Methacrylate-Containing n-Derivatives of N,N-Diethyl-4-(Phenyldiazenyl)Aniline as Initiators in Two-Photon Polymerization

Мұқаба

Дәйексөз келтіру

Толық мәтін

Ашық рұқсат Ашық рұқсат
Рұқсат жабық Рұқсат берілді
Рұқсат жабық Тек жазылушылар үшін

Аннотация

The possibility of using a number of methacrylate-containing N,N-diethyl-4-(phenyldiazenyl)anilines with various para-substituents with respect to the azo group (-H, -Br, -NO2) as photoinitiators of radical polymerization is considered. The electrochemical and photoluminescent properties of these compounds have been studied. In the presence of azo dyes, two-photon photopolymerization of pentaerythritol triacrylate was carried out by focused radiation from a femtosecond laser with a wavelength of 780 nm. Structures with minimum linear element sizes of 94 ± 5 nm were obtained by DLW nanolithography, as well as 3D microstructures of complex architecture.

Толық мәтін

Рұқсат жабық

Авторлар туралы

M. Arsenyev

G.A. Razuvaev Institute of Organometallic Chemistry of the Russian Academy of Sciences

Email: zhiganshinae@mail.ru
Ресей, Nizhny Novgorod

E. Zhiganshin

G.A. Razuvaev Institute of Organometallic Chemistry of the Russian Academy of Sciences

Хат алмасуға жауапты Автор.
Email: zhiganshinae@mail.ru
Ресей, Nizhny Novgorod

D. Kolymagin

Moscow Institute of Physics and Technology (National Research University)

Email: zhiganshinae@mail.ru
Ресей, Dolgoprudny

V. Ilyichev

G.A. Razuvaev Institute of Organometallic Chemistry of the Russian Academy of Sciences

Email: zhiganshinae@mail.ru
Ресей, Nizhny Novgorod

R. Kovylin

G.A. Razuvaev Institute of Organometallic Chemistry of the Russian Academy of Sciences

Email: zhiganshinae@mail.ru
Ресей, Nizhny Novgorod

A. Vitukhnovsky

Moscow Institute of Physics and Technology (National Research University); P.N. Lebedev Physical Institute of the Russian Academy of Sciences

Email: zhiganshinae@mail.ru
Ресей, Dolgoprudny; Moscow

S. Chesnokov

G.A. Razuvaev Institute of Organometallic Chemistry of the Russian Academy of Sciences

Email: zhiganshinae@mail.ru
Ресей, Nizhny Novgorod

Әдебиет тізімі

  1. Jaiswal A., Rastogi C. K., Rani S., Singh G. P. et al. // iScience. 2023. V. 26. № 106374.
  2. Zhiganshina E.R., Arsenyev M.V., Chesnokov S.A. // Polym. Sci., B. 2023. V. 65. P. 247.
  3. Zhiganshina E.R., Arsenyev M.V., Chubich D.A. et al. // Eur. Polym. J. 2021. V. 162. P. 110917.
  4. Liu Y.J., Yang J.Y., Nie Y.M. et al. // Microfluid Nanofluidics. 2015. V. 18. P. 427.
  5. Sakellari I., Yin X., Nesterov M.L., Terzaki K. et al. // Adv. Opt. Mater. 2017. V. 5. № 1700200.
  6. Rakhymzhanov A., Gueddida A., Alonso-Redondo E., et al. // Appl. Phys. Lett. 2016. V.108. № 201901.
  7. Zheng C., Jin F., Zhao Yu. et al. // Sens. Actuators B Chem. 2020. V. 304. № 127345.
  8. Otuka A.J.G., Torres B.B.M., Dipold J. et al. // Opt. Mater. Express. 2020. V. 10. № 8. P. 1792.
  9. Fominykh O.D., Sharipova A.V., Balakina M.Yu. // Comput. Mater. Sci. 2019. V. 168. P. 32.
  10. Lu Y., Hasegawa F., Goto T. et al. // J. Mater. Chem. 2003. V. 14. P. 75.
  11. Beharry A.A., Sadovski O., Woolley G.A. // J. Am. Chem. Soc. 2011. V. 133. P. 19684.
  12. Vivas M.G., Silva D.L., De Boni L. et al. // J. Phys. Chem. B. 2012. V. 116. P. 14677.
  13. Zhou L., Mao J., Ren Y. et al. // Small. 2018. V. 14. № 1703126.
  14. Ghanavatkar C.W., Mishra V.R., Nagaiyan S. // Dyes Pigm. 2021. V. 191. № 109367.
  15. Xu L., Zhang J., Yin L. et al. // J. Mater. Chem. C. 2020. V. 8. P. 6342.
  16. McKenzie L.K., Bryant H.E., Weinstein J.A. // Coord. Chem. Rev. 2019. V. 379. P. 2.
  17. Balakina M.Yu., Shalin N.I., Sharipova A.V., Fominykh O.D. // Mol. Phys. 2020. V. 118. № 21–22. P. 1.
  18. Mendonca C.R., Baldacchini T., Tayalia P., Mazur E. // J. Appl. Phys. 2007. V. 102. № 1. P. 013109.
  19. Tribuzi V., Fonseca R.D., Correa D.S., Mendonca C.R. // Opt. Mater. Express. 2013. V. 3. № 1. P. 21.
  20. Turro N.J. Modern Molecular Photochemistry. University Science Books, 1991. P. 628.
  21. Vijayakumar C., Balan B., Kim M.-J., Takeuchi M. // J. Phys. Chem. C. 2011. V. 115. P. 4533.
  22. Lim S.L., Li N.-J., Lu J.-M. et al. // ACS Appl. Mater. Interfaces. 2009. V. 1. № 1. P. 60.
  23. Qiu F.X., Zhang Q., Yang D.Y. // Mater. Sci. Forum. 2010. V. 663–665. P. 645.
  24. Armarego W.L.F., Chai C.L.L. Purification of laboratory chemicals. Amsterdam: Elsevier Inc. Butterworth-Heinemann, 2003.
  25. Eltaboni F., Bader N., El-Kailany R. et al. // J. Chem. Rev. 2022. V. 4. № 4. Р. 313.

Қосымша файлдар

Қосымша файлдар
Әрекет
1. JATS XML
Жүктеу
2. Scheme 1

Жүктеу (121KB)
Метадеректер
3. Fig. 1. CVA curves of azo dyes 1 (a), 2 (b), 3 (c) and 4 (d). MeCN, Ag/AgCl/KCl(us.), 0.1 M (NBu4)ClO4, scanning speed – 200 mV s-1

Жүктеу (245KB)
Метадеректер
4. Fig. 2. Luminescence spectra of polymer samples based on PET and azo dyes 1 (a), 2 (b), 3 (c), 4 (d). In all graphs: curve 1 – Polypet without azo dye; curve 2 – spectrum of polypet with dye registered at room temperature; 3 – spectrum A polypet with a dye registered at 77 K. The excitation wavelength is 405 nm, the radiation power is 100 MW

Жүктеу (391KB)
Метадеректер
5. Fig. 3. SEM-image of linear elements from the composition K5 at magnification × 18000 times

Жүктеу (201KB)
Метадеректер
6. Fig. 4. SEM images of cylindrical spiral 3D microstructures obtained on the K5 composition at magnification of ×400 (a) and ×2500 (b) times

Жүктеу (151KB)
Метадеректер

© Russian Academy of Sciences, 2024