Skip to main content
Log in

Synthesis and Structure of Triphenylbismuth Dicarboxylates Ph3Bi[OC(O)R]2 (R = CH2C6H4F-3, C6H3F2-2,3, C6HF4-2,3,4,5)

  • Published:
Russian Journal of General Chemistry Aims and scope Submit manuscript

Abstract

Bismuth compounds Ph3Bi[OC(O)R]2 (R = CH2C6H4F-3, C6H3F2-2,3, C6HF4-2,3,4,5) were synthesized by the reaction of triphenylbismuth with a carboxylic acid and tert-butyl hydroperoxide (1 : 2 : 1 mol.) in diethyl ether. Structural features of these compounds were determined by the single crystal X-ray analysis method. Bismuth atoms in triphenylbismuth dicarboxylates have distorted trigonal-bipyramidal coordination with oxygen atoms in axial positions. The presence of intramolecular contacts Bi···O(=C) [2.833(8)–3.136(9) Å] causes an increase in one of CBiC bond angles to 151.07(15)°, 142.0(3)°, 138.53(14)°, respectively, due to a decrease in the other two angles.

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.

Scheme
Fig. 1.
Fig. 2.

Similar content being viewed by others

REFERENCES

  1. Zhang, X.-Y., Wu, R.-X., Bi, C.-F., Zhang, X., and Fan, Y.-H., Inorg. Chim. Acta, 2018, vol. 483, p. 129. https://doi.org/10.1016/j.ica.2018.07.02

    Article  CAS  Google Scholar 

  2. Oliveira, L.G.D., Silva, M.M., de Paula, F.C.S., Pereira-Maia, E.C., Donnici, C.L., de Simone, C.A., Frezard, F., da Silva Junior, E.N., and Demicheli, C., Molecules, 2011, vol. 16, p. 10314. https://doi.org/10.3390/molecules161210314

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Duffin, R.N., Blair, V.L., Kedzierski, L., and Andrews, P.C., Dalton Trans., 2018, vol. 47, p. 971. https://doi.org/10.1039/c7dt04171c

    Article  CAS  PubMed  Google Scholar 

  4. Duffin, R.N., Blair, V.L., Kedzierski, L., and Andrews, P.C., J. Inorg. Biochem., 2018, vol. 189, p. 151. https://doi.org/10.1016/j.jinorgbio.2018.08.015

    Article  CAS  PubMed  Google Scholar 

  5. Ong, Y.C., Blair, V.L., Kedzierski, L., and Andrews, P.C., Dalton Trans., 2014, vol. 43, p. 12904. https://doi.org/10.1039/c4dt00957f

    Article  CAS  PubMed  Google Scholar 

  6. Ong, Y.C., Blair, V.L., Kedzierski, L., Tuck, K.L., and Andrews, P.C., Dalton Trans., 2015, vol. 44, p. 18215. https://doi.org/10.1039/c5dt03335g

    Article  CAS  PubMed  Google Scholar 

  7. Andleeb, S., Imtiaz-ud-Din, Rauf, K.M., Azam, S.S, and Haq, I.-u., Appl. Organomet. Chem., 2019, vol. 33, p. e5061. https://doi.org/10.1002/aoc.5061

  8. Dodonov, V.A., Gushchin, A.V., and Brilkina, T.G., Zh. Obshch. Khim., 1985, vol. 55, no. 1, p. 73.

    CAS  Google Scholar 

  9. Verkhovykh, V.A., Kalistratova, O.S., Grishina, A.I., Artemova, V.G, and Gushchin, F.V., Bull. South Ural State Univ., Ser. Chem., 2015, vol. 7, no. 3, p. 61.

    Google Scholar 

  10. Gushchin, F.V., Kalistratova, O.S., Maleeva, A.I., and Kuropatov, V.A., Bull. South Ural State Univ., Ser. Chem., 2016, vol. 8, no. 1, p. 51. https://doi.org/10.14529/chem160108

    Article  Google Scholar 

  11. Gushchin, A.V., Shashkin, D.V., Prytkova, L.K., Somov, N.V., Baranov, E.V., Shavyrin, A.S., and Rykalin, V.I., Russ. J. Gen. Chem., 2011, vol. 81, no. 3, p. 493. https://doi.org/10.1134/S107036321103008X

    Article  CAS  Google Scholar 

  12. Gusakovskaya, A.A., Kalistratova, O.S., Andreev, P.V., Chuprunov, E.V., Kalistratova, O.S., and Gusakovskaya, A.A., Kristallogr., 2018, vol. 63, no. 2, p. 203. https://doi.org/10.7868/S0023476118020066

    Article  Google Scholar 

  13. Sharutin, V.V. and Mosunova, T.V., Vestn. YuRGU, Ser. Khim., 2020, vol. 12, no. 3, p. 7. https://doi.org/10.14529/chem200301

    Article  Google Scholar 

  14. Sencurin, V.S., Vestn. YuRGU, Ser. Khim., 2020, vol. 12, no. 4, p. 72. https://doi.org/10.14529/chem200404

    Article  Google Scholar 

  15. Sharutin, V.V. and Sharutina, O.K., Russ. J. Gen. Chem., 2021, vol. 91, no. 4, p. 598. https://doi.org/10.31857/S0044460X21040156

    Article  Google Scholar 

  16. Sharutin, V.V., Poddel’sky, A.I., and Sharutina, O.K., Russ. J. Coord. Chem., 2020, vol. 46, no. 10, p. 663. https://doi.org/10.1134/S1070328420100012

    Article  CAS  Google Scholar 

  17. Da Silva, J.G., Berbet, F.M., Da Silva, S.M., Rodrigues, B.L., Beraldo, H., Melo, M.N., Frézard, F., and Demicheli, C., Molecules, 2014, vol. 19, p. 6009. https://doi.org/10.3390/molecules19056009

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Batsanov, S.S., Zh. Neorg. Khim., 1991, vol. 36, no. 12, p. 3015.

    CAS  Google Scholar 

  19. SMART and SAINT-Plus. Version 5.0. Data Collection and Processing Software for the SMART System. Madison (WI, USA): Bruker AXS Inc., 1998.

  20. SHELXTL/PC. Version 5.10. An Integrated System for Solving, Refining and Displaying Crystal Structures from Diffraction Data. Bruker AXS Inc., Madison, USA, 1998.

  21. Dolomanov, O.V., Bourhis, L.J., Gildea, R.J., Howard, K., and Puschmann, H., J. Appl. Cryst., 2009, vol. 42, p. 339. https://doi.org/10.1107/S0021889808042726

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to V. V. Sharutin.

Ethics declarations

No conflict of interest was declared by the authors.

Additional information

Translated from Zhurnal Obshchei Khimii, 2021, Vol. 91, No. 5, pp. 758–762 https://doi.org/10.31857/S0044460X21050139.

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. & Koscheeva, L.V. Synthesis and Structure of Triphenylbismuth Dicarboxylates Ph3Bi[OC(O)R]2 (R = CH2C6H4F-3, C6H3F2-2,3, C6HF4-2,3,4,5). Russ J Gen Chem 91, 840–843 (2021). https://doi.org/10.1134/S1070363221050133

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1070363221050133

Keywords:

Navigation