for the construction of tetra- and pentacyclic fused systems based on sigma(H)-adducts of 6-nitro-1,2,4-triazolo[1,5-a]pyrimidine with pi-excessive heteroaromatic compounds. The method involves the reduction of the nitro group accompanied by the aromatization of the dihydropyrimidine ring and followed by the cyclocondensation of the amino derivative with aldehydes

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2009, 58 (6), 1309-1314.pdf
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13.
Инвентарный номер: нет.
   

   
    Development of a method for the thiocarbamoylation of polyepichlorohydrin with a high degree of functionalization / A. P. Rodionova, A. V. Mekhaev, O. V. Koryakova [et al.] // Russian chemical bulletin. - 2021. - Vol. 70, № 6. - P1167-1173
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
POLYEPICHLOROHYDRIN -- THIOUREA -- SYNTHESIS IN GEL
Аннотация: The conditions for the homogeneous functionalization of polyepichlorohydrin (PECH) with thiourea by the “synthesis in gel” method were experimentally selected. The best solvent for this process is 1,4-dioxane. The reaction mixture visually represents a physical gel in the range of polymer concentrations from 6 to 20%. The composition of the products was characterized by the data of elemental analysis, and specific features of their structure were established using FT-IR spectroscopy and thermogravimetry with the simultaneous IR spectrometric identification of the decomposition products. Thiourea was shown to react with PECH as an ambident nucleophile with the formation of both groups of N-substituted thiourea and fragments of isothiuronium salt. The total degree of functionalization was 90%. The crosslinking of the macromolecules proceeds simultaneously due to which the obtained products with different degrees of functionalization are insoluble in organic solvents. The thiocarbamoylated PECH derivative demonstrates antiselectivity to CuII ions in the sorption of the metal ions of the Irving—Williams series.

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14.
Инвентарный номер: нет.
   
   E 27

   
    Efficient large (ca. 40 g) laboratory scale preparation of (S)- and (R)-valine tert-butyl esters [Text] / V. P. Krasnov, G. L. Levit, I. M. Bukrina, A. M. Demin, O. N. Chupakhin, Ji Uk Yoo // Tetrahedron: Asymmetry . - 2002. - Vol. 13, № 17. - P1911-1914
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A large laboratory scale (ca. 40 g) method for the preparation of enantiomerically pure (S)- and (R)-valine tert-butyl esters has been developed. The method involves three steps: preparation of N-TFA-valines, preparation of valine tert-butyl esters using 2-methylpropene in dioxane in the presence of sulfuric acid, and isolation of the target compounds as the acetate derivative. The overall yield is up to 70% relative to the starting valine, ee being more than 98% (by HPLC)????

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15.
Инвентарный номер: нет.
   
   F 76

   
    Formation of polynuclear palladium complexes with the benzimidazole-2-thiolate anion [Electronic resource] / M. O. Talismanova, A. A. Sidorov, G. G. Aleksandrov, V. N. Charushin, S. K. Kotovskaya, I. L. Eremenko, I. I. Moiseeva // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2008. - Vol. 57, № 1. - P47-55
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The reactions of palladium(II) salts with 2-mercaptobenzimidazole (HL) and its 5,6-difluorinated derivative (HLF) were investigated. In the presence of hydrochloric acid, PdCl2 and K2PdCl4 react with HL and HLF in the ethanol—water and acetonitrile—water systems to form the mono-nuclear dicationic complexes [Pd(HL)4]Cl2 (1) and [Pd(LF)4]Cl2 (2). In the absence of HCl, the reactions afford the tetranuclear complex Pd4[(L)2(3-S,N-(L))2(S,N-(L))4] (3). The reaction of triethylamine with an ethanolic solution of 3 leads to degradation of 3 and the formation of the lantern-type dinuclear complex Pd2[2-(L)4] (4), in which the palladium atoms are in the nonequivalent coordination environment, PdN4 and PdS4. The reaction of K2PdCl4 with HL or HLF in the THF—water or acetonitrile—water systems (for the reaction with HLF) in the presence of Et3N produces the lantern-type dinuclear complexes Pd2[(?S,N-(L3))4] and Pd2[(S,N)(LF))4] (5), in which the metal atoms are in the equivalent coordination environment (cis-PdN2S2)

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2008, 57 (1), 47.pdf
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16.
Инвентарный номер: нет.
   
   H 10

   
    H-1 and C-13-NMR investigations on-adduct formation of 1,2,4-triazine 4-oxides and 3-chloro-6-phenyl-1,2,4-triazine with liquid ammonia and alkylamines [Text] / A. Rykowski, O. N. Chupakhin, D. N. Kozhevnikov, V. N. Kozhevnikov, V. L. Rusinov, der Plas H. C. Van // Heterocycles. - 2001. - Т. 55, № 1. - P127-133
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: 1H- and 13C-NMR spectra of the ?-adducts formed between 6-phenyl-1,2,4-triazine 4-oxide (1a), 3-ethyl-6-phenyl-1,2,4-triazine 4-oxide (1b) and liquid ammonia, methylamine or dimethylamine are described, together with 1H NMR spectra of 3-chloro-6-phenyl-1,2,4-triazine (7) in liquid ammonia. The results of the NMR study have shown that the carbon C-5 in 1a-b and 7 is the preferred site for nucleophilic attack by liquid ammonia and alkylamines at low temperatures (from -75° to -20°C). The ?-adduct (5e) formed between 1a and dimethylamine at -75°C on heating to -20°C irreversibly converts to open-chain product (3a), via intermediary C-3 ?-adduct (6). The amination of 7 into 3-amino-6-phenyl-1,2,4-triazine (10) occurs via SN(AE) mechanism involving the isomerisation of the C-5 ?-adduct (8) into the C-3 ?-adduct (9) as confirmed by a 15N study with labeled liquid ammonia.

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17.
Инвентарный номер: нет.
   
   H 43

   
    Heavy metals removal by flocculation/precipitation using N-(2-carboxyethyl)chitosans [Text] / S. YU. Bratskaya, A. V. Pestov, Yu. G. Yatluk, V. A. Avramenko // Colloids and Surfaces A: Physicochemical and Engineering Aspects. - 2009. - Vol. 339, № 1-3. - P140-144
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Here we report on solution properties and flocculation performance of polyampholyte chitosan derivatives - N-carboxyethylated chitosans (CEC) - synthesized "in gel" by treatment of chitosan with acrylic acid. We show that carboxyethylation with the substitution degrees (DS) from 0.7 to 1.6 yields water-soluble derivatives, whose isoelectric points (IEP) range from 6.30 to 3.55. At pH 7.5 interaction of negatively charged CEC derivatives with positively charged colloids of the heavy metal hydroxides (Zn2+, Cu2+, Ni2+), serving as a model of postgalvanic wastewaters, results in lowering of electrokinetic potential of the hydroxide colloids and their precipitation at appropriate flocculant dose. Investigations of CEC flocculation performance depending on pH and DS show that the efficiency of metal removal decreases in the row Cu2+ Zn2+ Ni2+ corresponding to the row of the hydroxocomplex stability for these metals. The higher was pH of the system and DS of CEC derivative, the narrower was the flocculation window and the stronger was negative effect of flocculant overdosing on the efficiency of heavy metal removal. Based on the estimation of floc settling rates and the residual metal concentrations, we have concluded that the optimal DS of CEC derivatives for the precipitation of metal hydroxides is 0.7-1.0

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18.
Инвентарный номер: нет.
   
   I-55

   
    Imidazole-containing chitosan derivative: a new synthetic approach and sorption properties [Electronic resource] / A. V. Pestov, S. YU. Bratskaya, Yu. A. Azarova, Yu. G. Yatluk // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2012. - Vol.61, №10. - С. 1959-1964. - Bibliogr. : p. 1963-1964 (33 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CHITOSAN -- SORBENT -- GOLD(III)
Аннотация: A novel method for the synthesis of a hetaryl containing chelate amino polymer, namely, N (4(5) imidazolylmethyl)chitosan (IMC), with a degree of substitution up to 0.3 was pro posed. The "synthesis in gel" approach involves direct substitution of the hydroxyl group in 4(5) imidazolylmethanol. The structures of these polymers were confirmed by 1H NMR data. For sorption studies, IMC samples were crosslinked with epichlorohydrin and diglycidyl ethers of ethylene glycol and diethylene glycol. The degrees of swelling and sorption properties of the polymers largely depend on the crosslinking agent and the degree of crosslinking. The sorption capacities of IMC for AuIII, PtIV, and PdII ions are higher than those of the nonmodified polymer. The extraction of noble metal ions from chloride solutions becomes more selective with increasing degree of crosslinking. The sorption capacity of IMC for CoII and NiII ions is higher than those of chitosan and its known N heterocyclic derivatives

\\\\expert2\\NBO\\Russian Chemical Bulletin\\2012, 61 (10), 1959-1964.pdf
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19.
Инвентарный номер: нет.
   
   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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20.
Инвентарный номер: нет.
   
   H 99

   
    Interaction of perfluorent-2-ene and its 2-amino-4-ivino derivative with ethylenediamine and with diethylenetriamine [Text] / V. I. Saloutin, Z. E. Skryabina, Ya. V. Burgart, O. N. Chupakhin, M. Fontaltaba, X. Solans, M. Fontbardia // Journal of Fluorine Chemistry. - 1994. - Vol. 69, N 1. - P25-29
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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