Abstract
Compound (7-NH3-L)2[B10H10] has been prepared and identified by elemental analysis and IR and UV spectroscopies. This compound as a potential inhibitor of free radicals and contains a representative of coumarins possessing biological activity and a representative of boron cluster anions widely used in various fields of science and technology. The radiation-chemical transformations of 7-amino-4-methylcoumarin in CH3CN, 96% C2H5OH, in the CH3CN/CF3COOH system, and in 20% aqueous solution (H3O)2[B10H10] have been first studied by UV spectroscopy.
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REFERENCES
S. Jamal and J. R. Casley-Smith, Ann. Trop. Med. Parasitol. 83, 287 (1989). https://doi.org/10.1080/00034983.1989.11812346
M. E. Marshal, J. L. Mochler, K. Edmonds, et al., Cancer. Res. Clin. Oncol. 120, 39 (1994). https://doi.org/10.1007/BF01377124
E. Perez-Rodriguez, J. Aguilera, and F. L. Figueroa, J. Exp. Bot. 54, 1093 (2003). https://doi.org/10.1093/jxb/erg111
R. H. Goodwin and C. Taves, Am. J. Bot. 37, 224 (1950). https://doi.org/10.1002/j.1537-2197.1950.tb12186.x
I. Korotkova, Y. A. Karbainov, and O. A. Avramchik, Anal. Bioanal. Chem. 327, 465 (2003). https://doi.org/10.1007/s00216-002-1687-y
B. B. Guilherme, da R. V. Damiana, M.-R. Alexander, et al., Mini-Rev. Med. Chem. 13, 318 (2013). https://doi.org/10.2174/138955713804999775
B. Halliwell and J. M. C. Gutteridge, Free Radicals in Biology and Medicine (University press, Oxford, 2007).
Y. Al-Majedy, A. Al-Amiery, A. A. Kadhum, A. BakarMohamad, Sys. Rev. Pharm. 8, 24 (2017). https://doi.org/10.5530/srp.2017.1.6
Y. Xue, Y. Liu, Q. Luo, et al., 122, 8520 (2018). https://doi.org/10.1021/acs.jpca.8b06787
S. N. Samovich, S. D. Brinkevich, and O. I. Shadyro, Rad. Phys. Chem. 100, 13 (2014). https://doi.org/10.1016/j.radphyschem.2014.03.015
I. G. Antropova, A. A. Fenin, and A. A. Revina, High Energy Chemistry 41, 61 (2007). https://doi.org/10.1134/S0018143907020026
D. R. Vianna, B. Guilherme, G. Meirelles, et al., Int. J. Mol. Sci. 13, 7260 (2012). https://doi.org/10.3390/ijms13067260
N. A. Gromak, F. A. Kolokolov, V. V. Dotsenko, et al., Russ. J. Gen. Chem. 91, 685 (2021). https://doi.org/10.1134/S1070363221040174
D. Ashok, K. Ramakrishna, N. Nagaraju, et al., Russ. J. Gen. Chem. 91, 711 (2021). https://doi.org/10.1134/S1070363221040216
T. M. Valova, O. V. Venidiktova, and V. A. Barachevsky, et al., Russ. J. Gen. Chem. 91, 2647 (2021). https://doi.org/10.1134/S1070363221120379
I. B. Sivaev, Chem. Heterocycl. Comp. 53, 638 (2017). https://doi.org/10.1007/s10593-017-2106-9
W. H. Knoth, Patent USA 3354121.
V. K. Skachkova, A. V. Grachev, L. V. Goeva, et al., Patent RF 2550156 C1.
L. N. Goswami, L. Ma, S. Chakravarty, et al., Inorg. Chem. 52, 1694 (2013). https://doi.org/10.1021/ic3017613
J. Plesek, Chem. Rev. 92, 269 (1992). https://doi.org/10.1021/ic3017613
I. B. Sivaev, V. I. Bregadze, and N. T. Kuznetsov, Russ. Chem. Bull. 51, 1362 (2002). https://doi.org/10.1023/A:1020942418765
I. B. Sivaev and V. I. Bregadze, Eur. J. Inorg. Chem. 11, 1433 (2009). https://doi.org/10.1002/ejic.200900003
F. Teixidor, C. Viñas, A. Demonceau, and R. Núñez, Pure Appl. Chem. 75, 1305 (2003). https://doi.org/10.1351/pac200375091305
R. B. King, Chem. Rev. 101, 1119 (2001). https://doi.org/10.1021/cr000442t
Z. Chen and R. B. King, Chem. Rev. 105, 3613 (2005). https://doi.org/10.1021/cr0300892
K. Yu. Zhizhin, A. P. Zhdanov, and N. T. Kuznetsov, Russ. J. Inorg. Chem. 55, 2089 (2010). https://doi.org/10.1134/S0036023610140019
I. B. Sivaev, A. V. Prikaznov, and D. Naoufal, Coll. Czech. Chem. Commun. 75, 1149 (2010). https://doi.org/10.1135/cccc2010054
I. B. Sivaev, Russ. J. Inorg. Chem. 64, 955 (2019). https://doi.org/10.1134/S003602361908014X
I. N. Klyukin, N. A. Selivanov, A. Y. Bykov, et al., Russ. J. Inorg. Chem. 65, 1547 (2020). https://doi.org/10.1134/S0036023620100113
A. V. Nelyubin, I. N. Klyukin, A. P. Zhdanov, et al., Russ. J. Inorg. Chem. 66, 139 (2021). https://doi.org/10.1134/S0036023621020133
E. Y. Matveev, I. V. Novikov, A. S. Kubasov, et al., Russ. J. Inorg. Chem. 66, 187 (2021). https://doi.org/10.1134/S0036023621020121
E. A. Malinina, S. E. Korolenko, A. P. Zhdanov, et al., J. Cluster Sci. 32, 755 (2021). https://doi.org/10.1007/s10876-020-01840-5
K. Fink and M. Uchman, Coord. Chem. Rev. 431, 213684 (2021). https://doi.org/10.1016/j.ccr.2020.213684
V. V. Avdeeva, T. M. Garaev, E. A. Malinina, et al., Russ. J. Inorg. Chem. 67, 28 (2022). https://doi.org/10.1134/S0036023622010028
E. Justus, D. T. Izteleuova, A. V. Kasantsev, et al., Collect. Czech. Chem. Commun. 72, 1740 (2007). https://doi.org/10.1135/cccc20071740
I. Kosenko, J. Laskova, A. Kozlova, et al., J. Organomet. Chem. 921, 121379 (2020). https://doi.org/10.1016/j.jorganchem.2020.121370
A. Serdyukov, I. Kosenko, A. Druzina, et al., J. Organomet. Chem. 946–947, 121905 (2021). https://doi.org/10.1016/j.jorganchem.2021.121905
H. C. Miller, N. E. Miller, and E. L. Muetterties, J. Am. Chem. Soc. 85, 3885 (1963). https://doi.org/10.1021/ja00906a033
E. A. Makhneva, A. V. Lipeeva, and E. E. Shul’ts, Russ. J. Org. Chem. 50, 662 (2014). https://doi.org/10.1134/S107042801405008X
D. J. Fuller, D. L. Kepert, B. W. Skelton, and A. H. White, Aust. J. Chem. 40, 2097 (1987). https://doi.org/10.1071/CH9872097
C. T. Chantler and E. N. Maslen, Acta Crystallogr., Sect. B: Struct. Sci., Cryst. Eng. Mater. 45, 290 (1989). https://doi.org/10.1107/S0108768189001138
V. V. Avdeeva, A. V. Vologzhanina, E. A. Malinina, and N. T. Kuznetsov, Crystals 9, 330 (2019). https://doi.org/10.3390/cryst9070330
S. E. Korolenko, A. S. Kubasov, L. V. Goeva, et al., Inorg. Chim. Acta 527, 120587 (2021). https://doi.org/10.1016/j.ica.2021.120587
E. A. Malinina, S. E. Korolenko, A. S. Kubasov, et al., J. Solid State Chem. 302, 122413 (2021). https://doi.org/10.1016/j.jssc.2021.122413
H. D. Burrows and E. M. Kosower, J. Phys. Chem. 78, 112 (1974). https://doi.org/10.1021/j100595a006
A. K. Pikayev, Modern Radiation Chemistry. Radiolysis of Gases and Liquids (Nauka, Moscow, 1986) [in Russian].
S. Lukáč, J. Teplý, and K. Vacek, J. Chem. Soc. Faraday Trans. 68, 1377 (1972). https://doi.org/10.1039/F19726801377
S. J. Newton, J. Chem. Phys. 26, 1764 (1957). https://doi.org/10.1063/1.1743630
J. N. Baxter and F. J. Johnston, Radiat. Res. 33, 311 (1968). https://doi.org/10.2307/3572482
M. Ntumann-Spallert and N. Getoff, Radiat. Phys. Chem. 13, 101 (1977). https://doi.org/10.1016/0146-5724(79)90056-6
G. R. Freeman, Radiation Chemistry of Ethanol: A Review of Data on Yields, Reaction Rate Parameters, and Spectral Properties of Transients (NBS, Washington, 1974).
I. P. Bell, M. A. J. Roders, H. D. J. Burrows, J. Chem. Soc., Faraday Trans. 73, 315 (1977). https://doi.org/10.1039/F19777300315
W. A. Mulac, A. Bromberg, and D. Meisel, Radiat. Phys. Chem. 26, 205 (1985). https://doi.org/10.1016/0146-5724(85)90187-6
T. H. Tran-Thi, A. M. Koulkes-Pujo, and L. Gilles, Radiat. Phys. Chem. 15, 209 (1980). https://doi.org/10.1016/0146-5724(80)90133-8
E. A. Malinina, V. V. Avdeeva, L. V. Goeva, et al., Russ. J. Inorg. Chem. 56, 687 (2011). https://doi.org/10.1134/S0036023611050160
G. Shoha, D. Schomburg, and W. N. Lipscomb, Cryst. Struct. Comm. 9, 429 (1980).
I. N. Polyakova, E. A. Malinina, V. V. Drozdova, et al., Crystallogr. Rep. 54, 831 (2009). https://doi.org/10.1134/S1063774509050149
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The study was performed within the framework of the State Assignment of the Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, in the field of fundamental research. The authors thank the Ministry of Science and Higher Education of the Russian Federation.
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The article is based on the abstracts of the XXVIII International Chugaev Conference on Coordination Chemistry, Tuapse, Russia, October 3–8, 2021.
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Goeva, L.V., Zhuchkova, A.F., Malinina, E.A. et al. Radiation-Chemical Transformations of 7-NH3-4-CH3-Coumarin Decahydro-closo-Decaborate as a Potential Inhibitor of Free Radicals. Russ. J. Inorg. Chem. 67, 1144–1150 (2022). https://doi.org/10.1134/S0036023622080149
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DOI: https://doi.org/10.1134/S0036023622080149