Skip to main content
Log in

Fluorine-Containing Tetraarylantimony Carboxylates: Synthesis and Structure

  • COORDINATION COMPOUNDS
  • Published:
Russian Journal of Inorganic Chemistry Aims and scope Submit manuscript

Abstract

Tetraarylantimony carboxylates Ph4SbOC(O)R (R = CF2Br (I), CF2CF2CF3 (II)), (4‑MeC6Н4)4SbOC(O)CF2CF3 (III), and (4-MeC6Н4)4SbOC(O)CF2CF2CF3 (IV) have been synthesized by the reaction between pentaarylantimony Ar5Sb (Ar = Ph, 4-MeC6H4) and fluorine-containing carboxylic acids. Despite an excess amount of carboxylic acid in the reaction mixture, it does not form any solvates Ar4SbOC(O)R ⋅ HOC(O)R with tetraarylantimony carboxylates. X-ray diffraction shows that the Sb atoms in complexes IIV have differently distorted trigonal bipyramidal coordination. Crystals of complexes III and IV contain two types of crystallographically independent molecules. The axial СSbO angles in complexes I, II, III, and IV are 175.32(14)°, 178.87(8)°, 178.56(13)° and 178.33(10)°, 178.16(13)°, and 179.58(15)°, respectively. The Sb–O and Sb–С bond lengths are 2.333(3) and 2.106(4)–2.151(5) Å in I, 2.340(2) and 2.101(2)–2.154(3) Å in II, 2.364(3), 2.411(3), and 2.096(4)–2.159(4) Å in III, and 2.376(3), 2.367(3), and 2.105(4)–2.161(4) Å in IV. The intramolecular Sb⋅⋅⋅O distances with the carbonyl oxygen atom are 3.506(4) Å (I), 3.517(6) Å (II), 3.565(6) Å (III), and 3.527(6) Å (IV), being ~0.2 Å smaller than the sum of Sb and O van der Waals radii. The second carbonyl oxygen atoms in crystals of complexes III and IV do not participate in the coordination with the central metal atom.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1.
Fig. 2.
Fig. 3.
Fig. 4.

Similar content being viewed by others

REFERENCES

  1. 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 

  2. 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 

  3. X. Y. Zhang, L. S. Cui, X. Zhang, et al., J. Mol. Struct. 1134, 742 (2017). https://doi.org/10.1016/j.molstruc.2017.01.039

    Article  CAS  Google Scholar 

  4. A. V. Gushchin, E. V. Grunova, D. V. Moiseev, et al., Izv. Russ. Akad. Nauk, Ser. Khim., No. 6, 1302 (2003).

  5. L. Quan, H.-D. Yin, J.-C. Cui, et al., J. Organomet. Chem. 694, 3708 (2009). https://doi.org/10.1016/j.jorganchem.2009.07.040

    Article  CAS  Google Scholar 

  6. 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 

  7. J.-S. Li, Y.-Q. Ma, J.-R. Cui, et al., Appl. Organomet. Chem. 15, 639 (2001). https://doi.org/10.1002/aoc.200

    Article  CAS  Google Scholar 

  8. Y.-Q. Ma, J.-S. Li, Z.-A. Xuan, et al., J. Organomet. Chem. 620, 235 (2001). https://doi.org/10.1016/S0022-328X(00)00799-3

    Article  CAS  Google Scholar 

  9. H.-D. Yin, L.-Y. Wen, J.-C. Cui, et al., Polyhedron 28, 2919 (2009). https://doi.org/10.1016/j.poly.2009.06.065

    Article  CAS  Google Scholar 

  10. J.-S. Li, R.-C. Liu, X.-B. Chi, et al., Inorg. Chim. Acta 357, 2176 (2004). https://doi.org/10.1016/j.ica.2003.12.012

    Article  CAS  Google Scholar 

  11. V. V. Sharutin and O. K. Sharutina, Russ. J. Inorg. Chem. 62, 905 (2017). https://doi.org/10.1134/S003602361707021X

    Article  CAS  Google Scholar 

  12. V. V. Sharutin, O. K. Sharutina, and V. S. Senchurin, Russ. J. Coord. Chem. 40, 109 (2014). https://doi.org/10.1134/S1070328414020109

    Article  CAS  Google Scholar 

  13. 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 

  14. V. V. Sharutin, O. K. Sharutina, Yu. O. Gubanova, et al., Russ. J. Inorg. Chem. 64, 1138 (2019). https://doi.org/10.1134/S0036023619090195

    Article  CAS  Google Scholar 

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

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

  17. 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 

  18. V. V. Sharutin, V. S. Senchurin, O. K. Sharutina, et al., Zh. Obshch. Khim. 66, 1755 (1996).

    CAS  Google Scholar 

  19. H. Schmidbaur and K. H. Mitschke, Angew. Chem., No. 83, 149 (1971). https://doi.org/10.1002/zaac.19713860204

  20. S. S. Batsanov, Russ. J. Inorg. Chem. 36, 1694 (1991).

    Google Scholar 

  21. V. V. Sharutin, V. S. Senchurin, O. K. Sharutina, et al., Russ. J. Inorg. Chem. 53, 1110 (2008). https://doi.org/10.1134/S0036023608070206

    Article  Google Scholar 

  22. S. P. Bone and D. B. Sowerby, Phosphorus, Sulfur Silicon Relat. Elem. 45, 23 (1989). https://doi.org/10.1080/10426508908046072

    Article  CAS  Google Scholar 

Download references

Funding

This work was financially supported within state task no. 4.6151.2017/8.9.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to A. N. Efremov.

Ethics declarations

The authors declare that they have no conflict of interests.

Additional information

Translated by E. Glushachenkova

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sharutin, V.V., Sharutina, O.K., Efremov, A.N. et al. Fluorine-Containing Tetraarylantimony Carboxylates: Synthesis and Structure. Russ. J. Inorg. Chem. 65, 502–506 (2020). https://doi.org/10.1134/S0036023620040178

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S0036023620040178

Keywords:

Navigation