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Synthesis and Structure of μ2-Oxobis(carboxylatotriarylantimony)

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Abstract

Binuclear antimony compounds with a bridging oxygen atom [Ph3SbOC(O)R]2O (R = CF2CF3, CF2CF2CF3), [(4-МеC6H4)3SbOC(O)CF2CF3]2O, [(3-FC6H4)3SbOC(O)R]2O (R = C6F5, CF2CF3) have been synthesized by reacting equimolar amounts of triarylantimony, carboxylic acid and tert-butyl hydroperoxide in diethyl ether. According to X-ray diffraction data, in the molecules of compounds obtained, the Sb atoms have a trigonal bipyramid coordination with carboxylate ligands and a bridging oxygen atom in axial positions. The intramolecular distances Sb···O with a carbonyl oxygen atom are less than the sum of the van der Waals radii of Sb and O by ~0.2–0.4 Å.

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References

  1. Ferguson, G., Kaither, B., Glidewell, С., Ferguson, G., Kaither, B., Glidewell, C., and Smith, S.J., J. Organomet. Chem., 1991, vol. 419, p. 283. doi https://doi.org/10.1016/0022-328X(91)80241-B

    Article  CAS  Google Scholar 

  2. Qin, W., Yasuike, S., Kakusawa, N., Qin, W., Yasuike, S., Kakusawa, N., Sugawara, Y., Kawahata, M., Yamaguchi, K., and Kurita, J., J. Organomet. Chem., 2008, vol. 693, p. 109. doi https://doi.org/10.1016/j.jorganchem.2007.10.030

    Article  CAS  Google Scholar 

  3. Sharutin, V.V. and Sharutina, O.K., Russ. Chem. Bull., 2017, vol. 66, p. 707. doi https://doi.org/10.1007/s11172-017-1796-6

    Article  CAS  Google Scholar 

  4. Sharutin, V.V., Sharutina, O.K., Reshetnikova, R.V., Lobanova, E.V., and Efremov, A.N., Russ. J. Inorg. Chem., 2017, vol. 62, p. 1450. doi https://doi.org/10.1134/S003602361711016X

    Article  CAS  Google Scholar 

  5. Sharutin, V.V., Sharutina, O.K., and Efremov, A.N., Russ. J. Inorg. Chem., 2016, vol. 61, p. 43. doi https://doi.org/10.1134/S003602361601023X

    Article  CAS  Google Scholar 

  6. Yu, L., Ma, Y-Q., Wang, G-C., and Li, J-S., Heteroatom. Chem., 2004, vol. 15, p. 32. doi https://doi.org/10.1002/hc.10208

    Article  CAS  Google Scholar 

  7. Yu, L., Ma, Y-Q., Liu, R-C., Yu, L., Ma, Y.Q., Liu, R.C., Wang, G.C., Li, J.S., Du, G.H., and Hu, J.J., Polyhedron, 2004, vol. 23, p. 823. doi https://doi.org/10.1016/j.poly.2003.12.002

    Article  CAS  Google Scholar 

  8. Hadjikakou, S.K., Ozturk, I.I., Banti, C.N., and Kourkoumelis, N., Hadjiliadis, N.J., Inorg. Biochem., 2015, vol. 153, p. 293. doi https://doi.org/10.1016/j.jinorgbio.2015.06.006

    Article  CAS  Google Scholar 

  9. Ali, M.I., Rauf, M.K., Badshah, A., Ali, M.I., Rauf, M.K., Badshah, A., Kumar, I., Forsyth, C.M., Junk, P.C., Kedzierski, L., and Andrews, P.C., Dalton Trans., 2013, vol. 42, p. 16733. doi https://doi.org/10.1039/C3DT51382C

    Article  CAS  PubMed  Google Scholar 

  10. Sharutin, V.V., Sharutina, O.K., and Senchurin, V.S., Russ. J. Coord. Chem., 2014, vol. 40, p. 109. doi https://doi.org/10.1134/S1070328414020109

    Article  CAS  Google Scholar 

  11. Quan, L., Yin, H., and Wang, D., Acta Crystallogr. (E), 2008, vol. 64, p. m349. doi https://doi.org/10.1107/S1600536808000676

  12. Quan, L., Yin, H., and Wang, D., Acta Crystallogr. (E), 2009, vol. 65, p. m99. doi https://doi.org/10.1107/S1600536808042335

  13. Gibbons, M.N. and Sowerby, D.B., J. Organomet. Chem., 1998, vol. 555, p. 271. doi https://doi.org/10.1016/S0022-328X(97)00759-6.

    Article  CAS  Google Scholar 

  14. Sharutin, V.V., Pakusina, A.P., Nasonova, N.V., Sharutina, O.K., Gerasimenko, A.V., ansd Pushilin, M.A., Khimiya i Komp’yuternoe Modelirovanie. Butrlovsk. Soobshch. (Chemistry and Computer Simulation. Butlerov Reports), 2002, no. 11, p. 13.

    Google Scholar 

  15. Bruker (1998). SMART and SAINT-Plus. Versions 5.0. Data Collection and Processing Software for the SMART System. Bruker AXS Inc., Madison, Wisconsin, USA.

  16. Bruker (1998). SHELXTL/PC. Versions 5.10. An Integrated System for Solving, Refining and Displaying Crystal Structures From Diffraction Data. Bruker AXS Inc., Madison, Wisconsin, USA.

    Google Scholar 

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

    Article  CAS  Google Scholar 

  18. Sharutin, V.V. and Senchurin, V.S., Imennye reaktsii v khimii elementorganicheskikh soedinenii (Nominal Reaction in Chemistry of Organoelemental Compounds), Celyabinsk: Izd. Tsentr YuUrGU, 2011.

    Google Scholar 

  19. Glidewell, C., J. Orgnomet. Chem., 1988, vol. 356, p. 151. doi https://doi.org/10.1016/0022-328X(88)83084-5

    Article  CAS  Google Scholar 

  20. Tiekink, E.R.T., J. Organomet. Chem., 1987, vol. 333, p. 199. doi https://doi.org/10.1016/0022-328X(87)85152-5

    Article  CAS  Google Scholar 

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Correspondence to V. V. Sharutin.

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Russian Text © V.V. Sharutin, O.K. Sharutina, A.N. Efremov, E.V. Artem’eva, 2019, published in Zhurnal Obshchei Khimii, 2019, Vol. 89, No. 1, pp. 89–94.

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Sharutin, V.V., Sharutina, O.K., Efremov, A.N. et al. Synthesis and Structure of μ2-Oxobis(carboxylatotriarylantimony). Russ J Gen Chem 89, 76–81 (2019). https://doi.org/10.1134/S1070363219010146

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