Skip to main content
Log in

Reaction of Triarylantimony Dibromides Ar3SbBr2 with Sodium Salts (X = NO3, NCS, F)

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

Abstract

Triarylantimony dibromides reacted with sodium nitrate, thiocyanate, and fluoride in aqueous acetone at room temperature to give bridged dinuclear antimony compounds [(4-MeC6H4)3SbONO2]2O, (Ph3SbNCS)2O, [(3-MeC6H4)3SbNCS]2O, and [(4-MeC6H4)3SbNCS]2O and mononuclear derivatives (2-MeC6H4)3Sb(NCS)2 and (3-FC6H4)3SbF2. The antimony atoms in these compounds have a distorted trigonal-bipyramidal configuration with electronegative atoms in the axial positions.

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

Similar content being viewed by others

REFERENCES

  1. Kocheshkov, K.A., Skoldinov, A.P., and Zemlyanskii, N.N., Metody elementoorganicheskoi khimii. Sur’ma, vismut (Methods of Organoelement Chemistry. Antimony, Bismuth), Moscow: Nauka, 1976.

  2. Sharutin, V.V., Poddel’skiy, A.I., and Sharutina, O.K., Russ. J. Coord. Chem., 2020, vol. 46, no. 10, p. 663. https://doi.org/10.31857/S0132344X20100011

    Article  CAS  Google Scholar 

  3. Chekhlov, A.N., Dokl. Akad. Nauk SSSR, 1993, vol. 328, no. 2, p. 205.

    CAS  Google Scholar 

  4. Sharutin, V.V., Senchurin, V.S., Sharutina, O.K., and Akulova, E.V., Russ. J. Gen. Chem., 2008, vol. 78, no. 12, p. 2344. https://doi.org/10.1134/S1070363208120098

    Article  CAS  Google Scholar 

  5. Sen, S., Ke, I.S., and Gabbai, F.P., J. Inorg. Chem., 2016, vol. 55, no. 18, p. 9162. https://doi.org/10.1021/acs.inorgchem.6b01290

    Article  CAS  Google Scholar 

  6. Jones, J.S., Wade, C.R., and Gabbai, F.P., Organometallics, 2015, vol. 34, no. 11, p. 2647. https://doi.org/10.1021/om501291g

    Article  CAS  Google Scholar 

  7. Otero, A. and Royo, P., J. Organomet. Chem., 1978, vol. 154, no. 1, p. 13. https://doi.org/10.1016/S0022-328X(00)82787-4

    Article  CAS  Google Scholar 

  8. Tolman, C.A., J. Am. Chem. Soc., 1970, vol. 92, no. 10, p. 2956. https://doi.org/10.1021/ja00713a007

    Article  CAS  Google Scholar 

  9. Zakharov, L.N., Domrachev, G.A., and Struchkov, Yu.T., J. Struct. Chem., 1983, vol. 24, no. 3, p. 392. https://doi.org/10.1007/BF00747800

    Article  Google Scholar 

  10. Vasil’ev, A.V., Grinenko, E.V., Shchukin, A.O., and Fedulina, T.G., Infrakrasnaya spektroskopiya organicheskikh i prirodnykh soedinenii (IR Spectroscopy of Organic and Natural Compounds), St. Petersburg: Sankt-Peterb. Gos. Lesotekh. Akad,, 2007.

  11. Tarasevich, B.N., IK spektry osnovnykh klassov organicheskikh soedinenii (IR Spectra of Main Classes of Organic Compounds), Moscow: Mosk. Gos. Univ., 2012.

  12. Sharutin, V.V., Sharutina, O.K., Molokova, O.V., Pakusina, A.P., Bondar’, E.N., Krivolapov, D.B., Gubaidullin, A.T., and Litvinov, I.A., Russ. J. Gen. Chem., 2001, vol. 71, no. 9, p. 1426. https://doi.org/10.1023/A:1013910120594

    Article  CAS  Google Scholar 

  13. Grigsby, E.W.J., Hart, R.D., Raston, C.L., Skelton, B.W., and White, A.H., Aust. J. Chem., 1997, vol. 50, no. 6, p. 675. https://doi.org/10.1071/C96042

    Article  Google Scholar 

  14. Tiekink, E.R.T., J. Organomet. Chem., 1987, vol. 333, no. 2, p. 199. https://doi.org/10.1016/0022-328X(87)85152-5

    Article  CAS  Google Scholar 

  15. Ouchi, A. and Sato, S., Bull. Chem. Soc. Jpn., 1988, vol. 61, no. 5, p. 1806. https://doi.org/10.1246/bcsj.61.1806

    Article  CAS  Google Scholar 

  16. Sharutin, V.V., Sharutina, O.K., Pakusina, A.P., and Smirnova, S.A., Russ. J. Inorg. Chem., 2009, vol. 54, no. 10, p. 1630. https://doi.org/10.1134/S0036023609100209

    Article  Google Scholar 

  17. Gibbons, M.N., Blake, A.J., and Sowerby, D.B., J. Organomet. Chem., 1997, vol. 543, no. 2, p. 217. https://doi.org/10.1016/S0022-328X(97)00208-8

    Article  CAS  Google Scholar 

  18. Balazs, L., Breunig, H.J., Ghesher, I., and Lork, E., J. Organomet. Chem., 2002, vol. 648, no. 1, p. 33. https://doi.org/10.1016/S0022-328X(01)01467-X

    Article  CAS  Google Scholar 

  19. Taylor, M.J., Baker, L.-J., Rickard, C.E.F., and Surman, P.W.J., J. Organomet. Chem., 1995, vol. 498, no. 1, p. S14. https://doi.org/10.1016/0022-328X(95)05555-4

  20. Almond, M.J., Drew, M.G.B., Rice, D.A., Salisbury, G., and Taylor, M.J., J. Organomet. Chem., 1996, vol. 522, no. 2, p. 265. https://doi.org/10.1016/0022-328X(96)06304-8

    Article  CAS  Google Scholar 

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

    CAS  Google Scholar 

  22. Sharutin, V.V., Pakusina, A.P., Sharutina, O.K., Platonova, T.P., Smirnova, S.A., Gerasimenko, A.V., and Pushilin, M.A., Butlerov. Soobshch., Khim. Komp’yut. Model., 2003, no. 1, p. 22.

    Google Scholar 

  23. Forster, G.E., Begley, M.J., and Sowerby, D.B., J. Organomet. Chem., 1996, vol. 507, nos. 1–2, p. 263. https://doi.org/10.1016/0022-328X(95)05775-K

    Article  CAS  Google Scholar 

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

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

  26. Dolomanov, O.V., Bourhis, L.J., Gildea, R.J., Howard, J.A.K., and Puschmann, H., J. Appl. Crystallogr., 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. 9, pp. 1438–1445 https://doi.org/10.31857/S0044460X21090158.

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. & Sopshina, D.M. Reaction of Triarylantimony Dibromides Ar3SbBr2 with Sodium Salts (X = NO3, NCS, F). Russ J Gen Chem 91, 1717–1723 (2021). https://doi.org/10.1134/S1070363221090152

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1070363221090152

Keywords:

Navigation