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Reactions of 5,6,10-{Cl(Ph3P)2Ru}-[5,6,10-(μ-H)3-10-H-exo-nido-7,8-C2B9H8] with bis(diphenylphosphino)methane and 1,2-bis(diphenylphosphino)benzene: specific features

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Abstract

Specific features of reactions of complex 5,6,10-{Cl(Ph3P)2Ru}-[5,6,10-(μ-H)3-10-H-exo-nido-7,8-C2B9H8] (1) with 1,2-bis(diphenylphosphino)benzene (dppbz) and bis(diphenylphosphino)methane (dppm) in acetonitrile in the presence of amines were studied. Novel closo-ruthenacarborane complexes containing the metal in a formal oxidation state of +2 were isolated. It was established that the reaction of 1 with dppbz affords a complex containing a coordinated acetonitrile molecule, whereas the reaction with dppm results in a tris(phosphine) complex with strongly sterically shielded ruthenium center. Reactions of the newly obtained compounds with carbon tetrachloride or hydrogen chloride give corresponding 17-electron complexes containing the metal atom in a formal oxidation state of +3. The reversibility of the RuII → RuIII redox transition in the compounds synthesized was investigated by cyclic voltammetry and the influence of the ligand environment on the values of the corresponding redox potentials was assessed.

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References

  1. S. E. Korolenko, V. V. Avdeeva, E. A. Malinina, N. T. Kuznetsov, Russ. J. Inorg. Chem., 2021, 66, 1350; DOI: https://doi.org/10.1134/S0036023621090047.

    Article  CAS  Google Scholar 

  2. I. B. Sivaev, I. D. Kosenko, Russ. Chem. Bull., 2021, 70, 753; DOI: https://doi.org/10.1007/s11172-021-3146-y.

    Article  CAS  Google Scholar 

  3. V. V. Avdeeva, E. A. Malinina, N. T. Kuznetsov, Russ. J. Inorg. Chem., 2020, 65, 335; DOI: https://doi.org/10.1134/S003602362003002X.

    Article  CAS  Google Scholar 

  4. V. V. Avdeeva, E. A. Malinina, K. Yu. Zhizhin, N. T. Kuznetsov, Russ. J. Inorg. Chem., 2020, 65, 514; DOI: https://doi.org/10.1134/S0036023620040026.

    Article  CAS  Google Scholar 

  5. R. J. Jeans, A. P. Y. Chan, L. E. Riley, J. Taylor, G. M. Rosair, A. J. Welch, I. B. Sivaev, Inorg. Chem., 2019, 58, 11751; DOI: https://doi.org/10.1021/acs.inorgchem.9b01774.

    Article  CAS  PubMed  Google Scholar 

  6. S. V. Timofeev, O. B. Zhidkova, K. Yu. Suponitsky, A. A. Anisimov, I. B. Sivaev, H. Yan, V. I. Bregadze, Inorg. Chim. Acta, 2021, 518, 120243; DOI: https://doi.org/10.1016/j.ica.2020.120243.

    Article  CAS  Google Scholar 

  7. E. V. Balagurova, I. A. Godovikov, I. T. Chizhevsky, Russ. Chem. Bull., 2020, 69, 1189; DOI: https://doi.org/10.1007/s11172-020-2888-2.

    Article  CAS  Google Scholar 

  8. J. J. Jones, A. P. M. Robertson, G. M. Rosair, A. J. Welch, Russ. Chem. Bull., 2020, 69, 1594; DOI: https://doi.org/10.1007/s11172-020-2940-2.

    Article  CAS  Google Scholar 

  9. R. Z. Yuan, P. F. Cui, S. T. Guo, G. X. Jin, Dalton Trans., 2021, 50, 1060, DOI: https://doi.org/10.1039/D0DT03832F.

    Article  CAS  PubMed  Google Scholar 

  10. A. P. Molotkov, M. M. Vinogradov, A. P. Moskovets, O. Chusova, S. V. Timofeev, V. A. Fastovskiy, Yu. V. Nelyubina, A. A. Pavlov, D. A. Chusov, D. A. Loginov, Eur. J. Inorg. Chem., 2017, 38–39, 4635; DOI: https://doi.org/10.1002/ejic.201700498.

    Article  Google Scholar 

  11. I. D. Grishin, N. A. Knyazeva, A. M. Penkal’, Russ. Chem. Bull., 2020, 69, 1520; DOI: https://doi.org/10.1007/s11172-020-2931-3.

    Article  CAS  Google Scholar 

  12. A. P. Molotkov, S. V. Timofeev, D. A. Loginov, Russ. Chem. Bull., 2021, 70, 1922; DOI: https://doi.org/10.1007/s11172-021-3297-x.

    Article  CAS  Google Scholar 

  13. S. Dworakowska, F. Lorandi, A. Gorczynski, K. Matyjaszewski, Adv. Sci., 2022, 9, 2106076; DOI: https://doi.org/10.1002/advs.202106076.

    Article  CAS  Google Scholar 

  14. I. D. Grishin, Polym. Sci., Ser. C, 2022, 64, 82; DOI: https://doi.org/10.1134/S1811238222700035.

    Article  CAS  Google Scholar 

  15. A. M. Zimina, N. A. Knyazeva, E. V. Balagurova, F. M. Dolgushin, N. V. Somov, D. L. Vorozhtsov, Yu. B. Malysheva, I. D. Grishin, J. Organomet. Chem., 2021, 946–947, 121908; DOI: https://doi.org/10.1016/j.jorganchem.2021.121908.

    Article  Google Scholar 

  16. I. D. Grishin, K. S. Agafonova, A. Yu. Kostyukovich, D. I. D’yachihin, I. A. Godovikov, F. M. Dolgushin, D. F. Grishin, I. T. Chizhevsky, Russ. Chem. Bull., 2016, 65, 1574; DOI: https://doi.org/10.1007/s11172-016-1484-y.

    Article  CAS  Google Scholar 

  17. A. A. Kaltenberg, A. M. Penkal’, N. V. Somov, I. D. Grishin, Russ. Chem. Bull., 2019, 68, 770; DOI: https://doi.org/10.1007/s11172-019-2484-5.

    Article  CAS  Google Scholar 

  18. A. A. Kaltenberg, N. V. Somov, Yu. B. Malysheva, N. A. Knyazeva, A. V. Piskunov, I. D. Grishin, J. Organomet. Chem., 2020, 917; DOI: https://doi.org/10.1016/j.jorganchem.2020.121291.

  19. I. T. Chizhevsky, I. A. Lobanova, P. V. Petrovskii, V. I. Bregadze, F. M. Dolgushin, A. I. Yanovsky, Yu. T. Struchkov, A. L. Chistyakov, I. V. Stankevich, C. B. Knobler, M. F. Hawthorne, Organometallics, 1999, 18, 726; DOI: https://doi.org/10.1021/om9806592.

    Article  CAS  Google Scholar 

  20. W. K. Wong, K. K. Lai, M. S. Tse, M. Ch. Tse, J. X. Gao, W. T. Wong, S. Chan, Polyhedron, 1994, 13, 2751; DOI: https://doi.org/10.1016/S0277-5387(00)83433-6.

    Article  CAS  Google Scholar 

  21. J. T. Mague, M. S. Balakrishna, Polyhedron, 1996, 15, 4259; DOI: https://doi.org/10.1016/0277-5387(96)00169-6.

    Article  CAS  Google Scholar 

  22. D. N. Cheredilin, F. M. Dolgushin, I. D. Grishin, E. V. Kolyakina, A. S. Nikiforov, S. P. Solodovnikov, M. M. Il’in, V. A. Davankov, I. T. Chizhevsky, D. F. Grishin, Russ. Chem. Bull., 2006, 55, 1163; DOI: https://doi.org/10.1007/s11172-006-0394-9.

    Article  CAS  Google Scholar 

  23. A. Flores-Figuero, O. Kaufhol, A. Hepp, R. Frohlich, F. E. Hahn, Organometallics, 2009, 28, 6362; DOI: https://doi.org/10.1021/om900703q.

    Article  Google Scholar 

  24. I. D. Grishin, K. S. Agafonova, A. P. Tyurin, D. I. D’yachihin, I. T. Chizhevsky, D. F. Grishin, Russ. Chem. Bull., 2014, 63, 945; DOI: https://doi.org/10.1007/s11172-014-0532-8.

    Article  CAS  Google Scholar 

  25. R. C. Clark, J. S. Reid, Acta Crystallogr., 1995, 51, 887; DOI: https://doi.org/10.1107/S0108767395007367.

    Article  Google Scholar 

  26. I. T. Chizhevsky, I. A. Lobanova, V. I. Bregadze, P. V. Petrovskii, V. A. Antonovich, A. V. Polyakov, A. I. Yanovskii, Yu. T. Struchkov, Mendeleev Commun., 1991, 1, 47; DOI: https://doi.org/10.1070/MC1991v001n02ABEH000027.

    Article  Google Scholar 

  27. G. M. Sheldrick, Acta Crystallogr., Sect. A, 2015, 71, 3; DOI: https://doi.org/10.1107/S2053273314026370.

    Article  Google Scholar 

  28. L. J. Farrugia, J. Appl. Crystallogr., 1999, 32, 837; DOI: https://doi.org/10.1107/S0021889899006020.

    Article  CAS  Google Scholar 

  29. M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, J. A. Montgomery Jr., T. Vreven, K. N. Kudin, J. C. Burant, J. M. Millam, S. S. Iyengar, J. Tomasi, V. Barone, B. Mennucci, M. Cossi, G. Scalmani, N. Rega, G. A. Petersson, H. Nakatsuji, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, M. Klene, X. Li, J. E. Knox, H. P. Hratchian, 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, P. Y. Ayala, K. Morokuma, G. A. Voth, P. Salvador, J. J. Dannenberg, V. G. Zakrzewski, S. Dapprich, A. D. Daniels, M. C. Strain, O. Farkas, D. K. Malick, A. D. Rabuck, K. Raghavachari, J. B. Foresman, J. V. Ortiz, Q. Cui, A. G. Baboul, S. Clifford, J. Cioslowski, B. B. Stefanov, G. Liu, A. Liashenko, P. Piskorz, I. Komaromi, R. L. Martin, D. J. Fox, T. Keith, M. A. Al-Laham, C. Y. Peng, A. Nanayakkara, M. Challacombe, P. M. W. Gill, B. Johnson, W. Chen, M. W. Wong, C. Gonzalez, J. A. Pople, Gaussian 03, Revision E.01, Gaussian, Inc., Wallingford, CT, 2004.

    Google Scholar 

  30. I. D. Grishin, I. T. Chizhevsky, J. Organomet. Chem., 2014, 760, 24; DOI: https://doi.org/10.1016/j.jorganchem.2014.01.016.

    Article  CAS  Google Scholar 

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Correspondence to I. D. Grishin.

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Dedicated to Academician of the Russian Academy of Sciences I. P. Beletskaya on the occasion of her anniversary.

This work was financially supported the Russian Federation Presidential Grant to young scientists–Doctors of Science (Project No. MD-1474.2022.1.3).

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, Vol. 72, No. 4, pp. 912–924, April, 2023.

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Kaltenberg, A.A., Zimina, A.M., Bashilova, A.D. et al. Reactions of 5,6,10-{Cl(Ph3P)2Ru}-[5,6,10-(μ-H)3-10-H-exo-nido-7,8-C2B9H8] with bis(diphenylphosphino)methane and 1,2-bis(diphenylphosphino)benzene: specific features. Russ Chem Bull 72, 912–924 (2023). https://doi.org/10.1007/s11172-023-3854-9

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  • DOI: https://doi.org/10.1007/s11172-023-3854-9

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