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Каталог библиотеки ИЭРиЖ УрО РАН
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1.

Вид документа : Статья из журнала
Шифр издания : 54
Автор(ы) : Ratner V. G., Lork E., Pashkevich K. I., Roeschenthaler G.-V.
Заглавие : (E)-1,1,1-trifluoro-4-phenyl-but-2-ene-4-one and trimethyl phosphite
Место публикации : Journal of Fluorine Chemistry. - 2000. - Vol. 102, № 1-2. - С. 73-77
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The interaction of (E)-1,1,1-trifluoro-4-phenyl-but-2-ene-4-one (1) with trimethyl phosphite affords in a [4 + 1] cycloaddition the 1,2?5-oxaphospholene 2 as a sole product which upon hydrolysis is transformed into the fluoroalkyl containing ?-ketophosphonate 4. When the reaction is carried out in the presence of small mounts of water, in addition to 2 as a main product, the phosphoric acid ester 6 of the enolic dimer of ketone 1 is also formed. The molecular structure of compound 6 (monoclinic P 2(1)/c with a = 2088.60(2), b = 1403.1(3), c = 1613.8(1) pm, ? = 90, ? = 100.97(1), ? = 90°, Z = 8) was determined, indicating two independent molecules with (RR) and (SS) configuration and disordered CF3 groups.????
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2.

Вид документа : Статья из журнала
Шифр издания : 54
Автор(ы) : Lipunova G. N., Nosova E. V., Mochul`skaya N. N., Andreiko A. A., Chasovskikh O. M., Charushin V. N.
Заглавие : 1,2,4-Triazino[5,6,1-i,j]quinolines: a new type of tricyclic analogs of fluoroquinolones [Electronic resource]
Место публикации : Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 2002. - Vol. 51, № 4. - С. 663-667
Систем. требования: http://www.springerlink.com/content/kwep81pgqyj1mtc3/fulltext.pdf
Примечания : 24.10.2011
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The interaction of C-aryl-substituted amidrazones and S-methylisothiosemicarbazide with 3-ethoxy-2-polyfluorobenzoylacrylates results in corresponding N-(quinolin-1-yl)amidines that undergo conversion into derivatives of 1,2,4-triazino[5,6,1-i,j]quinoline by heating in acetic anhydride
\\\\Expert2\\nbo\\Russian Chemical Bulletin\\2002, 51 (4), 663.pdf
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3.

Вид документа : Статья из журнала
Шифр издания : 54/A 10
Автор(ы) : Bazhin D. N., Kudyakova Yu.S., Roeschenthaler G.-V., Burgart Ya. V., Slepukhin P. A., Isenov M. L., Saloutin V. I., Charushin V. N.
Заглавие : A Convenient Approach to CF3-Containing N-Heterocycles Based on 2-Methoxy-2-methyl-5-(trifluoromethyl)furan-3(2H)-one [Электронный ресурс]
Место публикации : European Journal of Organic Chemistry. - 2015. - № 23. - С. 5236-5245
Систем. требования: http://apps.webofknowledge.com/
Примечания : Bibliogr. : p. 5245 (23 ref.). - 18.01.16
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): 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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4.

Вид документа : Статья из журнала
Шифр издания : 54/A 53
Автор(ы) : Khomutov O. G., Filyakova V. I., Kutchin A.V., Pashkevich K. I.
Заглавие : An efficient synthesis of alkylfluoroalkylketones
Место публикации : Journal of Fluorine Chemistry. - 1992. - Vol. 58, № 2-3. - С. 161
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Interaction of fluoroacyl chlorides with lithium tetraalkylaluminates II prepared by the hydroalumination of alkenes I results in fluorinated ketones III with yields of 65–70%.??RF = CF3, H(CF2)2, C4F9, C6F13 R1 = C3H7, C4H9, C6H13, C7H15??The reaction is simple and does not require an argon atmosphere, as is needed for most reactions of organoaluminum compounds????
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5.

Вид документа :
Шифр издания : 54/A 62
Автор(ы) : Gorbunova T. I., Zapevalov A. Ya., Bazhin D. N., Korshunov L. G., Gaviko V.S., Saloutin V. I.
Заглавие : Antifriction properties of new fluorine-containing derivatives of natural graphite
Место публикации : Russian Journal of Applied Chemistry. - 2012. - Vol.85, №1. - С. 102-107
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): 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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6.

Вид документа : Статья из журнала
Шифр издания : 54/A 62
Автор(ы) : Kogan G., Skorik Yu.A., Zitnanova I., Krizkova L., Durackova Z., Gomes C. A. R., Yatluk Yu. G., Krajcovic J.
Заглавие : Antioxidant and antimutagenic activity of N-(2-carboxyethyl)chitosan
Место публикации : Toxicology and Applied Pharmacology . - 2004. - Vol. 201, № 3. - С. 303-310: ил.
Примечания : Библиогр.: с. 309-310 (49 ref.)
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The antioxidant and antimutagenic activities of the novel carboxyethyl derivatives of chitosan with three different degrees of substitution have been assayed in vitro in the unicellular flagellate Euglena gracilis subjected to the action of genotoxic agents acridine orange and ofloxacin. It has been demonstrated that chitosan derivatives exhibit concentration-dependent protective antigenotoxic activity against both mutagens. It is suggested that different mechanisms may be involved in its protective action—antioxidant activity in case of ofloxacin-induced DNA damage, as well as possible interaction with the cell membrane that prevents acridine orange from reaching the genetic compartments and subsequent damaging DNA through intercalative binding. Direct adsorption of acridine orange on chitosan derivatives was ruled out as a possible mechanism of protection on the basis of spectrophotometric measurements. Dependence of the antimutagenic properties of the studied chitosan derivatives on the degree of substitution was reversed in experiments involving acridine orange and ofloxacin, which also indicated different mechanisms of protection involved in these two cases.????
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7.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Sravya G., Khasanov A. F., Krinochkin A. P., Kopchuk D. S., Slepukhin P. A., Rahman M., Zyryanov G. V., Rusinov V. L., Chupakhin O. N., Padmavathi V.
Заглавие : Aryne-mediated transformations of 3-(α- or γ-r-2-pyridyl)-1,2,4-triazines: id diels-alder reaction vs domino transformation
Место публикации : Polycyclic aromatic compounds. - 2021. - Vol. 42, № 8. - С. 4937-4947
Ключевые слова (''Своб.индексиров.''): 3-(α- or γ-r-pyridin-2-yl)-1,2,4-triaizines--influence of substituent--arynes
Аннотация: Interaction of 3-(α- or γ-R-pyridin-2-yl)-1,2,4-triazines (R = Me, CO2Me) with arynes affords either the domino-transformation products, pyrido[1,2-a]indoles, or Diels-Alder reaction ones, isoquinolines. The influence of the nature and/or position of the substituent on the reaction pathway is discussed.
doi.org/10.1080/10406638.2021.1962371
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8.

Вид документа : Статья из журнала
Шифр издания : 54/B 12
Автор(ы) : Egorova D. O., Gorbunova T. I., Pervova M. G., Demakov V. A.
Заглавие : Bacterial degradation of a mixture obtained through the chemical modification of polychlorinated biphenyls by polyethylene glycols [Электронный ресурс]
Место публикации : Applied Biochemistry and Microbiology. - 2014. - Vol. 50, № 7. - С. 722-729
Систем. требования: http://download-v2.springer.com/static/pdf/131/art%253A10.1134%252FS0003683814070023.pdf?token2=exp=1428652880~acl=%2Fstatic%2Fpdf%2F131%2Fart%25253A10.1134%25252FS0003683814070023.pdf*~hmac=3182eca3e5ccea6ab1f49dd6b89a557b80a88fa01d0e203f57bcd3fed34fc4d2
Примечания : Bibliogr. : p. 729 (29 ref.). - 10.04.15
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): bacterial degradation--chemical modification--polyethylene glycols
Аннотация: Polychlorinated biphenyls (PCBs), also known by the trade name Sovol, are toxic industrial wastes. They have been subjected to chemical treatment by polyethylene glycols (PEGs) and potassium hydroxide. As a result of the interaction of the Sovol with various molecular mass PEGs (MMPEG-4 ∼ 200, MMPEG-22 ∼ 1000), water-soluble mixtures M1 and M2 containing mono(polyethylene glycol)oxy-derivatives (PCB-PEG-4 and PCB-PEG-22), polychlorobiphenylols, and unreacted PCB congeners (PCB 44, PCB 47, PCB 49, PCB 52, and PCB 66) were obtained. It was shown for the first time that mixtures M1 and M2 are susceptible to bacterial degradation without their fractionation. According to the gas-liquid chromatography with flame-ionization and mass-spectrometric detection, the Rhodococcus wratislaviensis KT112-7 strain degraded all of the chemical compounds occurring in the mixtures. In a 5-day experiment, it was found that the KT112-7 strain decomposes mono(polyethylene glycol)oxy-derivatives completely (by 100%) and polychlorobiphenylols and PCB congeners by 90–95% in the M1 and M2 mixtures. The culture medium did not contain transformation products, whereas free chlorine ions were accumulated (72–94% of the maximum possible amount). Thus, the use of the chemical modification and consecutive bacterial degradation provided an effective destruction of technical PCB mixtures with a high content of highly chlorinated congeners
\\\\expert2\\nbo\\Applied Biochemistry and Microbiology\\2014, v.50, N 7, p.722-729.pdf
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9.

Вид документа : Статья из журнала
Шифр издания : 54/C 45
Автор(ы) : Ivshina N. N., Bartashevich E. V., Potemkin V. A., Grishina M. A., Ishmetova R. I., Rusinov G. L., Latosh N. I., Slepukhin P. A., Charushin V. N.
Заглавие : Changes in the vibrational characteristics of substituted 1,2,4,5-tetrazines after complexation with 1,2,3-benzotriazole: A theoretical study [Electronic resource]
Место публикации : Journal of Structural Chemistry. - 2009. - Vol. 50, № 6. - С. 1053-1058
Систем. требования: http://www.springerlink.com/content/ag50570h40011132/fulltext.pdf
Примечания : 2.11.2011 г.
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The complexation of 3,6-substituted 1,2,4,5-tetrazines with benzotriazole was studied theoretically based on the vibrational spectra. For model complexes, the energy was minimized by the geometrical parameters, and the spectral characteristics were calculated by the PM3 method. The shift of the bond vibration frequencies of the atoms involved in complexation after the formation of different various intermolecular contacts was determined. This made it possible to determine the type of intermolecular interaction and suggest the structures of the complexes
\\\\Expert2\\nbo\\Journal of Structural Chemistry\\2009, V. 50, N 6, p.1053.pdf
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10.

Вид документа : Статья из журнала
Шифр издания : 54/C 51
Автор(ы) : Bushkova O. V., Andreev O. L., Batalov N. N., Shkerin S. N., Kuznetsov M. V., Koryakova O. V., Song E. N., Chung H. J.
Заглавие : Chemical interactions in the cathode half-cell of lithium-ion batteries: Part I. Thermodynamic simulation
Место публикации : Journal of Power Sources. - 2006. - Vol. 157, № 1. - С. 477-482
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The method of thermodynamic simulation was used to study chemical interactions in the cathode half-cell of lithium-ion battery, which contained LiCoO2 as cathode active material and a LiPF6 solution as the electrolyte. It was shown that in the temperature range 298–400 K in thermodynamic equilibrium state a layer of solid products of chemical reaction formed on the cathode/electrolyte interface. The layer predominantly consisted of LiF and LiPO3 in the molar ratio about 2:1 (corresponding to the volume ratio 2:3). In equilibrium state also some soluble interaction products formed, namely: CoF2 (considerable quantity), POF3 and PF5. The concentration of the later two substances was small, but it increased with increase of the temperature. Furthermore, in equilibrium state oxygen gas formed as a product of chemical interactions in cathode half-cell.????Thermodynamic characteristics of Co2O3 and LiCoO2 compounds were determined using a set of calculation methods??
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11.

Вид документа : Статья из журнала
Шифр издания : 54/C 52
Автор(ы) : Chizhov D. L., Roeschenthaler G.-V.
Заглавие : Reaction of trifluoromethylated beta-alkoxyenones with tris(trimethylsilyl) phosphite: A temperature influence on regioselectivity
Место публикации : Journal of Fluorine Chemistry. - 2006. - Vol. 127, № 2. - С. 235-239
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The interaction of tris(trimethylsilyl) phosphite (TMSO)3P and E-trifluoromethyl-alkoxyenones CF3C(O)CHCHOEt and CF3C(O)CHC(OMe)Me yielded mixtures of E-1,2- and Z-1,4-adducts, CF3C(OTMS)[P(O)(OTMS)2]CCH(OAlk)R 2 and CF3(OTMS)CCHCR(OAlk)[P(O)(OTMS)2] 3 where R and Alk = H and Me, or both Me. Conversion of these 1,2-adducts to 1,4-isomers was effected by increased temperature or by exposure to more tris(trimethylsilyl) phosphite. Acid hydrolysis of 2b (R and Alk = Me) gave ketophosphonic acid CF3C(OH)[P(O)(OH)2]CH2COMe in 88% yield, whereas hydrolysis of 2a (R = H and Alk = Et) with KOH in methanol gave CF3C(OH)[P(O)(OK)2]CHCHOEt in 37% yield. Acid hydrolysis of 3a (R = H and Alk = Et) and 3b (R and Alk = Me) gave phosphonic acid CF3C(OH)2CHCHP(O)(OH)2 in 82% yield and trifluoromethylated 1,2,5,4-oxaphosphol-3-en
\\\\Expert2\\nbo\\Journal of Fluorine Chemistry\\2006, v.127, p.235.pdf
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12.

Вид документа : Статья из журнала
Шифр издания : 54/C 91
Автор(ы) : Pestov A. V., Slepukhin P. A., Virovets A. V., Podberezskaya N. V. , Yatluk Yu. G.
Заглавие : Crystal structure of N-(2-hydroxyethyl)-beta-alanine and racemic mixture of the coordination stereoisomers of N-(2-hydroxyethyl)-beta-alaninatonickel(II) [Electronic resource]
Место публикации : Journal of Structural Chemistry. - 2008. - Vol. 49, № 1. - С. 102-108
Систем. требования: http://www.springerlink.com/content/m543016419774u52/fulltext.pdf
Примечания : 2.11.2011 г.
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: N-(2-Hydroxyethyl)-?-alaninatonickel(II) was synthesized by the interaction of basic nickel carbonate with N-(2-hydroxyethyl)-?-alanine. The structures of the chelating agent and its nickel complex were studied by single crystal X-ray diffraction. In the synthesized compound, the nickel ion lies at the center of an octahedron of the N and 2O donor atoms of two tridentate ligands, each ligand having a meridional conformation. The ligands around the central atom are arranged in perpendicular planes. This coordination of two ligands yields two stereoisomers, whose cocrystallization affords a racemate
\\\\Expert2\\nbo\\Journal of Structural Chemistry\\2008, V. 49, N 1, p.102.pdf
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13.

Вид документа : Статья из журнала
Шифр издания : 54/D 29
Автор(ы) : Khristoforov R. R., Suchareva B. S., Dixon H. B. F., Sparkers M. J., Krasnov V. P., Bukrina I. M., Grishakov A. N.
Заглавие : Decarboxylation and side transamination when glutamate decarboxylase from Escherichia coli acts on substrate analogues modified at C-3 and C-4
Место публикации : Biochemistry. - 1996. - Vol. 61, N 3. - С. 343-348
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The interaction of glutamate decarboxylase with aspartate and glutamate analogues modified at C-3 and C-4 was studied. 3-Arsonoalanine, 3-phosphonoalanine, 2-amino-4-arsonobutyric acid, 2-amino-4-phospho-nobutyric acid, a mixture of diastereoisomers of 4-(methylthio)glutamic acid, and erythro-4-(methylthio)glutamic acid were shown to be poor substrates for the enzyme.
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14.

Вид документа : Статья из сборника (однотомник)
Шифр издания : 54/D 45
Автор(ы) : Deryabina T. G., Utepova I. A., Chupakhin O. N.
Заглавие : Interaction 3-(2-hydroxy-2-aryl/hetaryl-vinil)-1H-quinoxalin-2-ones with hydrazine hydrate : доклад, тезисы доклада
Место публикации : Fifth International Conference on Organic Chemistry for young Scientists (InterYCOS-2009) "Universities Contribution in the Organic Chemistry Progress", devoted to the 175 th anniversary of D.I.Mendeleevs birthday and 80th anniversary of the Chemistry department of St. Petersburg State University foundation, Saint-Petersburg, 22-25 june 2009 : abstr. - СПб., 2009. - С. 117 (P-1-19)
Примечания : Bibliogr. : p. 117 (1 ref.)
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
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15.

Вид документа : Статья из журнала
Шифр издания : 54/E 97
Автор(ы) : Golberg A., Aleksandrov G. G., Bogomyakov A. S., Kiskin M. A., Kolotilov S. V., Utepova I. A., Sidorov A. A., Chupakhin O. N., Eremenko I. L.
Заглавие : Exchange Interactions in Cobalt(II) and Nickel(II) Complexes Containing M-4(mu(3)-OH)(2) Metal Cores with Distorted Rhombic Topology [Электронный ресурс]
Место публикации : Theoretical and Experimental Chemistry . - 2015. - Vol. 50, № 6. - С. 364-370
Систем. требования: http://apps.webofknowledge.com/
Примечания : Bibliogr. : p. 369-370 (21 ref.). - 20.01.2016
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): pentanuclear complex--cobalt(ii)--tetranuclear complex
Аннотация: Antiferromagnetic interactions between the Co2+ or Ni2+ ions were found in complexes [(mu(3) aEuroaEuro parts per thousand L)(2)Co (5) (II) (mu aEuroaEuro parts per thousand OH)(2)(Piv)(7)(NO3)] and [(mu(3) aEuroaEuro parts per thousand L)(2)(HPiv)Ni (4) (II) (mu(3) aEuroaEuro parts per thousand OH)(2)(Piv)(4)(NO3)(2)] (Piv(-) = pivalic acid anion, L = 1,1'-dipyridazinylferrocene) possessing a metal core with distorted rhombic topology M-4(mu(3)-OH)(2). In contrast to the case of symmetrical analogs, the signs of all the exchange interaction parameters J were determined unambiguously.
\\\\expert2\\nbo\\Theoretical and Experimental Chemistry\\2015, V.50, № 6, p.364-370.pdf
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16.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Edilova Y. O., Burgart Y. V., Saloutin V. I., Bazhin D. N., Kudyakova Y. S., Kiskin M. A.
Заглавие : Expanding 1,2,4-triketone toolbox for use as fluorinated building blocks in the synthesis of pyrazoles, pyridazinones and β-diketohydrazones
Место публикации : Journal of fluorine chemistry. - 2022. - Vol. 253. - Ст.109932
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Fluorinated lithium β-diketonates bearing a methyl acetal group behave in the condensation reactions with hydrazines as trielectrophilic building blocks for the preparation of pyrazoles, pyridazinones and β-diketohydrazones. For the first time, solvent-induced regioisomeric and heterocyclic ring size-controlled formation was observed for 1,2,4-triketone analogues. Fluoroalkylated acetyl NH-pyrazoles or substituted 5-RF-pyrazoles were obtained from the acid-catalyzed cyclocondensation of lithium β-diketonates with (aryl)hydrazines in ethanol. In methanol solvent acetyl-containing 3-CF3-pyrazoles were isolated because of inverse nucleophilic attack of arylhydrazines. The use of aprotic acetonitrile in the condensation resulted in regioselective trifluorinated pyridazinones and fluorinated β-diketohydrazones formation via initial acetal fragment interaction with N,N-dinucleophile.
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17.

Вид документа : Статья из журнала
Шифр издания : 54/E 97
Автор(ы) : Khasanov A. F., Kopchuk D. S., Kovalev I. S., Taniya O. S., Giri K., Slepukhin P. A., Santra S., Rahman M., Majee A., Charushin V. N., Chupakhin O. N.
Заглавие : Extended cavity pyrene-based iptycenes for the turn-off fluorescence detection of RDX and common nitroaromatic explosives
Место публикации : New Journal of Chemistry. - 2017. - Vol. 41, № 6. - С. 2309-2320
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Ключевые слова (''Своб.индексиров.''): pyrene (chemical)--fluorescence--rdx (cyclonite)
Аннотация: Extended cavity pyrene-based iptycenes have been synthesized by using the Diels–Alder reaction between in situ generated dehydropyrenes and anthracene. The photophysical properties and the interaction of these iptycenes with nitro-explosive components were studied both in solution and in the solid state by using fluorescence spectroscopy and X-ray crystallography, respectively. Due to the presence of both the large iptycene cavity and the central pyrene core, an unprecedently high fluorescence-quenching response towards non-aromatic and non-planar 1,3,5-trinitroperhydro-1,3,5-triazine (RDX) has been observed both in solution (with an apparent Stern–Volmer constant value aKSV up to 1.53 × 103 M−1) and in the vapor phase (50–75% fluorescence quenching of the PU films doped with chemosensors). In the case of nitroaromatic explosives, nitrobenzene (NB), 2,4-DNT, TNT, and 2,4,6-trinitrophenol (TNP or picric acid, PA), pyrene-based iptycenes also demonstrate a good fluorescence-quenching response both in solutions (with apparent Stern–Volmer constant values aKSV = 0.4–8.0 × 103 M−1) and in the vapor phase (up to 90% fluorescence quenching of the PU films doped with chemosensors). The “sphere of action” fluorescence quenching model was suggested.
\\\\Expert2\\NBO\\New Journal of Chemistry\\2017 v.41 p.2309-2320.pdf
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18.

Вид документа : Статья из журнала
Шифр издания : 54/F 70
Автор(ы) : Khudina O. G., Burgart Ya. V., Saloutin V. I., Chupakhin O. N.
Заглавие : Fluoroalkyl-containing 2-arylhydrazono-1,3-dicarbonyl compounds in the reactions with ethylenediamine and polyethylenepolyamines
Место публикации : Journal of Fluorine Chemistry. - 2004. - Vol. 125, № 3. - С. 401-407: ил.
Примечания : Библиогр.: с. 407 (15 ref.)
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Acyclic N,N?-(poly)ethylene-bis(2-arylazo-1,3-aminovinylketones) are the main products in the reactions of fluoroalkyl-containing 2-arylhydrazono-1,3-diketones with ethylenediamine, diethylenetriamine and triethylenetetramine. Nickel(II) and copper(II) chelates were obtained from N,N'-ethylene-bis(2-arylazo-1,3-aminovinylketones). 2-Arylhydrazono-3-fluoroacyl esters formed N,N?-ethylenediamides of 2-arylhydrazono-3-fluoroacylpropionic acids with ethylenediamine. Interaction of 2-arylhydrazono-3-fluoroacyl esters with diethylenetriamine and triethylenetetramine resulted in and decomposition products.????
\\\\Expert2\\nbo\\Journal of Fluorine Chemistry\\2004, v.125, p.401.pdf
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19.

Вид документа : Статья из журнала
Шифр издания : 54/G 65
Автор(ы) : Gorbunova T. I., Zapevalov A. Ya., Saloutin V. I.
Заглавие : Synthesis of oxyranes based on 1,1,2,3,3-pentafluoro-1,5-hexadiene [Electronic resource]
Место публикации : Russian Chemical Bulletin (Translation of Izvestiya Akademii Nauk, Seriya Khimicheskaya). - 1995. - Vol. 44, № 8. - С. 1470-1473
Систем. требования: http://www.springerlink.com/content/p38p768256481080/fulltext.pdf
Примечания : 26.10.2011 г.
ББК : 54
Предметные рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Interaction of 1,1,2,3,3-pentafluoro-1,5-hexadiene with Br2 in a MeCOOH medium results in the product of selective bromination of the hydrocarbon double bond,i.e., 5,6-dibromo-1,1,2,3,3-pentafluoro-1-hexene. Epoxidation of the latter with H2O2 in an alkaline medium followed by debromination afforded 5,6-epoxy-4,4,5,6,6-pentafluoro-1-hexene for the first time
\\\\Expert2\\nbo\\Russian Chemical Bulletin\\1995, 44 (8), 1470.pdf
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20.

Вид документа : Статья из журнала
Шифр издания : 54/H 43
Автор(ы) : Bratskaya S.YU., Pestov A. V., Yatluk Yu. G., Avramenko V.A.
Заглавие : Heavy metals removal by flocculation/precipitation using N-(2-carboxyethyl)chitosans
Место публикации : Colloids and Surfaces A: Physicochemical and Engineering Aspects. - 2009. - Vol. 339, № 1-3. - С. 140-144
ББК : 54
Предметные 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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