This article is cited in 14 scientific papers (total in 14 papers)
First representatives of macrocyclic poly(diazene oxide furazans): 3,4:7,8:11,12:15,16-tetrafurazano-1,2,5,6,9,10,13,14-octaazacyclohexadeca-1,3,5,7,9,11,13,15-octaene 1,9- and 1,10-dioxides; 1,5,9,13-tetraoxide and its crystal structure
Abstract:
Macrocyclic poly(diazene oxide furazans) have been synthesised for the first time: the tetraoxide was prepared by the oxidation of diazene fragments in the tetradiazenofurazan macrocycle, and the dioxides were synthesised by the intramolecular and intermolecular oxidative cyclisation of structures already containing diazene oxide fragments. The structure of the tetraoxide derivative has been established by X-ray diffraction analysis.
Document Type:
Article
Language: English
Citation:
V. A. Eman, M. S. Sukhanov, O. V. Lebedev, L. V. Batog, L. S. Konstantinova, V. Yu. Rozhkov, M. O. Dekaprilevich, Yu. T. Struchkov, L. I. Khmel'nitskii, “First representatives of macrocyclic poly(diazene oxide furazans): 3,4:7,8:11,12:15,16-tetrafurazano-1,2,5,6,9,10,13,14-octaazacyclohexadeca-1,3,5,7,9,11,13,15-octaene 1,9- and 1,10-dioxides; 1,5,9,13-tetraoxide and its crystal structure”, Mendeleev Commun., 7:1 (1997), 5–7
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This publication is cited in the following 14 articles:
V.P. Sinditskii, A.V. Burzhava, A.B. Sheremetev, “Macrocyclic tetra(azo-) and tetra(azoxyfurazan)s: Comparative study of decomposition and combustion with linear analogs”, Energetic Materials Frontiers, 2:2 (2021), 87
Owen T. O'Sullivan, Michael J. Zdilla, “Properties and Promise of Catenated Nitrogen Systems As High-Energy-Density Materials”, Chem. Rev., 120:12 (2020), 5682
Leonid L. Fershtat, Nina N. Makhova, “1,2,5‐Oxadiazole‐Based High‐Energy‐Density Materials: Synthesis and Performance”, ChemPlusChem, 85:1 (2020), 13
Yanyang Qu, Sergey P. Babailov, “Azo-linked high-nitrogen energetic materials”, J. Mater. Chem. A, 6:5 (2018), 1915
Alireza Salimi Beni, Maryam Zarandi, “Application of DFT and MP2 calculations on structural and water-assisted proton transfer in 3-amino-4-nitrofurazan”, Russ. J. Phys. Chem., 90:2 (2016), 374
Aleksei B. Sheremetev, Boris V. Lyalin, Andrei M. Kozeev, Nadezhda V. Palysaeva, Marina I. Struchkova, Kyrill Yu. Suponitsky, “A practical anodic oxidation of aminofurazans to azofurazans: an environmentally friendly route”, RSC Adv., 5:47 (2015), 37617
Kyrill Yu. Suponitsky, Konstantin A. Lyssenko, Ivan V. Ananyev, Andrei M. Kozeev, Aleksei B. Sheremetev, “Role of Weak Intermolecular Interactions in the Crystal Structure of Tetrakis-furazano[3,4-c:3′,4′-g:3″,4″-k:3‴,4‴-o][1,2,5,6,9,10,13,14]octaazacyclohexadecine and Its Solvates”, Crystal Growth & Design, 14:9 (2014), 4439
Jacqueline M. Veauthier, David E. Chavez, Bryce C. Tappan, Damon A. Parrish, “Synthesis and Characterization of Furazan Energetics ADAAF and DOATF”, Journal of Energetic Materials, 28:3 (2010), 229
M. A. Epishina, A. S. Kulikov, N. N. Makhova, “Synthesis of macrocyclic systems from 4,4′-diamino-3,3′-bi-1,2,5-oxadiazole and 3(4)-amino-4(3)-(4-amino-1,2,5-oxadiazol-3-yl)-1,2,5-oxadiazole 2-oxides”, Russ Chem Bull, 57:3 (2008), 644
Aleksei B. Sheremetev, Nataliya S. Aleksandrova, Dmitrii E. Dmitriev, Boris B. Averkiev, Mikhail Yu. Antipin, “Synthesis and x-ray study of novel azofurazan-annulated macrocyclic lactams”, Journal of Heterocyclic Chemistry, 42:4 (2005), 519
Aleksei B. Sheremetev, Elena V. Shatunova, Boris B. Averkiev, Dmitrii E. Dmitriev, Viktor A. Petukhov, Mikhail Yu. Antipin, “Chromophoric macrocycles from the oxidation of bis(aminofurazanylic) ethers of 1,2‐diols”, Heteroatom Chemistry, 15:2 (2004), 131
Aleksei B. Sheremetev, Nina N. Makhova, Willy Friedrichsen, Advances in Heterocyclic Chemistry, 78, 2001, 65
V. A. EMAN, M. S. SUKHANOV, O. V. LEBEDEV, L. V. BATOG, L. S. KONSTANTINOVA, V. YU. ROZHKOV, M. O. DEKAPRILEVICH, YU. T. STRUCHKOV, L. I. KHMEL'NITSKII, “ChemInform Abstract: First Representatives of Macrocyclic Poly(diazene oxide furazans): 3,4: 7,8:11,12:15,16‐Tetrafurazano‐1,2,5,6,9,10,13,14‐octaazacyclohexadeca‐ 1,3,5,7,9,11,13,15‐octaene 1,9‐ and 1,10‐dioxides (VI) and (IV), resp.; 1,5,9,13‐Tetraoxide (II) and Its Crystal Structure”, ChemInform, 28:28 (1997)
S. G. Zlotin, E. A. Vinogradova, O. A. Luk'yanov, “Synthesis of 3,4:7,8:11,12-trifurazano-1,2,5,6,9,10-hexaazacyclododeca-1,3,5,7,9,11-hexaene-1,5,9-trioxide”, Mendeleev Commun., 7:1 (1997), 7–8
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