Abstract:
The oxidative intermolecular cyclocondensation of 3,4-diaminofurazan and 4,4′-diamino-3,3′-azofurazan has been carried out by treating them with mixtures of Pb(OAc)4 and Bu4NBr, Br2 or NaBr to give previously unknown macrocyclic compounds: polydiazenofurazans possessing differing numbers of units.
Document Type:
Article
Language: English
Citation:
V. E. Eman, M. S. Sukhanov, O. V. Lebedev, L. V. Batog, L. S. Konstantinova, V. Yu. Rozhkov, L. I. Khmel'nitskii, “Polydiazenofurazans: novel macrocyclic systems”, Mendeleev Commun., 6:2 (1996), 66–67
Linking options:
https://www.mathnet.ru/eng/mendc4917
https://www.mathnet.ru/eng/mendc/v6/i2/p66
This publication is cited in the following 13 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
Leonid L. Fershtat, Nina N. Makhova, “1,2,5‐Oxadiazole‐Based High‐Energy‐Density Materials: Synthesis and Performance”, ChemPlusChem, 85:1 (2020), 13
Andrei I. Stepanov, Vladimir S. Sannikov, Dmitry V. Dashko, Alexey G. Roslyakov, Alexander A. Astrat'ev, Elena V. Stepanova, “A rational method of synthesis and chemical properties of 5-(4-aminofurazan-3-yl)-1-hydroxytetrazole”, Chem Heterocycl Comp, 53:6-7 (2017), 746
Indranirekha Saikia, Arun Jyoti Borah, Prodeep Phukan, “Use of Bromine and Bromo-Organic Compounds in Organic Synthesis”, Chem. Rev., 116:12 (2016), 6837
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
L. V. Batog, L. S. Konstantinova, A. S. Kulikov, N. N. Makhova, “Synthesis of 4,4′-bis(dichloroamino)- and 4,4′-bis(chloroamino)-3,3′-azofurazans, the first representatives of dichloroamino- and chloroaminofurazans”, Russ Chem Bull, 62:6 (2013), 1388
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, “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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