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A STUDY OF CRYSTAL STRUCTURES OF TETRA(p-TOLYL)ANTIMONY 2,4,6-TRICHLOROPHENOXIDE AND 3,4,5-TRIFLUOROBENZOATE

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Abstract

Tetra(p-tolyl)antimony 2,4,6-trichlorophenoxide p-Tol4SbOC6H2Cl3-2,4,6 (1) and tetra(p-tolyl)antimony 3,4,5-trifluorobenzoate p-Tol4SbOС(O)C6H2F3-3,4,5 (2) are synthesized by the interaction of penta(p-tolyl)antimony with equimolar amounts of 2,4,6-trichlorophenol and 3,4,5-trifluorobenzoic acid in a benzene solution. Compounds 1 and 2 are also obtained by ligand redistribution reactions between penta(p-tolyl)antimony and symmetric antimony derivatives p-Tol3SbХ2. The crystal structures and structural features of compounds 1 and 2, in which antimony atoms have a trigonal bipyramidal coordination of substituents with axially located oxygen-containing ligands, are determined by single crystal X-ray diffraction.

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REFERENCES

  1. Cambridge Crystallografic Datebase. Release 2020. University of Cambridge, UK.

  2. J. Kopf, G.Vetter, and G. Klar. Z. Anorg. Allg. Chem., 1974, 409, 285.

  3. G.-C. Wang, J. Xiao, L. Yu, J.-S. Li, J.-R. Cui, R.-Q. Wang, and F.-X. Ran. J. Organomet. Chem., 2004, 689, 1631.

  4. R. Ruther, F. Huber, and and H. Preut. J. Organomet. Chem., 1985, 295, 21.

  5. I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, and A. A. Rakhanskii. Russ. J. Gen. Chem., 2014, 84, 1371.

  6. G.-C. Wang, Y.-N. Lu, J. Xiao, L. Yu, H.-B. Song, J.-S. Li, J.-R. Cui, R.-Q. Wang, and F.-X. Ran. J. Organomet. Chem., 2005, 690, 151.

  7. V. A. Trush, K. E. Gubina, V. M. Amirkhanov, J. Swiatek-Kozlowska, and K. V. Domasevitch. Polyhedron, 2005, 24, 1007

  8. H. Yamamichi, S. Matsukawa, S. Kojima, K. Ando, and Y. Yamamoto. Heteroat. Chem., 2011, 22, 553.

  9. J.-S. Li, R.-C. Liu, X.-B. Chi, G.-C. Wang, and Q.-S. Guo. Inorg. Chim. Acta, 2004, 357, 2176.

  10. V. E. Shklover, Yu. T. Struchkov, V. A. Dodonov, T. I. Zinov′eva, and V. L. Antonovskii. Metalloorg. Khim., 1988, 1, 1140.

  11. A. V. Ivanov, A. P. Pakusina, M. A. Ivanov, V. V. Sharutin, A. V. Gerasimenko, O. N. Anzutkin, G. Grobner, and W. Forsling. Dokl. Akad. Nauk SSSR, 2005, 401, 643.

  12. A. P. M. Robertson, S. S. Chitnis, H. A. Jenkins, R. McDonald, M. J. Ferguson, and N. Burford. Chem. – Eur. J., 2015, 21, 7902.

  13. K. Shen, W. E. McEwen, S. J. La Placa, W. C. Hamilton, and A. P. Wolf. J. Am. Chem. Soc., 1968, 90, 1718.

  14. M. Yang, N. Pati, G. Belanger-Chabot, M. Hirai, and F. P. Gabbai. Dalton Trans., 2018, 47, 11843.

  15. K. V. Domasevich, V. V. Skopenko, R. Kempe, A. A. Mokhir, J. Sieler, and E. Hoyer. Russ. J. Inorg. Chem., 1998, 43, 192.

  16. K. Akiba, H. Fujishima, A. Ohtani, S. Kojima, and Y. Yamamoto. Bull. Soc. Chim. Belg., 1997, 106, 577.

  17. C. Ma, Q. Zhang, J. Sun, and R. Zhang. J. Organomet. Chem., 2006, 691, 2567.

  18. G. M. Arvanitis, M. E. Berardini, T. B. Acton, and P. E. Dumas. Phosphorus, Sulfur Silicon Relat. Elem., 1993, 82, 127.

  19. N. Dinsdale, J. C. Jeffrey, R. J. Kilby, S. M. Mansell, O. C. Presly, and C. A. Russell. Inorg. Chim. Acta, 2007, 360, 418.

  20. C. L. Perrin and Y.-J. Kim. Inorg. Chem., 2000, 39, 3902.

  21. B. Pan and F. P. Gabbai. J. Am. Chem. Soc., 2014, 136, 9564.

  22. K. V. Domasevich, A. N. Chernega, S. V. Lindeman, and Yu. T. Struchkov. Zh. Neorg. Khim., 1995, 40, 426.

  23. K. V. Domasevitch, N. N. Gerasimchuk, and A. Mokhir. Inorg. Chem., 2000, 39, 1227.

  24. V. V. Sharutin, O. K. Sharutina, and V. S. Senchurin. Russ. J. Inorg. Chem., 2017, 62, 295.

  25. V. V. Sharutin, O. K. Sharutina, and V. S. Senchurin. Russ. J. Coord. Chem., 2016, 42, 32.

  26. D. V. Lyakaev, A. V. Markina, E. V. Khabarova, N. N. Smirnova, A. V. Knyazev, V. V. Sharutin, and O. K. Sharutina. Russ. J. Phys. Chem., 2018, 92, 1659.

  27. V. V. Sharutin, O. K. Sharutina, Y. O. Gubanova, and O. S. Eltsov. Inorg. Chim. Acta, 2019, 494, 211.

  28. S. P. Bone and D. B. Sowerby. Phosphorus, Sulfur Silicon Relat. Elem., 1989, 45, 23.

  29. H.-D. Yin, L.-Y. Wen, J.-C. Cui, and W.-K. Li. Polyhedron, 2009, 28, 2919.

  30. L. Quan, H.-D. Yin, J.-C. Cui, M. Hong, and D.-Q. Wang. J. Organomet. Chem., 2009, 694, 3708.

  31. L.-Y. Wen, H.-D. Yin, W.-K. Li, and D.-Q. Wang. Inorg. Chim. Acta, 2010, 363, 676.

  32. R.-C. Liu, Y.-Q. Ma, L. Yu, J.-S. Li, J.-R. Cui, and R.-Q. Wang. Appl. Organomet. Chem., 2003, 17, 662.

  33. S. P. Bone and D. B. Sowerby. J. Chem. Res., 1979, 82, 1029.

  34. J.-S. Li, Y.-Q. Ma, J.-R. Cui, and R.-Q. Wang. Appl. Organomet. Chem., 2001, 15, 639.

  35. Y.-Q. Ma, J.-S. Li, Z. Xuan, and R.-С. Liu. J. Organomet. Chem., 2001, 620, 235.

  36. L. Quan, H. Yin, J. Cui, M. Hong, L. Cui, M. Yang, and D. Wang. J. Organomet. Chem., 2009, 694, 3683.

  37. P. M. Millington and D. B. Sowerby. J. Chem. Soc., Dalton Trans., 1992, 7, 1199.

  38. V. V. Sharutin, O. K. Sharutina, A. N. Efremov, and P. V. Andreev. Russ. J. Inorg. Chem., 2017, 62, 1320.

  39. V. V. Sharutin and O. K. Sharutina. Russ. J. Inorg. Chem., 2017, 62, 905.

  40. K. A. Kocheshkov, A. P. Skoldinov, and N. N. Zemlyansky. Metody jelementoorganicheskoj Himii. Sur′ma, vismut (Methods of the Organometallic Chemistry. Antimony, Bismuth) [in Russian]. Nauka: Moscow, 1976.

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

  42. Bruker. SHELXTL/PC. Versions 5.10. An Integrated System for Solving, Refining and Displaying Crystal Structures from Diffraction Data. Bruker AXS Inc.: Madison, Wisconsin, USA, 1998.

  43. O. V. Dolomanov, L. J. Bourhis, R. J. Gildea, J. A. K. Howard, and H. Puschmann. J. Appl. Crystallogr., 2009, 42, 339.

  44. B. N. Tarasevich. IK Spektry Osnovnyh Klassov Organicheskih Soedinenij (IR Spectra of the Main Classes of Organic Compounds) [in Russian]. MGU: Moscow, 2012.

  45. S. S. Batsanov. Russ. J. Inorg. Chem., 1991, 36, 1694.

  46. A. Mukherjee, S. Tothadi, and G. R. Desiraju. Acc. Chem. Res., 2014, 47, 2514.

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Correspondence to A. N. Efremov.

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Sharutin, V.V., Sharutina, O.K. & Efremov, A.N. A STUDY OF CRYSTAL STRUCTURES OF TETRA(p-TOLYL)ANTIMONY 2,4,6-TRICHLOROPHENOXIDE AND 3,4,5-TRIFLUOROBENZOATE. J Struct Chem 61, 1414–1421 (2020). https://doi.org/10.1134/S0022476620090085

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