Mononuclear diphenyltin (IV) complexes with salicylaldimine Schiff bases. Synthesis, structure, electrochemical properties
- Authors: Shangin P.G.1, Klok V.A.1, Krylova I.V.1, Minyaev M.E.1, Tretyakov E.V.1, Syroeshkin M.A.1, Pechennikov V.M.2, Egorov M.P.1, Nikolaevskaya E.N.1
-
Affiliations:
- Zelinsky Institute of Organic Chemistry Russian Academy of Sciences, Moscow, Russia
- First Moscow State Medical University, Moscow, Russia
- Issue: Vol 51, No 9 (2025)
- Pages: 541-555
- Section: Articles
- URL: https://bakhtiniada.ru/0132-344X/article/view/309077
- DOI: https://doi.org/10.31857/S0132344X25090017
- EDN: https://elibrary.ru/lietyl
- ID: 309077
Cite item
Abstract
New mononuclear tin(IV) complexes were obtained by condensation diphenyltin oxide Ph2SnO with a number of Schiff bases containing hydrazone fragment. The structure of the complexes was confirmed by 1H, 13C and 119Sn NMR spectroscopy, as well as by X-ray diffraction analysis (CCDC 2443096 (IV) и 2443095 (V)). The electronic and redox properties of complexes I–V, including the value of the energy gap, were studied using UV spectroscopy and cyclic voltammetry. Electrochemical oxidation and reduction of complexes I, II, IV and V are irreversible and accompanied by further chemical transformations. Unlike them electroreduction of complex III with a pincer ligand leads to the formation of persistent anion-radical particles.
About the authors
P. G. Shangin
Zelinsky Institute of Organic Chemistry Russian Academy of Sciences, Moscow, Russia
Email: en@ioc.ac.ru
V. A. Klok
Zelinsky Institute of Organic Chemistry Russian Academy of Sciences, Moscow, Russia
Email: en@ioc.ac.ru
I. V. Krylova
Zelinsky Institute of Organic Chemistry Russian Academy of Sciences, Moscow, Russia
Email: en@ioc.ac.ru
M. E. Minyaev
Zelinsky Institute of Organic Chemistry Russian Academy of Sciences, Moscow, Russia
Email: en@ioc.ac.ru
E. V. Tretyakov
Zelinsky Institute of Organic Chemistry Russian Academy of Sciences, Moscow, Russia
Email: en@ioc.ac.ru
M. A. Syroeshkin
Zelinsky Institute of Organic Chemistry Russian Academy of Sciences, Moscow, Russia
Email: en@ioc.ac.ru
V. M. Pechennikov
First Moscow State Medical University, Moscow, Russia
Email: en@ioc.ac.ru
M. P. Egorov
Zelinsky Institute of Organic Chemistry Russian Academy of Sciences, Moscow, Russia
Email: en@ioc.ac.ru
E. N. Nikolaevskaya
Zelinsky Institute of Organic Chemistry Russian Academy of Sciences, Moscow, Russia
Author for correspondence.
Email: en@ioc.ac.ru
References
- Schiff H. // Ann. Der Chem. Und Pharm. 1864. V. 131. P. 118. https://doi.org/10.1002/jlac.18641310113
- Raczuk E., Dmochowska B., Samaszko-Fiertek J. et al. // Molecules. 2022. V. 27. P. 787. https://doi.org/10.3390/molecules27030787
- Middya P., Roy D., Chattopadhyay S. // Inorg. Chim. Acta. 2023. V. 548. P. 121377. https://doi.org/10.1016/j.ica.2023.121377
- Cozzi P.G. // Chem. Soc. Rev. 2004. V. 33. P. 410. https://doi.org/10.1039/b307853c
- Fal.lah-Mehrjardi M., Kargar H., Munawar K.S. // Inorg. Chim. Acta. 2024. V. 560. P. 121835. https://doi.org/10.1016/j.ica.2023.121835
- Juyal. V.K., Pathak A., Panwar M. et al. // J. Organomet. Chem. 2023. V. 999. P. 122825. https://doi.org/10.1016/j.jorganchem.2023.122825
- Iacopetta D., Catalano A., Ceramella J. et al. // Molecules. 2025. V. 30. P. 207. https://doi.org/10.3390/molecules30020207
- Jeevadason A.W., Murugavel K.K., Neelakantan M.A. // Renew. Sustain. Energy Rev. 2014. V. 36. P. 220. https://doi.org/10.1016/j.rser.2014.04.060
- Zhang J., Xu L., Wong W.-Y. // Coord. Chem. Rev. 2018. V. 355. P. 180. https://doi.org/10.1016/j.ccr.2017.08.007
- Akbulatov A.F., Akyeva A.Y., Shangin P.G. et al. // Membranes. 2023. V. 13. P. 439. https://doi.org/10.3390/membranes13040439
- Nikolaevskaya E.N., Syroeshkin M.A., Egorov M.P. // Mend. Comm. 2023. V. 33. P. 733. https://doi.org/10.1016/j.mencom.2023.10.001
- Krylova I.V., Proshutinskaya V. Yu., Labutskaya L.D. et al. // J. Organomet. Chem. 2025. V. 1028. P. 123527. https://doi.org/10.1016/j.jorganchem.2025.123527
- Baryshnikova S.V., Bellan E.V., Poddel’sky A.I. et al. // Eur. J. Inorg. Chem. 2016. V. 2016. P. 5230. https://doi.org/10.1002/ejic.201600885
- Baryshnikova S.V., Poddel’sky A.I., Bellan E.V. et al. // Inorg. Chem. 2020. V. 59. P. 6774. https://doi.org/10.1021/acs.inorgchem.9b03757
- Baryshnikova S.V., Bellan E.V., Poddel’sky A.I. et al. // Inorg. Chem. Comm. 2016. V. 69. P. 94. https://doi.org/10.1016/j.inoche.2016.05.003
- Smolyaninov I.V., Burmistrova D.A., Pomortseva N.P. et al. // Russ. J. Coord. Chem. 2023. V. 49. P. 124. https://doi.org/10.1134/S1070328423700446
- Protasenko N.A., Baryshnikova S.V., Cherkasov A.V. et al. // Russ. J. Coord. Chem. 2022. V. 48. P. 478. https://doi.org/10.1134/S1070328422070077
- Krylova I.V., Saverina E.A., Rynin S.S. et al. // Mend. Comm. 2020. V. 30. P. 563. https://doi.org/10.1016/j.mencom.2020.09.003
- Krylova I.V., Labutskaya L.D., Markova M.O. et al. // New J. Chem. 2023. V. 47. P. 11890. https://doi.org/10.1039/d3nj01993d
- Piskunov A.V., Trofimova O.Yu., Fukin G.K. et al. // Dalton Trans. 2012. V. 41. P. 10970. https://doi.org/10.1039/c2dt30656e
- Perrin D.D., Armarego W.L.F., Perrin D.R. Purification of Laboratory Chemicals. Oxford: Pergamon Press, 1988.
- Joseph J., Mary N.L., Sidambaram R. // Synth. React. Inorg. Met. Org. Chem. 2010. V. 40. P. 930. https://doi.org/10.1080/15533174.2010.522661
- Tian F.-F., Jiang F.-L., Han X.-L. et al. // J. Phys. Chem. B. 2010. V. 114. P. 14842. https://doi.org/10.1021/jp105766n
- Das K., Dutta M., Das B. et al. // Adv. Synt. Catal. 2019. V. 361. P. 2965. https://doi.org/10.1002/adsc.201900107
- Lüning U., Baumstark R., Peters K. et al. // Liebigs Ann. Chem. 1990. P. 129. https://doi.org/10.1002/jlac.199019900124
- Bessega T., Chaves O.A., Martins F. M. et al. // Inorg. Chim. Acta. 2019. V. 496. P. 119049. https://doi.org/10.1016/j.ica.2019.119049
- Sukanya P., Reddy C.V., Bhargavi G. // Crystal. Rep. 2020. V. 65. P. 72. https://doi.org/10.1134/s1063774520010253
- CrysAlisPro. Version 1.171.41. Rigaku Oxford Diffraction, 2021.
- Sheldrick G.M. // Acta Cryst. 2015. V. A71(1). P. 3. http://doi.org/10.1107/S2053273314026370
- Sheldrick G.M. // Acta Cryst. 2015. V. C71(1). P. 3. http://doi.org/10.1107/S2053229614024218
- Dolomanov O.V., Bourhis L.J., Gildea R.J. et al. // J. Appl. Cryst. 2009. V. 42(2). P. 229. http://doi.org/10.1107/S0021889808042726
- Cordero B., Gómez V., Platero-Prats A.E. et al. // Dalton Trans. 2008. P. 2832. https://doi.org/10.1039/B801115J
- Piskunov A.V., Aivaz’yan I.A., Fukin G.K. et al. // Inorg. Chem. Commun. 2006. V. 9. P. 612. https://doi.org/10.1016/j.inoche.2006.03.012
- Piskunov A.V., Chegerev M.G., Fukin G.K. et al. // J. Organomet. Chem. 2016, V. 803. P. 51. https://doi.org/10.1016/j.jorganchem.2015.12.012
- Piskunov A., Mescheryakova I., Fukin G. et al. // Chem. Eur. J. 2008. V. 14. P. 10085. https://doi.org/10.1002/chem.200801203
- Piskunov A.V., Mescheryakova I.N., Fukin G.K. et al. // Heteroatom Chem. 2009. V. 20. P. 332. https://doi.org/10.1002/hc.20555
- Maurya R.M., Jayaswal. M.N., Puranik V.G. et al. // Polyhedron. 1997. V. 16. P. 3977. https://doi.org/10.1016/S0277-5387(97)00187-3
Supplementary files
