Mixed-Ligand Coordination Compounds of Copper with Pyrocatechol Derivatives and 2-Hetarylbenzimidazoles

Cover Page

Cite item

Full Text

Abstract

Four new mixed-ligand copper-containing coordination compounds were synthesized, with the organic ligands, one of which (O,O-ligand) is bis-tert-butyl-substituted pyrocatechol, and the second (N,N-ligand) is 2-pyridylbenzimidazole or 2-imidazolylbenzothiazole. The structure of the obtained complexes was established based on the data of elemental analysis, electron spectroscopy, and electrochemical studies using cyclic voltammetry and rotating disk electrode voltammetry. It was shown that the resulting complexes with 2-pyridylbenzimidazole ligand contain Cu2+, and complexes with 2-imidazolylbenzothiazole contain Cu+.

About the authors

Elena S. Barskaya

Lomonosov Moscow State University

Author for correspondence.
Email: elenakovaleva2010@gamil.com
Russian Federation, 1-3 Leninskie Gory, Moscow, 119991, Russia

Anna A. Moiseeva

Lomonosov Moscow State University

Email: moiseeva.1955@mail.ru
Russian Federation, 1-3 Leninskie Gory, Moscow, 119991, Russia

Elena K. Beloglazkina

Lomonosov Moscow State University

Email: beloglazki@mail.ru
Russian Federation, 1-3 Leninskie Gory, Moscow, 119991, Russia

References

  1. G. Speier, Z. Tyeklár, P. Tóth, E. Speier, S. Tisza, A. Rockenbauer, A. M. Whalen, N. Alkire, C. G. Pierpont Inorg. Chem., 2001, 40, 5653. doi: 10.1021/ic010373g.
  2. O.-S. Jung, C. G. Pierpont Inorg. Chem., 1994, 33, 2227. doi: 10.1021/ic00088a027.
  3. D.N. Hendrickson, C.G. Pierpont Spin Crossover in Transition Metal Compounds II, 2004, 234, 63. doi: 10.1007/b95413.
  4. A. Caneschi, A. Cornia, A. Dei Inorg. Chem., 1998, 37, 3419. doi: 10.1021/ic971083w.
  5. H. Ohtsu, K. Tanaka Angew. Chem. Int. Ed., 2004, 43, 6301. doi: 10.1002/anie.200460023.
  6. N. Shaikh, S. Goswami, A. Panja, X.-Y. Wang, S. Gao, R.J. Butcher, P. Banerjee Inorg. Chem., 2004, 43, 5908. doi: 10.1021/ic049579i.
  7. C. Drouz, M. Vlasiou, A.D. Keramidas Dalton Trans., 2013, 42, 11831. doi: 10.1039/C3DT50619C.
  8. K.P. Butin, E.K. Beloglazkin, N.V Zyk Russ. Chem. Rev., 2005, 74, 531. doi: 10.1070/RC2005v074n06ABEH000977.
  9. C.G. Pierpont, A.S. Attia Collect. Czech. Chem. Commun., 2001, 66, 33. doi: 10.1135/cccc20010033.
  10. G. Speier, S. Tisza, Z. Tyeklar, C.W. Lange, C.G. Pierpont Inorg. Chem., 1994, 33, 2041. doi: 10.1021/ic00087a047.
  11. F. Zhao, W. Wang, W. Lu, L. Xu, Sh.Yang, X.-M. Ca, M. Zhou, M. Lei, M. Ma, H.-J. Xu, F. Cao Eur. J. Med. Chem., 2018, 146, 451. doi: 10.1016/j.ejmech.2018.01.041.
  12. D. Dooley, M. McGuirl, D. Brown, P.N. Turowski, W.S. Mclntire, P.F. Knowles Nature, 1991, 349, 262. doi: 10.1038/349262a0.
  13. E.S. Barskaya, E.K. Beloglazkina, A.G. Mazhuga, I.V. Yudin, N.V. Zyk Russ. Chem. Bull., 2015, 64, 1975. doi: 10.1007/s11172-015-1103-3.
  14. E.S. Barskaya, V.V. Shorokhov, A.V. Rzheutsky, A.D. Khudyakov, I.V. Yudin, V.A. Tafeenko, N.V. Zyk, E.K. Beloglazkina Russ. Chem. Bull., 2019, 68, 638. doi: 10.1007/s11172-019-2468-5.
  15. T.M. Khomenko, O.V. Salomatina, S.Yu. Kurbakova, I.V. Il’ina, K.P. Volcho, N.I. Komarova, D.V. Korchagina, N.F. Salakhutdinov, A.G. Tolstikov Russ. J. Org. Chem., 2006, 42, 1653. doi: 10.1134/S1070428006110091.

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2024 Barskaya E.S., Moiseeva A.A., Beloglazkina E.K.

Согласие на обработку персональных данных

 

Используя сайт https://journals.rcsi.science, я (далее – «Пользователь» или «Субъект персональных данных») даю согласие на обработку персональных данных на этом сайте (текст Согласия) и на обработку персональных данных с помощью сервиса «Яндекс.Метрика» (текст Согласия).