共查询到20条相似文献,搜索用时 31 毫秒
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A. M. Golyakov A. N. Borisov G. A. Shagisultanova A. L. Shpilev 《Russian Journal of General Chemistry》2011,81(9):1867-1872
The electrochemical oxidation of N,N′-bis(3-methoxysalicylidene)-1,3-propylenediamine leads to the formation of conducting polymer on the electrode surface. The
decisive role of phenol oxygen in the formation of the polymeric forms of azomethine bases was elucidated. Optimal conditions
for the synthesis of the polymer in the potentiostatic conditions were revealed. The coefficient of the charge diffusion and
the activation barrier for the charge transfer in the polymer bulk in the electrolyte medium were determined. 相似文献
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A. D. Dubonosov V. P. Rybalkin Ya. Yu. Vorob’eva V. A. Bren’ V. I. Minkin S. M. Aldoshin V. V. Tkachev A. V. Tsukanov 《Russian Chemical Bulletin》2004,53(10):2248-2252
It was shown by electron absorption spectroscopy and X-ray diffraction analysis that steric strains in photochromic 2-(N-acyl-N-arylaminomethylene) benzo[b]thiophen-3(2H)-one molecules ortho-substituted in the N-phenyl ring increase the quantum yield of the N→O photoinduced rearrangement in accord with an increase in the steric constant of the ortho-substituent.__________Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 2151–2155, October, 2004. 相似文献
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Dmitry S. Goncharov Ivan V. Kulakov Alexander S. Fisyuk 《Chemistry of Heterocyclic Compounds》2017,53(12):1335-1339
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E. G. Mesropyan A. S. Galstyan A. A. Avetisyan 《Russian Journal of Organic Chemistry》2010,46(9):1296-1300
The preparation of N-(oxiran-2-ylmethyl)-N-ethylaniline was developed. The compound was used in the synthesis of new N-derivatives of aromatic amines containing vicinal
aminoalcohol moieties. 相似文献
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V. Yu. Korotaev Yu. A. Skorik A. Yu. Barkov M. I. Kodess A. Ya. Zapevalov 《Russian Chemical Bulletin》2005,54(11):2545-2549
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.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2465–2469, November, 2005. 相似文献
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A. D. Sinitsa A. A. Shalimov A. M. Nesterenko D. M. Malenko 《Russian Chemical Bulletin》2005,54(3):752-757
In the study of reactions of N-alkyl- and N-aryltrihalogenoacetamides with PCl5, it was demonstrated for the first time that 3-alkyl(aryl)-2,2,2,4 tetrachloro-4-trihalomethyl-1,3,2-λ5-oxazaphosphetanes are intermediates in the synthesis of trihaloacetimidoyl chlorides. According to quantum-chemical calculations, acyclic N-tetrachlorophosphoranes, which are the primary products in the reactions of trihaloacetamides with PCl5, undergo rapid cyclization into the corresponding phosphorates and subsequent 1,3-chlorotropic migration gives rise to oxazaphosphetanes with the five-coordinate P atom.__________Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp. 739-744, March, 2005. 相似文献
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3-Acetyl-6-(o-methyl benzoyl)-N-ethylcarbazole was prepared through successive o-methyl benzoylation and acetylation of N-ethylcarbazole in one pot. The overall yield was 85.6% and the structure was confirmed by 1H-NMR and 13C-NMR. A preliminary investigation had also been carried out on the mechanism of the o-methyl benzoylation of N-ethylcarbazole. 相似文献
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Yu. A. Aizina I. B. Rozentsveig I. V. Ushakova G. G. Levkovskaya A. N. Mirskova 《Russian Journal of Organic Chemistry》2005,41(1):91-94
Reactions of N-(2,2,2-trichloroethylidene)arenesulfonamides with thiophene, 2-chlorothiophene, and 2,5-dichlorothiophene, as well as of N-(2,2,2-trichloro-1-hydroxyethyl)arenesulfonamides with 2-chlorothiophene, lead to formation of the corresponding N-(2,2,2-trichloro-1-thienylethyl)arenesulfonamides. Alkaline hydrolysis of the latter occurs selectively at the trichloromethyl group to give N-arylsulfonyl-α-thienylglycines.__________Translated from Zhurnal Organicheskoi Khimii, Vol. 41, No. 1, 2005, pp. 93–96.Original Russian Text Copyright © 2005 by Aizina, Rozentsveig, Ushakova, Levkovskaya, Mirskova. 相似文献
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Cho Rong Kim Hyun Ji Kang Chi Won Kim Kyung Ho Yoo Ok-Sang Jung 《Transition Metal Chemistry》2009,34(6):579-584
The reaction of (COD)PdCl2 (COD = 1,5-cyclooctadiene) with (3-Py)2SiMe2 (bis(3-pyridyl)dimethylsilane) in acetone produces single crystals consisting of cyclodimers, [PdCl2((3-Py)2SiMe2)]2, whereas the similar reaction in a mixture of dichloromethane and ethanol yields amorphous submicrospheres consisting of
cyclotrimers, [PdCl2((3-Py)2SiMe2)]3. In a boiling chloroform solution, the cyclodimers are completely converted to the cyclotrimers. The structures of both cyclic
species are locked at temperatures below 0 °C. The cyclotrimer equilibrates to the cyclodimer, the cyclotrimer, and cyclotrimeric
mono-DMF adduct, [Pd3Cl5(DMF)((3-Py)2SiMe2)3]Cl in the mole ratio of 6:1:5 in DMF solution at room temperature. The cyclodimer finally reaches the equilibrium in the
same condition.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
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S. Yu. Bylikin A. G. Shipov E. P. Kramarova O. B. Artamkina Vad. V. Negrebetskii Yu. I. Baukov 《Russian Journal of General Chemistry》2004,74(9):1356-1358
N-[(Chlorodimethylgermyl)methyl]lactams and -amides containing a five-coordinate germanium atom react with Grignard reagents chemoselectively by the Ge-Cl bond to form four-coordinate germanium compounds. The method of competitive reactions was used to establish that respective five-coordinate germanium and silicon compounds are almost equally reactive toward Grignard reagents but much more reactive than model four-coordinate germanium and silicon compounds.Translated from Zhurnal Obshchei Khimii, Vol. 74, No. 9, 2004, pp. 1462–1465.Original Russian Text Copyright © 2004 by Bylikin, Shipov, Kramarova, Artamkina, Negrebetskii, Baukov.This revised version was published online in April 2005 with a corrected cover date. 相似文献
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Pyridine N-oxide reacts with 2- and 3-aminopyridines and their N-p-tolylsulfonyl derivatives in alkaline medium in the presence of p-toluenesulfonyl chloride to give N-p-tolylsulfonyl-2,2′- and 2,3′-dipyridylamines, respectively, as a result of reductive acylamination. In the reactions with 4-aminopyridine and 4-p-tolylsulfonyl-aminopyridine, their N-p-tolylsulfonyl- and N,N-bis(p-tolylsulfonyl) derivatives are formed, while reductive acylamination does not occur.__________Translated from Zhurnal Organicheskoi Khimii, Vol. 41, No. 1, 2005, pp. 128–130.Original Russian Text Copyright © 2005 by Solekhova, Kurbatov. 相似文献