New macrocyclic bis-1,10-phenanthroline-2,9-diamides. synthesis and stereodynamics in solutions

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New examples of macrocyclic 1,10-phenanthroline-2,9-diamides containing simultaneously two phenanthroline moiety in their structure have been obtained. The structure of the obtained compounds was confirmed by NMR spectroscopy and other methods. New macrocyclic phenanthrolines expectedly exhibit complex stereodynamic behavior in solutions. This effect was studied using 1H NMR spectroscopy at various temperatures.

作者简介

Yu. Ustynyuk

Moscow State University

V. Petrov

Moscow State University

P. Lemport

Moscow State University

V. Roznyatovsky

Moscow State University

V. Nenajdenko

Moscow State University

Email: nenajdenko@gmail.com

参考

  1. Ustynyuk Yu.A., Borisova N.E., Babain V.A., Gloriozov I.P., Manuilov A.Y., Kalmykov S.N., Alyapyshev M.Yu., Tkachenko L.I., Kenf E.V., Ustynyuk N.A. Chem. Commun. 2015, 51, 7466-7469. doi: 10.1039/c5cc01620g
  2. Leoncini A., Huskens J., Verboom W. Chem. Soc. Rev. 2017, 46, 7229-7273. doi: 10.1039/C7CS00574A
  3. Alyapyshev M., Babain V., Kirsanov D. Energies. 2022, 15, 7380. doi: 10.3390/en15197380
  4. Wang Y., Yang Y., Wu Y., Li J., Hu B., Cai Y., Yuan L., Feng W. Inorg. Chem. 2023, 62, 4922-4933. doi: 10.1021/acs.inorgchem.2c04384
  5. Alyapyshev M., Ashina J., Dar'in D., Kenf E., Kirsanov D., Tkachenko L., Legin A., Starova G., Babain V. RSC Adv. 2016, 6, 68642-68652. doi: 10.1039/c6ra08946a
  6. Xiao C.-L., Wu Q.-Y., Wang C.-Z., Zhao Y.-L., Chai Z.-F., Shi W.-Q. Inorg. Chem. 2014, 53, 10846-10853. doi: 10.1021/ic500816z
  7. Bencini A., Lippolis V. Coord. Chem. Rev. 2010, 254, 2096-2180. doi: 10.1016/j.ccr.2010.04.008
  8. Colombo F., Annunziata R., Raimondi L., Benaglia M. Chirality. 2006, 18, 446-456. doi: 10.1002/chir.20283
  9. Lemport P.S., Petrov V.S., Matveev P.I., Leksina U.M., Roznyatovsky V.A., Gloriozov I.P., Yatsenko A.V., Tafeenko V.A., Dorovatovskii P.V., Khrustalev V.N., Budylin G.S., Shirsin E.A., Markov V.Y., Goryunkov A.A., Petrov V.G., Ustynyuk Y.A., Nenajdenko V.G. Int. J. Mol. Sci. 2023, 24, 10261. doi: 10.3390/ijms241210261
  10. Lemport P.S., Evsiunina M.V., Matveev P.I., Petrov V.S., Pozdeev A.S., Khult E.K., Nelyubina Yu.V., Isakovskaya K.L., Roznyatovsky V.A., Gloriozov I.P., Tarasevich B.N., Aldoshin A.S., Petrov V.G., Kalmykov S.N., Ustynyuk Yu.A., Nenajdenko V.G. Inorg. Chem. Front. 2022, 9, 4402-4412. doi: 10.1039/D2QI00803C
  11. Петров В.С., Авакян Н.А., Лемпорт П.С., Матвеев П.И., Евсюнина М.В., Рознятовский В.А., Тарасевич Б.Н., Исаковская К.Л., Устынюк Ю.А., Ненайденко В.Г. Изв. Ан. Сер. хим. 2023, 72, 697-705.
  12. Petrov V.S., Avagyan N.A., Lemport P.S., Matveev P.I., Evsiunina M.V., Roznyatovsky V.A., Tarasevich B.N., Isakovskaya K.L., Ustynyuk Y.A., Nenajdenko V.G. Russ. Chem. Bull. 2023, 72, 697-705. doi: 10.1007/s11172-023-3834-7
  13. Lemport P.S., Matveev P.I., Yatsenko A.V., Evsiunina M.V., Petrov V.S., Tarasevich B.N., Roznyatovsky V.A., Dorovatovskii P.V., Khrustalev V.N., Zhokhov S.S., Solov'ev V.P., Aslanov L.A., Petrov V.G., Kalmykov S.N., Nenajdenko V.G., Ustyniuk Yu.A. RSC Adv. 2020, 10, 26022-26033. doi: 10.1039/D0RA05182A
  14. Avagyan N.A., Lemport P.S., Lysenko K.A., Gudovanny A.O., Roznyatovsky V.A., Petrov V.S., Vokuev M.F., Ustynyuk Y.A., Nenajdenko V.G. Molecules. 2022, 27, 4705. doi: 10.3390/molecules27154705
  15. Ustynyuk Yu. A., Lemport P.S., Roznyatovsky V.A., Lyssenko K.A., Gudovannyy A.O., Matveev P.I., Khult E.K., Evsiunina M.V., Petrov V.G., Gloriozov I.P., Pozdeev A.S., Petrov V.S., Avagyan N.A., Aldoshin A.S., Kalmykov S.N., Nenajdenko V.G. Molecules. 2022, 27, 3114. doi: 10.3390/molecules27103114
  16. Райхардт К. Растворители и эффекты среды в органической химии. Ред. В.С. Петросян. М.: Мир, 1991.

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