Skip to main content
SpringerLink
Log in

Synthesis of Ni(II) complexes with chiral derivatives of cyclohexane-1,2-diamine, bycyclo[2.2.2]octane-2,3-diamine, and 1,2-diphenylethane-1,2-diamine

  • Published:
Russian Journal of General Chemistry Aims and scope Submit manuscript

Abstract

Chiral ligands—derivatives of (1R,2R)-cyclohexane-1,2-diamine, (1R,2R)-diphenylethane-1,2-diamine, and (2S,3S)-bicyclo[2.2.2]octane-2,3-diamine—and octahedral Ni(II) complexes on their basis have been synthesized.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Log in via an institution

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Suga, H., Furihata, Y., Sakamoto, A., Itoh, K., Okumura, Y., Tsuchida, T., Kakehi, A., and Baba, T., J. Org. Chem., 2011, vol. 76, p. 7377. doi 10.1021/jo201061f.

    Article  CAS  Google Scholar 

  2. Suga, H., Adachi, Y., Fujimoto, K., Furihata, Y., Tsuchida, T., Kakehi, A., and Baba, T., J. Org. Chem., 2009, vol. 74, p. 1099. doi 10.1021/jo802392c

    Article  CAS  Google Scholar 

  3. Suga, H., Funyu, A., and Kakehi, A., Org. Lett., 2007, vol. 9, p. 97. doi 10.1021/ol062675y

    Article  CAS  Google Scholar 

  4. Suga, H., Nakajima, T., Itoh, K., and Kakehi, A., Org. Lett., 2005, vol. 7, p. 1431. doi 10.1021/ol050397h

    Article  CAS  Google Scholar 

  5. Lu, Z., Wilsily, A., and Fu, G.C., J. Am. Chem. Soc., 2011, vol. 133, no. 22, p. 8154. doi 10.1021/ja203560q

    Article  CAS  Google Scholar 

  6. Owston, N.A. and Fu, G.C., J. Am. Chem. Soc., 2010, vol. 132, p. no. 34, p. 11908. doi 10.1021/ja105924f

    Article  CAS  Google Scholar 

  7. Saito, B. and Fu, G.C., J. Am. Chem. Soc., 2008, vol. 130, no. 21, p. 6694. doi 10.1021/ja8013677

    Article  CAS  Google Scholar 

  8. Fossey, J.S., Matsubara, R., Vital, P., and Kobayashi, S., Org. Biomol. Chem., 2005, vol. 3, p. 2910. doi 10.1039/B505404D

    Article  CAS  Google Scholar 

  9. Evans, D.A. and Seidel, D., J. Am. Chem. Soc., 2005, vol. 127, no. 28, p. 9958. doi 10.1021/ja052935r

    Article  CAS  Google Scholar 

  10. Evans, D.A., Shizue, M., and Seidel, D., J. Am. Chem. Soc., 2007, vol. 129, no. 37, p. 11583. doi 10.1021/ja0735913

    Article  CAS  Google Scholar 

  11. Reznikov, A.N. and Klimochkin, Y.N., Russ. J. Org. Chem., 2012, vol. 48, no. 12, p. 1526. doi 10.1134/S1070428012120056

    Article  CAS  Google Scholar 

  12. Reznikov, A.N., Sybiryakova, A.E., Rybakov, V.B., and Klimochkin, Yu.N., Tetrahedron Asym., 2015, vol. 26, p. 1050. doi 10.1016/j.tetasy.2015.08.003

    Article  CAS  Google Scholar 

  13. Reznikov, A.N., Sibiryakova, A.E., and Klimochkin, Yu.N., Russ. J. Gen. Chem., 2014, vol. 84, no. 11, p. 2280. doi 10.1134/S1070363214110437

    Article  CAS  Google Scholar 

  14. Reznikov, A.N., Sibiryakova, A.E., and Klimochkin, Yu.N., Russ. J. Org. Chem., 2014, vol. 50, no. 11, p. 1695. doi 10.1134/S107042801411027X

    Article  CAS  Google Scholar 

  15. Reznikov, A.N., Golovin, E.V., and Klimochkin, Yu.N., Russ. J. Org. Chem., 2013, vol. 49, no. 5, p. 663. doi 10.1134/S1070428013050047

    Article  CAS  Google Scholar 

  16. Reznikov, A.N., Osyanin, V.A., and Klimochkin, Yu.N., Izv. Vuzov, Ser. Khim. Khin. Tekhnol., 2012, vol. 55, no. 12, p. 86.

    CAS  Google Scholar 

  17. Reznikov, A.N. and Klimochkin, Yu.N., RF Patent 2488576, 2013; Byull. Izobret., 2013, no. 21.

  18. Reznikov, A.N., Sidnin, E.A., and Klimochkin, Yu.N., RF Patent 2529996, 2014; Byull. Izobret., 2014, no. 28.

  19. Reznikov, A.N., Sidnin, E.A., and Klimochkin, Yu.N., RF Patent 2555370, 2015; Byull. Izobret., 2015, no. 19.

  20. Reznikov, A.N., Sidnin, E.A., and Klimochkin, Yu.N., Russ. J. Org. Chem., 2013, vol. 49, no. 11, p. 1600. doi 10.1134/S1070428013110067

    Article  CAS  Google Scholar 

  21. Sidnin, E.A., Reznikov, A.N., Shiryayev, V.A., and Klimochkin, Yu.N., Russ. J. Org. Chem., 2014, vol. 50, no. 11, p. 1579. doi 10.1134/S1070428014110074

    Article  CAS  Google Scholar 

  22. Ihara, Y. and Tsuchiya, R., Bull. Chem. Soc. Japan, 1984, vol. 57, no. 10, p. 2829. doi 10.1246/bcsj.57.2829

    Article  CAS  Google Scholar 

  23. Ihara, Y., Fukuda, Y., and Sone, K., Inorg. Chem., 1987, vol. 26, no. 22, p. 3745. doi 10.1021/ic00269a025

    Article  CAS  Google Scholar 

  24. Yang, D., Li, D., Wang, L., Zhao, D., and Wang, R., J. Org. Chem., 2015, vol. 80, no. 9, p. 4336. doi 10.1021/acs.joc.5b00013

    Article  CAS  Google Scholar 

  25. Meshkovaya, V.V., Yudashkin, A.V., Bushueva, P.Y., Eremeeva, N.B., and Klimochkin, Y.N., Tetrahedron, 2014, vol. 70, no. 19, p. 3211. doi 10.1016/j.tet.2014.02.092

    Article  CAS  Google Scholar 

  26. Kusakov, M.M., Shimanko, N.A., and Shishkina, M.V., Ul’trafioletovye spektry pogloshheniya aromaticheskikh uglevodorodov (UV Absorption Spectra of Aromatic Hydrocarbons), Moscow: Akad. Nauk SSSR, 1963, p. 7.

    Google Scholar 

  27. Ihara, Y. and Toda, R., Thermochim. Acta, 1994, vol. 237, no. 1, p. 167. doi 10.1016/0040-6031(94)85196-4

    Article  CAS  Google Scholar 

  28. Gonzalez, E., Rodrigue-Witchel, A., and Reber, C., Coord. Chem. Rev., 2007, vol. 251, p. 351. doi 10.1016/j.ccr.2006.08.011

    Article  CAS  Google Scholar 

  29. Ihara, Y., Fukui, T., and Sone, K., Bull. Chem. Soc. Japan, 1986, vol. 59, no. 6, p. 1825. doi 10.1246/bcsj.59.1825

    Article  CAS  Google Scholar 

  30. Cho, J., Lee, Y.-M., Kim, S.Y., and Nam, W., Polyhedron, 2010, vol. 29, p. 446. doi 10.1016/j.poly.2009.06.071

    Article  CAS  Google Scholar 

  31. Moreno-Lara, B., Carabineiro, S.A., Krishnamoorthy, P., Rodriguez, A.M., Mano, J.F., Manzano, B.R., Jalon, F.A., and Gomes, P.T., J. Organomet. Chem., 2015, vols. 799–800, p. 90. doi 10.1016/j.jorganchem.2015.09.004

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Samara State Technical University, ul. Molodogvardeyskaya 244, Samara, 443100, Russia

    A. E. Sibiryakova, A. N. Reznikov & Yu. N. Klimochkin

  2. Lomonosov Moscow State University, Moscow, Russia

    V. B. Rybakov

Authors
  1. A. E. Sibiryakova
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. A. N. Reznikov
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. V. B. Rybakov
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Yu. N. Klimochkin
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to A. E. Sibiryakova.

Additional information

Original Russian Text © A.E. Sibiryakova, A.N. Reznikov, V.B. Rybakov, Yu.N. Klimochkin, 2016, published in Zhurnal Obshchei Khimii, 2016, Vol. 86, No. 11, pp. 1834–1840.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sibiryakova, A.E., Reznikov, A.N., Rybakov, V.B. et al. Synthesis of Ni(II) complexes with chiral derivatives of cyclohexane-1,2-diamine, bycyclo[2.2.2]octane-2,3-diamine, and 1,2-diphenylethane-1,2-diamine. Russ J Gen Chem 86, 2477–2483 (2016). https://doi.org/10.1134/S107036321611013X

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S107036321611013X

Keywords

Search

Navigation