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2.
A. S. Peregudov L. N. Usatova E. I. Smyslova E. I. Fedin D. N. Kravtsov 《Russian Chemical Bulletin》1995,44(8):1513-1519
It has been shown by the19F NMR method that the relative polarities of nitrogenelement bonds in 2-(4-fluorophenyl)benzimidazole and its PhHg and PPh3Au derivatives increase in the order N-H19F NMR. It has been found that these reactions occur by a bimolecular associative mechanism and that the N-H bond is substantially less reactive than the N-Hg and N-Au bonds, which have identical reactivities within the limits of sensitivity of the method used.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1574–1580, August, 1995.This work was carried out with financial support from the Russian Foundation for Basic Research (Project No. 93-03-5528). 相似文献
3.
V. V. Shaposhnikova D. S. Sharapov I. A. Kaibova V. V. Gorlov S. N. Salazkin L. V. Dubrovina T. P. Bragina V. V. Kazantseva K. A. Bychko A. A. Askadskii A. S. Tkachenko G. G. Nikiforova P. V. Petrovskii A. S. Peregudov 《Polymer Science Series A》2007,49(10):1071-1078
Exchange reactions that may proceed in the course of polycondensation during formation of a polymer from 4,4′-difluorobenzophenone and 4,4′-(isopropylidene)diphenol have been studied. It has been shown that the molecular mass of the polymer decreases under the action of 4,4′-(isopropylidene)diphenol diphenolate. The nucleophilic substitution of the activated aryl halide in DMAA in the presence of potassium carbonate yields high-molecular-mass block copoly(arylene ether ketones) based on 4,4′-difluorobenzophenone and a number of bisphenols. It was demonstrated the synthetic procedure and the chemical structure of block copoly(arylene ether ketones) strongly affect the onset temperature of softening and the mechanical characteristics of the films based on these polymers. 相似文献
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F. I. Zubkov V. P. Zaitsev A. A. Orlova A. S. Peregudov N. M. Mikhailova A. V. Varlamov 《Russian Journal of Organic Chemistry》2007,43(8):1202-1208
Dimethyl acetylenedicarboxylate reacts with 4-substituted and 3,4-fused 2-furyl-1,2,3,4-tetrahydroquinoline derivatives at the furan fragment according to the [4 + 2]-cycloaddition pattern. The reaction is not stereoselective, and it yields two diastereoisomeric 7-oxabicyclo[2.2.1]hepta-2,5-dienes whose structure was determined by X-ray analysis and NMR spectroscopy. 相似文献
6.
D. N. Kravtsov A. S. Peregudov L. S. Golovchenko E. I. Smyslova 《Russian Chemical Bulletin》1996,45(5):1194-1199
19F NMR spectroscopy was used to study the exchange reactions involving 4-fluorothiophenoxides, 4-nitrophenoxides, chlorides, and acetates of arylmercury and triphenylphosphinegold. The analysis of the data on equilibrium constants allows one to obtain information on the comparative chemical hardness of ArHg+ and Ph3PAu+ cations. The increase in the electron-donating ability of aryl ligands enhances the chemical hardness of ArHg+ cations, their influence being best described by 0 constants of substituted phenyl groups.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 1255–1260, May, 1996. 相似文献
7.
Compounds of general formulatrans-ArNi(PR3)2OAr' (R = Et, cyclohexyl; Ar = 2-MeC6H4, 2-FC6H4; Ar' = 4-FC6H4, 4-NO2C6H4) were synthesized by the reaction of Ar'OK with cationic nickel complexes generated by treatment of ArNi(PR3)2Cl with TlBF4. Syntheses of 4-fluorophenoxide complexes, ArNi(PR3)2OC6H4F-4, additionally give some quantities oftrans-[ArNi(PR3)2OC6H4F-4][HOC6H4F-4] adducts. Exchange reactions MeC6H4Ni(PEt3)2OC6H4F-4 + XC6H4OH 2-MeC6H4Ni(PEt3)2OC6H4X + 4-FC6H4OH were studied in THF. The equilibrium is shifted to the right as the acidity of ArOH increases. A linear relationship between lgK
eq and pK
a of XC6H4OH in DMSO was found. A conclusion concerning the strong polarization of the Ni-O bond was made on the basis of an analysis of the chemical shifts of fluorine atoms in 2-MeC6H4Ni(PEt3)2OC6H4F-4.Translated fromIvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2266–2271, November, 1995. 相似文献
8.
S. Pasynkiewicz K.B. Starowieyski A.S. Peregudov D.N. Kravtsov 《Journal of organometallic chemistry》1977,132(2):191-201
Intramolecular coordination in dimethylaluminium phenoxides (with an ortho-substituted ring) was investigated. Only strongly donating groups in the phenoxy ring (COOMe) displayed strong intramolecular coordination. All compounds investigated formed donor-acceptor complexes with hexamethylphosphoramide (HMPA). Dimethylaluminium methylsalicilate coordinated HMPA without splitting the intramolecular carbonyl oxygen—aluminium bond, which suggests formation of the pentacoordinated aluminium atom. 相似文献
9.
V. A. Vasnev G. D. Markova M. L. Keshtov A. S. Peregudov A. R. Khokhlov 《Polymer Science Series A》2006,48(8):773-778
Copolyterephthalates of bis(4-hydroxy-3-methylphenyl)-2,2-propane and N-methyldiethanolamine and their hydrochloric salts of various compositions and microstructures have been prepared by the copolycondensation of hydrophilic and hydrophobic comonomers. It has been shown that the transition from random proteinlike structures to the block structures makes it possible to preserve biomimetic properties of the copolymers at a smaller content of charged units in macromolecules. The ability of charged polymers to survive in aqueous solutions has been used for the synthesis of copolyterephthalate of N-bis(hydroxyethyl)tetradecylmethylammonium bromide and N-methyldiethanolamine demonstrating fungicidal activity. 相似文献
10.