Zobrazeno 1 - 10
of 23
pro vyhledávání: '"M. P. Prigozhina"'
Autor:
J. Y. Sanchez, E. G. Bulycheva, V. Yu. Voitekunas, A. E. Osolodkov, Mikhail D. Dutov, Svyatoslav A. Shevelev, Marc J.M. Abadie, Olga V. Serushkina, Cristina Iojoiu, A. L. Rusanov, Vasily V. Mezhnev, M. P. Prigozhina, L. G. Komarova, M. G. Bugaenko
Publikováno v:
Polymer Science Series B. 51:465-470
New poly(arylene ethers) containing side sulfo groups have been synthesized through the copolycondensation of 3,5-dinitrodiphenyl sulfone 4′-sulfonic acid and 4,4′-dichlorodiphenyl sulfone with bicyclic aromatic bisphenols under the conditions of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3c077cb401e55a40e3efe1000858902
https://doi.org/10.1134/s1560090409110074
https://doi.org/10.1134/s1560090409110074
Benzophenone-Type Unsymmetrical Substituted Aromatic Diamines and Organosoluble Polyimides Therefrom
Autor:
Yulia S. Yakovleva, Alexander L. Rusanov, R. S. Begunov, Ludmila G. Komarova, M. P. Prigozhina
Publikováno v:
High Performance Polymers. 21:729-743
Benzophenone-type unsymmetrical substituted aromatic diamines of general formula were prepared starting with p-nitrobenzoyl chloride and substituted benzenes. Interaction of the diamines obtained with aromatic tetracarboxylic acids dianhydrides under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8a1770a0b68f280e8627b42685bb26e
https://doi.org/10.1177/0954008308099187
https://doi.org/10.1177/0954008308099187
Autor:
V. Yu. Voytekunas, Marc J.M. Abadie, Mikhail D. Dutov, L. G. Komarova, Svyatoslav A. Shevelev, A. L. Rusanov, Andrey A. Askadskii, Olga V. Serushkina, M. P. Prigozhina
Publikováno v:
Polymer Science Series B. 50:70-74
Aromatic polyethers with phenylsulfone side groups were obtained via the reaction of aromatic nucleophile substitution using 3,5-dinitrodiphenylsulfone as an electrophilic monomer activated by meta-substituents. The polymers are characterized by solu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f300c313d0cc71d0a87886f77295913
https://doi.org/10.1134/s1560090408030056
https://doi.org/10.1134/s1560090408030056
Publikováno v:
Polymer Science Series B. 50:6-10
Asymmetric aromatic diamines of the benzophenone series (3,4′-diamino-4-methylbenzophenone and 3,4′-diamino-4-methoxybenzophenone) were synthesized via the Friedel-Crafts reaction of 4-nitrobenzoyl chloride with an equimolar amount of toluene or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ba957dd5a7fbc54aa728de65015a443
https://doi.org/10.1134/s1560090408010028
https://doi.org/10.1134/s1560090408010028
Autor:
A. Yu. Leikin, M. P. Prigozhina, L. G. Komarova, A. L. Rusanov, D. Yu. Likhachev, Andrey A. Askadskii, I. I. Brodskii, R. S. Begunov
Publikováno v:
Polymer Science Series B. 49:22-25
A new phenoxy-substituted aromatic diamine, 3,4′-diamino-4-phenoxybenzophenone, was synthesized by a four-step process using p-nitrobenzoyl chloride and chlorobenzene as initial compounds. By interaction of the obtained diamine with aromatic tetrac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d244b81ecd130469846b47c58e63e7b5
https://doi.org/10.1134/s156009040701006x
https://doi.org/10.1134/s156009040701006x
Autor:
N. N. Ul’yanova, L. G. Komarova, Yu. N. Sazanov, Olga V. Okatova, A. L. Rusanov, Peter N. Lavrenko, M. P. Prigozhina
Publikováno v:
Polymer Science Series A. 49:349-354
For a number of new polyimides prepared from 3,5-diaminodiphenyl oxide, 2-methyl-3,5-diaminodiphenyl sulfide, and various dianhydrides of aromatic tetracarboxylic acids, the hydrolytic stability in DMF and 96% H2SO4 and the thermooxidative stability
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf884102ee0837ebb2c61360eb7765d2
https://doi.org/10.1134/s0965545x07030169
https://doi.org/10.1134/s0965545x07030169
Autor:
Rusanov Aleksandr L, Andrey A. Askadskii, Olga V. Serushkina, A. Kh. Shakhnes, L. G. Komarova, M. P. Prigozhina, Mikhail D. Dutov, Svyatoslav A. Shevelev
Publikováno v:
Polymer Science Series B. 48:209-212
A new fluorinated diamine, 3,5-diamino-4-methyl-2′,3′,5′,6′-tetrafluoro-4′-trifluoromethyldiphenyloxide, was synthesized by interaction of 2,6-diamino-p-cresol with perfluorotoluene via aromatic nucleophilic substitution. New aromatic polyi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6ff6501723e2632c12cc72c29367b60
https://doi.org/10.1134/s1560090406070141
https://doi.org/10.1134/s1560090406070141
Autor:
Mikhail D. Dutov, Svyatoslav A. Shevelev, L. G. Komarova, Vladimir A. Tartakovsky, M. P. Prigozhina, A. L. Rusanov
Publikováno v:
International Journal of Energetic Materials and Chemical Propulsion. 5:1031-1047
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ee2432882f7657a1cc82c458def283f
https://doi.org/10.1615/intjenergeticmaterialschemprop.v5.i1-6.1060
https://doi.org/10.1615/intjenergeticmaterialschemprop.v5.i1-6.1060
Autor:
E. G. Bulycheva, V.A. Tartakovskiy, L. G. Komarova, Olga V. Serushkina, M. P. Prigozhina, I.A. Vatsadse, L. B. Elshina, Mikhail D. Dutov, Svyatoslav A. Shevelev, A. L. Rusanov
Publikováno v:
Polymer. 41:5021-5037
New condensation monomers—primarily diamines containing phenoxy, thiophenoxy and phenylsulphone substituents were obtained from 2,4,6-trinitrotoluene (TNT). Interaction of some dinitro compounds containing strong electron-withdrawing groups in meta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ca5478d14faecd7116c2f62ea9213c6
https://doi.org/10.1016/s0032-3861(99)00564-9
https://doi.org/10.1016/s0032-3861(99)00564-9
Autor:
O. Yu. Sapozhnikov, L. G. Komarova, M. P. Prigozhina, Mikhail D. Dutov, Svyatoslav A. Shevelev, A. L. Rusanov, M. A. Korolev
Publikováno v:
High Performance Polymers. 11:395-403
The interaction of the demethylation product of 1, 3, 5-trinitrobenzene—2, 4, 6-trinitrotoluene—with fluorinated alcohols followed by reduction of the perfluoroalkoxy-substituted m-dinitrobenzenes thus formed led to the formation of new fluorinat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e21f6cfd202410c344a995603623fd16
https://doi.org/10.1088/0954-0083/11/4/305
https://doi.org/10.1088/0954-0083/11/4/305