Journal of Cluster Science

, Volume 28, Issue 6, pp 3103–3114 | Cite as

Synthesis, Structure and Magnetism of Coordination Polymers Based on [{Re4Te4(CN)12]4− Cluster Anions and [Ln(phen)(H2O)3Ln(phen)(H2O)2(μ-OH)2]4+ (Ln = Dy, Ho, Er) Dimeric Fragments

  • Yulia M. Litvinova
  • Yakov M. Gayfulin
  • Artem S. Bogomyakov
  • Denis G. Samsonenko
  • Yuri V. Mironov
Original Paper

Abstract

Three new polymeric compounds of general formula {[Ln(phen)(H2O)3Ln(phen)(H2O)2(μ-OH)2][Re4Te4(CN)12]}·H2O (Ln = Dy, Ho, Er) were obtained by self-assembly reaction of [Re4Te4(CN)12]4– cluster anions, Ln3+ cations and 1,10-phenthroline (phen) in a solvothermal conditions. Single-crystal X-Ray diffraction showed that structure of compounds consist of non-charged ladder-type chains formed by [Re4Te4(CN)12]4− cluster anions and dimeric cationic complexes [Ln(phen)(H2O)3Ln(phen)(H2O)2(μ-OH)2]4+. Chains are packed parallel and linked with each other by a system of hydrogen bonds. The magnetic susceptibility of compounds is determined by exchange coupled Ln3+ ions in dimeric cationic fragments. The anisotropy effects take place and cause non-linear field dependencies of magnetization for the complexes.

Keywords

Rhenium cluster Lanthanides Coordination polymer Crystal structure Magnetic properties 

Notes

Acknowledgement

This work was supported by the Russian Science Foundation (Project No. 14-23-00013).

References

  1. 1.
    S. R. Batten, S. M. Neville, and D. R. Turner Coordination polymers: design, analysis and application (Royal Society of Chemistry, Cambridge, 2009).Google Scholar
  2. 2.
    S. Kaskel (ed.), The Chemistry of Metal-Organic Frameworks: Synthesis, Characterization, and Applications, (Wiley-VCH Verlag GmbH & Co., Weinheim, Germany, 2016).Google Scholar
  3. 3.
    H. Furukawa, K. E. Cordova, M. O’Keeffe, and O. M. Yaghi (2013). Science 341, 974.CrossRefGoogle Scholar
  4. 4.
    O. M. Yaghi, M. O’Keeffe, N. W. Ockwig, H. K. Chae, M. Eddaoudi, and J. Kim (2003). Nature 423, 705.CrossRefGoogle Scholar
  5. 5.
    E. V. Alexandrov, A. V. Virovets, V. A. Blatov, and E. V. Peresypkina (2015). Chem. Rev. 115, 12286.CrossRefGoogle Scholar
  6. 6.
    K. R. Dunbar, R.A. Heintz and K.D. Karlin (eds.), In Progress in Inorganic Chemistry (John Wiley & Sons, Inc., 2007), vol 45, p 283.Google Scholar
  7. 7.
    N. G. Naumov, A. V. Virovets, and V. E. Fedorov (2000). J. Struct. Chem. 41, 499.CrossRefGoogle Scholar
  8. 8.
    V. E. Fedorov, N. G. Naumov, Y. V. Mironov, A. V. Virovets, S. B. Artemkina, K. A. Brylev, S. S. Yarovoi, O. A. Efremova, and U.-H. Peak (2002). J. Struct. Chem. 43, 669.CrossRefGoogle Scholar
  9. 9.
    Y. Kim, V. E. Fedorov, and S.-J. Kim (2009). J. Mater. Chem. 19, 7178.CrossRefGoogle Scholar
  10. 10.
    N. G. Naumov, D. V. Soldatov, J. A. Ripmeester, S. B. Artemkina, and V. E. Fedorov (2001). Chem. Commun. 2001, 571.CrossRefGoogle Scholar
  11. 11.
    M. V. Bennett, L. G. Beauvais, M. P. Shores, and J. R. Long (2001). J. Am. Chem. Soc. 123, 8022.CrossRefGoogle Scholar
  12. 12.
    O. A. Efremova, Y. V. Mironov, and V. E. Fedorov (2006). Eur. J. Inorg. Chem. 2006, 2533.CrossRefGoogle Scholar
  13. 13.
    Y. M. Gayfulin, N. V. Kuratieva, Y. M. Litvinova, and Y. V. Mironov (2016). Rus. J. Coord. Chem. 42, 423.CrossRefGoogle Scholar
  14. 14.
    Y. M. Litvinova, Y. M. Gayfulin, D. G. Samsonenko, A. S. Bogomyakov, W. H. Shon, S.-J. Kim, J.-S. Rhyee, and Y. V. Mironov (2016). Polyhedron 115, 174.CrossRefGoogle Scholar
  15. 15.
    Y. M. Litvinova, Y. M. Gayfulin, D. G. Samsonenko, D. A. Piryazev, and Y. V. Mironov (2016). J. Mol. Struct. 1107, 109.CrossRefGoogle Scholar
  16. 16.
    O. A. Efremova, Y. M. Gayfulin, Y. V. Mironov, N. V. Kuratieva, A. I. Smolentsev, and V. E. Fedorov (2012). Polyhedron 31, 515.CrossRefGoogle Scholar
  17. 17.
    J.-C. G. Bunzli and C. Piguet (2005). Chem. Soc. Rev. 34, 1048.CrossRefGoogle Scholar
  18. 18.
    A. Earnshow, Introduction to magnetochemistry (Academic press London and New York, 1968).Google Scholar
  19. 19.
    E. G. Moore, A. P. S. Samuel, and K. N. Raymond (2009). Acc. Chem. Res. 42, 542.CrossRefGoogle Scholar
  20. 20.
    L.-J. Xu, G.-T. Xu, and Z.-N. Chen (2014). Coord. Chem. Rev. 273, 47.CrossRefGoogle Scholar
  21. 21.
    R. Sessoli and A. K. Powell (2009). Coord. Chem. Rev. 253, 2328.CrossRefGoogle Scholar
  22. 22.
    Y. V. Mironov, A. V. Virovets, S. B. Artemkina, and V. E. Fedorov (1999). J. Struct. Chem. 40, 313.CrossRefGoogle Scholar
  23. 23.
    CrysAlisPro Version 1.171.34.49, Agilent Technologies, (2011).Google Scholar
  24. 24.
    G. M. Sheldrick (2008). Acta Crystallogr. A 64, 112.CrossRefGoogle Scholar
  25. 25.
    Y. M. Gayfulin, A. I. Smolentsev, and Y. V. Mironov (2015). J. Coord. Chem. 68, 409.CrossRefGoogle Scholar
  26. 26.
    Y. M. Litvinova, N. V. Kuratieva, Y. M. Gayfulin, V. A. Logvinenko, A. Y. Andreeva, E. V. Korotaev, and Y. V. Mironov (2015). Polyhedron 102, 27.CrossRefGoogle Scholar
  27. 27.
    J.-P. Zhao, B.-W. Hu, F.-C. Liu, X. Hu, Y.-F. Zeng, and X.-H. Bu (2007). CrystEngComm 9, 902.CrossRefGoogle Scholar
  28. 28.
    Y.-Q. Zheng, L.-X. Zhou, J.-L. Lin, S.-W. Zhang, and Z. Anorg (2001). Allg. Chem. 627, 2425.CrossRefGoogle Scholar
  29. 29.
    W. L. Leong and J. J. Vittal (2011). Chem. Rev. 111, 688.CrossRefGoogle Scholar
  30. 30.
    A. N. Sokolov and L. R. MacGillivray (2006). Cryst. Growth Des. 6, 2615.CrossRefGoogle Scholar
  31. 31.
    N. F. Chilton, R. P. Anderson, L. D. Turner, A. Soncini, and K. S. Murray (2013). J. Comput. Chem. 34, 1164.CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC 2017

Authors and Affiliations

  • Yulia M. Litvinova
    • 1
  • Yakov M. Gayfulin
    • 1
  • Artem S. Bogomyakov
    • 2
    • 3
  • Denis G. Samsonenko
    • 1
    • 2
  • Yuri V. Mironov
    • 1
    • 2
  1. 1.Nikolaev Institute of Inorganic ChemistrySB RASNovosibirskRussia
  2. 2.Novosibirsk State UniversityNovosibirskRussia
  3. 3.International Tomography CenterSB RASNovosibirskRussia

Personalised recommendations