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1.
Инвентарный номер: нет.
   
   G 33


    Gein, V. L.
    A novel four-component synthesis of ethyl 6-amino-4-aryl-5-cyano-2,4-dihydropyrano[2,3-c]pyrazole-3-carboxylates [Electronic resource] / V. L. Gein, T. M. Zamaraeva, P. A. Slepukhin. - [Б. м. : б. и.]. - Bibliogr. : p. 4528 (26 ref.). - Б. ц.
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
MULTICOMPONENT REACTION -- AROMATIC ALDEHYDES -- SODIUM DIETHYLOXALOACETATE
Аннотация: Ethyl 6-amino-4-aryl-5-cyano-2,4-dihydropyrano[2,3-с]pyrazole-3-carboxylates were synthesized via a four-component reaction of the sodium salt of diethyloxaloacetate, an aromatic aldehyde, hydrazine hydrate, and malononitrile. The products were obtained in moderate to high yields.

\\\\expert2\\nbo\\Tetrahedron Letters\\2014, v. 55, p. 4525.pdf
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2.
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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3.
Инвентарный номер: нет.
   


   
    The electrochemical behavior’s character of a potential antiviral drug 3-nitro-4-hydroxy-7-methylthio-4H-[1,2,4]triazolo[5,1-c][1,2,4]triazinide monohydrate / P. N. Mozharovskaia, A. V. Ivoilova, R. A. Drokin [и др.] // Chimica Techno Acta. - 2022. - Vol. 9, № 4. - Ст. 20229426
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
NITROHETEROCYCLIC COMPOUNDS -- ANTIVIRAL ACTIVITY -- CYCLIC VOLTAMMETRY
Аннотация: The results of this study of the electrochemical transformation of 3-R-4-hydroxy-1,4-dihydro-7-X-1,2,4-triazolo[5,1-c][1,2,4] obtained by voltammetry are presented. It was found that 3-R-4-hydroxy-1,4-dihydro-7-X-1,2,4-triazolo[5,1-c][1,2,4] derivatives are capable of electrochemical reduction in the potential range of -0.28 to -0.33 V (relative to Ag/AgCl) in Britton-Robinson buffer at pH = 2. The electrochemical behavior of the sodium salt of 3-nitro-4-hydroxy-7-methylthio-4H-[1,2,4]triazolo[5,1-c][1,2,4]triazinide monohydrate (compound 1), which in silico modeling predicted possible biological activity against various tick-borne encephalitis and Coxsackie B3 viruses. At the potentials of the first stage of electroreduction at pH = 2, the main transformation process is the three-electron reduction scheme of the nitro group of compound 1. It was established that compound 1 in an aprotic medium is reduced in ionic form, most likely in the form of an ion pair with the Na+ cation, and in an aqueous medium in the form of a protonated particle. Based on this, a scheme was proposed for the probable electrochemical transformation of the studied compound.

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4.
Инвентарный номер: нет.
   
   T 82


   
    Transesterification of dialkyl carbonates with fluorine-containing alcohols / A. M. Semenova, M. G. Pervova, M. A. Ezhikova [et al.] // Russian chemical bulletin. - 2021. - Vol. 70, № 5. - P933-936
ББК Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Reactions of transesterification of dimethyl, diethyl and dibutyl carbonates with 2,2,3,3-tetrafluoroethyl-, 2,2,3,3,4,4,5,5-octafluorobutyl- and 2,2,3,3,4,4,5,5,6,6,7,7-dodecafluorohexyl-carbinols were investigated in the presence of various catalysts. It was found that the conversion of starting dialkyl carbonate increases upon increasing the length of fluorine-containing radical in the presence of sodium alkoxide. It was shown that the maximum conversion of dimethyl carbonate (90%) was achieved in its reaction with 2,2,3,3,4,4,5,5-octafluoropentan-1-ol upon using catalysts such as K2CO3, NaOH, and sodium alkoxide. To achieve similar values of the conversion, Ti(OEt)4 and Ti(OiPr)4 should be used in the cases of diethyl and dibutyl carbonates, respectively.

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5.
Инвентарный номер: нет.
   


   
    Alternative approaches to the synthesis of polyfluoroalkyl-containing 1-methyl-4-nitrosopyrazoles / N. A. Agafonova, Y. V. Burgart, N. A. Gerasimova [et al.] // Russian chemical bulletin. - 2021. - Vol. 70, № 6. - P1135–1140
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
4,4,4-TRIFL UORO-3,3-DIHYDROXY-2-(HYDROXYIMINO)BUTAN-1-ONES -- POLYFL UOROALKYL2-HYDROXYIMINO-1,3-DIKETONES -- 1-METHYL-4-NITROSOPYRAZOLES -- MYCOSTATIC ACTIVITY
Аннотация: We studied different approaches to the synthesis of polyfluoroalkyl-containing 1-methyl-4-nitrosopyrazoles, which are based on the cyclization of 4,4,4-trifluoro-3,3-dihydroxy-2-hydroxyimino-1-R-butan-1-ones or 2-hydroxyimino-1,3-diketones with methylhydrazine and on a one-pot sequential treatment of 1,3-diketones with sodium nitrite and methylhydrazine. It was found that the regioselectivity of the formation of 1-methyl-4-nitrosopyrazoles is affected by the steric factors of 1,3-dicarbonyl reagents. The study of the mycostatic effect of 4-nitrosopyrazoles showed that the introduction of a bulky polyfluoroalkyl or tert-butyl substituent leads to a decrease in their activity.

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6.
Инвентарный номер: нет.
   
   T 70


    Tokareva, M. A.
    Reaction of sodium 4-acetyl-1-phenyl-1h-1,2,3-triazol-5-olate with 1,2,3-thiadiazole-4-carboxylic acid hydrazide / M. A. Tokareva, K. L. Obydennov, P. A. Slepukhin, O. A. Vysokova, T. V. Gluchareva // Современные синтетические методологии для создания лекарственных препаратов и функциональных материалов (MOSM2018): вторая международная научно-практическая конференция : материалы и доклады. - Екатеринбург, 2019. - С. 134-135
ББК Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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7.
Инвентарный номер: нет.
   
   G 33


    Gein, V. L.
    Diethyl oxalacetate sodium salt as a reagent to obtain functionalized spiro[indoline-3,4’-pyrano[2,3-c]pyrazoles] / V. L. Gein, T. M. Zamaraeva, P. A. Slepukhin // Tetrahedron Letters. - 2017. - Vol. 58. - С. 134-136. - Bibliogr. : p. 136 (27 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
3,4’-PYRANO[2,3-C]PYRAZOLES -- INDOLINE -- SODIUM SALT

\\\\expert2\\NBO\\Tetrahedron Letters\\2017, v. 58, p. 134-136.pdf
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8.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis of podands modified with thiosemicarbazide and fluoroalkyl(hydroxy)pyrazoline fragments / V. I. Filyakova, P. A. Slepukhin, N. S. Boltacheva, E. B. Letova, V. N. Charushin // Russian Journal of General Chemistry. - 2017. - Vol. 87, № 5. - P957-962
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PODANDES -- X-RAY DIFFRACTION ANALYSIS -- ACETIC ACID -- ORGANIC ACIDS
Аннотация: 1,8-Bis(diisothiosemicarbazido)-3,6-dioxaoctane have been synthesized by subsequent treatment of 2,2 -(ethylenedioxy)bisethylamine with carbon disulfide, sodium chloroacetate, and hydrazine hydrate. 1,8-Bis- (diisothiosemicarbazido)-3,6-dioxaoctane has reacted with lithium 1,1-difluoropenta-2,4-dionate in glacial acetic acid to yield 1,8-bis[5R*,5 R*(5-hydroxy-5-difluoromethyl-4,5-dihydro-3-methyl-1H-pyrazol-1-yl)-1-carbothioamido]-3,6-dioxaoctane. The molecular and crystal structure of the product has been determined by X-ray diffraction analysis.

\\\\Expert2\\NBO\\Russian Journal of General Chemistry\\2017 V 87 P957.pdf
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9.
Инвентарный номер: нет.
   
   N 91


   
    Nucleophilic dimerization of indoline under oxidative conditions [Electronic resource] / I. S. Kovalev, D. S. Kopchuk, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin // Mendeleev Communications. - 2014. - Vol.24, №1. - С. 40-41. - Bibliogr. : p. 41 (10 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
INDOLINE -- HYDROGEN PEROXIDE -- METHANOL
Аннотация: Oxidation of indoline with 30% hydrogen peroxide in methanol in the presence of sodium tungstate affords the dimeric 3-oxo-1’H,3H- 2,3’-biindole-1-oxide.

\\\\expert2\\nbo\\Mendeleev Communications\\2014, v.24 (1), p. 40.pdf
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10.
Инвентарный номер: нет.
   
   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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11.
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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12.
Инвентарный номер: нет.
   
   P 41


   
    Pentacyanoferrate(II) complexes with N-containing derivatives of chitosan and polyallylamine: Synthesis and cesium uptake properties [Electronic resource] / S. YU. Bratskaya, V. V. Zheleznov, Y. O. Privar, A. Mechaev, A. V. Pestov // Colloids and Surfaces A: Physicochemical and Engineering Aspects. - 2014. - Vol. 460. - С. 145-150
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
SODIUM AMINOPRUSSIDE -- POLYMER LIGANDS (CHITOSAN) -- POLYALLYLAMINE
Аннотация: Here we report on synthesis of new organic–inorganic materials based on products of interaction between sodium aminoprusside and polymer ligands (chitosan (CS), N-2-(2-pyridyl)ethylchitosan (2-PC), N-2-(4-pyridyl)ethylchitosan (4-PC), N-(4-methyl-5-imidazolyl)methylchitosan (IC), N-(2-cyanoethyl)chitosan (CC), polyallylamine (PA), N-(2-pyridyl)methyl-polyallylamine (PMPA), N-2-(2-pyridyl)ethyl-polyallylamine (PEPA), N-(4-methyl-5-imidazolyl)methyl-polyallylamine (IPA) and poly(2-vinylpyridine) (PVP)). The composition of the obtained materials was characterized using the element analysis and X-ray diffraction; the Fourier transform infrared (FT-IR) spectroscopy and thermogravimetric analysis data were used to propose the structure of the formed complexes. It was established that ion and ligand exchange were the main reactions, through which sodium aminoprusside interacts with water-soluble polymer salts. Reactivity in complex formation reaction of unmodified polymers changes in a row: PA > CS > PVP. Modification of chitosan with 2-(4-pyridyl)ethyl and 2-cyanoethyl moieties enhances reactivity of chitosan to the level of PA, while introduction of 2-(2-pyridyl) and (4-methyl-5-imidazolyl)methyl moieties, on the contrary, decreases reactivity of chitosan to that of PVP. At the same time, functionalization of PA with 2-pyridylalkyl groups decreases its reactivity in reaction with aminoprusside ion. Thus, reactivity of all studied polymeric matrices changes in the row: PA ≈ 4-PC ≈ CC > CS > 2-PC ≈ IPA ≈ IC > PMPA > PVP > PEPA. The distribution coefficients with respect to cesium ions have been determined for the synthesized complexes in cobalt(II) form. It has been shown that the complex of chitosan with pentacyanoferrate(II) has higher distribution coefficient with respect to Cs+ ions, as compared to its N-derivatives and synthetic polymers. Organic–inorganic materials obtained in the matrix of synthetic polymers have shown higher tendency to peptization and, therefore, lower sorption capacities and distribution coefficients

\\\\expert2\\nbo\\Colloids and Surfaces A\\2014, v.460, p.145-150.pdf
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13.
Инвентарный номер: нет.
   
   N 91


   
    Nucleophilic dimerization of indoline under oxidative conditions [Electronic resource] / I. S. Kovalev, D. S. Kopchuk, G. V. Zyryanov, V. L. Rusinov, O. N. Chupakhin // Mendeleev Communications. - 2014. - Vol. 24, № 1. - С. 40-41
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
INDOLINE -- HYDROGEN PEROXIDE -- SODIUM TUNGSTATE AFFORDS
Аннотация: Oxidation of indoline with 30% hydrogen peroxide in methanol in the presence of sodium tungstate affords the dimeric 3-oxo-1’H,3H- 2,3’-biindole-1-oxide

\\\\expert2\\nbo\\Mendeleev Communications\\2014, v.24, p. 40-41.pdf
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14.
Инвентарный номер: нет.
   
   K 96


    Kuznetsov, V. A.
    Synthesis of epsilon-caprolactone with stable hydrogen peroxide adducts / V. A. Kuznetsov, M. G. Pervova, Yu. G. Yatluk // Russian Journal of Applied Chemistry. - 2013. - Vol.86, №2. - С. 176-181. - Библиогр.: с. 181 (16 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CYCLOHEXANONE -- E-CAPROLACTONE -- HEXAFLUOROISOPROPANOL
Аннотация: Oxidation of cyclohexanone to ɛ-caprolactone with stable industrially manufactured hydrogen peroxide derivatives: adduct with urea (urea hydrogen peroxide), sodium perborate, sodium percarbonate (Persol), magnesium monoperphthalate (Dismozon) was studied. Oxidation with urea hydrogen peroxide is the most efficient in hexafluoroisopropanol in the case of preliminary removal of urea in the form of an oxalate. Oxidation with sodium perborate and percarbonate provides high yields in trifluoroacetic acid. The lowest cost process consists in interaction with sodium monoperphthalate (Persol and phthalic anhydride) in an aqueous medium

\\\\expert2\\NBO\\Russian Journal of Applied Chemistry\\2013, v. 86, N 2, p.176.pdf
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15.
Инвентарный номер: нет.
   
   S 98


   
    Synthesis in a gel and sorption properties of N-2-sulfoethyl chitosan / A. V. Pestov, Yu. S. Petrova, A. V. Bukharova, L. K. Neudachina, O. V. Koryakova, E. G. Matochkina, M. I. Kodess, Yu. G. Yatluk // Russian Journal of Applied Chemistry. - 2013. - Vol.86, №2. - С. 269-272. - Библиогр.: с. 272 (24 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CHELATES -- AMINO-CONTAINING POLYMER -- N-2-SULFOETHYL CHITOSAN
Аннотация: A new procedure was developed for preparation of chelate amino-containing polymer N-2-sulfoethyl chitosan by synthesis in a gel through the reaction between chitosan and sodium 2-bromoethanesulfonate, yielding a polymer with the degree of substitution of up to 0.5. The structure of the resulting polymers was confirmed by 1H NMR spectroscopy. The sorption characteristics with respect to transition and alkaline-earth metal ions were determined for the cross-linked polymers

\\\\expert2\\NBO\\Russian Journal of Applied Chemistry\\2013, v. 86, N 2, p.269.pdf
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16.
Инвентарный номер: нет.
   
   T 44


   
    Thermodynamic modeling of the reaction of polychlorinated biphenyls with sodium methoxide [Electronic resource] / T. V. Kulikova, A. V. Maiorova, K. Yu. Shunyaev, T. I. Gorbunova, V. I. Saloutin, O. N. Chupakhin // Russian Journal of General Chemistry. - 2013. - Vol.83, №5. - С. 893-900. - Библиогр.: с. 900 (17 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
THERMODYNAMIC MODELING -- SODIUM METHOXIDE -- POLYCHLORINATED BIPHENYLS
Аннотация: Thermochemical parameters, like standard enthalpy of formation (ΔH 298 0), enthalpy increment from 0 to 298 K (H 298 0 - H 0 0), standard heat capacity (C p298 0) and its temperature dependence [Cp(T)], and entropy (S 298 0), were calculated for the gaseous methoxy derivatives formed from polychlotinated biphenyl (PCB) congeners. Thermodynamic modeling and the HSC software were used to evaluate the reactivity of PCB congeners toward sodium methoxide in DMSO, and the calculation results were compared with experimental data

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17.
Инвентарный номер: нет.
   
   P 41


   
    Pentacyanoferrate(II) complexes with chitosan [Electronic resource] / S. YU. Bratskaya, Y. O. Privar, O. V. Korjakova, A. Mechaev, A. V. Pestov // Polymer Engineering and Science . - 2013. - Article in Press
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
SODIUM AMINOPRUSSIDE -- POLYMER LIGAND (CHITOSAN) -- X-RAY DIFFRACTION
Аннотация: New organic-inorganic materials based on products of interaction between sodium aminoprusside and polymer ligand (chitosan) have been synthesized. The composition of the obtained materials was characterized using the element analysis and X-ray diffraction; the Fourier transform infrared (FT-IR) spectroscopy and Thermogravimetric analysis data were used to propose the structure of the formed complexes. It was established that ion and ligand exchange were the main reactions at interaction of sodium aminoprusside with water-soluble chitosan salts. The comparative estimation of the sorption capacity with respect to cesium ions was performed for the synthesized complexes. It has been shown that the complex of chitosan with pentacyanoferrate(II) in the form of cobalt(II) salt has higher distribution coefficient with respect to Cs+ ions, as compared to cobalt aminoprusside. The maximum sorption capacity value for Cs+ was evaluated from the sorption isotherm and found to be equal to 0.3 mmol/g

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18.
Инвентарный номер: нет.
   
   N 89


   
    Novel bis[(1,2,3-triazolyl)methyl]carborane derivatives via regiospecific copper-catalyzed 1,3-dipolar cycloaddition / V. A. Ol'shevskaya, E. V. Verbitskiy, G. L. Rusinov, V. N. Charushin, Evamarie Hey-Hawkins // Polyhedron. - 2012. - Vol.42, №1. - С. 302-306
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CARBORANES -- CARBABORANES -- TRIFLATES
Аннотация: 1,2-Bis(azidomethyl)-о-carborane and 1,7-bis(azidomethyl)-m-carborane, prepared from the corresponding carboranylmethyl triflates and sodium azide, were conveniently functionalized by azide–alkyne cycloaddition affording novel bis[(1,2,3-triazolyl)methyl]carborane derivatives. Regiospecificity of this process was achieved by employing copper(II) acetate hydrate. Reaction of bis[(1,2,3-triazolyl)methyl]carborane derivatives with MeI yielded 3-methyl-1,2,3-triazolium carborane salts

\\\\Expert2\\nbo\\Polyhedron\\2012. v.42. p.302.pdf
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19.
Инвентарный номер: нет.
   
   R 30


   
    Reactivity features of polychlorobiphenyl congeners in the nucleophilic substitution reactions / T. I. Gorbunova, M. G. Pervova, V. I. Saloutin, O. N. Chupakhin // Russian Journal of General Chemistry. - 2012. - Vol. 82, № 1. - С. 138-143. - Bibliogr. : p. 143 (18 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
POLYCHLORINATED-BIPHENYLS -- IRON -- DECHLORINATION -- NANOPARTICLES -- PCBS
Аннотация: Groups of congeners and individual congeners of polychlorobiphenyls contributing to the composition of the technical mixture "Sovol" (PCB 60, PCB 64, PCB 70, PCB 74, PCB 97, PCB 101, PCB 105, PCB 110, PCB 118, PCB 138, PCB 149, PCB 156, and PCB 163) were synthesized by the reaction of aryl-aryl coupling. The interaction of the congeners with sodium methoxide was performed and their complete conversion was proved. By means of gas chromatography-mass spectrometry the PCBs methoxy derivatives were identified. The data on the reactivity of the individual polychlorobiphenyl congeners were precised

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20.
Инвентарный номер: нет.
   
   E 97


   
    Extraction of vanadium (IV) with DI-2-ethylhexylphosphoric acid [Электронный ресурс] / L. D. Kurbatova, P. A. Slepukhin, D. I. Kurbatov, E. V. Zabolotskaya // Phosphorus, Sulfur, and Silicon and the Related Elements. - 2012. - Vol.187, №9. - P1032-1037
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ELECTRONIC SPECTRA -- ESR SPECTROSCOPY -- VANADIUM
Аннотация: It was established with the use of electron and ESR spectroscopic methods that in the presence of sodium sulfate, the extraction of vanadium (IV) with di-2-ethylhexylphosphoric acid takes place by a cation-exchange mechanism giving rise to two complex compounds of vanadium (IV) oxocation with sulfuric and di-2-ethylhexylphosphoric acid anions. The vanadium (IV) oxocation sulfate complex extracted in the solid state was examined with X-ray structural analysis. It was shown that the vanadium (IV) oxocation sulfate complex trihydrate crystallizes in the centrosymmetrical space group to form dimers with bridging sulfate groups

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