Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Vladimir A. Zalomlenkov"'
Autor:
Kyrill Yu. Suponitsky, Ivan V. Fedyanin, Valentina A. Karnoukhova, Vladimir A. Zalomlenkov, Alexander A. Gidaspov, Vladimir V. Bakharev, Aleksei B. Sheremetev
Publikováno v:
Molecules, Vol 26, Iss 24, p 7452 (2021)
Co-crystallization is an elegant technique to tune the physical properties of crystalline solids. In the field of energetic materials, co-crystallization is currently playing an important role in the engineering of crystals with improved performance.
Externí odkaz:
https://doaj.org/article/b59eb20d9dab40a19c99727162c47901
Autor:
Vladimir V. Bakharev, Alexander А. Gidaspov, Vladimir А. Zalomlenkov, Victor E. Parfenov, Olga V. Golovina, Pavel А. Slepukhin
Publikováno v:
Chemistry of Heterocyclic Compounds. 58:153-158
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::788b011d8d7a7ded2e5b8bef1fd91a61
https://doi.org/10.1007/s10593-022-03068-9
https://doi.org/10.1007/s10593-022-03068-9
Autor:
Alexander A. Lashakov, Vladimir A. Zalomlenkov, Kyrill Yu. Suponitsky, Svetlana V. Osintseva, Aleksei A. Anisimov, Ivan V. Ananyev, Alexander A. Gidaspov
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:266-273
It is well known that the densest molecular crystals formed by molecules consisting of C, H, N, O, and F atoms are those of polynitro compounds that do not and cannot participate in strong intermolecular interactions. At the same time, many “typica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d5d75acfa7eb2f9fa16ff613da711ce
https://doi.org/10.1007/s10593-021-02903-9
https://doi.org/10.1007/s10593-021-02903-9
Autor:
Vladimir A. Zalomlenkov, Marina I. Struchkova, Victor E. Parfenov, Aleksei B. Sheremetev, Vladimir V. Bakharev, David B. Lempert, Nadezhda V. Palysaeva, Evgeniy V. Yurtaev, Kyrill Yu. Suponitsky, Alexander A. Gidaspov
Publikováno v:
RSC Advances. 6:34921-34934
The multicomponent reaction of 2,4,6-trichloro-1,3,5-triazine with potassium trinitromethane and trinitroethanol was exploited for the first synthesis of the hetaryl trinitroethyl ether, 2,4-bis(2,2,2-trinitroethoxy)-6-trinitrometyl-1,3,5-triazine 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a835af4634391ddd7c5b7a3dd4432016
https://doi.org/10.1039/c6ra05826d
https://doi.org/10.1039/c6ra05826d
Autor:
Victor E. Parfenov, Alexander A. Gidaspov, Olga V. Golovina, Pavel A. Slepukhin, Vladimir V. Bakharev, Vladimir A. Zalomlenkov
Publikováno v:
Chemistry of Heterocyclic Compounds. 53:822-824
The reaction of 3-methyl-5-trinitromethyltetrazolо[1,5-а][1, 3, 5]triazin-7-one with water led to the opening of 1,3,5-triazine ring and preservation of trinitromethyl group in the product. The obtained N-(1-methyltetrazol-5-yl)trinitroacetimidamid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4cc8f0f76f7df509f1e0de1a878ec54
https://doi.org/10.1007/s10593-017-2130-9
https://doi.org/10.1007/s10593-017-2130-9
Autor:
Vladimir V. Bakharev, Yuliya T. Palatova, Irina S. Nazarova, Alexander A. Gidaspov, Vladimir A. Zalomlenkov
Publikováno v:
ChemInform. 42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2319c7c1ea7cd387379c7e97c1de1ffa
https://doi.org/10.1002/chin.201144251
https://doi.org/10.1002/chin.201144251