Spectral-kinetic studies of some homodimeric styrylcyanine dyes in solutions

Capa

Citar

Texto integral

Acesso aberto Acesso aberto
Acesso é fechado Acesso está concedido
Acesso é fechado Somente assinantes

Resumo

The spectral and kinetic characteristics of the dye Sbt ((E)-2-(4-(dimethylamino)styryl)-3-methylbenzo[d]thiazol-3-ium iodide) and its homodimers Dbt-5, Dbt-10 in chloroform and its binary mixtures with solvents of different polarity were studied. It was found that with an increase in the proportion of hexane in chloroform solutions of the studied dyes, non-fluorescent H-aggregates are formed. It was found that the spectral and photophysical parameters of the studied dyes depend on the polarity and viscosity of the solvents. Quantum-chemical calculations of the charge distribution and potential energy in the ground and excited states for the molecules of the studied compounds were carried out. Sbt and Dbt-10 dyes are characterized by higher values of quantum yields and lifetime of the excited state in a viscous medium, which is associated with the formation of the TICT (twisted intramolecular charge transfer) state. The transition of molecules to this state leads to effective quenching of fluorescence.

Sobre autores

A. Yarmukhamedov

Samarkand State University named after Sh. Rashidov

Samarkand, Uzbekistan

E. Kurtaliev

Samarkand State University named after Sh. Rashidov

Email: kurtaliev@rambler.ru
Samarkand, Uzbekistan

I. Khairov

Samarkand State University named after Sh. Rashidov

Samarkand, Uzbekistan

N. Nizomov

Samarkand State University named after Sh. Rashidov

Samarkand, Uzbekistan

M. Malikov

Samarkand State University named after Sh. Rashidov

Samarkand, Uzbekistan

Bibliografia

  1. Shettigar S., Umesh G., Poornesh P., Manjunatha K.B., Asiri A.M. // Dyes Pigm. 2009. V. 83. № 2. P. 207.
  2. Berdnikova D.V., Sosnin N.I., Fedorova O.A., Ihmels H. // Org. Biomol. Chem. 2018. V. 16. P. 545.
  3. Matiukas A., Mitrea B.G., Qin M., Pertsov A.M., Shvedko A.G., Warren M.D., Zaitsev A.V., Wuskell J.P., Wei M., Watras J., Loew L.M. // Heart Rhythm. 2007. V. 4. № 11. Р. 1441.
  4. Li Q., Lee J.-S., Ha Ch., Park Ch. B., Yang G., Gan W.B., Chang Y.T. // Angew. Chem. 2004. V. 116. P. 6491.
  5. Martins S., Avo J., Lima J., Nogueira J., Andrade L., Mendes A., Pereira A., Branco P.S. // J. Photochem. Photobiol. A. 2018. V. 353. P. 564.
  6. Lee Ch.Ch., Hu A.T. // Dyes Pigm. 2003. V. 59. № 1. P. 63.
  7. Behera P.K., Mohapatra S., Patel S., Mishra B.K. // J. Photochem. Photobiol. 2005. V. 169. P. 253.
  8. Kurtaliev E.N. // Spectrochim. Acta A Mol. Biomol. Spectrosc. 2011. V. 81. № 1. P. 449.
  9. Lebedeva A.Yu., Fedorova O.A., Tsvetkov V.B., Grinberg V.Y., Grinberg N.V., Burova T.V., Dubovik A.S., Babievsky K.K., Fedorov Y.V. // Dyes Pigm. 2018. V. 157. P. 80.
  10. Kurtaliev E.N, Nizomov N.N, Yarmukhamedov A.Sh. // J. Mol. Struc. 2020. V. 1203. P. 1.
  11. Kurtaliev E.N., Yarmukhamedov A.Sh., Djamalova A.A., Nizomov N., Terekhov S.N. // J. Fluoresc. 2024.
  12. Kovalska V.B., Kryvorotenko D.V., Balanda A.O., Losytskyy M.Yu., Tokar V.P., Yarmoluk S.M. // Dyes and Pigm. 2005. V. 67. P. 47.
  13. Tokar V.P., Losytskyy M.Yu., Kovalska V.B., Kryvorotenko D.V., Balanda A.O., Prokopets V.M., Galak M.P., Dmytruk I.M., Yashchuk V.M., Yarmoluk S.M. // J. Fluoresc. 2006. V. 16. № 6. P. 783.
  14. Arbeloa F.L., Ojeda P.R., Arbeloa I.L. // J. Lumin. 1989. V. 44. № 1–2. P. 105
  15. http://www. openmopac.net
  16. Stewart J.P. // J. Comput. Aided Mol. Desing. 1990. V. 4. P. 1.
  17. Sulatskaya A.I., Sulatsky M.I., Povarova O.I, Rodina N.P., Kuznetsova I.M., Lugovskii A.A, Voropay E.S., Lavysh A.V., Maskevich A.A., Tureverov K.K. // Dyes and Pigm. 2018. V. 157. P. 385.
  18. Deng Y., Yuan W., Jia Zh., Liu G. // J. Phys. Chem. B 2014. V. 118. P. 14536.
  19. Nizomov N., Kurtaliev E.N., Rahimov S.I. // J. Mol. Struc. 2012. V. 1029. P.142.
  20. Kobayashi N. // J-Aggregates. World scientific, Singapore. 1996. P. 228.
  21. Heyne B. // Photochem. Photobiol. Sci. 2016. V.15. P.1103.
  22. Ищенко А.А. Структура и спектрально-люминесцентные свойства полиметиновых красителей. Науково думка: Киев. 1994. 246 с.
  23. Maskevich A.A., Stsiapura V.I., Kuzmitsky V.A., Kuznetsova I.M., Povarova O.I., Uversky V.N., Tureverov K.K. // J. Proteome Res. 2007. V. 6. P. 1382.
  24. Jana R., Seth D. // J. Photoch. Photobio. A. 2022. V. 427. P. 113842.

Arquivos suplementares

Arquivos suplementares
Ação
1. JATS XML

Declaração de direitos autorais © Russian Academy of Sciences, 2025

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).