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.
Similar content being viewed by others
REFERENCES
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.
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
Chekhlov, A.N., Dokl. Akad. Nauk SSSR, 1993, vol. 328, no. 2, p. 205.
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
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
Jones, J.S., Wade, C.R., and Gabbai, F.P., Organometallics, 2015, vol. 34, no. 11, p. 2647. https://doi.org/10.1021/om501291g
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
Tolman, C.A., J. Am. Chem. Soc., 1970, vol. 92, no. 10, p. 2956. https://doi.org/10.1021/ja00713a007
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
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.
Tarasevich, B.N., IK spektry osnovnykh klassov organicheskikh soedinenii (IR Spectra of Main Classes of Organic Compounds), Moscow: Mosk. Gos. Univ., 2012.
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
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
Tiekink, E.R.T., J. Organomet. Chem., 1987, vol. 333, no. 2, p. 199. https://doi.org/10.1016/0022-328X(87)85152-5
Ouchi, A. and Sato, S., Bull. Chem. Soc. Jpn., 1988, vol. 61, no. 5, p. 1806. https://doi.org/10.1246/bcsj.61.1806
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
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
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
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
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
Batsanov, S.S., Zh. Neorg. Khim., 1991, vol. 36, no. 12, p. 3015.
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.
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
SMART and SAINT-Plus. Version 5.0. Data Collection and Processing Software for the SMART System, Madison WI, USA: Bruker AXS, 1998.
SHELXTL/PC. Version 5.10. An Integrated System for Solving, Refining and Displaying Crystal Structures from Diffraction Data, Madison WI, USA: Bruker AXS, 1998.
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
Author information
Authors and Affiliations
Corresponding author
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
About this article
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
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1134/S1070363221090152