Lanthanide Complexes with 1,4,7-Trimethyl-1,4,7-triazacyclononane

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Resumo

The reaction of 1,4,7-trimethyl-1,4,7-triazacyclononane with samarium, gadolinium, and terbium chloride tetrahydrofuranates gives mononuclear complexes [LnCl3(Me3tacn)(THF)n] (Me3tacn = 1,4,7-trimethyl-1,4,7-triazacyclononane; Ln = Sm (I), Gd (II), n = 1; Ln = Tb (III), n = 0). The treatment of complexes I or II with 1,2,4-triphenylcyclopentadienyl potassium affords mono(cyclopentadienyl) complexes [CpPh3LnCl2(Me3tacn)] (CpPh3 = = 1,2,4-triphenylcyclopentadienyl; Ln = Sm (IV), Gd (V)). Complexes IV and V are formed even when a twofold excess of CpPh3K is used. The molecular structure of complexes IV was established by X-ray diffraction analysis (CCDC nos. 2299485 (I), 2299487 (II), 2299486 (III), 2305352 (IV), 2306051 (V)).

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Sobre autores

S. Degtyareva

Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences; Higher School of Economics

Email: kostya@xray.ineos.ac.ru
Rússia, Moscow; Moscow

D. Bardonov

Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences; Higher School of Economics

Email: kostya@xray.ineos.ac.ru
Rússia, Moscow; Moscow

K. Lysenko

Higher School of Economics; Lomonosov Moscow State University

Autor responsável pela correspondência
Email: kostya@xray.ineos.ac.ru
Rússia, Moscow; Moscow

M. Minyaev

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

Email: kostya@xray.ineos.ac.ru
Rússia, Moscow; Moscow

I. Nifantyev

Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences; Higher School of Economics; Lomonosov Moscow State University

Email: kostya@xray.ineos.ac.ru
Rússia, Moscow; Moscow; Moscow

D. Roitershtein

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

Email: roiter@yandex.ru
Rússia, Moscow; Moscow; Moscow

Bibliografia

  1. Ortu, F., Chem. Rev., 2022, vol. 122, no. 6, p. 6040.
  2. Baisch, U., DellʹAmico, D.B., Calderazzo, F., et al., Inorg. Chim. Acta, 2004, vol. 357, no. 5, p. 1538.
  3. Rogers, R.D., Voss, E.J., and Etzenhouser, R.D., Inorg. Chem., 1988, vol. 27, no. 3, p. 333.
  4. Gompa, T.P., Rice, N.T., Russo, D.R., et al., Dalton Trans., 2019, vol. 48, no. 23, p. 8030.
  5. Petricek, S., Demsar, A., and Golic, L., Polyhedron, 1998, vol. 18, nos. 3–4, p. 529.
  6. Li, J.-S., Neumuller, B., and Dehnicke, K., Z. Anorg. Allg. Chem., 2002, vol. 628, no. 1, p. 45.
  7. Bardonov, D.A., Komarov, P.D., Ovchinnikova, V.I., et al., Organometallics, 2021, vol. 40, no. 9, p. 1235.
  8. Sadrtdinova, G.I., Bardonov, D.A., Lyssenko, K.A., et al., Mendeleev Commun., 2023, vol. 33, no. 3, p. 357.
  9. Mortis, A., Maichle-Mossmer, C., and Anwander, R., Organometallics, 2023, vol. 42, no. 11, p. 1158.
  10. Bigmore, H.R., Lawrence, S.C., Mountford, P., et al., Dalton Trans., 2005, vol. 34, no. 4, p. 635.
  11. Lawrence, S.C., Ward, B.D., Dubberley, S.R., et al., Chem. Commun., 2003, vol. 39, no. 23, p. 2880.
  12. Barisic, D., Diether, D., Maichle-Mossmer, C., et al., J. Am. Chem. Soc., 2019, vol. 141, no. 35, p. 13931.
  13. Bambirra, S., Meetsma, A., and Hessen, B., Acta Crystallogr., Sect. E: Struct. Rep. Online, 2007, vol. 63, no. 12, p. m2891.
  14. Wedal, J.C., Ziller, J.W., and Evans, W.J., Dalton Trans., 2023, vol. 52, no. 15, p. 4787.
  15. Wedal, J.C., Murillo, J., Ziller, J.W., et al., Inorg. Chem., 2023, vol. 62, no. 15, p. 5897.
  16. Hajela, S., Schaefer, W.P., and Bercaw, J.E., J. Organomet. Chem., 1997, vol. 532, nos 1-2, p. 45.
  17. Curnock, E., Levason, W., Light, M.E., et al., Dalton Trans., 2018, vol. 47, no. 17, p. 6059.
  18. Edelmann, F.T. and Poremba, P., Synthetic Methods of Organometallic and Inorganic Chemistry (Herrman/Brauer), Edelmann, F.T. and Herrmann, W.A., Eds., Stuttgart, 1997, p. 34.
  19. Hirsch, S.S. and Bailey, W.J., Org. Chem., 1978, vol. 43, no. 21, p. 4090.
  20. Madison, S.A. and Batal, D.J., US Patent 5284944A, 1994.
  21. APEX-III, Madison: Bruker AXS Inc., 2019.
  22. Krause, L., Herbst-Irmer, G.M., Sheldrick, D., et al., J. Appl. Crystallogr., 2015, vol. 48, p. 3.
  23. CrysAlisPro. Rigaku Oxford Diffraction, Version 1.171.42, 2023.
  24. Sheldrick, G.M., Acta Crystallogr., Sect. A: Found. Adv., 2015, vol. 71, p. 3.
  25. Sheldrick, G.M., Acta Crystallogr., Sect. C: Struct. Chem., 2015, vol. 71, p. 3.
  26. Cirera, J., Ruiz, E., and Alvarez, S., Organometallics, 2005, vol. 24, no. 7, p. 1556.
  27. Stellfeldt, D., Meyer, G., and Deacon, G.B., Z. Anorg. Allg. Chem., 1999, vol. 625, no. 8, p. 1252.
  28. Evans, W.J., Gummerschmeir, T.S., and Ziller, J.W., Appl. Organomet. Chem., 1995, vol. 9, nos 5-6, p. 437.
  29. Bienfait, A.M., Wolf, B.M., Tornroos, K.W., et al., Organometallics, 2016, vol. 35, no. 21, p. 3743.
  30. Roitershtein, D.M., Puntus, L.N., Vinogradov, A.A., et al., Inorg. Chem., 2018, vol. 57, no. 16, p. 10199.
  31. Degtyareva, S.S., Bardonov, D.A., Lysenko, K.A., et al., Russ. J. Coord. Chem., 2023, vol. 49, no. 8, p. 513. https://doi.org/10.1134/S107032842370063X

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1. JATS XML
2. Scheme 1. Synthesis of complexes I and II

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3. Fig. 1. Molecular structure of complex I in the representation of atoms by ellipsoidal thermal vibrations (ρ = 50%). Hydrogen atoms and disorder of the coordinated THF molecule are not shown to simplify the figure

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4. Fig. 2. 1H NMR spectrum of complex I. The insert shows an enlarged fragment of the spectrum with the signal at 4.46 m.d.

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5. Scheme 2. Synthesis of complex III

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6. Fig. 3. Molecular structure of complex III in the representation of atoms by thermal vibration ellipsoids (ρ = 50%). Hydrogen atoms and disorder of the {TbCl3} fragment are not shown

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7. Scheme 3. Synthesis of complexes IV and V

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8. Fig. 4. Molecular structure of complex IV in the representation of atoms by thermal vibration ellipsoids (ρ = 50%). Hydrogen atoms, THF molecule and disorder of one of the phenyl substituents are not shown

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