Synthesis and structures of mixed-ligand lead(II) complexes with decahydro-closo-decaborate anion and azheterocyclic ligands

Cover Page

Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

Lead(II) complexation reactions were studied in the presence of salts of the closo-decaborate anion [B10H10]2– and azaheterocyclic ligands 2,2΄-bipyridyl (bipy) or 1,10-phenanthroline (phen) in water and organic solvents (acetonitrile, DMF). Binuclear complex Pb(bipy)2[B10H10] and polymer complex [Pb(phen)[B10H10]] were isolated. The effect of solvents and reagent ratios on the composition and structures of the final complexes was studied. The complex compounds were identified by elemental analysis, IR spectroscopy, and X-ray powder diffraction. The structure of complex [Pb(bipy)2[B10H10]]2 ⋅ 2CH3CN (CCDC no. 2325841) was determined by single-crystal X-ray diffraction.

Full Text

Restricted Access

About the authors

V. V. Avdeeva

Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences

Author for correspondence.
Email: avdeeva.varvara@mail.ru
Russian Federation, Moscow

A. S. Kubasov

Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences

Email: avdeeva.varvara@mail.ru
Russian Federation, Moscow

I. V. Kozerozhets

Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences

Email: avdeeva.varvara@mail.ru
Russian Federation, Moscow

S. E. Nikiforova

Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences

Email: avdeeva.varvara@mail.ru
Russian Federation, Moscow

E. A. Malinina

Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences

Email: avdeeva.varvara@mail.ru
Russian Federation, Moscow

N. T. Kuznetsov

Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences

Email: avdeeva.varvara@mail.ru
Russian Federation, Moscow

References

  1. Greenwood N.N., Earnshaw A. Chemistry of the Elements. School of Chemistry, University of Leeds, U. K. Butterworth-Heinemann, 1997.
  2. Boron Science: New Technologies and Applications / Ed. Hosmane N. S. CRC Press, 2012.
  3. Boron-Based Compounds: Potential and Emerging Applications in Medicine / Eds. Hey-Hawkins E., Viñas Teixidor C. John Wiley & Sons Ltd., 2018. https://doi.org/10.1002/9781119275602
  4. King R.B. // Chem. Rev. 2001. V. 101. P. 1119. https://doi.org/10.1021/cr000442t
  5. Chen Z., King R.B. // Chem. Rev. 2005. V. 105. P. 3613. https://doi.org/10.1021/cr0300892
  6. Ren L., Han Y., Hou X., Wu J. // Chem. 2021. V. 7. P. 3442. https://doi.org/10.1016/j.chempr.2021.11.003
  7. Klyukin I.N., Vlasova Yu.S., Novikov A.S. et al. // Symmetry. 2021. V. 13. P. 464. https://doi.org/10.3390/sym13030464
  8. Kal’tenberg A.A., Bashilova A.D., Somov N.V. et al. // Russ. J. Inorg. Chem. 2023. V. 68. P. 1247. https://doi.org/10.1134/S0036023623700286
  9. Stogniy M.Y., Bogdanova E.V., Anufriev S.A. et al. // Russ. J. Inorg. Chem. 2022. V. 67. P. 1537. https://doi.org/10.1134/S0036023622600848
  10. Núñez R., Romero I., Teixidor F., Viñas C. // Chem. Soc. Rev. 2016. V. 45. P. 5147. https://doi.org/10.1039/C6CS00159A
  11. Las’kova Y.N., Serdyukov A.A., Sivaev I.B. // Russ. J. Inorg. Chem. 2023. V. 68. P. 621. https://doi.org/10.1134/S0036023623600612
  12. Malinina E.A., Kubasov A.S., Nikiforova S.E. et al. // Polyhedron. 2024. V. 247. P. 116710. https://doi.org/10.1016/j.poly.2023.116710
  13. Exner R.M., Jenne C., Wegener B. // Z. Anorg. Allg. Chem. 2021. V. 647. P. 500. https://doi.org/10.1002/zaac.202000479
  14. Avdeeva V.V., Buzanov G.A., Malinina E.A. et al. // Crystals. 2020. V. 10. P. 389. https://doi.org/10.3390/cryst10050389
  15. Avdeeva V.V., Kubasov A.S., Golubev A.V. et al. // Inorg. Chim. Acta. 2023. V. 556. P. 121675. https://doi.org/10.1016/j.ica.2023.121675
  16. Zhdanov A.P., Voinova V.V., Klyukin I.N. et al. // Russ. J. Coord. Chem. 2019. V. 45. P. 563. https://doi.org/10.1134/S1070328419080098
  17. Malischewski M., Peryshkov D.V., Bukovsky E.V. et al. // Inorg. Chem. 2016. V. 55. P. 12254. https://doi.org/10.1021/acs.inorgchem.6b01980
  18. Volkov O., Hu C., Paetzold P. // Z. Anorg. Allg. Chem. 2005. V. 631. P. 1107. https://doi.org/10.1002/zaac.200400518
  19. Avdeeva V.V., Vologzhanina A.V., Korolenko S.E. et al. // Polyhedron. 2022. V. 223. P. 115932. https://doi.org/10.1016/j.poly.2022.115932
  20. Tiritiris I., Schleid T. // Z. Anorg. Allg. Chem. 2004. V. 630. P. 1555. https://doi.org/10.1002/zaac.200400167
  21. Tiritiris I., Schleid, T. // Z. Anorg. Allg. Chem. 2003. V. 629. P. 581. https://doi.org/10.1002/ZAAC.200390095
  22. Avdeeva V.V., Malinina E.A., Zhizhin K.Yu., Kuznetsov N.T. // Russ. J. Coord. Chem. 2021. V. 47. P. 519. https://doi.org/10.1134/S1070328421080017
  23. Malinina E.A., Kubasov A.S., Matveev E.Y. et al. // Polyhedron. 2023. V. 242. P. 116516. doi: 10.1016/j.poly.2023.116516
  24. Matveev E.Y., Avdeeva V.V., Kubasov A.S. et al. // Inorganics. 2023. V. 11. P. 144. https://doi.org/10.3390/inorganics11040144
  25. Lagun V.L., Katser S.B., Orlova A.M. et al. // Russ. J. Coord. Chem. 1992. V. 84. P. 365.
  26. Malinina E.A., Solntsev K.A., Butman L.A., Kuznetsov N.T. // Russ. J. Coord. Chim. 1989. V. 15. P. 1039.
  27. Lagun V.L., Orlova A.M., Katser S.V., et al. // Russ. J. Coord. Chem. 1994. V. 20. P. 431.
  28. Lagun V.L., Solntsev K.A., Katser S.V. et al. // Russ. J. Coord. Chem. 1994. V. 20. P. 504.
  29. Tiritiris I., Van N.-D., Schleid T. // Z. Anorg. Allg. Chem. 2011. V. 637. P. 682. https://doi.org/10.1002/zaac.201000457
  30. Avdeeva V.V., Vologzhanina A.V., Buzin M.I. et al. // Chem. Eur. J. 2017. V. 23. P. 16819. https://doi.org/10.1002/chem.201703285
  31. Avdeeva V.V., Polyakova I.N., Goeva L.V. et al. // Russ. J. Inorg. Chem. 2014. V. 59. P. 1247. https://doi.org/10.1134/S0036023614110047
  32. Malinina E.A., Goeva L.V., Kuznetsov N.T. // Russ. J. Inorg. Chem. 2009. V. 54. P. 417. https://doi.org/10.1134/S0036023609030152
  33. Matveev E.Y., Avdeeva V.V., Kubasov A.S. et al. // Inorganics. 2023. V. 11. P. 144. https://doi.org/10.3390/inorganics11040144
  34. Matveev E.Y., Dontsova O.S., Avdeeva V.V. et al. // Molecules. 2023. V. 28. P. 8073. https://doi.org/10.3390/molecules28248073
  35. Miller H.C., Miller N.E., Muetterties E.L. // J. Am. Chem. Soc. 1963. V. 85. P. 3885. https://doi.org/10.1021/ja00906a033
  36. Bruker, SAINT, Bruker AXS Inc., Madison, WI, 2018.
  37. Krause L., Herbst-Irmer R., Sheldrick G.M., Stalke D., J. Appl. Crystallogr. 2015. V. 48. P. 3. https://doi.org/10.1107/S1600576714022985
  38. Sheldrick G.M. // Acta Crystallogr. C. 2015. V. 71. P. 3.
  39. Dolomanov O.V., Bourhis L.J., Gildea R.J. et al. // J. Appl. Cryst. 2009. V. 42. P. 339.
  40. Turner M.J., McKinnon J.J., Wolff S.K. et al. // CrystalExplorer17.5. Perth: University of Western Australia, 2017).

Supplementary files

Supplementary Files
Action
1. JATS XML
2. Scheme 1: Synthesis of the compounds discussed in this work.

Download (229KB)
3. Fig. 1. Structure of complex I - CH3CN: structure fragment (a), packing fragment (b).

Download (670KB)
4. Fig. 2. dnorm-Hirschfeld surface of the [B10H10]2- anion in the structure of I (a); 2D-section of the Hirschfeld surface of the anion (b) and the contact boundaries of H...H (c), H...Pb (d) and H...N (e).

Download (430KB)
5. Fig. 3. Theoretical X-ray diffraction of the complex [Pb(Bipy)[B10H10]] [26] (blue) and practical X-ray diagram of complex II (red).

Download (131KB)

Copyright (c) 2024 Российская академия наук