Problems of synthesis of mercapto derivatives from corresponding hydroxy derivatives of polyphenylenes

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Abstract

In order to study the possibility of creating new anisotropic nanocomposites based on organic molecules containing mercapto groups for specific interaction with nanoparticles, the possibility of converting hydroxy derivatives of polyphenylenes into the corresponding thiols was studied.

About the authors

A. V Finko

Moscow State University;A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences

Email: finko.alexander@gmail.com

A. S Saakian

Moscow State University

Email: finko.alexander@gmail.com

V. S Bezborodov

Belarusian State Technological University

Email: finko.alexander@gmail.com

S. G Mikhalyonok

Belarusian State Technological University

Email: finko.alexander@gmail.com

R. V Talroze

A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences

Email: finko.alexander@gmail.com

References

  1. Shivakumar U., Mirzaei J., Feng X., Sharma A., Moreira P., Hegmann T. Liq. Cryst. 2011, 38, 1495-1514. doi: 10.1080/02678292.2011.605477
  2. Mundoor H., Park S., Senyuk B., Wensink H., Smalyukh I. Science. 2018, 360, 768-771. doi: 10.1126/science.aap9359
  3. Shen Y., Dierking I. Appl. Sci. 2019, 9, 2512. doi: 10.3390/app9122512
  4. Ezhov A.A., Derikov Y.I., Chernikova E.V., Abramchuk S.S., Shandryuk G.A., Merekalov A.S., Panov V.I., Talroze R.V. Polymer. 2015, 77, 113-121. doi: 10.1016/j.polymer.2015.09.029
  5. Rodarte A.L., Cisneros F., Hein J., Ghosh S., Hirst L.S. Photonics. 2015, 2, 855-864. doi: 10.3390/photonics2030855
  6. Cresta V., Romano G., Kolpak A., Zalar B., Domenici V. Polymers. 2018, 10, 773. doi: 10.3390/polym10070773
  7. Bugakov M., Boiko N., Samokhvalov P., Zhu X., Mouller M., Shibaev V. J. Mater. Sci. C. 2019, 7, 4326-4331. doi: 10.1039/C9TC00610A
  8. Soule E.R., Milette J., Reven L., Rey A.D. Soft Matter. 2012, 8, 2860-2866. doi: 10.1039/C2SM07091J
  9. Milette J., Cowling S.J., Toader V., Lavigne C., Saez I.M., Lennox R.B., Goodby J.W., Reven L. Soft Matter. 2012, 8, 173-179. doi: 10.1039/c1sm06604h
  10. Mirzaei J., Urbanski M., Yu K., Kitzerow H.-S., Hegmann T. J. Mater. Chem. 2011, 21, 12710-12716. doi: 10.1039/C1JM11832C
  11. Bezborodov V.S., Finko A.V., Mikhalyonok S.G., Derikov Y.I., Shandryuk G.A., Kuz'menok N.M., Arol A.S., Karpov O.N., Talroze R.V. Liq. Cryst. 2021, 48, 1544-1554. doi: 10.1080/02678292.2021.1884912
  12. Merekalov A.S., Shandryuk G.A., Bezborodov V.S., Otmakhova O.A., Mikhalyonok S.G., Kuz'menok N.M., Arol A.S., Osipov M.F., Talroze R.V. J. Mol. Liq. 2019, 276, 588-594. doi: 10.1016/j.molliq.2018.12.036
  13. Priscilla P., Malik P., Supreet, Kumar A., Castagna R., Singh G. Crit. Rev. Solid State Mater. Sci. 2022, 48, 57-92. doi: 10.1080/10408436.2022.2027226
  14. Milette J., Toader V., Soulé E.R., Lennox R.B., Rey A.D., Reven L. Langmuir. 2013, 29, 1258-1263. doi: 10.1021/la304189n
  15. Żurowska M., Filipowicz M., Czerwiński M., Szala M. Liq. Cryst. 2019, 46, 299-308. doi: 10.1080/02678292.2018.1499147
  16. Newman M.S., Karnes H.A. J. Org. Chem. 1966, 31, 3980-3984. doi: 10.1021/jo01350a023
  17. Kwart H., Evans E.R. J. Org. Chem. 1966, 31, 410-413. doi: 10.1021/jo01340a015
  18. Faucher A-M., White P.W., Brochu C., Grand-Maître C., Rancourt J., Fazal G. J. Med. Chem. 2004, 47, 18-21. doi: 10.1021/jm034206x
  19. Sasnouski G., Lapanik V., Bezborodov V., Dabrowski R., Dziaduszek J. Phase Transit. 2014, 87, 783-789. doi: 10.1080/01411594.2014.893341

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