Аннотация:
Fully aromatic C60Cl30 is much more difficult to reduce than non-aromatic C60Cl24; the anion radicals C60Cln− (n = 24, 30) are unstable and undergo rapid decomposition with loss of Cl− anions and partial substitution of chlorine atoms by organic groups.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
P. A. Troshin, O. A. Troshina, S. M. Peregudova, E. I. Yudanova, A. G. Buyanovskaya, D. V. Konarev, A. S. Peregudov, A. N. Lapshin, R. N. Lyubovskaya, “Chemical and electrochemical reduction of the highly chlorinated fullerenes C60Cl24 and C60Cl30”, Mendeleev Commun., 16:4 (2006), 206–208
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3589
https://www.mathnet.ru/rus/mendc/v16/i4/p206
Эта публикация цитируется в следующих 15 статьяx:
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Dmitri V. Konarev, Natalia A. Romanova, Roman A. Panin, Alexey A. Goryunkov, Sergey I. Troyanov, Rimma N. Lyubovskaya, “Magnetic Coupling and Optical Properties of the S6‐Dodecakis(trifluoromethyl)fullerene Radical Anions in the Layered Salt (PPN+)[C60(CF3)12.-]”, Chemistry A European J, 20:18 (2014), 5380
Hua Liang, Ke Dai, Ru‐Fang Peng, Shi‐Jin Chu, “An Isomer of C60Cl10 Free of Skew‐Pentagonal‐Pyramidal C60Cl6 Substructure”, Chemistry A European J, 20:48 (2014), 15742
A. I. Kotel'nikov, A. Yu. Rybkin, N. S. Goryachev, A. Yu. Belik, A. B. Kornev, P. A. Troshin, “Photodynamic activity of a hybrid nanostructure based on a polycationic fullerene derivative and phthalocyanine dye photosens”, Dokl Phys Chem, 452:2 (2013), 229
A. B. Kornev, A. S. Peregudov, V. M. Martynenko, G. V. Guseva, T. E. Sashenkova, A. Yu. Rybkin, I. I. Faingold, D. V. Mishchenko, R. A. Kotelnikova, N. P. Konovalova, J. Balzarini, P. A. Troshin, “Synthesis and biological activity of a novel water-soluble methano[60]fullerene tetracarboxylic derivative”, Mendeleev Commun., 23:6 (2013), 323–325
A. V. Barinov, N. S. Goryachev, D. A. Poletaeva, A. Yu. Rybkin, A. B. Kornev, P. A. Troshin, F. J. Schmitt, G. Renger, H. J. Eichler, A. I. Kotelnikov, “Photodynamic activity of hybrid nanostructure on the basis of polycationic fullerene derivative and xanthene dye eosine Y”, Nanotechnol Russia, 7:7-8 (2012), 409
D.Sh. Sabirov, R.R. Garipova, R.G. Bulgakov, “General formula for accurate calculation of halofullerenes polarizability”, Chemical Physics Letters, 523 (2012), 92
E. A. Khakina, A. S. Peregudov, S. I. Troyanov, P. A. Troshin, “Synthesis and study of trannulene derivatives of fullerenes”, Russ Chem Bull, 61:2 (2012), 264
Alexey B. Kornev, Ekaterina A. Khakina, Sergey I. Troyanov, Alla A. Kushch, Alexander Peregudov, Alexey Vasilchenko, Dmitry G. Deryabin, Vyacheslav M. Martynenko, Pavel A. Troshin, “Facile preparation of amine and amino acid adducts of [60]fullerene using chlorofullerene C60Cl6 as a precursor”, Chem. Commun., 48:44 (2012), 5461
Alexey B. Kornev, Alexander S. Peregudov, Vyacheslav M. Martynenko, Jan Balzarini, Bart Hoorelbeke, Pavel A. Troshin, “Synthesis and antiviral activity of highly water-soluble polycarboxylic derivatives of [70]fullerene”, Chem. Commun., 47:29 (2011), 8298
Ekaterina A. Khakina, Sergey I. Troyanov, Alexander S. Peregudov, Ilya V. Soulimenkov, Natalya V. Polyakova, Pavel A. Troshin, “The Remarkable Chemistry of Trannulenes: Green Fluorinated Fullerenes with Unconventional Aromaticity”, Chemistry A European J, 16:43 (2010), 12947
Alexey A. Goryunkov, Eugenia S. Kornienko, Tatyana V. Magdesieva, Andrey A. Kozlov, Vsevolod A. Vorobiev, Stanislav M. Avdoshenko, Ilya N. Ioffe, Oleg M. Nikitin, Vitality Yu. Markov, Pavel A. Khavrel, Andrey Kh. Vorobiev, Lev N. Sidorov, “Electrochemical, ESR and theoretical studies of [6,6]-opened C60(CF2), cis-2-C60(CF2)2 and their anions”, Dalton Trans., 2008, no. 48, 6886
Pavel A. Troshin, Olesya A. Troshina, Svetlana M. Peregudova, Evgeniya I. Yudanova, Anastasiya G. Buyanovskaya, Dmitry V. Konarev, Alexander S. Peregudov, Alexander N. Lapshin, Rimma N. Lyubovskaya, “Chemical and Electrochemical Reduction of the Highly Chlorinated Fullerenes C60Cl24 and C60Cl30.”, ChemInform, 38:1 (2007)
Adam D. Darwish, “Fullerenes”, Annu. Rep. Prog. Chem., Sect. A: Inorg. Chem., 103 (2007), 370
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