L. I. Komarova
Russian Academy of Sciences
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Russian Chemical Bulletin | 1983
V.V. Korshak; V. A. Pankratov; L. I. Komarova; Ts. M. Frenkel; A. M. Fainleib; S.V. Vinogradova
ConclusionsIn the case of the reaction of triphenylcyanurate and phenyl glycidyl ether, we showed that the oxirane rings may react at high temperature with the cyanurate rings to form isocyanurate fragments, which, in turn, react with excess epoxide to form oxazolidone rings.
Polymer Science Series A | 2008
K. I. Donetskii; A. N. Ryabev; V. V. Shaposhnikova; S. N. Salazkin; L. I. Komarova; O. V. Afonicheva
A number of amorphous copoly(arylene ether ketones) with side reactive groups (carboxyl and phthalimidine) have been synthesized via the nucleophilic substitution of a halogen atom in activated aryl halide. The said copolymers exhibit an increased onset temperature of softening (170–250°C) and good mechanical characteristics: in the case of films, the breaking strength is 88.5–119 MPa, while for plastics, the notched specific impact strength varies from 16 to 22 kJ/m2 and the bending strength is in the range of 135–217 MPa.
Russian Chemical Bulletin | 1976
V. V. Korshak; S.V. Vinogradova; G. N. Melekhina; S. N. Salazkin; L. I. Komarova; P. V. Petrovskii; P. O. Okulevich
A method has been developed for the isolation of 2,4-dibenzoylisophthalic and 2,5-dibenzoylterephthalic acids from the mixtures formed during the Friedel-Crafts condensation of pyromellitic dianhydride with benzene. The structure of the acids obtained has been investigated by PMR and DR speetroscopy. The ability of 2,5-dibenzoylterephthalic acid to undergo tautomeric interconversions (normal or cyclic forms) has been discovered.
Russian Chemical Bulletin | 1971
S.V. Vinogradova; V. A. Pankratov; V.V. Korshak; L. I. Komarova
1. The interaction of dimethylformamide with thionyl chloride was investigated at various temperatures. 2. At the beginning of the interaction of dimethylformamide with thionyl chloride, an unstable addition product of thionyl chloride at the carbonyl oxygen of dimethylformamide is formed
Polymer Science Series B | 2012
E. M. Chistyakov; V. V. Kireev; S. N. Filatov; I. V. Terekhov; M. I. Buzin; L. I. Komarova
Polymer Science Series C | 2009
A. N. Ryabev; K. I. Donetskii; S. N. Salazkin; V. V. Shaposhnikova; L. I. Komarova; V. V. Kazantseva; K. A. Bychko; A. A. Askadskii; A. S. Tkachenko
\begin{gathered} \hfill \\ [(CH_3 )_2 \mathop N\limits^ \oplus = C\begin{array}{*{20}c} / \\ \backslash \\ \end{array} \begin{array}{*{20}c} {O - SO - Cl} \\ H \\ \end{array} ]Cl^ \ominus \hfill \\ \end{gathered}
Polymer Science U.s.s.r. | 1981
S.V. Vinogradova; V. A. Pankratov; Ts.M. Frenkel; L.F. Larina; L. I. Komarova; V.V. Korshak
Polymer Science Series B | 2011
A. N. Ryabev; S. N. Salazkin; V. V. Shaposhnikova; L. I. Komarova; V. V. Kazantseva; T. P. Bragina; A. S. Tkachenko
3. The adduct of dimethylformamide with thionyl chloride initially formed decomposes along two competing pathways: with liberation of SO2 and formation of the immonium chloride chloride
Polymer Science Series A | 2014
V. G. Vasil’ev; L. A. Wasserman; G. G. Nikiforova; L. I. Komarova; Galina I. Timofeeva; I. G. Plashchina; S. N. Salazkin; V. S. Papkov
Russian Chemical Bulletin | 1996
Ts. M. Frenkel; A.E. Shvorak; V.A. Pankratov; L. I. Komarova; A. K. Bonetskaya; M. A. Kravchenko
\begin{gathered} \hfill \\ [(CH_3 )_2 \mathop N\limits^ \oplus = C\begin{array}{*{20}c} / \\ \backslash \\ \end{array} \begin{array}{*{20}c} {Cl} \\ H \\ \end{array} ]Cl^ \ominus , \hfill \\ \end{gathered}