1. Berezin, B.D. (1985) Porphyrins: spectroscopy, electrochemistry, application. M.: Nauka (in Russian).
2. Abramov, I.G., Baklagin, V.L., Makarova, E.S. & Kleikova, D.E. (2021) Nitrogen-containing heterocyclic O , and s-nucleophiles in reactions with 4-nitrophthalonitrile and 4-bromo-5-nitrophthalonitrile, From Chemistry Towards Technology Step-By-Step, 2(4), pp. 43-49 [online]. Available at: http://chemintech.ru/index.php/tor/2021-2-4 (in Russian).
3. Koifman, O.I. (2020) Macroheterocyclic compounds – a key building block in new functional materials and molecular devices, Macroheterocycles, (13), pp. 311-467. DOI:https://doi.org/10.6060/mhc200814k.
4. Masa, J., Ozoemena, K., Schuhmann, W. & Zagal, J.H. (2012) Oxygen reduction reaction using N4 metallomacrocyclic catalysts: fundamentals on rational catalyst design, J. Porphyrins and Phtalocyanines, (16), pp. 761-784. DOI:https://doi.org/10.1142/S1088424612300091.
5. Kuzmin, S.M., Chulovskaya, S.A., Parfenyuk, V.I. & Koifman, O.I. (2020) Poly-5,10,15,20-tetrakis(4-hydroxyphenyl)porphyrin as a material for photovoltaic devices, Mendeleev Communications, 30(6), pp. 777 780. DOI:https://doi.org/10.1016/j.mencom.2020.11.030.
6. Zamadar, M., Orr, Ch. & Uherek, M. (2016) Water Soluble Cationic Porphyrin Sensor for Detection of Hg2+, Pb2+, Cd2+ and Cu2+, Journal of Sensors, (216). DOI:https://doi.org/10.1155/2016/1905454.
7. Grin, M.A., Suvorov, N.V. & Mironov, A.F. (2020) Natural chlorins as a promising platform for creating targeted theranostics in oncology, Mendeleev Communications, 30(4), pp. 406-418. DOI:https://doi.org/10.1016/j.mencom.2020.07.003.
8. Kustov, A.V., Berezin, D.B., Strelnikov, A.I. & Lapochkina, N.P. (2020) Antitumour and antimicrobial photodynamic therapy: mechanisms, targets, clinical and laboratory studies. M.: Largo (in Russian).
9. Giancola, C., Caterino, M., D'Aria, F., Kustov, A.V., Belykh, D.V., Khudyaeva, I.S., Starseva, O.M., Berezin, D.B., Pylina, Y.I., Usacheva, T. & Amato, J. (2020) Selective binding of a bioactive porphyrin-based photosensitizer to the G-quadruplex from the KRAS oncogene promoter, International Journal of Biological Macromolecules, (145), pp. 244-251. DOI:https://doi.org/10.1016/j.ijbiomac.2019.12.152.
10. Kruk, N.N. (2019) Structure and optical properties of tetrapyrrole compounds. Minsk: BSTU (in Russian).
11. Gu, J, Peng, Y, Zhou, T, Ma, J., Pang, H. & Yamauchi, Y. (2022) Porphyrin-based framework materials for energy conversion, Nano Research Energy, 1(e9120009). DOI:https://doi.org/10.26599/NRE.2022.9120009.
12. Berezina, N.M., Berezin, M.B. & Semeikin, A.S. (2019) Solvation interactions and photostability of tetrakis(1-methylpyridyl)porphyrin derivatives, Journal of Molecular Liquids, (290). DOI:https://doi.org/10.1016/j.molliq.2019.111196.
13. Amorim, C.F., Iglesias, B.A., Pinheiro, T.R., Lacerda, L.E., Sokolonski, A.R., Pedreira, B.O., Moreira, K.S., Burgo, L.T.A., Meyer, R., Azevedo, V. & Portela, R.W. (2023) Photodynamic inactivation of different Candida species and inhibition of biofilm formation induced by water-soluble porphyrins, Photodiagnosis and Photodynamic Therapy, 42(103343). DOI:https://doi.org/10.1016/j.pdpdt.2023.103343.
14. Fialkov, Y., Ya. (1990) Solvent as a chemical process control tool. L.: Khimiya (in Russian).
15. Himanshu, P. & Khare, A. (2005) Cryoscopic studies of α-amino acids in water, Journal of Molecular Liquids, (122), pp. 61-64.
16. Berezina, N.M., Berezin, M.B., Minh, D.N. & Bazanov, M.I. (2017) Solvation and coordination interactions of tetrapyridylporphyrin in aqueous solutions. Thermal stability, Rossijskij zhurnal obshhej khimii, 87(3), pp. 639-650. DOI:https://doi.org/10.1134/S1070363217030422 (in Russian).
17. Berezina, N.M., Bazanov, M.I. Semeikin, A.S. &, Berezin, M.B. (2009) The physicochemical properties of complexones, tetrapyridylporphin derivatives, Zhurnal Fizicheskoj Khimii, 83(5), pp. 903-910 (in Russian).
18. Berezina, N.M., Bazanov, M.I. Semeikin, A.S. & Berezin, M.B. The physicochemical properties of complexones, tetrapyridylporphin derivatives, Russian Journal of Physical Chemistry, 85(5), pp. 785-791. DOI:https://doi.org/10.1134/S0036024409050185.