Novel Cobalt Bis-o-semiquinonato Complexes with Bidentate N-Donor Ligands

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Resumo

Two new cobalt bis-o-semiquinonato complexes, (Pyz-Phen)Co(3,6-DBSQ)2 (I) and (Bpyz)Co(3,6-DBSQ)2 (II) (Pyz-Phen = pyrazino[2,3-f][1,10]phenanthroline, Bpyz = bipyrazine, 3,6-DBSQ = 3,6-di-tert-butyl-o-benzoquinone radical anion), were synthesized. According to X-ray diffraction data, both complexes have a trigonal-prismatic geometry of the inner coordination sphere. The distribution of C–O and Co–O bond lengths, which reflects the valence state of the metal and the ligands, indicates that the complexes are formed by cobalt(II) surrounded by two semiquinone radical anions. The results of magnetochemical measurements show that the pyrazino[2,3-f][1,10]phenanthroline complex is a derivative of low-spin divalent cobalt, whereas its bipyrazine structural analogue is a high-spin cobalt(II) derivative.

Sobre autores

A. Zolotukhin

Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences, Nizhny Novgorod, Russia

Email: aaz@iomc.ras.ru
Россия, Нижний Новгород

M. Bubnov

Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences, Nizhny Novgorod, Russia

Email: aaz@iomc.ras.ru
Россия, Нижний Новгород

R. Rumyantsev

Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences, Nizhny Novgorod, Russia

Email: aaz@iomc.ras.ru
Россия, Нижний Новгород

G. Fukin

Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences, Nizhny Novgorod, Russia

Email: aaz@iomc.ras.ru
Россия, Нижний Новгород

A. Bogomyakov


International Tomography Center, Siberian Branch, Russian Academy of Sciences, Novosibirsk, Russia

Email: aaz@iomc.ras.ru
Россия, Новосибирск

V. Cherkasov

Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences, Nizhny Novgorod, Russia

Autor responsável pela correspondência
Email: aaz@iomc.ras.ru
Россия, Нижний Новгород

Bibliografia

  1. Pierpont C.G. // Coord. Chem. Rev. 2001. V. 216–217. P. 99. https://doi.org/10.1016/S0010-8545(01)00309-5
  2. Tezgerevska T., Alley K.G., Boskovic C. // Coord. Chem. Rev. 2014. V. 268. P. 23. https://doi.org/10.1016/j.ccr.2014.01.014
  3. Золотухин А.А., Бубнов М.П., Черкасов В.К. и др. // Коорд. химия. 2018. 44. № 2. С. 123 (Zolotukhin A.A., Bubnov M.P., Cherkasov V.K. et al. // Russ. J. Coord. Chem. 2018. V. 44. P. 272). https://doi.org/10.7868/S0132344X18020056
  4. Buchanan R.M., Pierpont C.G. // J. Am. Chem. Soc. 1980. V. 102. P. 4951. https://doi.org/10.1021/ja00535a021
  5. Абакумов Г.А., Черкасов В.К., Бубнов М.П. и др. // Докл. РН. 1993. Т. 328. № 3. С. 332 (Abakumov G.A., Cherkasov V.K., Bubnov M.P. et al. // Dokl. Akad. Nauk. 1993. V. 328. P. 332). https://doi.org/S0020-1693(22)00023-8/h0080
  6. Roux C., Adams D.M., Itie J.P. et al. // Inorg. Chem. 1996. V. 35. P. 2846. https://doi.org/10.1021/ic951080o
  7. Markevtsev I.N., Monakhov M.P., Platonov V.V. et al. // J. Magn. Magn. Mater. 2006. V. 300. P. e407. https://doi.org/10.1016/j.jmmm.2005.10.134
  8. Yokoyama T., Okamoto K., Nagai K. et al. // Chem. Phys. Lett. 2001. V. 345. P. 272. https://doi.org/10.1016/S0009-2614(01)00888-0
  9. Francisco T.M., Gee W.J., Shepherd H.J. // J. Phys. Chem. Lett. 2017. V. 8. № 19. P. 4774. https://doi.org/10.1021/acs.jpclett.7b01794
  10. Lukyanov A. Yu. Bubnov M.P., Skorodumova N.A. et al. // Solid State Sci. 2015. V. 48. P. 13. https://doi.org/10.1016/j.solidstatescienes.2015.06.011
  11. Jung O.-S., Jo D.H., Lee Y.-A. et al. // Inorg. Chem. 1997. V. 36. P. 19. https://doi.org/10.1021/ic961214d
  12. Zolotukhin A.A., Bubnov M.P., Arapova A.V. et al. // Inorg. Chem. 2017. V. 56. P. 14751. https://doi.org/10.1021/acs.inorgchem.7b02597
  13. Adams D.M., Dei A., Rheingold A.L. et al. // J. Am. Chem. Soc. 1993. V. 115. P. 8221. https://doi.org/10.1021/ja00071a035
  14. Арапова А.В., Бубнов М.П., Абакумов Г.А. и др. // Журн. физ. химии. 2009. Т. 83. № 8. С. 1417.
  15. Jung O.-S., Pierpont C.G. // Inorg. Chem. 1994. V. 33. P. 2227. https://doi.org/10.1021/ic00088a027
  16. Protasenko N.A., Poddel’sky A.I., Bogomyakov A.S. et al. // Polyhedron. 2013. V. 49. P. 239. https://doi.org/10.1016/j.poly.2012.10.016
  17. Zolotukhin A.A., Bubnov M.P., Bogomyakov A.S. et al. // Inorg. Chim. Acta. 2020. V. 502. 119346. https://doi.org/10.1016/j.ica.2019.119346
  18. Gomez-Coca S., Cremades E., Aliaga-Alcalde N. et al. // J. Am. Chem. Soc. 2013. V. 135. P. 7010. https://doi.org/10.1021/ja4015138
  19. Novikov V.V., Pavlov A.A., Nelyubina Y.V. et al. // J. Am. Chem. Soc. 2015. V. 137. P. 9792. https://doi.org/10.1021/jacs.5b05739
  20. Perrin D.D., Armarego W.L.F., Perrin D.R. Purification of Laboratory Chemicals. Oxford: Pergamon Press, 1980.
  21. Litvinenko A.S., Mikhaleva E.A., Kolotilov S.V., Pavlishchuk V.V. // Theor. Exp. Chem. 2011. V. 46. P. 422. https://doi.org/10.1007/s11237-011-9174-1
  22. Rigaku Oxford Diffraction. CrysAlis Pro Software System. Version 1.171.38.46. Wroclaw (Poland): Rigaku Corporation, 2015.
  23. SAINT. Data Reduction and Correction Program. Madison (WI, USA): Bruker AXS, 2014.
  24. Kraus L., Herbst-Irmer R., Sheldrick G.M., Stalke D. // J. Appl. Crystallogr. 2015. V. 48. P. 3. https://doi.org/10.1107/S1600576714022985
  25. Sheldrick G.M. // Acta Crystallogr. A. 2015. V. 71. P. 3. https://doi.org/10.1107/S2053273314026370
  26. Sheldrick G.M. // Acta Crystallogr. C. 2015. V. 71. P. 3. https://doi.org/10.1107/S2053229614024218
  27. Pierpont C.G., Buchanan R.M. // Coord. Chem. Rev. 1981. V. 38. P. 45. https://doi.org/10.1016/S0010-8545(00)80499-3
  28. Brown S.N. // Inorg. Chem. 2012. V. 51. P. 1251. https://doi.org/10.1021/ic202764j
  29. Adams D.M., Dei A., Rheingold A.L. et al. // Angew. Chem. Int. Ed. 1993. V. 32. P. 880. https://doi.org/10.1002/anie.199308801
  30. Wang J.-H., Dai J.-W., Li Z.-Y. et al. // New J. Chem. 2020. V. 44. P. 8471. https://doi.org/10.1039/D0NJ00767F
  31. Janiak C. // Dalton Trans. 2000. P. 3885. https://doi.org/10.1039/b003010o
  32. Guda A.A., Chegerev M., Starikov A.G. et al. // J. Phys.: Condens. Matter. 2021. V. 33. 215405. https://doi.org/10.1088/1361-648X/abe650
  33. Protasenko N.A., Poddel’sky A.I. // Theor. Exp. Chem. 2020. V. 56. P. 338. https://doi.org/10.1007/s11237-020-09663-1
  34. Graf M., Wolmershauser G., Kelm H. et al. // Angew. Chem. Int. Ed. 2010. V. 49. P. 950. https://doi.org/10.1002/anie.200903789
  35. Фарус О.А., Балашев К.П., Иванов М.А. и др. // Журн. общ. химии. 2006. T. 76. С. 328.
  36. Kawanishi Y., Kitamura N., Tazuke S. // Inorg. Chem. 1989. V. 28. P. 2968. https://doi.org/10.1021/ic00314a019
  37. Hendrickson D.N., Pierpont C.G. // Top. Curr. Chem. 2004. V. 234. P. 63. https://doi.org/10.1007/b95413
  38. Jung O.-S., Pierpont C.G. // J. Am. Chem. Soc. 1994. V. 116. P. 1127. https://doi.org/10.1021/ja00082a043

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