Trinuclear Lutetium(III) Cyclopentadienyl Complex with the 2,2´-Bipyridine Dianion

Cover Page

Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription or Fee Access

Abstract

The reaction of lutetium cyclopentadienyl anthracenide complex (C5H5)Lu(C14H10)(THF)2] with 1 equiv. of 2,2´-bipyridine in THF gives the trinuclear complex [{(η5-C5H5)Lu}3(μ₂-Bipy)₃] (I), containing a 2,2´-bipyridine dianion. The complex was isolated as a powder with the composition I·0.1(C14H10)·0.8(C7H8). The recrystallization from a toluene/hexane mixture resulted in the crystals of I·0.084(C14H10)·0.831(C7H8)· · 0.500(C6H14), which were studied by X-ray diffraction (monoclinic group P21/c; CCDC no. 2311508). Complex I has an unusual μ22N1,N1´:η4N1,C2,C2´,N1´-bridging coordination of the dianion.

Full Text

Restricted Access

About the authors

D. A. Bardonov

Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences; Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences; National Research University, Higher School of Economics

Email: mminyaev@ioc.ac.ru
Russian Federation, Moscow; Moscow; Moscow

D. M. Roitershtein

Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences; Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: mminyaev@ioc.ac.ru
Russian Federation, Moscow; Moscow

D. I. Nasyrova

Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences; Moscow Institute of Physics and Technology

Email: mminyaev@ioc.ac.ru
Russian Federation, Moscow; Dolgoprudnyi, Moscow oblast

M. E. Minyaev

Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Author for correspondence.
Email: mminyaev@ioc.ac.ru
Russian Federation, Moscow

References

  1. Evans W.J. // Polyhedron. 1987. V. 6. P. 803.
  2. Bochkarev M.N. // Chem. Rev. 2002. V. 102. P. 2089.
  3. Fryzuk M.D., Love J.B., Rettig S.J. // J. Am. Chem. Soc. 1997. V. 119. P. 9071.
  4. Scholz J., Scholz A., Weimann R. et al. // Angew. Chem. Int. Ed. 1994. V. 33. P. 1171.
  5. Fedushkin I.L., Petrovskaya T.V., Girgsdies F. et al. // Angew. Chem. Int. Ed. 1999. V. 38. P. 2262.
  6. Roitershtein D., Domingos A., Pereira L.C J. et al. // Inorg. Chem. 2003. V. 42. P. 7666.
  7. Stennett C.R., Nguyen J.Q., Ziller J.W., Evans W.J. // Organometallics. 2023. V. 42. P. 696.
  8. Shibata Y., Nagae H., Sumiya S. et al. // Chem. Sci. 2015. V. 6, P. 5394.
  9. Chen C., Hu Z.-B., Ruan H. et al. // Organometallics. 2020. V. 39, P. 4143.
  10. Roitershtein D.M., Rybakova L.F., Petrov E.S. // J. Organomet. Chem. 1993. V. 460. P. 39.
  11. Ellis J.E., Minyaev M.E., Nifant´ev I.E., Churakov A.V. // Acta Crystallogr. C. 2018. V. 74. P. 769.
  12. Groom C.R., Allen F.H. // Angew. Chem. Int. Ed. 2014. V. 53. P. 662.
  13. Groom C.R., Bruno I.J., Lightfoot M.P., Ward S.C. // Acta Crystallogr. B. 2016. V. 72. P. 171.
  14. Wen Q., Feng B., Xiang L. et al. // Inorg.Chem. 2021. V. 60. P. 13913.
  15. Petrovskaya T.V., Fedyushkin I.L., Nevodchikov V.I. et al. // Russ. Chem. Bull. 1998. V. 47. P. 2271.
  16. Halbach R. L., Nocton G., Amaro-Estrada J.I. et al. // Inorg. Chem. 2019. V. 58. P. 12083.
  17. Ortu F., Zhu H., Boulon M.-E., Mills D.P. // Inorganics. 2015. V. 3. P. 534.
  18. Ortu F., Liu J., Burton M. et al. // Inorg. Chem. 2017. V. 56. P. 2496.
  19. Jacquot L., Xemard M., Clavaguera C., Nocton G. // Organometallics. 2014. V. 33. P. 4100.
  20. Bochkarev M.N., Fedushkin I.L., Nevodchikov V.I. et al. // J. Organomet. Chem. 1996. V. 524, P. 125.
  21. Bochkarev M.N., Petrov B.I., Fedyushkin I.L. et al. // Russ. Chem. Bull. 1997. V. 46. P. 371.
  22. Huang W., Abukhalil P.M., Khan S.I., Diaconescu P.L. // Chem. Commun. 2014. V. 50. P. 5221.
  23. Tupper K.A., Tilley T.D. // J. Organomet. Chem. 2005. V. 690. P. 1689.
  24. Quitmann C.C., Muller-Buschbaum K. // Z. Anorg. Allg. Chem. 2005. V. 631. P. 2651.
  25. Fedyushkin I.L., Petrovskaya T.V., Girgsdies F. et al. // Russ. Chem. Bull. 2000. V. 49. P. 1869.
  26. Chen C., Hu Z.-B., Ruan H. et al. // Organometallics. 2020. V. 39. P. 4143.
  27. Shibata Y., Nagae H., Sumiya S. et al. // Chem. Sci. 2015. V. 6. P. 5394.
  28. Edelmann F.T., Poremba P. // Synthetic Methods of Organometallic and Inorganic Chemistry (Herrman/Brauer) / Eds. Edelmann F.T., Herrmann W.A.: Stuttgart (Germany): Verlag, 1997. P. 34.
  29. Roitershtein D.M., Minyaev M.E., Mikhailyuk A.A. et al. // Russ. Chem. Bull. 2007. V. 56. P. 1978.
  30. Roitershtein D.M., Ellern A.M., Antipin M.Yu. et al. // Mendeleev Commun. 1992. V. 2. P. 118.
  31. CrysAlisPro. Vversion 1.171.42.89a. Rigaku Oxford Diffraction, 2023.
  32. Sheldrick G.M. // Acta Crystallogr. A. 2015. V. 71. P. 3.
  33. Dolomanov O.V., Bourhis L.J., Gildea R.J. et al. // J. Appl. Cryst. 2009. V. 42. P. 339.
  34. Sheldrick G.M. // Acta Crystallogr. C. 2015. V. 71. P. 3.
  35. Shen W.-Z., Trötscher-Kausa G., Lippert B. // Dalton Trans. 2009. P. 8203.
  36. Shannon R.D. // Acta Crystallogr. A. 1976. V. 2. P. 751.
  37. Schulze B.M., Watkins D.L., Zhang J. et al. // Org. Biomol. Chem. 2014. V. 12. P. 7932.

Supplementary files

Supplementary Files
Action
1. JATS XML
2. Scheme 1. Synthesis of [{(η⁵-C₅H₅)Lu}₃(μ₂-Bipy)₃].

Download (94KB)
3. Fig. 1. Molecular structure of {[(η⁵-C₅H₅)Lu]₃ [μ₂-κ²N¹,N¹´:η4N¹,C²,C²´,N¹´-Bipy]₃} (I): atoms ((a), hydrogen atoms are not shown) and non-coordinating organic molecules (b), the minor component of disorder, anthracene, is shown by open lines) in I · 0.084(C₁₄H₁₀) · 0.831(C₇H₈) · 0.500(C₆H₁₄) (p = 50%).

Download (606KB)

Copyright (c) 2024 Российская академия наук