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Tris(fluorophenyl)antimony Dicarboxylates (4-FC6H4)3Sb[OC(O)R]2 (R = CH2Cl, C6F5, C6F4H-2, CF2CF3, CF2CF2CF3) and (3-FC6H4)3Sb[OC(O)C6F4H-2]2: Synthesis and Structure

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Abstract

Tris(4-fluorophenyl)antimony dicarboxylates (4-FC6H4)3Sb[OC(O)R]2, where R = CH2Cl (I), C6F5 (II), C6F4H-2 (III), CF2CF3 (IV), CF2CF2CF3 (V), and (3-FC6H4)3Sb[OC(O)C6F4H-2]2 (VI) have been synthesized by the reaction of tris(fluorophenyl)antimony with chloroacetic, pentafluorobenzoic, tetrafluorobenzoic, pentafluoropropionic, and heptafluorobutyric acids in the presence of tert-butyl hydroperoxide. According to X-ray diffraction data, the Sb atoms in complexes IVI have trigonal bipyramidal coordination. The axial OSbO angles are 177.68(9)°, 177.44(12)°, 176.59(7)°, 179.59(6)°, 179.63(9)°, and 175.72(12)°. The Sb–O and Sb–С bond lengths are 2.125(2), 2.136(2) and 2.101(3)–2.112(3) Å in I, 2.118(3), 2.119(3) and 2.094(5)–2.109(5) Å in II, 2.120(2), 2.137(2) and 2.114(2)–2.122(3) Å in III, 2.133(2), 2.153(2) and 2.086(2)–2.098(2) Å in IV, 2.146(3), 2.164(3) and 2.090(4)–2.093(4) Å in V, 2.123(3), 2.140(3) and 2.109(5)–2.122(5) Å in VI.

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REFERENCES

  1. M. I. Ali, M. K. Rauf, A. Badshah, et al., Dalton Trans. 42, 16733 (2013). https://doi.org/10.1039/C3DT51382C

    Article  CAS  PubMed  Google Scholar 

  2. R. N. Duffin, V. L. Blair, L. Kedzierski, et al., Dalton Trans. 47, 971 (2018). https://doi.org/10.1039/c7dt04171c

    Article  CAS  PubMed  Google Scholar 

  3. L. Yu, Y.-Q. Ma, R.-C. Liu, et al., Polyhedron 23, 823 (2004). https://doi.org/10.1016/j.poly.2003.12.002

    Article  CAS  Google Scholar 

  4. S. K. Hadjikakou, I. I. Ozturk, C. N. Banti, et al., J. Inorg. Biochem. 153, 293 (2015). https://doi.org/10.1016/j.jinorgbio.2015.06.006

    Article  CAS  PubMed  Google Scholar 

  5. A. Islam, B. L. Rodrigues, I. M. Marzano, et al., Eur. J. Med. Chem. 109, 254 (2016). https://doi.org/10.1016/j.ejmech.2016.01.003

    Article  CAS  PubMed  Google Scholar 

  6. N. M. Polychronis, C. N. Banti, C. P. Raptopoulou, et al., Inorg. Chim. Acta 489, 39 (2019). https://doi.org/10.1016/j.ica.2019.02.004

    Article  CAS  Google Scholar 

  7. E. I. Gkaniatsou, C. N. Banti, N. Kourkoumelis, et al., J. Inorg. Biochem. 150, 108 (2015). https://doi.org/10.1016/j.jinorgbio.2015.04.014

    Article  CAS  PubMed  Google Scholar 

  8. T. C. Thepe, R. J. Garascia, M. A. Selvoski, et al., Ohio J. Sci. 77, 134 (1977).

    CAS  Google Scholar 

  9. V. V. Sharutin, O. K. Sharutina, and A. R. Kotlyarov, Russ. J. Inorg. Chem. 60, 465 (2015). https://doi.org/10.1134/S0036023615040221

    Article  CAS  Google Scholar 

  10. V. V. Sharutin, O. K. Sharutina, and V. S. Senchurin, Russ. J. Inorg. Chem. 60, 1093 (2015). https://doi.org/10.1134/S0036023615060145

    Article  CAS  Google Scholar 

  11. V. V. Sharutin and O. K. Sharutina, Russ. Chem. Bull. 66, 707 (2017). https://doi.org/10.1007/s11172-017-1796-6

    Article  CAS  Google Scholar 

  12. V. V. Sharutin and O. K. Sharutina, Russ. J. Gen. Chem. 86, 1902 (2016). https://doi.org/10.1134/S107036321608020X

    Article  CAS  Google Scholar 

  13. L. Yu, Y.-Q. Ma, G.-C. Wang, and J.-S. Li, Heteroat. Chem. 15, 32 (2004). https://doi.org/10.1002/hc.10208

    Article  CAS  Google Scholar 

  14. SMART and SAINT-Plus: Data Collection and Processing Software for the SMART System, Versions 5.0 (Bruker, Madison, WI, USA, 1998).

  15. SHELXTL/PC: An Integrated System for Solving, Refining and Displaying Crystal Structures from Diffraction Data, Versions 5.10 (Bruker, Madison, WI, USA, 1998).

  16. O. V. Dolomanov, L. J. Bourhis, R. J. Gildea, et al., J. Appl. Crystallogr. 42, 339 (2009). https://doi.org/10.1107/S0021889808042726

    Article  CAS  Google Scholar 

  17. V. V. Sharutin and V. S. Senchurin, Named Reactions in Organoelemental Chemistry (YuUrGU Press, Che-lyabinsk, 2011) [in Russian].

  18. B. Kaither and C. Glidewell, et al., J. Organomet. Chem. 419, 283 (1991). https://doi.org/10.1016/0022-328X(91)80241-B

    Article  Google Scholar 

  19. L. Wen, H. Yin, W. Li, et al., Inorg. Chim. Acta 363, 676 (2010). https://doi.org/10.1016/j.ica.2009.11.022

    Article  CAS  Google Scholar 

  20. V. V. Sharutin, V. S. Senchurin, O. K. Sharutina, et al., Vestn. Yuzhn. Ural. Gos. Univ., Ser. Khim. 6 (33), 47 (2011).

    Google Scholar 

  21. L. Saleem, A. A. Altaf, A. Badshah, et al., Inorg. Chim. Acta 474, 148 (2018). https://doi.org/10.1016/j.ica.2018.01.036

    Article  CAS  Google Scholar 

  22. L. Quan, H. Yin, and D. Wang, Acta Crystallogr., Sect. E: Struct. Rep. Online 64, m1503 (2008). https://doi.org/10.1107/S1600536808033783

    Article  CAS  Google Scholar 

  23. M. Hong, H. -D. Yin, W. -K. Li, et al., Inorg. Chem. Commun. 14, 1616 (2011). https://doi.org/10.1016/j.inoche.2011.06.023

    Article  CAS  Google Scholar 

  24. L. Wen, H. Yin, and C. Wang, Acta Crystallogr., Sect. E: Struct. Rep. Online 65, m1442 (2009). https://doi.org/10.1107/S160053680904358X

    Article  CAS  Google Scholar 

  25. A. V. Guschin, O. S. Kalistratova, R. A. Verkhovykh, et al., Vestn. Lobachev. State Univ. Nizh. Nov. 1, 86 (2013).

  26. I. A. Letyanina, A. V. Markin, N. N. Smirnova, et al., J. Therm. Anal. Calorim. 125, 339 (2016). https://doi.org/10.1007/s10973-016-5401-2

    Article  CAS  Google Scholar 

  27. S. Sarwar, T. Iftikhar, M. K. Rauf, et al., Inorg. Chim. Acta 476, 12 (2018). https://doi.org/10.1016/j.ica.2018.02.005

    Article  CAS  Google Scholar 

  28. R. Mushtaq, M. K. Rauf, M. Bond, et al., Appl. Organomet. Chem. 30, 465 (2016). https://doi.org/10.1002/aoc.3456

    Article  CAS  Google Scholar 

  29. G. K. Fukin, M. A. Samsonov, O. S. Kalistratova, et al., Struct. Chem. 27, 357 (2016). https://doi.org/10.1007/s11224-015-0604-x

    Article  CAS  Google Scholar 

  30. M. Hong and Y. Yang, et al., J. Coord. Chem. 68, 2938 (2015). https://doi.org/10.1080/00958972.2015.1060322

    Article  CAS  Google Scholar 

  31. P. V. Andreev, N. V. Somov, O. S. Kalistratova, et al., Acta Crystallogr., Sect. E: Struct. Rep. Online 69, m167 (2013). https://doi.org/10.1107/S1600536813004674

    Article  CAS  Google Scholar 

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Funding

The National South Ural State Research University is grateful to the Ministry of Education and Science of the Russian Federation for financial support (grant no. 4.6151.2017/8.9).

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Correspondence to A. N. Efremov.

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Translated by E. Glushachenkova

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Sharutin, V.V., Sharutina, O.K., Efremov, A.N. et al. Tris(fluorophenyl)antimony Dicarboxylates (4-FC6H4)3Sb[OC(O)R]2 (R = CH2Cl, C6F5, C6F4H-2, CF2CF3, CF2CF2CF3) and (3-FC6H4)3Sb[OC(O)C6F4H-2]2: Synthesis and Structure. Russ. J. Inorg. Chem. 65, 992–998 (2020). https://doi.org/10.1134/S0036023620070190

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