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Effect of Bridging Group Nature on the Extraction Ability of Diphenylphosphorylketones toward Actinides and Lanthanides

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Abstract

Effect of structure of phosphorylketones containing flexible alkyl and conformationally rigid fragments in the linker on extraction ability toward actinides and lanthanides has been studied. It has been shown that the introduction of conformationally rigid cycloalkanediyl and alkenediyl fragments in the bridge between P=O and C=O groups in the structure of molecule decreases efficiency of extractants for both actinides and lanthanides. At the same time, the introduction of flexible alkyl groups in linker structure increases complexing and extraction ability. This dependence has been explained theoretically by modeling complexation (DFT, PBE, cc-pVDZ), monodentate coordination was observed for all studied phosphorylalkanones

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REFERENCES

  1. Assessment of Partitioning Processes for Transmutation of Actinides IAEA (Vienna, 2010, IAEA-TECDOC-1648).

  2. B. Ya. Zil’berman, E. A. Puzikov, D. V. Ryabkov, et al., At. Energy 107, 333 (2009). https://doi.org/10.1007/s10512-010-9233-z

    Article  CAS  Google Scholar 

  3. Ion Exchange and Solvent Extraction: A Series of Advances, Ed. by B. A. Moyer (CRC Press, New York, 2010).

    Google Scholar 

  4. A. M. Rozen, Ros. Khim. Zh. 40, 42 (1996).

    CAS  Google Scholar 

  5. T. A. Mastryukova, O. I. Artyushin, I. L. Odinets, and I. G. Tananaev, Ros. Khim. Zh. 49, 86 (2005).

    CAS  Google Scholar 

  6. A. M. Rozen and B. V. Krupnov, Russ. Chem. Rev. 65, 973 (1996). https://doi.org/10.1070/RC1996v065n11ABEH000241

    Article  Google Scholar 

  7. P. Matveev, P. K. Mohapatra, S. N. Kalmykov, et al., Solvent Extr. Ion Exch. 679 (2020). https://doi.org/10.1080/07366299.2020.1856998

  8. T. Ya. Medved’, M. K. Chmutova, N. P. Nesterova, et al., Izv. AN SSSR, Ser. Khim. 9, 2112 (1981).

    Google Scholar 

  9. M. K. Chmutova, N. E. Kochetkova, O. E. Koiro, et al., J. Radioanal. Chem. 80, 63 (1983). https://doi.org/10.1007/BF02517648

    Article  Google Scholar 

  10. B. F. Myasoedov, M. K. Chmutova, N. E. Kochetkova, et al., Solvent Extr. Ion Exch. 4, 61 (1986). https://doi.org/10.1080/07366298608917853

    Article  CAS  Google Scholar 

  11. M. N. Litvina, M. K. Chmutova, Yu. M. Kulyako, and B. F. Myasoedov, Radiochemistry 43, 66 (2001). https://doi.org/10.1023/A:1012878106998

    Article  CAS  Google Scholar 

  12. E. V. Sharova, O. I. Artyushin, I. L. Odinets, Russ. Chem. Rev. 83, 95 (2014). https://doi.org/10.1070/RC2014v083n02ABEH004384

    Article  CAS  Google Scholar 

  13. D. A. Tatarinov, V. F. Mironov, A. A. Kostin, et al., Russ. Gen. Chem. 80, 1377 (2010). https://doi.org/10.1134/S1070363210070297

    Article  CAS  Google Scholar 

  14. G. V. Bodrin, E. I. Goryunov, I. B. Goryunova, et al., Dokl. Chem. 447, 269 (2012). https://doi.org/10.1134/S0012500812120014

    Article  CAS  Google Scholar 

  15. E. I. Goryunov, G. V. Bodrin, I. B. Goryunova, et al., Russ. Chem. Bull. 62, 780 (2013). https://doi.org/10.1007/s11172-013-0106-1

    Article  CAS  Google Scholar 

  16. A. M. Safiulina, A. G. Matveeva, A. V. Lizunov, et al., Dokl. Chem. 460, 57 (2015). https://doi.org/10.1134/S001250081502007X

    Article  CAS  Google Scholar 

  17. A. M. Safiulina, N. E. Borisova, A. V. Lizunov, et al., Russ. J. Inorg. Chem. 67, 524 (2022). https://doi.org/10.1134/S0036023622040167

    Article  CAS  Google Scholar 

  18. Yu. G. Elistratova, A. R. Mustafina, D. A. Tatarinov, et al., Russ. Chem. Bull. 60, 790 (2011). https://doi.org/10.1007/s11172-011-0126-7

    Article  CAS  Google Scholar 

  19. A. G. Matveeva, E. I. Goryunov, A. M. Tu, et al., Russ. Chem. Bull. 63, 2493 (2014). https://doi.org/10.1007/s11172-014-0767-4

    Article  CAS  Google Scholar 

  20. A. G. Matveeva, A. M. Tu, A. M. Safiulina, et al., Russ. Chem. Bull. 62, 1309 (2013). https://doi.org/10.1007/s11172-013-0184-0

    Article  CAS  Google Scholar 

  21. S. Mazzotta, L. Gramigna, L. Bernardi, et al., Org. Proc. Res. Dev. 14, 687 (2010). https://doi.org/10.1021/op1000308

    Article  CAS  Google Scholar 

  22. R. J. Giguere and B. Herberich, Synth. Commun. 21, 2197 (1991). https://doi.org/10.1080/00397919108055453

    Article  CAS  Google Scholar 

  23. S. B. Savvin, Organic Reagents of the Arsenazo III Group (Atomizdat, Moscow, 1971) [in Russian].

    Google Scholar 

  24. D. N. Laikov, Chem. Phys. Lett. 416, 116 (2005). https://doi.org/10.1016/j.cplett.2005.09.046

    Article  CAS  Google Scholar 

  25. D. N. Laikov, Chem. Phys. Lett. 281, 151 (1997). https://doi.org/10.1016/S0009-2614(97)01206-2

    Article  CAS  Google Scholar 

  26. J. P. Perdew, K. Burke, and M. Ernzerhof, Phys. Rev. Lett. 77, 3865 (1996). https://doi.org/10.1103/PhysRevLett.77.3865

    Article  CAS  PubMed  Google Scholar 

  27. J. P. Perdew, K. Burke, and M. Ernzerhof, Phys. Rev. Lett. 78, 1396 (1997). https://doi.org/10.1103/PhysRevLett.78.1396

    Article  CAS  Google Scholar 

  28. A. M. Safiulina, A. G. Matveeva, T. K. Dvoryanchikova, et al., Russ. Chem. Bull. 61, 392 (2012). https://doi.org/10.1007/s11172-012-0055-0

    Article  CAS  Google Scholar 

  29. A. G. Matveeva, M. S. Grigor’ev, T. K. Dvoryanchikova, et al., Russ. Chem. Bull. 61, 399 (2012). https://doi.org/10.1007/s11172-012-0056-z

    Article  CAS  Google Scholar 

  30. C. Reichardt and T. Welton, Solvents and Solvent Effects in Organic Chemistry (Wiley-VCH Verlag GmbH & Co. KGaA, 2011).

  31. R. Babecki, A. W. G. Platt, and D. R. Russell, Inorg. Chim. Acta 171, 25 (1990). https://doi.org/10.1016/S0020-1693(00)84658-7

    Article  CAS  Google Scholar 

  32. U. Casellato, P. A. Vigato, and M. Vidali, Coord. Chem. Rev. 36, 183 (1981). https://doi.org/10.1016/S0010-8545(00)80500-7

    Article  CAS  Google Scholar 

  33. D. J. McCabe, E. N. Duesler, and R. T. Paine, Inorg. Chim. Acta 147, 265 (1988). https://doi.org/10.1016/S0020-1693(00)83383-6

    Article  CAS  Google Scholar 

  34. S. M. Bowen, E. N. Duesler, and R. T. Paine, Inorg. Chem. 21, 261 (1982). https://doi.org/10.1021/ic00131a048

    Article  CAS  Google Scholar 

  35. S. M. Bowen, E. N. Duesler, and R. T. Paine, Inorg. Chim. Acta 61, 155 (1982). https://doi.org/10.1016/S0020-1693(00)89134-3

    Article  CAS  Google Scholar 

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Funding

This work was performed under the State Assignment for 2023 of the Ministry of Science and Higher Education of the Russian Federation for the Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences (INEOS RAS) (no. 075-03-2023-642). The study of the obtained compounds was supported by the Ministry of Science and Higher Education of the Russian Federation using equipment (NMR spectrometers) of the Center for Molecular Structure Studies, INEOS RAS. Computations were performed under the State assignment for the Moscow State University “Solving problems of nuclear power and environmental safety and materials diagnostics using ionizing radiation” (Project no. 122030200324-1).

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Translated by I. Kudryavtsev

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Safiulina, A.M., Borisova, N.E., Lizunov, A.V. et al. Effect of Bridging Group Nature on the Extraction Ability of Diphenylphosphorylketones toward Actinides and Lanthanides. Russ. J. Inorg. Chem. 68, 1650–1656 (2023). https://doi.org/10.1134/S0036023623602118

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