Abstract
The reaction of tris(2-methoxy-5-chlorophenyl)antimony with pentafluoropropionic, heptafluorobutanoic, pentafluorobenzoic, or 2-methoxybenzoic acids in the presence of hydrogen peroxide (1 : 2 : 1 molar ratio) in diethyl ether has afforded tris(2-methoxy-5-chlorophenyl)antimony dicarboxylates (2-MeO-5-ClC6H3)3Sb[OC(O)R]2, R = C2F5, C3F7, C6F5, or C6H4ОMe-2. Structures of the synthesized compounds have been investigated.
Similar content being viewed by others
REFERENCES
Iftikhar, T., Rauf, M.K., Sarwar, S., Badshah, A., Waseem, D., Tahir, M.N., Khan, A., Khan, K.M., and Khan, G.M., J. Organomet. Chem., 2017, vol. 851, p. 89. https://doi.org/10.1016/j.jorganchem.2017.09.002
Mushtaq, R., Rauf, M.K., Bond, M., Badshah, A., Ali, M.I., Nadhman, A., and Yasinzai, M., Appl. Organomet. Chem., 2016, vol. 30, no. 6, p. 465. https://doi.org/10.1002/aoc.3456
Mushtaq, R., Rauf, M.K., Bolte, M., Nadhman, A., Badshah, A., Tahir, M.N., and Yasinzai, M., Appl. Organomet. Chem., 2017, vol. 31, no. 5, p. e3606. https://doi.org/10.1002/aoc.3606
Ali, M.I., Rauf, M.K., Badshah, A., Kumar, I., Forsyth, C.M., Junk, P.C., Kedzierski, L., and Andrews, P.C., J. Chem. Soc. Dalton Trans., 2013, vol. 42, no. 48, p. 16733. https://doi.org/10.1039/c3dt51382c
Ma, Y.Q., Yu, L., and Li, J.S., Heteroatom. Chem., 2002, vol. 13, no. 4, p. 299. https://doi.org/10.1002/hc.10033
Islam, A., Da Silva, J.G., Berbet, F.M., Da Silva, S.M., Rodriques, B.L., Beraldo, H., Melo, M.N., Frezard, F., and Demicheli, C., Molecules, 2014, vol. 19, no. 5, p. 6009. https://doi.org/10.3390/molecules19056009
Liu, R.C., Ma, Y.Q., Yu, L., Li, J.S., Cui, J.R., and Wang, R.Q., Appl. Organomet. Chem., 2003, vol. 17, no. 9, p. 662. https://doi.org/10.1002/aoc.491
Li, J.S., Liu, R.C., Chi, X.B., Wang, G.C., and Guo, Q.S., Inorg. Chim. Acta, 2004, vol. 357, no. 7, p. 2176. https://doi.org/10.1016/j.ica.2003.12.012
Ma, Y., Li, J., Xuan, Z., and Liu, R., J. Organomet. Chem., 2001, vol. 620, nos. 1‒2, p. 235. https://doi.org/10.1016/S0022-328X(00)00799-3
Li, J.S., Ma, Y.Q., Cui, J.R., and Wang, R.Q., Appl. Organomet. Chem., 2001, vol. 15, no. 7, p. 639. https://doi.org/10.1002/aoc.200
Zhang, X.-Y., Cui, L., Zhang, X., Jin, F., and Fan, Y.-H., J. Mol. Struct., 2017, vol. 134, p. 742. https://doi.org/10.1016/j.molstruc.2017.01.039
Lowe, K. and Powell, R., J. Fluor. Chem., 2001, vol. 109, no. 1, p. 1. https://doi.org/10.1016/S0022-1139(01)00371-2
Smart, B.E., J. Fluor. Chem., 2001, vol. 109, no. 1, p. 3. https://doi.org/10.1016/S0022-1139(01)00375-X
Park, B.K. and Kitteringham, N.R., Drug Metab. Rev., 1994, vol. 26, no. 3, p. 605. https://doi.org/10.3109/03602539408998319
Maienfisch, P. and Hall, R.G., Chimia Int. J. Chem., 2004, vol. 58, no. 3, p. 93. https://doi.org/10.2533/000942904777678091
Wen, L., Yin, H., Quan, L., and Wang, D., Acta Crystallogr. (E), 2008, vol. 64, no. 10, p. m1303. https://doi.org/10.1107/s1600536808029656
Ferguson, G., Kaitner, B., Glidewell, C., and Smith, S., J. Organomet. Chem., 1991, vol. 419, no. 3, p. 283. https://doi.org/10.1016/0022-328x(91)80241-b
Zhang, X.-Y., Cui, L., Zhang, X., Jin, F., and Fan, Y.-H., J. Mol. Struct., 2017, vol. 1134, p. 742. https://doi.org/10.1016/j.molstruc.2017.01.039
Quan, L., Yin, H., Cui, L., Yang, M., and Wang, D., Acta Crystallogr., 2009, vol. 65, no. 6, p. m656. https://doi.org/10.1107/s1600536809017449
Sharutin, V.V. and Sharutina, O.K., Russ. J. Inorg. Chem., 2021, vol. 66, no. 3, p. 361. https://doi.org/10.1134/S0036023621030153
Sharutin, V.V., Sharutina, O.K., Russ. J. Gen. Chem., 2021, vol. 91, no. 4, p. 672. https://doi.org/10.1134/S1070363221040150
Sharutin, V.V., Poddel’sky, A.I., Sharutina, O.K., Russ. J. Coord. Chem., 2020, vol. 46, no. 10, p. 663. https://doi.org/10.1134/S1070328420100012
Vasil’ev, A.V., Grinenko, E.V., Shchukin, A.O., and Fedulina, T.G., Infrakrasnaya spektroskopiya organicheskikh i prirodnykh soedinenii (Infrared Spectroscopy of Organic and Natural Compounds), St. Petersburg: SPbGLTA, 2007.
Tarasevich, B.N., IK spektry osnovnykh klassov organicheskikh soedinenii (IR Spectra of the Main Classes of Organic Compounds), Moscow: MGU, 2012.
Batsanov, S.S., Zh. Neorg. Khim., 1991, vol. 36, no. 12, p. 3015.
Sharutin, V.V., Sharutina, O.K., Pakusina, A.P., and Bel’skii, V.K., Zh. Obshch. Khim., 1997, vol. 67, no. 9, p. 1536.
SMART and SAINT-Plus. Version, 5.0. Data Collection and Processing Software for the SMART System. Madison (WI, USA): Bruker AXS Inc., 1998.
SHELXTL/PC. Version 5.10. An Integrated System for Solving, Refining and Displaying Crystal Structures from Diffraction Data. Bruker AXS Inc., Madison: (WI, USA), 1998.
Dolomanov, O.V., Bourhis, L.J., Gildea, R.J., Howard, J.A.K., and Puschmann, H., J. Appl. Cryst., 2009, vol. 42, p. 339. https://doi.org/10.1107/S0021889808042726
Sharutin, V.V. and Sharutina, O.K., Russ. J. Gen. Chem., 2020, vol. 90, no. 10, p. , 1901. https://doi.org/10.1134/S1070363220100138
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. 1446–11452 https://doi.org/10.31857/S0044460X2109016X.
Rights and permissions
About this article
Cite this article
Sharutin, V.V., Sharutina, O.K. & Khaybullina, O.A. Tris(2-methoxy-5-chlorophenyl)antimony Dicarboxylates as Novel Hypercoordinate Antimony Compounds. Russ J Gen Chem 91, 1724–1729 (2021). https://doi.org/10.1134/S1070363221090164
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1134/S1070363221090164