The Synthesis and Structural Features of Tetra(para-tolyl)antimony Derivatives

Reviews and Advances in Chemistry - Tập 12 - Trang 248-254 - 2023
V. V. Sharutin1
1South Ural State University, Chelyabinsk, Russia

Tóm tắt

The interaction of penta(para-tolyl)antimony with oximes and carboxylic acids in benzene synthesized oximates and carboxylates of tetra(para-tolyl)antimony p-Tol4SbX (X = ON=CHR, R = CHCHPh (1), С6H4(Br-3) (2); X = OC(O)R', R' = CH2OС6H3Cl2-2,4 (3), CF2CF2C(O)OH (4). The structure of compounds 1–4 was established by X-ray diffraction analysis (XRD). According to XRD data, the antimony atoms in complexes 1–3 have the coordination of a distorted trigonal bipyramid with three aryl ligands in the equatorial plane, while the CSbO axial angles are 178.94(5)°, 174.4(2)° and 176.95(5)°. Crystal 4 consists of distorted tetrahedral cations of tetra(para-tolyl)stibonium (CSbC angles 106.6(2)°−112.46(19)°) and singly charged anions of tetrafluoroethanedioic acid. Complete tables of atomic coordinates, bond lengths, and bond angles for compounds 1, 2, 3, 4 have been deposited at the Cambridge Crystallographic Data Center (CCDC 2130472, 2131085, 2131084, 2126158; [email protected]; http://www.ccdc.cam.ac.uk ).

Tài liệu tham khảo

Kocheshkov, K.A., Skoldinov, A.P., and Zemlyansky, N.N., Metody elementoorganicheskoi khimii. Sur’ma, vismut (Methods of Organoelement Chemistry: Antimony, Bismuth), Moscow: Nauka, 1976. 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 Akatova, K.N., Bochkova, R.I., Lebedev, V.A., Sharutin, V.V., and Belov, N.V., Dokl. Akad. Nauk SSSR, 1983, vol. 268, no. 6, p. 1389. Sharutin, V.V., Sharutina, O.K., Pakusina, A.P., Smirnova, S.A., and Pushilin, M.A., Russ. J. Coord. Chem., 2005, vol. 31, no. 2, p. 117. Sharutin, V.V., Sharutina, O.K., Platonova, T.P., Pakusina, A.P., Gerasimenko, A.V., Gerasimenko, E.A., Bukvetsky, B.V., and Popov, D.Yu., Russ. J. Coord. Chem., 2003, vol. 29, no. 1, p. 13. Sharutin, V.V., Sharutina, O.K., Panova, L.P., and Belsky, V.K., Russ. J. Gen. Chem., 1997, vol. 67, no. 9, p. 1531. Sharutin, V.V., Pakusina, A.P., Egorova, I.V., Ivanenko, T.K., Gerasimenko, A.V., and Sergienko, A.S., Russ. J. Coord. Chem., 2003, vol. 29, no. 5, p. 336. Sharutin, V.V., Sharutina, O.K., Pakusina, A.P., and Belsky, V.K., Russ. J. Gen. Chem., 1997, vol. 67, no. 9, p. 1536. Sharutin, V.V., Sharutina, O.K., Tarasova, T.A., Harsika, A.N., and Belsky, V.K., Russ. J. Gen. Chem., 1999, vol. 69, no. 12, p. 1979. Sharutin, V.V., Sharutina, O.K., Platonova, T.P., Pakusina, A.P., and Toichkina, O.N., Russ. J. Gen. Chem., 2000, vol. 70, no. 11, p. 1932. Sharutin, V.V., Sharutina, O.K., Molokova, O.V., Pakusina, A.P., Gerasimenko, A.V., and Sergienko, A.S., Russ. J. Coord. Chem., 2002, vol. 28, no. 8, p. 581. Sharutin, V.V., Sharutina, O.K., Molokova, O.V., Ettenko, E.N., Krivolapov, D.B., Gubaidullin, A.T., and Litvinov, I.A., Russ. J. Gen. Chem., 2001, vol. 71, no. 8, p. 1317. Sharutin, V.V., Sharutina, O.K., Osipov, P.E., Vorobieva, E.B., Muslin, D.V., and Belsky, V.K., Russ. J. Gen. Chem., 2000, vol. 70, no. 6, p. 931. Sopshina, D.M., Vestn. Yuzhno-Ural. Gos. Univ., Ser. Khim., 2022, vol. 14, no. 1, p. 50. https://doi.org/10.14529/chem220106 Efremov, A.N. and Sharutin, V.V., Vestn. Yuzhno-Ural. Gos. Univ., Ser. Khim., 2021, vol. 13, no. 1, p. 47. https://doi.org/10.14529/chem210105 Sharutina, O.K., Vestn. Yuzhno-Ural. Gos. Univ., Ser. Khim., 2021, vol. 13, no. 4, p. 63. https://doi.org/10.14529/chem210404 Senchurin, V.S. and Orlenko, E.D., Vestn. Yuzhno-Ural. Gos. Univ., Ser. Khim., 2019, vol. 11, no. 2, p. 66. https://doi.org/10.14529/chem190207 Sharutin, V.V., Sharutina, O.K., Bondar, E.A., Pakusina, A.P., Adonin, N.Yu., and Starichenko, V.F., Russ. J. Coord. Chem., 2002, vol. 28, no. 5, p. 356. Sharutin, V.V., Sharutina, O.K., Efremov, A.N., and Andreev, P.V., Russ. J. Inorg. Chem., 2017, vol. 62, no. 10, p. 1330. https://doi.org/10.7868/S0044457X17100075 Sharutin, V.V. and Sharutina, O.K., Russ. J. Inorg. Chem., 2017, vol. 62, no. 7, p. 925. https://doi.org/10.7868/S0044457X17070224 Sharutin, V.V., Sharutina, O.K., Senchurin, V.S., and Somov, N.V., Russ. J. Inorg. Chem., 2016, vol. 61, no. 8, p. 1017. https://doi.org/10.7868/S0044457X16080146 Sharutin, V.V., Sharutina, O.K., and Efremov, A.N., Russ. J. Struct. Chem., 2020, vol. 61, no. 9, p. 1490. https://doi.org/10.26902/JSC_id60682 Sharutin, V.V., Sharutina, O.K., and Efremov, A.N., Russ. J. Inorg. Chem., 2020, vol. 65, no. 1, p. 49. https://doi.org/10.31857/S0044457X20010158 Sharutin, V.V., Sharutina, O.K., Efremov, A.N., and Artemyeva, E.V., Russ. J. Inorg. Chem., 2020, vol. 65, no. 4, p. 482. https://doi.org/10.31857/S0044457X20040170 Bruker SMART and SAINT-Plus, Data Collection and Processing Software for the SMART system, ver. 5.0, Madison: Bruker AXS, 1998. Bruker SHELXTL/PC, An Integrated System for Solving, Refining and Displaying Crystal Structures from Diffraction Data, ver. 5.10, Madison: 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 Cordero, B., Gómez, V., Platero-Prats, A.E., Revés, M., Echeverría, J., Cremades, E., Barragána, F., and Alvarez, S., Dalton Trans., 2008, no. 21, p. 2832. https://doi.org/10.1039/B801115J