Synthesis and structural features of Co(II) compounds with 3-arylidene-1-pyrroline derivatives and monocarboxylic acids anions

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Abstract

A series of acetate and trifluoroacetate compounds of cobalt(II) with derivatives of 3-arylidene-1-pyrrolines (X-L; X = Cl, OH) as N-donor ligands was synthesized. Varying the synthesis and crystallization conditions made it possible to obtain coordination compounds of various compositions and structures: a tetranuclear complex based on a cubane fragment {Co4(OH)4}4– — [Co4(OH)4(Cl–L)4(OAc)4] (I), a 1D-polymer complex [Co(H2O)(Cl–L)2(CF3COO)1.167(OAc)0.833]n (II) or a molecular complex [Co(OH–L)2(OAc)2] (III). The synthesized compounds were characterized by X-ray diffraction, IR spectroscopy and CHN analysis. The structure and crystal packing of the obtained complexes were analyzed in detail, the main structure-forming non-covalent interactions in crystals were identified.

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About the authors

Yu. K. Voronina

N. S. Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences

Author for correspondence.
Email: juliavoronina@mail.ru
Russian Federation, Moscow

O. V. Zvereva

N. S. Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences; A. N. Nesmeyanov Institute of Organoelement Compounds of the Russian Academy of Sciences

Email: juliavoronina@mail.ru
Russian Federation, Moscow; Moscow

M. A. Shmelev

N. S. Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences

Email: juliavoronina@mail.ru
Russian Federation, Moscow

E. N. Zorina-Tikhonova

N. S. Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences

Email: juliavoronina@mail.ru
Russian Federation, Moscow

A. V. Rogachev

MIREA — Russian Technological University

Email: juliavoronina@mail.ru
Russian Federation, Moscow

A. A. Sidorov

N. S. Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences

Email: juliavoronina@mail.ru
Russian Federation, Moscow

I. L. Eremenko

N. S. Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences

Email: juliavoronina@mail.ru
Russian Federation, Moscow

References

  1. Keller L.-A., Merkel O., Popp A. // Drug Deliv Transl Res. 2022. V. 12. № 4. P. 735.
  2. Jeong W.Y., Kwon M., Eun Choi H., Su Kim K. // Biomater Res. 2021. V. 25. № 1. P. 24.
  3. Thomford N.E., Senthebane D.A., Rowe A. et al. // Int. J. Mol. Sci. 2018. V. 19. № 6. Р. 1578.
  4. Krasnovskaya O., Naumov A., Guk D. et al. // Int. J. Mol. Sci. 2020. V. 21. № 11. Р. 3965.
  5. Psomas G. // Coord. Chem. Rev. 2020. V. 412. P. 213259.
  6. Ghanghas P., Choudhary A., Kumar D., Poonia K. // Inorg. Chem. Commun. 2021. V. 130. P. 108710.
  7. El-Gammal O.A., Mohamed F.S., Rezk G.N., ElBindary A.A. // J. Mol. Liq. 2021. V. 330. P. 115522.
  8. Pellei M., Del Bello F., Porchia M., Santini C. // Coord. Chem. Rev. 2021. V. 445. P. 214088.
  9. Uvarova M.A., Lutsenko I.A., Shmelev M.A. et al // New. J. Chem. 2024. V. 48. № 2. P. 717.
  10. Shmelev M.A., Chistyakov A.S., Razgonyaeva G.A. et al. // Crystals. 2022. V. 12. № 4. Р. 508.
  11. Leung C.-H., Zhong H.-J., Chan D. S.-H. et al. // Coord. Chem. Rev. 2013. V. 257. № 11‒12. P. 1764.
  12. Ronconi L., Sadler P.J. // Coord. Chem. Rev. 2007. V. 251. № 13‒14. P. 1633.
  13. Liu W., Gust R. // Coord. Chem. Rev. 2016. V. 329. P. 191.
  14. Bazhina E.S., Bovkunova A.A., Shmelev M.A. et al. // Inorg. Chim. Acta. 2023. V. 547. Р. 121359.
  15. Klintworth R., de Koning C.B., Opatz T., Michael J.P. // J. Org. Chem. 2019. V. 84. № 17. P. 11025.
  16. Saraswat P., Jeyabalan G., Hassan M.Z. et al. // Synth. Commun. 2016. P. 1643.
  17. Ahmad Bhat A., Singh I., Tandon N., Tandon R. // Eur. J. Med. Chem. 2023. V. 246. P. 114954.
  18. Fernandes L. de P., Silva J.M.B., Martins D.O.S. et al. // Int. J. Mol. Sci. 2020. V. 21. № 21. P. 8355.
  19. Delehanty J.B., Bongard J.E., Thach D.C. et al. // J. Biol. Chem. 2008. V. 16. № 2. P. 830.
  20. Smolobochkin, A.V., Gazizov, A.S., Melyashova, A.S. et al. // RSC Advances. 2017. V. 7. № 80. P. 50955.
  21. Rizbayeva T.S., Smolobochkin A.V, Gazizov A.S. et al. // J. Org. Chem. 2023. V. 88. P. 11855.
  22. Sheldrick G.M. // Acta Crystallogr. C. 2015. V. 71. P. 3.
  23. Dolomanov O.V., Bourhis L.J., Gildea R.J. et al. // J. Appl. Cryst. 2009. V. 42. P. 339.
  24. Casanova D., Llunell M., Alemany P., Alvarez S. et al. // Chem. Eur. J. 2005. V. 11. P. 1479.
  25. Lee S.Y., Kim N., Lee M.M. et al. // Dalton Trans. 2016. V. 45. P. 1727.
  26. Nguyen A.I., Wang J., Levine D.S. et al. // Chem. Sci. 2017. V. 8. P. 4274.
  27. Zhao H., Bacsa J., Dunbar K.R. // Acta Crystallogr. E. 2004. V. 60. P. m637.
  28. Fomina I.G., Dobrokhotova Zh.V, Aleksandrov G.G. et al. // Russ. Chem. Bull. 2009. V. 58. P. 11.
  29. Newton G.N., Cooper G.J.T., Kögerler P. et al. // J. Am. Chem. Soc. 2008. V. 130. P. 790.
  30. Cooper G.J.T., Newton G.N., Kogerler P. et al. // Angew. Chem. Int. Ed. 2007. V. 46. P. 1340.
  31. Andaloussi Y.H., Sensharma D., Bezrukov A.A et al. // Cryst. Growth. Des. 2023. V. 23. P. 3019. https://doi.org/10.1021/acs.cgd.3c00094
  32. Zvereva O.V., Rizbaeva T.S., Shmelev M.A. et al. // J. Struct. Chem. 2024. V. 65. № 7. P. 1439.

Supplementary files

Supplementary Files
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2. Fig. 1. Structure of the molecule (a) and fragment of the crystal packing (b) of compound I.

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3. Fig. 2. Structure of the monomer fragment (a), fragment of the polymer chain (b) and fragment of the crystal packing (c) of coordination polymer II.

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4. Fig. 3. Structure of the complex (a) and a fragment of the crystal packing (b) of complex III.

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5. Scheme 1. Synthesis of complexes I–III.

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