Abstract
The reaction of oxygen with the nitrosyl iron complex [Fe(SC(NH2)2)2(NO)2]+ (complex 1) was studied. According to the results obtained, three main directions of transformation of complex 1 under aerobic conditions can be distinguished: (i) reversible binding of complex 1 with oxygen leading to a sharp decrease in the oxygen concentration at the initial moment, (ii) irreversible spontaneous transformation of complex 1 without participation of oxygen accompanied by the elimination of thio ligands and NO groups, and (iii) irreversible reaction of complex 1 with oxygen to form oxygen coordination products (at the iron atom, Fe-N bond, and two N atoms of nitrosyl ligands), which then reversibly transform into oxidation products. The latter process is accompanied by an increase in the absorbance in the experimental UV spectra and the formation of nitrates and nitrites in the reaction system.
Article PDF
Similar content being viewed by others
Avoid common mistakes on your manuscript.
References
N. S. Bryan, D. J. Lefer, Mol. Pharmacol., 2019, 96, 109; DOI: https://doi.org/10.1124/mol.118.113910.
L. J. Ignarro, J. Physiol. Pharmacol., 2002, 53, 503.
S. Korde Choudhari, M. Chaudhary, S. Bagde, A. R. Gadbail, V. Joshi, World J. Surg. Oncol., 2013, 11, 118; DOI: https://doi.org/10.1186/1477-7819-11-118.
N. Lehnert, E. Kim, H. T. Dong, J. B. Harland, A. P. Hunt, E. C. Manickas, K. M. Oakley, J. Pham, G. C. Reed, V. S. Alfaro, Chem. Rev., 2021, 121, 14682; DOI: https://doi.org/10.1021/acs.chemrev.1c00253.
C.-Y. Chiang, M. Y. Darensbourg, J. Biol. Inorg. Chem., 2006, 11, 359; DOI: https://doi.org/10.1007/s00775-006-0084-y.
A. F. Vanin, S. V. Kiladze, L. N. Kubrina, Biofizika [Biophysics], 1975, 20, 1068–1072 (in Russian).
T. Ueno, T. Yoshimura, Jpn J. Pharmacol., 2000, 82, 95; DOI: https://doi.org/10.1254/jjp.82.95.
H. Lewandowska, M. Kalinowska, K. Brzóska, K. Wójciuk, G. Wójciuk, M. Kruszewski, Dalton Trans., 2011, 40, 8273; DOI: https://doi.org/10.1039/C0DT01244K.
N. I. Neshev, E. M. Sokolova, G. I. Kozub, T. A. Kondrat’eva, N. A. Sanina, Russ. Chem. Bull., 2020, 69, 1987; DOI: https://doi.org/10.1007/s11172-020-2989-y.
N. S. Emel’yanova, L. G. Gutsev, O. V. Pokidova, A. F. Shestakov, N. A. Sanina, S. M. Aldoshin, Inorg. Chim. Acta, 2021, 522, 120361; DOI: https://doi.org/10.1016/j.ica.2021.120361.
A. Banerjee, S. Sen, A. Paul, Chem. — A Eur. J., 2018, 24, 3330; DOI: https://doi.org/10.1002/chem.201705726.
O. V. Pokidova, N. S. Emel’yanova, B. L. Psikha, A. V. Kulikov, B. A. Tretyakov, A. I. Kotel’nikov, N. A. Sanina, S. M. Aldoshin, Inorg. Chim. Acta, 2020, 502, 119369; DOI: https://doi.org/10.1016/j.ica.2019.119369.
H. L. K. Wah, M. Postel, F. Tomi, Inorg. Chem., 1989, 28, 233; DOI: https://doi.org/10.1021/ic00301a015.
N. A. Sanina, N. S. Emel’yanova, A. N. Chekhlov, A. F. Shestakov, I. V. Sulimenkov, S. M. Aldoshin, Russ. Chem. Bull., 2010, 59, 1126; DOI: https://doi.org/10.1007/s11172-010-0215-z.
N. A. Sanina, S. M. Aldoshin, N. Y. Shmatko, D. V. Korchagin, G. V. Shilov, N. S. Ovanesyan, A. V. Kulikov, Inorg. Chem. Commun., 2014, 49, 44; DOI: https://doi.org/10.1016/j.inoche.2014.09.016.
N. A. Sanina, N. Y. Shmatko, D. V. Korchagin, G. V. Shilov, A. A. Terent’ev, T. S. Stupina, A. A. Balakina, N. V. Komleva, N. S. Ovanesyan, A. V. Kulikov, S. M. Aldoshin, J. Coord. Chem., 2016, 69, 812; DOI: https://doi.org/10.1080/00958972.2016.1142536.
N. Sanina, N. Shmatko, T. Stupina, A. Balakina, A. Terent’ev, Molecules, 2017, 22, 1426; DOI: https://doi.org/10.3390/molecules22091426.
V. M. Ignat’ev, N. S. Emel’yanova, N. A. Sanina, Russ. Chem. Bull., 2020, 69, 2265; DOI: https://doi.org/10.1007/s11172-020-3045-7.
N. A. Sanina, L. A. Syrtsova, N. I. Shkondina, T. N. Rudneva, E. S. Malkova, T. A. Bazanov, A. I. Kotel’nikov, S. M. Aldoshin, Nitric Oxide, 2007, 16, 181; DOI: https://doi.org/10.1016/j.niox.2006.10.005.
G. Geraci, L. J. Parkhurst, Q. H. Gibson, J. Biol. Chem., 1969, 244, 4664; DOI: https://doi.org/10.1016/S0021-9258(18)93675-6.
M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, G. Scalmani, V. Barone, B. Mennucci, G. A. Petersson, H. Nakatsuji, M. Caricato, X. Li, H. P. Hratchian, F. Izmaylov, J. Bloino, G. Zheng, J. L. Sonnenberg, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven, J. A. Montgomery, Jr., J. E. Peralta, F. Ogliaro, M. Bearpark, J. J. Heyd, E. Brothers, K. N. Kudin, V. N. Staroverov, T. Keith, R. Kobayashi, J. Normand, K. Raghavachari, A. Rendell, J. C. Burant, S. S. Iyengar, J. Tomasi, M. Cossi, N. Rega, J. M. Millam, M. Klene, J. E. Knox, J. B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R. E. Stratmann, O. Yazyev, A. J. Austin, R. Cammi, C. Pomelli, J. W. Ochterski, R. L. Martin, K. Morokuma, V. G. Zakrzewski, G. A. Voth, P. Salvador, J. J. Dannenberg, S. Dapprich, A. D. Daniels, O. Farkas, J. B. Foresman, J. V. Ortiz, J. Cioslowski, D. J. Fox, GAUSSIAN 09, Revision D.01, Gaussian, Inc., Wallingford (CT), 2013.
O. V. Pokidova, N. S. Emel’yanova, A. Y. Kormukhina, V. O. Novikova, A. V. Kulikov, A. I. Kotelnikov, N. A. Sanina, Dalton Trans., 2022, 51, 6473; DOI: https://doi.org/10.1039/d2dt00291d.
O. V. Pokidova, A. Y. Kormukhina, A. I. Kotelnikov, T. N. Rudneva, K. A. Lyssenko, N. A. Sanina, Inorg. Chim. Acta, 2021, 524, 120453; DOI: https://doi.org/10.1016/j.ica.2021.120453.
A. F. Vanin, A. P. Poltorakov, V. D. Mikoyan, L. N. Kubrina, D. S. Burbaev, Nitric Oxide, 2010, 23, 136; DOI: https://doi.org/10.1016/j.niox.2010.05.285.
O. V. Pokidova, N. S. Emel’yanova, B. L. Psikha, N. A. Sanina, A. V. Kulikov, A. I. Kotel’nikov, S. M. Aldoshin, J. Mol. Struct., 2019, 1192, 264; DOI: https://doi.org/10.1016/j.molstruc.2019.05.005.
L. J. Ignarro, J. M. Fukuto, J. M. Griscavage, N. E. Rogers, R. E. Byrns, Proc. Natl. Acad. Sci., 1993, 90, 8103; DOI: https://doi.org/10.1073/pnas.90.17.8103.
M. N. Möller, N. Rios, M. Trujillo, R. Radi, A. Denicola, B. Alvarez, J. Biol. Chem., 2019, 294, 14776; DOI: https://doi.org/10.1074/jbc.REV119.006136.
C. Helms, D. B. Kim-Shapiro, Free Radic. Biol. Med., 2013, 61, 464; DOI: https://doi.org/10.1016/j.freeradbiomed.2013.04.028.
E. Antonini, M. Brunori, in North-Holland Research Monographs. Frontiers of Biology, Eds E. L. Tatum, A. Neuberger, North-Holland Publishing Company, Amsterdam-London, 1971, Vol. 21, p. 276.
N. S. Emel’yanova, N. Yu. Shmatko, N. A. Sanina, S. M. Aldoshin, Russ. Chem. Bull., 2017, 66, 1842; DOI: https://doi.org/10.1007/s11172-017-1955-9.
D. Ampadu Boateng, M. D. Word, L. G. Gutsev, P. Jena, K. M. Tibbetts, J. Phys. Chem. A, 2019, 123, 1140; DOI: https://doi.org/10.1021/acs.jpca.8b11723.
Author information
Authors and Affiliations
Corresponding author
Additional information
Dedicated to Academician of the Russian Academy of Sciences V. A. Tartakovsky on the occasion of his 90th birthday.
This work was carried out in terms of state assignment (state registration Nos AAAA-A19-119071890015-6 and AAAA-A19-119111390022-2).
No human or animal subjects were used in this research.
The authors declare no competing interests.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1604–1613, August, 2022.
Rights and permissions
About this article
Cite this article
Pokidova, O.V., Psikha, B.L., Emel’yanova, N.S. et al. Features of the decomposition of the nitrosyl iron complex with thiourea ligands under aerobic conditions: experiment and kinetic and quantum chemical modeling. Russ Chem Bull 71, 1604–1613 (2022). https://doi.org/10.1007/s11172-022-3569-0
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11172-022-3569-0