Synthesis of triethylene glycol-substituted phenylterpyridine with a terminal aurophilic group and its coordination compound with Rh(III) for adsorption on the gold surface

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A method has been developed for the preparation of a conjugate of 4-substituted phenylterpyridine and lipoic acid with a triethylene glycol linker between the terpyridine and sulfur-containing fragments. A coordination compound of the obtained terpyridine with Rh(III) have been synthesized. The ability of the resulting ligand and rhodium complex to be chemisorbed on the surface of gold electrodes with the formation of an Au-S bond have been shown using the cyclic voltammetry.

作者简介

I. Salimova

Lomonosov Moscow State University

Email: bel@org.chem.msu.ru

A. Moiseeva

Lomonosov Moscow State University

Email: bel@org.chem.msu.ru

N. Zyk

Lomonosov Moscow State University

Email: bel@org.chem.msu.ru

E. Beloglazkina

Lomonosov Moscow State University

Email: bel@org.chem.msu.ru

参考

  1. Shorokhov V.V., Presnov D.E., Amitonov S.V., Pashkin Y.A., Krupenin V.A. Nanoscale. 2017, 9, 613-620. doi: 10.1039/C6NR07258E
  2. Dagesyan S.A., Shorokhov V.V., Presnov D.E., Soldatov E.S., Trifonov A.S., Krupenin V.A. Nanotechnology. 2017, 28, 225-304. doi: 10.1088/1361-6528/aa6dea
  3. Gale P.A., Howe E.N.W., Wu X. Anion Receptor Chem. 2016, 1, 351-422. doi: 10.1016/j.chempr.2016.08.004
  4. Saleem M., Lee K.H. RSC Adv. 2015, 5, 72150-72287. doi: 10.1039/C5RA11388A
  5. Mital M., Ziora Z., Coord. Chem. Rev. 2018, 375, 434-458. doi: 10.1016/j.ccr.2018.02.013
  6. Mielke J., Leyssner F., Koch M., Meyer S., Luo Y., Selvanathan S., Haag R., Tegeder P., Grill L., ACS Nano. 2011, 5, 2090. doi: 10.1021/nn103297e
  7. Гайдамаченко В.Р., Белоглазкина Е.К., Петров Р.А., Дагесян С.А., Сапков И.В., Солдатов Е.С. Вестн. МГУ. Сер. 3: Физика, астрономия. 2018, 73, 70-76.
  8. Gaydamachenko V.R., Beloglazkina E.K., Petrov R.A., Dagesyan S.A., Sapkov I.V., Soldatov E.S. Moscow Univ. Phys. Bull. 2018, 73, 193-198. doi: 10.3103/S0027134918020066
  9. Davidson R., Liang J. H., Milan D.C., Mao B.W., Nichols R.J., Higgins S.J., Yufit D.S., Beeby A., Low P.G. Inorg. Chem. 2015, 54, 5487-5494. doi: 10.1021/acs.inorgchem.5b00507
  10. Brooke R.J., Jin C., Szumski D.S., Nichols R.J., Mao B.-W., Thygesen K.S., Schwarzacher W. Nano Lett. 2015, 15, 275-280. doi: 10.1021/nl503518q
  11. Chappell S., Brooke C., Nichols R.J., Cook L.J.K., Halcrow M., Ulstrup J., Higgins S.J. Faraday Disc. 2016, 193, 113-131. doi: 10.1039/c6fd00080k
  12. Osorio H.M., Catarelli S., Cea P., Gluyas J.B.G., Hartl F. J. Am. Chem. Soc. 2015, 137, 14319-14328. doi: 10.1021/jacs.5b08431
  13. Salimova I.O., Berezina A.V., Shikholina I.A., Zyk N.V., Beloglazkina E.K. Polyhedron. 2021, 200, 115149. doi: 10.1016/j.poly.2021.115149
  14. Салимова И.О., Березина А.В., Моисеева А.А., Зык Н.В., Белоглазкина Е.К. Изв. Акад. наук. Сер. хим. 2022, 71, 267-275.
  15. Salimova I.O., Berezina A.V., Moiseeva A.A., Zyk N.V., Beloglazkina E.K. Russ. Chem. Bull. 2022, 71, 267-275. doi: 10.1007/s11172-022-3407-4
  16. Pineux F., Federico S., Klotz K.-N., Kachler S., Michiels C., Sturlese M., Prato M., Giampiero S., Moro S., Bonifazi D. ChemMedChem. 2020, 15, 1909-1920. doi: 10.1002/cmdc.202000466
  17. Brönnimann S., Zilian A., Güdel H.U., Ludi A. Inorganica Chim. Acta. 1990, 173, 159-162. doi: 10.1016/S0020-1693(00)80208-X
  18. Bora T., Singh M.M. J. Inorg. Nucl. Chem. 1976, 38, 1815-1820. doi: 10.1016/0022-1902(76)80095-4
  19. Bratsos I., Alessio E., Ringenberg M.E., Rauchfuss T.B. Inorg. Synth. 2010, 35, 148-152. doi: 10.1002/9780470651568.ch8
  20. James B.R., Morris R.H. Can. J. Chem. 1980, 58, 399-408. doi: 10.1139/v80-064
  21. Paul J., Spey S., Adams H., Thomas J.A. Inorg. Chim. Acta. 2004, 357, 2827-2832. doi: 10.1016/j.ica.2003.12.023
  22. Paul J., Spey S., Adams H., Thomas J.A., Inorg. Chim. Acta. 2004, 357, 2827-2832. doi: 10.1016/j.ica.2003.12.023
  23. Ulman A. Chem. Rev. 1996, 96, 1533-1554. doi: 10.1021/cr9502357
  24. Mikel C., Potvin P.G. Polyhedron. 2002, 21, 49-54. doi: 10.1016/S0277-5387(01)00959
  25. Roy S., Saha S., Majumdar R., Roy M., Dighe R.R., Chakravarty A.R. Polyhedron. 2010, 29, 3251-3256. doi: 10.1016/j.poly.2010.09.002
  26. Beley M., Collin J.-P. J. Mol. Catal. 1993, 79, 133-140. doi: 10.1016/0304-5102(93)85096-C
  27. Cao Q., Li Y., Freisinger E., Qin P., Sigel R., Mao Z.-W. Inorg. Chem. Front. 2017, 4, 10-32. doi: 10.1039/C6QI00300A
  28. Ромашкина Р.Б., Мажуга А.Г., Белоглазкина Е.К., Пичугина Д.А., Аскерка М.С., Моисеева А.А., Рахимов Р.Д., Зык Н.В. Изв. Акад. наук. Сер. хим. 2022, 61, 2265-2281.
  29. Romashkina R.B., Majouga A.G., Beloglazkina E.K., Pichugina D.A., Askerka M.S., Moiseeva A.A., Rakhimov R.D., Zyk N.V. Russ. Chem. Bull. 2012, 61, 2265-2281. doi: 10.1007/s11172-012-0322-0

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