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Synthesis, structure, and properties of rare earth chloride complexes {[Ap´Y(THF)](μ2-Cl)23-Cl)Li(THF)}2, {[Ap9MeLn(THF)](μ2-Cl)3Li(THF)2}2 (Ln = Y, Nd, Sm), and {[Ap*Ln(THF)](μ2-Cl)3Li(THF)2}2 (Ln = Nd, Sm) containing amidopyridinate ligands

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Abstract

New amidopyridinate chloride complexes {[Ap´Y(THF)](μ2-Cl)23-Cl)Li(THF)}2, {[Ap9MeLn(THF)](μ2-Cl)3Li(THF)2}2 (Ln = Y, Nd, Sm), and {[Ap*Ln(THF)](μ2-Cl)3Li(THF)2}2 (Ln = Nd, Sm) were synthesized by the exchange reactions of lithium amidopyridinates ApLi(OEt2) (Ap´ is N-(2,6-diisopropylphenyl)-6-(2,6-dimethylphenyl)pyridine-2-amine; Ap9Me is N-mesityl-6-(2,4,6-triisopropylphenyl)pyridine-2-amine; Ap* is N-(2,6-diisopropylphenyl)-6-(2,4,6-triisopropylphenyl)pyridine-2-amine) with anhydrous rare earth chlorides. The X-ray diffraction study showed that the amidopyridinate chloride derivatives are heterobimetallic ate-complexes, in which two rare earth metal atoms are linked by bridging chloride ligands and bridging Cl—Li—Cl groups. The three-component system {[Ap*Nd(THF)](μ2-Cl)3Li(THF)2}2—AlBui 3—[Ph3C][B(C6F5)4] (1: 10: 1 molar ratio) catalyzes the isoprene polymerization.

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References

  1. R. D. Shannon, Acta Cryst., 1976, A32, 751.

    Article  CAS  Google Scholar 

  2. A. A. Trifonov, Russ. Chem. Rev., 2007, 76, 1051 [Usp. Khim., 2007, 76, 1122].

    Article  CAS  Google Scholar 

  3. F. Estler, G. Eickerling, E. Herdtweck, R. Anwander, Organometallics, 2003, 22, 1212.

    Article  CAS  Google Scholar 

  4. H. Sugiyama, S. Gambarotta, G. P. A. Yap, D. R. Wilson, S. K.-H. Thiele, Organometallics, 2004, 23, 5054.

    Article  CAS  Google Scholar 

  5. W. P. Kretschmer, A. Meetsma, B. Hessen, T. Schmalz, S. Qayyum, R. Kempe, Chem. Eur. J., 2006, 12, 8969.

    Article  CAS  Google Scholar 

  6. G. G. Skvortsov, G. K. Fukin, A. A. Trifonov, A. Noor, C. Doering, R. Kempe, Organometallics, 2007, 26, 5770.

    Article  CAS  Google Scholar 

  7. D. M. Lyubov, C. Doring, G. K. Fukin, A. V. Cherkasov, A. S. Shavyrin, R. Kempe, A. A. Trifonov, Organometallics, 2008, 27, 2905.

    Article  CAS  Google Scholar 

  8. D. M. Lyubov, G. K. Fukin, A. V. Cherkasov, A. S. Shavyrin, A. A. Trifonov, L. Luconi, C. Bianchini, A. Meli, G. Giambastiani, Organometallics, 2009, 28, 1227.

    Article  CAS  Google Scholar 

  9. G. Li, M. Lamberti, M. Mazzeo, D. Pappalardo, G. Roviello, C Pellecchia, Organometallics, 2012, 31, 1180.

    Article  CAS  Google Scholar 

  10. C. Doring, R. Kempe, Eur. J. Inorg, Chem., 2009, 412.

    Google Scholar 

  11. D. M. Lyubov, L. Luconi, A. Rossin, G. Tuci, A. V. Cherkasov, G. K. Fukin, G. Giambastiani, A. A. Trifonov, Chem. Eur. J., 2014, 20, 3487.

    Article  CAS  Google Scholar 

  12. N. M. Scott, R. Kempe, Eur. J. Inorg. Chem., 2005, 1319.

    Google Scholar 

  13. C. Doering, W. Kretschmer, R. Kempe, Eur. J. Inorg. Chem., 2010, 18, 2853.

    Article  Google Scholar 

  14. D. M. Lyubov, C. Doering, S. Yu. Ketkov, R. Kempe, A. A. Trifonov, Chem. Eur. J., 2011, 17, 3824.

    Article  CAS  Google Scholar 

  15. D. M. Lyubov, A. V. Cherkasov, G. K. Fukin, S. Yu Ketkov, A. S. Shavyrin, A. A. Trifonov, Dalton Trans., 2014, 43, 14450.

    Article  CAS  Google Scholar 

  16. V. Rad´kov, V. Dorcet, J.-F. Carpentier, A. Trifonov, E. Kirillov, Organometallics, 2013, 32, 1517.

    Article  Google Scholar 

  17. V. Rad´kov, T. Roisnel, A. Trifonov, J.-F. Carpentier, E. Kirillov, Eur. J. Inorg. Chem., 2014, 25, 4168.

    Article  Google Scholar 

  18. L. Luconi, D. M. Lyubov, A. Rossin, T. A. Glukhova, A. V. Cherkasov, G. Tuci, G. K. Fukin, A. A. Trifonov, G. Giambastiani, Organometallics, 2014, 33, 7125.

    Article  CAS  Google Scholar 

  19. D. M. Lyubov, L. Luconi, A. Rossin, G. Tuci, A. V. Cherkasov, G. K. Fukin, G. Giambastiani, A. A. Trifonov, Chem. Eur. J., 2014, 20, 3487.

    Article  CAS  Google Scholar 

  20. A. V. Karpov, A. S. Shavyrin, A. V. Cherkasov, G. K. Fukin, A. A. Trifonov, Organometallics, 2012, 31, 5349.

    Article  CAS  Google Scholar 

  21. D. M. Lyubov, C. Doering, S. Yu. Ketkov, R. Kempe, A. A. Trifonov, Chem. Eur. J., 2011, 17, 3824.

    Article  CAS  Google Scholar 

  22. S. Qayyum, G. G. Skvortsov, G. K. Fukin, A. A. Trifonov, W. P. Kretschmer, C. Doering, R. Kempe, Eur. J. Inorg. Chem., 2010, 248.

    Google Scholar 

  23. W. P. Kretschmer, A. Meetsma, B. Hessen, N. M. Scott, S. Qayyum, R. Kempe, Zeitschrift Anorg. Allgem. Chemie, 2006, 632, 1936.

    Article  CAS  Google Scholar 

  24. G. W. Rabe, C. D. Bérubé, G. P. A. Yap, Inorg. Chem., 2001, 40, 4780.

    Article  CAS  Google Scholar 

  25. E. N. Kirillov, A. A. Trifonov, S. E. Nefedov, I. L. Eremenko, F. T. Edelmann, M. N. Bochkarev, Z. Naturforsch., 1999, 54b, 1379.

    Google Scholar 

  26. M. D. Taylor, C. P. Carter, J. Inorg. Nucl. Chem., 1962, 24, 87.

    Article  Google Scholar 

  27. G. M. Sheldrick, SHELXTL v. 6.12, Structure Determination Software Suite, 2000, Bruker AXS, Madison, Wisconsin, USA

  28. G. M. heldrick, SADABS v. 2.01, Bruker/Siemens Area Detector Absorption Correction Program, 1998, Bruker AXS, Madison, Wisconsin, USA.

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Correspondence to A. A. Trifonov.

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Dedicated to Academician of the Russian Academy of Sciences V. I. Minkin on the occasion of his 80th birthday.

Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp. 0618—0625, March, 2015.

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Lyubov, D.M., Rad´kov, V.Y., Tolpygin, A.O. et al. Synthesis, structure, and properties of rare earth chloride complexes {[Ap´Y(THF)](μ2-Cl)23-Cl)Li(THF)}2, {[Ap9MeLn(THF)](μ2-Cl)3Li(THF)2}2 (Ln = Y, Nd, Sm), and {[Ap*Ln(THF)](μ2-Cl)3Li(THF)2}2 (Ln = Nd, Sm) containing amidopyridinate ligands. Russ Chem Bull 64, 618–625 (2015). https://doi.org/10.1007/s11172-015-0908-4

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  • DOI: https://doi.org/10.1007/s11172-015-0908-4

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