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1.
Инвентарный номер: нет.
   


   
    2,3-Epoxyperfluoro-2-methylpentane in reactions with urea and thiourea [Electronic resource] / T. I. Filyakova, V. I. Saloutin, A. Ya. Zapevalov, P. A. Slepukhin, M. I. Kodess, V. I. Saloutin // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2011. - Vol. 47, № 5. - P650-658 : рис., табл. - Bibliogr. : p. 658 (24 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: 2,3-Epoxyperfluoro-2-methylpentane reacts with thiourea in protic (methanol, 2-propanol) and aprotic (dioxane) solvents, and also with urea in acetonitrile affording unexpected products: 1-(2,2,3,3,3-pentafluoropropionyl)-2-(2,2,2-trifluoro-1-trifluoro-methylethyl)isothiourea, and 1-(2,2,3,3,3-pentafluoropropionyl)-3-(2,2,2-trifluoro-1-trifluoro-methylethyl)urea respectively that result from the rearrangement of the intermediately formed ketone in the process of the intramolecular “haloform” cleavage. At the same time in dioxane the 2,3-epoxyperfluoro-2-methylpentane reacts with urea with the formation of a heterocyclic compound, 2-amino-4-pentafluoroethyl-5,5-bis(trifluoromethyl)-4,5-dihydrooxazol-4-ol. From 1-(2,2,3,3,3-pentafluoropropionyl)-2-(2,2,2-trifluoro-1-trifluoromethylethyl)isothiourea and Cu(OAc)2 a stable fluorine-containing chelate complex was obtained

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2011, 47 (5), 650-658.pdf
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2.
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    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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3.
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   A 10


   
    A new application of derivatives of polychlorobiphenyls and polyethylene glycols / T. I. Gorbunova, M. G. Pervova, E. B. Trushina, S. V. Pavlysko, A. Ya. Zapevalov, V. I. Saloutin // Russian Journal of Applied Chemistry. - 2012. - Vol.85, №10. - С. 1622-1626
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
POLYCHLOROBIPHENYLS -- POLYETHYLENE GLYCOLS -- SYNTHESIS
Аннотация: The reaction of congeners of Sovol technical mixture of polychlorobiphenyls with polyethylene glycols was studied. Mixtures of hydroxy and mono(polyethylene glycol)oxy derivatives were obtained. The mixtures synthesized, which are of low hazard, were used as additives to industrial oil to improve its tribological char

\\\\Expert2\\nbo\\Russian Journal of Applied Chemistry\\2012, v. 85, N 10, p.1662.pdf
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4.
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   A 10


   
    A route to fluorocontaining 1,3-thiazolines via internal polyfluorooxiranes [Electronic resource] / L. V. Saloutina, A. Ya. Zapevalov, M. I. Kodess, V. I. Saloutin, O. N. Chupakhin // Mendeleev Communications. - 1999. - N 6. - P231-232 . - ISSN 0959-9436
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The reaction of internal fluoroolefin oxides with thiourea results in 2-amino-5-fluoro-4-hydroxy-4,5-di(polyfluoroalkyl)-1,3-thiazolines, providing a route to an unknown type of fluorine-containing thiazolines with two fluoroalkyl substituents

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5.
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   A 10


   
    A route to fluorocontaining N,S-heterocycles via octafluoro-2,3-epoxybutane [Text] / L. V. Saloutina, A. Ya. Zapevalov, V. I. Saloutin, P. A. Slepukhin, M. I. Kodess, V. E. Kirichenko, M. G. Pervova, O. N. Chupakhin // Journal of Fluorine Chemistry. - 2007. - Vol. 128, № 7. - P769-778
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The reaction of octafluoro-2,3-epoxybutane 1 with 2-aminothiophenol gave three kinds of novel fluorocontaining N,S-heterocyclic compounds depending on the solvent nature: 2,3-bis(trifluoromethyl)-3,4-dihydro-2H-1,4-benzothiazin-2-ol 2, 2-trifluoromethyl-2-[1-(2-aminophenylthio)-2,2,2-trifluoroethyl]-1,3-benzothiazolidine 6 and 5a,11a-bis(trifluoromethyl)-5a,6,11a,12-tetrahydro-5,11-dithia-6,12-diazanaphthacene 5. Use of the toluene, dioxane, tetrahydrofuran, acetonitrile and dimethoxyethane gave the unexpected dihydrobenzothiazine 2 (RS,SR RR,SS) in good to moderate yields. In dimethylsulfoxide and N,N-dimethylacetamide, unusual cyclization occurred resulting in benzothiazolidine 6 (RS,SR/RR,SS 1:1) in moderate yields. Formation of minor 1,1,1,3,4,4,4-heptafluoro-3-(2-aminophenylthio)-2,2-dihydroxybutane 4 which was converted into bis(benzothiazine) 5 was observed in all solvents tested with the exception of toluene and dioxane. The molecular structure of the RS,SR-diastereomer of dihydrobenzothiazine 2, bis(benzothiazine) 5 and the RS,SR-diastereomer of benzothiazolidine 6 has been established by X-ray crystallography.

\\\\Expert2\\nbo\\Journal of Fluorine Chemistry\\2007, v.128. p.769.pdf
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6.
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   A 10


   
    A study of the physico-chemical features of the [(perfluoroalkyl)methyl]oxirane amino derivatives based on the hexafluoropropylene oxide trimer / D. N. Bazhin, T. I. Gorbunova, A. Ya. Zapevalov, I. V. Beketov, V. I. Saloutin // Russian Journal of General Chemistry. - 2011. - Vol.81, №9. - С. 1829-1833
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
PHYSICO-CHEMICAL FEATURES -- HEXAFLUOROPROPYLENE -- OXIDE TRIMER
Аннотация: The 1,2-epoxy-4,6,6,7,9,9,10,10,11,11,11-undecafluoro-4,7-bis(trifluoromethyl)-5,8-dioxaundecane was synthesized for the first time on the basis of the hexafluoropropylene oxide trimer. We showed that it reacted with diethylamine, morpholine, or N-methylpiperazine to afford the product of regioselective cleavage of the oxirane ring. The processing of nano-sized copper powder with a solution of the obtained hydroxyamine solution in acetone allowed the formation of the hydrophobic metal coating

\\\\Expert2\\nbo\\Russian Journal of General Chemistry\\2012, V. 81, N 9, p. 1829–1833.pdf
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7.
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   A 20


   
    Addition of polyfluoroalkyl iodides to allyl glycidyl ether [Electronic resource] / D. N. Bazhin, T. I. Gorbunova, A. Ya. Zapevalov, V. I. Saloutin // Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2007. - Vol. 56, № 8. - P1534-1536. - Библиогр. : с. 1536 (24 назв.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Addition of polyfluoroalkyl iodides to the double bond of allyl glycidyl ether occurred under mild conditions (20-25 °C, MeCN/H2O, Na2S2O4, NaHCO3) with retention of the oxirane ring.

\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2007, 56 (8), 1534-1536.pdf
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8.
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   A 25


   
    Aggregative stability of the CdS nanoparticles-H2O colloidal dispersion system in the presence of surfactants / N. S. Kozhevnikova, T. I. Gorbunova, A. S. Vorokh, D. N. Bazhin, A. Ya. Zapevalov, V. I. Saloutin, A. A. Rempel, O. N. Chupakhin // Doklady Chemistry. - 2012. - Vol.443, №1. - С. 86-90
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CdS -- COLLOIDAL DISPERSION SYSTEM -- AGGREGATIVE STABILITY

\\\\Expert2\\nbo\\Doklady Chemistry\\2012, v. 443, N 1, p. 86-90.pdf
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9.
Инвентарный номер: нет.
   
   A 62


   
    Antifriction properties of fluorine-containing poly(ethylene glycol) esters / T. I. Gorbunova, D. N. Bazhin, A. Ya. Zapevalov, L. G. Korshunov, I. V. Beketov, V. I. Saloutin // Russian Journal of Applied Chemistry. - 2012. - Vol.85, №2. - С. 267-271
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ANTIFRICTION PROPERTIES -- FLUORINE-CONTAINING POLY(ETHYLENE GLYCOL) ESTERS -- EQUILIBRIUM MIXTURES
Аннотация: Equilibrium mixtures of fluorine-containing mono- and diesters based on poly(ethylene glycol) (M = 1000) were synthesized. The effect of these compounds on antifriction properties of industrial oil was studied

\\\\Expert2\\nbo\\Russian Journal of Applied Chemistry\\2012, v. 85, N 2, p.267.pdf
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10.
Инвентарный номер: нет.
   
   A 62


   
    Antifriction properties of new fluorine-containing derivatives of natural graphite / T. I. Gorbunova, A. Ya. Zapevalov, D. N. Bazhin, L. G. Korshunov, V. S. Gaviko, V. I. Saloutin // Russian Journal of Applied Chemistry. - 2012. - Vol.85, №1. - С. 102-107
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ANTIFRICTION PROPERTIES -- FLUORINE-CONTAINING DERIVATIVES -- GRAPHITE
Аннотация: Interaction of natural graphite with potassium salts of perfl uoro(ω-chloroperfl uoro)carboxylic acids in the presence of potassium persulfate was studied. The derivatives obtained were used as independent lubricants for a chromium-containing-steel friction pair

\\\\Expert2\\nbo\\Russian Journal of Applied Chemistry\\2012, v. 85, N 1, p.102.pdf
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