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Dive into the research topics where L. I. Komarova is active.

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Featured researches published by L. I. Komarova.


Russian Chemical Bulletin | 1983

Reaction of cyanurates with the epoxide ring

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

Synthesis and Properties of Copoly(arylene ether ketones) with Side Reactive Groups

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

Structure of the dibenzoylphthalic acids obtained by condensation of pyromellitic dianhydride with benzene

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

Investigation of the reaction of thionyl chloride with dimethylformamide

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

Thermal polycondensation of hexa-p-hydroxymethylphenoxycyclotriphosphazene

E. M. Chistyakov; V. V. Kireev; S. N. Filatov; I. V. Terekhov; M. I. Buzin; L. I. Komarova


Polymer Science Series C | 2009

Chemical transformations of poly(arylene ether ketones) containing side functional groups

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

The polycyclotrimerization of isocyanates

S.V. Vinogradova; V. A. Pankratov; Ts.M. Frenkel; L.F. Larina; L. I. Komarova; V.V. Korshak


Polymer Science Series B | 2011

Comb-shaped homo- and copoly(arylene ether ketones) containing hydrophilic groups in side chains

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

Structuring in solutions of polydiphenylenesulfophthalide salts and their combined systems with a cationic surfactant

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

The nature of active centers in cyclotrimerization of isocyanates catalyzed by the tertiary amine—α-oxide—proton donor system 1. The role of the proton donor

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}

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S. N. Salazkin

Russian Academy of Sciences

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Ts. M. Frenkel

A. N. Nesmeyanov Institute of Organoelement Compounds

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V.V. Korshak

Moscow State University

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A. N. Ryabev

Russian Academy of Sciences

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G. G. Nikiforova

Russian Academy of Sciences

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L. V. Dubrovina

Russian Academy of Sciences

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V. S. Papkov

Russian Academy of Sciences

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