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Zirconium Complexes [Ph3PR] +2 [ZrCl6]2–, R = Et, CH2Ph, CH2C(O)OMe: Synthesis and Structure

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Abstract

The complexes [Ph3PR] +2 [ZrCl6]2–, R = Et (I), CH2Ph (II) (1: 1 solvate with acetonitrile), and CH2C(O)OMe (III) have been synthesized by the reaction between zirconium tetrachloride and triphenylorganyl phosphonium chlorides in acetonitrile and structurally characterized. The phosphorus atoms in triphenylorganyl phosphonium cations have a distorted tetrahedral coordination: the CPC angles are 108.29(9)°–110.84(8)° (I), 106.91(8)°—112.21(8)° (II), and 107.26(9)°–112.83(9)° (III), and the P–C bond lengths are 1.793(2)–1.803(2) Å (I), 1.791(2)–1.824(2) Å (II), and 1.784(2)–1.811(2) Å (III). The Zr–Cl distances in the centrosymmetric octahedral anions [ZrCl6]2– of complex I are 2.4625(11)–2.4634(11) Å. The octahedral configuration of anions in complexes II and III is distorted: the trans-ClZrCl angles are 176.80(2)°, 177.12(2)°, 179.80(2)° (II) and 175.53(3)°, 175.97(2)°, 177.75(2)° (III), and the Zr–Cl bonds are 2.4489(11)–2.4953(15) Å (II) and 2.4510(8)−2.4864(9) Å (III).

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References

  1. U. M. Dzhemilev, O. S. Vostrikova, and A. G. Ibragimov, Russ. Chem. Rev. 55, 66 (1986).

    Article  Google Scholar 

  2. I. Schwartz and J. Labinger, Angew. Chem., Int. Ed. Engl. 15, 333 (1976). doi 10.1002/anie.197603331

    Article  Google Scholar 

  3. J. Schwartz, Pure Appl. Chem. 52, 733 (1980). doi 10.1351/pac198052030733

    Article  CAS  Google Scholar 

  4. J. S. Rogers, G. C. Bazan, and C. K. Sperry, J. Am. Chem. Soc. 119, 9305 (1997). doi 10.1021/ja971976n

    Article  CAS  Google Scholar 

  5. K.-T. Wang, Y.-X. Wang, B. Wang, et al., Dalton Trans. 45, 10308 (2016). doi 10.1039/C6DT01391K

    Article  CAS  PubMed  Google Scholar 

  6. S. M. Yu, U. Tritschler, I. Göttker-Schnetmann, and S. Mecking, Dalton Trans. 39, 4612 (2010). doi 10.1039/B916289E

    Article  CAS  PubMed  Google Scholar 

  7. D. A. X. Fraser, Z. R. Turner, J.-Ch. Buffet, and D. O’Hare, Organometallics 35, 2664 (2016). doi 10.1021/acs.organomet.6b00417

    Article  CAS  Google Scholar 

  8. N. Nakata, T. Toda, Y. Saito, et al., Polymers 8, 31 (2016). doi 10.3390/polym8020031

    Article  CAS  PubMed Central  Google Scholar 

  9. G. W. Theaker, C. Morton, and P. Scott, Macromolecules 44, 1393 (2011). doi 10.1021/ma102835p

    Article  CAS  Google Scholar 

  10. Th. Holtrichter-Rößmann, I. Häger, C.-G. Daniliuc, et al., Organometallics 35, 1906 (2016). doi 10.1021/acs.organomet.6b00240

    Article  CAS  Google Scholar 

  11. Sh. Yuan, L. Wang, Y. Hua, et al., J. Chem. Sci. 71, 1019 (2016). doi 10.1007/s12039-016-1109-x

    CAS  Google Scholar 

  12. T. Cuenca, J. C. Flores, and P. Royo, J. Organomet. Chem. 462, 191 (1993). doi 10.1016/0022-328X(93)83357-2

    Article  CAS  Google Scholar 

  13. X. Xu, G. Kehr, C. G. Daniliuc, and G. Erker, J. Am. Chem. Soc. 137, 4550 (2015). doi 10.1021/jacs.5b01623

    Article  CAS  PubMed  Google Scholar 

  14. G. Blay, I. Fernandez, A. Monleon, et al., Org. Lett. 9, 2601 (2007). doi 10.1021/ol0710820

    Article  CAS  PubMed  Google Scholar 

  15. G. Blay, I. Fernandez, A. Monleon, et al., Org. Lett. 11, 441 (2009). doi 10.1021/ol802509m

    Article  CAS  PubMed  Google Scholar 

  16. L.-P. Mo and Zh.-H. Zhang, Curr. Org. Chem. 15, 3800 (2011). doi 10.2174/138527211797884520

    Article  CAS  Google Scholar 

  17. E. Hartmann, K. Dehnicke, D. Fenske, et al., Z. Naturforsch., B: Chem. Sci. 44, 1155 (1989). doi 10.1515/znb-1989-1001

    Article  CAS  Google Scholar 

  18. L. Chen and F. A. Cotton, Inorg. Chem. 35, 7364 (1996). doi 10.1021/ic960454q

    Article  CAS  PubMed  Google Scholar 

  19. L. Chen, F. A. Cotton, and W. F. Wojtczak, Inorg. Chem. 36, 4047 (1997). doi 10.1021/ic960173i

    Article  CAS  Google Scholar 

  20. S. G. Minasian, K. S. Boland, R. K. Feller, et al., Inorg. Chem. 51, 5728 (2012). doi 10.1021/ic300179d

    Article  CAS  PubMed  Google Scholar 

  21. F. Gauch and J. Strahle, Z. Anorg. Allg. Chem. 626, 1153 (2000). https://doi.org/10.1002/(SICI)1521-3749(200005)626:5<1153:: AID-ZAAC1153>3.0.CO;2-0.

    Article  CAS  Google Scholar 

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

    Google Scholar 

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

  24. O. V. Dolomanov, L. J. Bourhis, R. J. Gildea, et al., J. Appl. Crystallogr. 42, 339 (2009). doi 10.1107/S0021889808042726

    Article  CAS  Google Scholar 

  25. V. V. Sharutin, O. K. Sharutina, V. S. Senchurin, et al., Russ. J. Inorg. Chem. 61, 451 (2016). doi 10.1134/S0036023616040173

    Article  CAS  Google Scholar 

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Correspondence to V. V. Sharutin.

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Original Russian Text © V.V. Sharutin, O.K. Sharutina, E.V. Lobanova, 2018, published in Zhurnal Neorganicheskoi Khimii, 2018, Vol. 63, No. 12, pp. 1549–1554.

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Sharutin, V.V., Sharutina, O.K. & Lobanova, E.V. Zirconium Complexes [Ph3PR] +2 [ZrCl6]2–, R = Et, CH2Ph, CH2C(O)OMe: Synthesis and Structure. Russ. J. Inorg. Chem. 63, 1558–1563 (2018). https://doi.org/10.1134/S0036023618120197

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  • DOI: https://doi.org/10.1134/S0036023618120197

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