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Ytterbium Complexes with Redox-Active N,N-Chelating Ligands

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Abstract

1,2-Bis[(2,6-dibenzhydryl-4-methylphenyl)imino]acenaphthene (ArBIG-bian) reacts with an excess of ytterbium metal in 1,2-dimethoxyethane (DME) to afford solvent-free ytterbium complex of ArBIG-bian dianion, [(ArBIG-bian)Yb]. The reaction of [(ArBIG-bian)Yb] with 2,2′-bipyridine (bpy) (1 to 2) in DME proceeds with the electron transfer from the metal to the bpy and results in ytterbium(III) derivative [(ArBIG-bian)Yb(bpy)2], containing both neutral and radical-anionic bpy ligands. The newly prepared compounds were characterized by IR, NMR spectroscopy. The molecular structure of [(ArBIG-bian)Yb(bpy)2] was determined by single crystal X-ray analysis.

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Fig. 1.

REFERENCES

  1. Hay, M.A., and Boskovic, C., Chem. Eur. J., 2021, vol. 27, p. 3608. https://doi.org/10.1002/chem.202003761

    Article  CAS  PubMed  Google Scholar 

  2. Tezgerevska, T., Alley, K.G., and Boskovic, C., Coord. Chem. Rev., 2014, vol. 268, p. 23. https://doi.org/10.1016/j.ccr.2014.01.014

    Article  CAS  Google Scholar 

  3. Fedushkin, I.L., Maslova, O.V., Morozov, A.G., Dechert, S., Demeshko, S., and Meyer, F., Angew. Chem. Int. Ed., 2012, vol. 51, p. 10584. https://doi.org/10.1002/anie.201204452

    Article  CAS  Google Scholar 

  4. Selektor, S.L., Shokurov, A.V., Arslanov, V.V., Gorbunova, Y.G., Birin, K.P., Raitman, O.A., Morote, F., Cohen-Bouhacina, T., Grauby-Heywang, C., and Tsivadze, A.Y., J. Phys. Chem. C., 2014, vol. 118, p. 4250. https://doi.org/10.1021/jp411936k

    Article  CAS  Google Scholar 

  5. Shokurov, A.V., Kutsybala, D.S., Martynov, A.G., Bakirov, A.V., Shcherbina, M.A., Chvalun, S.N., Gorbunova, Y.G., Tsivadze, A.Yu., Zaytseva, A.V., Novikov, D., Arslanov, V.V., and Selektor, S.L., Langmuir, 2020, vol. 36, p. 1423. https://doi.org/10.1021/acs.langmuir.9b03403

    Article  CAS  PubMed  Google Scholar 

  6. Kutsybala, D.S., Shokurov, A.V., Martynov, A.G., Yagodin, A.V., Arslanov, V.V., Gorbunova, Y.G., and Selektor, S.L., Symmetry, 2022, vol. 14, p. 340. https://doi.org/10.3390/sym14020340

  7. Fedushkin, I.L., Maslova, O.V., Baranov, E.V., and Shavyrin, A.S., Inorg. Chem., 2009, vol. 48, p. 2355. https://doi.org/10.1021/ic900022s

  8. Jung, O.-S., Jo, D.H., Lee, Y.-A., Sohn, Y.S., and Pierpont, C.G., Inorg. Chem., 1998, vol. 37, p. 5875. https://doi.org/10.1021/ic9805372

  9. Bubnov, M.P., Skorodumova, N.A., Arapova, A.V., Smirnova, N.N., Samsonov, M.A., Fukin, G.K., Cherkasov, V.K., and Abakumov, G.A., Inorg. Chem., 2015, vol. 54, p. 7767. https://doi.org/10.1021/acs.inorgchem.5b00716

    Article  CAS  PubMed  Google Scholar 

  10. Buchanan, R.M. and Pierpont, C.G., J. Am. Chem. Soc., 1980, vol. 102, p. 4951. https://doi.org/10.1021/ja00535a021

    Article  CAS  Google Scholar 

  11. Fedushkin, I.L., Yambulatov, D.S., Skatova, A.A., Baranov, E.V., Demeshko, S., Bogomyakov, A.S., Ovcharenko, V.I., and Zueva, E.M., Inorg. Chem., 2017, vol. 56, p. 9825. https://doi.org/10.1021/acs.inorgchem.7b01344

    Article  CAS  PubMed  Google Scholar 

  12. Lukina, D.A., Skatova, A.A., Sokolov, V.G., Baranov, E.V., Demeshko, S., Ketkov, S.Yu., and Fedushkin, I.L., Dalton Trans., 2020, vol. 49, p. 14445. https://doi.org/10.1039/D0DT02963G

    Article  CAS  PubMed  Google Scholar 

  13. Sokolov, V.G., Lukina, D.A., Skatova, A.A., Fedushkin, I.L., Baranov, E.V., and Kiskin, M.A., J. Struct. Chem., 2023, vol. 64, p. 1724. https://doi.org/10.1134/S0022476623090159

    Article  CAS  Google Scholar 

  14. Sokolov, V.G., Lukina, D.A., Skatova, А.А., Moskalev, M.V., Baranov, E.V., and Fedushkin, I.L. Russ. Chem. Bull., 2021, vol. 70, p. 2119. https://doi.org/10.1007/s11172-021-3323-z

  15. Schultz, M., Boncella, J.M., Berg, D.J., Tilley, T.D., and Andersen, R.A., Organometallics, 2002, vol. 21, p. 460. https://doi.org/10.1021/om010661k

    Article  CAS  Google Scholar 

  16. Zwart, F.J., Reus, B., Laporte, A.A.H., Sinha, V., and Bruin, B., Inorg. Chem., 2021, vol. 60, p. 3274. https://doi.org/10.1021/acs.inorgchem.0c03685

  17. Chisholm, M.N., Huffman, J.C., Rothwell, I.P., Bradley, P.G., Kress, N., and Woodruff, W.H., J. Am. Chem. Soc., 1981, vol. 103, p. 4945. https://doi.org/10.1021/ja00406a048

    Article  CAS  Google Scholar 

  18. Janiak C., J. Chem. Soc., Dalton Trans., 2000, p. 3885. https://doi.org/10.1039/B003010O

  19. Rigaku Oxford Diffraction. (2021). CrysAlis Pro software system, version 1.171.41.122a, Rigaku Corporation, Wroclaw, Poland.

  20. Sheldrick, G.M., Acta Crystallogr. (A), 2015, vol. 71, p. 3. https://doi.org/10.1107/S2053273314026370

  21. Sheldrick, G.M., Acta Crystallogr. (C), 2015, vol. 71, p. 3. https://doi.org/10.1107/S2053229614024218

    Article  CAS  Google Scholar 

  22. Moskalev, M.V., Razborov, D.A., Bazanov, A.A., Sokolov, V.G., Koptseva, T.S., Baranov, E.V., and Fedushkin, I.L., Mendeleev Commun., 2020, vol. 30, p. 94. https://doi.org/10.1016/j.mencom.2020.01.031

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Funding

This work was carried out within the state assignment of the Ministry of Science and Higher Education of the Russian Federation using the equipment of the Center for Collective Use “Analytical Center of the IOMC RAS” with the financial support of the grant “Ensuring the development of the material and technical infrastructure of the centers for collective use of scientific equipmen” (unique identifier RF-2296.61321X0017, agreement number 075-15-2021-670).

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Correspondence to I. L. Fedushkin.

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I.L. Fedushkin is a member of the Editorial Board of the Russian Journal of General Chemistry. The remaining authors declare no conflict of interest.

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To the 35th Anniversary of the founding of the G.A. Razuvaev Institute of Organometallic Chemistry of the Russian Academy of Sciences

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Lukina, D.A., Skatova, A.A., Kozlova, E.A. et al. Ytterbium Complexes with Redox-Active N,N-Chelating Ligands. Russ J Gen Chem 93 (Suppl 3), S782–S787 (2023). https://doi.org/10.1134/S1070363223160168

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