UDC 547.791.8

SYNTHESIS OF UV ABSORBERS BASED ON N‑(2‑AMINOARYL)BENZOTRIAZOLE DERIVATIVES Synthesis of UV absorbers based on N‑(2‑aminoaryl)benzotriazole derivatives

Published in From Chemistry Towards Technology Step-By-Step · Volume 7, Issue 3, 2026 · Pages 113–122 · Rubric: Scientific articles
DOI: https://doi.org/10.52957/2782-1900-2026-7-3-113-122
Received: 08.06.2026 Accepted: 12.08.2026 Published: 02.10.2026 Language of publication: ENG
Through the aromatic nucleophilic substitution and reduction reactions, we obtain mixtures of 1-(2-NH2-4-CF3-phenyl)-1H- and 2-(2-NH2-4-CF3-phenyl)-2H-benzotriazoles, containing 1- and 2‑substituted isomers in various ratios. The UV absorption intensity of these amino compound mixtures was studied. All mixtures of aminobenzotriazole derivatives had absorption in the ranges of 280–200 nm, 315–280 nm, and 400–315 nm. An increase in the content of the 2‑substituted isomer in the mixture resulted in their higher ability to absorb UVA and UVB radiation. When the 1‑substituted derivative predominated in the mixture, UVC radiation was absorbed more intensely. The most promising mixture was found to be one containing the 1- and 2‑substituted isomers in a ratio of 1 : 0.49. It exhibited continuous and significant absorption over the entire studied UV spectral range. Quantum chemical calculations showed the hypsochromic shift of the absorption maxima in the UV spectrum of the 1‑substituted isomer is due to steric hindrance. It makes the molecule substantially non‑planar and disrupts the conjugation between the benzotriazole and aniline moieties. It increases both the energy gap between the HOMO and LUMO and in the energy of electronic transitions.
UV absorbers, N-(2-aminoaryl)benzotriazoles, SNAr reaction, reduction, UV spectra, wavelength range 280–200 nm, 315–280 nm and 400–315 nm, quantum chemical modeling
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1. Lu T., Solis-Ramos E., Yi Y., Kumosa M. UV degradation model for polymers and polymer matrix composites. Pol. Deg. and Stab., 2018, 154, 203-210. DOI:https://doi.org/10.1016/j.polymdegradstab.2018.06.004.

2. Wypych G. Handbook of UV degradation and stabilization. Elsevier, 2020, 518 p. URL: www.sciencedirect.com/book/9781927885574/handbook-of-uv-degradation-and-stabilization.

3. Rabek J. F. Polymer photodegradation: mechanisms and experimental methods. Springer Science & Business Media, 2012, 664 p. URL: https://link.springer.com/book/10.1007/978-94-011-1274-1.

4. Bisht P., Pandey K.K., Barshilia H.C. Photostable transparent wood composite functionalized with an UV absorber. Polym. Degrad. Stab., 2021, 189, Article 109600. DOI:https://doi.org/10.1016/j.polymdegradstab.2021.109600. EDN: https://elibrary.ru/RRJZXZ

5. Cormack P.A.G., Erdemli O.C., Sankey S.W. Polymerizable UV absorbers for the UV stabilization of polyesters. I. Design, synthesis and polymerization of a library of UV absorbing monomers. Arkivoc, 2021, 6. 148-173. DOI:https://doi.org/10.24820/ark.5550190.p011.575. EDN: https://elibrary.ru/AANTJZ

6. Zhang Y., Naebe M. Lignin: A review on structure, properties, and applications as a light-colored UV absorber. ACS Sustainable Chem. Eng., 2021, 9(4), 1427-1442. DOI:https://doi.org/10.1021/acssuschemeng.0c06998. EDN: https://elibrary.ru/MKGGYM

7. El-Hiti G.A., Ahmed D.S., Yousif E., Al-Khazrajy O.S., Abdallh M., Alanazi S.A. Modifications of polymers through the addition of ultraviolet absorbers to reduce the aging effect of accelerated and natural irradiation. Polymers, 2021, 14(1), 20. DOI: https://doi.org/10.3390/polym14010020. EDN: https://elibrary.ru/EOPDHK

8. Lefedova O.V., Nemtzeva M.P. Liquid-phase hydrogenation of 2-nitro-2'-hydroxy-5'-methylazobenzene on skeletal nickel to obtain a photo-stabilizing composition. ChemChemTech, 2025, 68(9), 106-114. DOI:https://doi.org/10.6060/ivkkt.20256809.7267. EDN: https://elibrary.ru/OZYJOR

9. Lefedova O.V., Nemtseva M.P. 2-(2-Hydroxy-5-methylphenyl)benzotriazole and Its Hydrogenation Products in Polystyrene Stabilization. Russ. J. Appl. Chem., 2012, 85(7), 1128-1132. DOI:https://doi.org/10.1134/S1070427212070245 EDN: https://elibrary.ru/RGMXRT

10. Cui Z., Li X., Wang X., Pei K., Chen W. Structure and properties of N-heterocycle-containing benzotriazoles as UV absorbers. J. Mol. Struct., 2013, 1054, 94-99. DOI:https://doi.org/10.1016/j.molstruc.2013.09.045.

11. Pijeau S., Foster D., Hohenstein E.G. Excited-state dynamics of a benzotriazole photostabilizer: 2-(2′-hydroxy-5′-methylphenyl)benzotriazole. J. Phys. Chem. A., 2017, 121(34), 6377-6387. DOI:https://doi.org/10.1021/acs.jpca.7b04504.

12. Kim S., Hwang T.G., Namgoong J.W., Kim H.M., Kim P.J. Effect of linker moiety on linear dimeric benzotriazole derivatives as highly stable UV absorber for transparent polyimide film. Dyes Pigm., 2020, 180, Article 108469. DOI:https://doi.org/10.1016/j.dyepig.2020.108469. EDN: https://elibrary.ru/KCLSTX

13. Naumov S., Herzog B., Abel B. Spectra and photorelaxation of hydroxyphenyl-benzotriazole-type UV absorbers: From monomers to nanoparticles. J. Phys. Chem. A., 2020, 124(4). 625-632. DOI:https://doi.org/10.1021/acs.jpca.9b09883. EDN: https://elibrary.ru/PADKUR

14. Wu F., Tan S., Fang Z., Deng J., He Z., Huang C., Au C., Yi B. Substituent Effects on the Ultraviolet Absorption Properties of 2,4-Dihydroxy Dibenzophenone. Molecules, 2022, 27(23), Article 8169. DOI:https://doi.org/10.3390/molecules27238169 EDN: https://elibrary.ru/KKQCBY

15. Huang Z., Ding A., Guo H., Lu G., Huang X. Construction of nontoxic polymeric UV-absorber with great resistance to UV-photoaging. Sc. Rep., 2016, 6(1), 1-12. DOI:https://doi.org/10.1038/srep25508.

16. Pospíšil J., Nešpurek S. Photostabilization of coatings. Mechanisms and performance. Prog. Polym. Sci., 2000, 25(9). P. 1261–1335 DOI:https://doi.org/10.1016/S0079-6700(00)00029-0.

17. Merrill J.R., Bennett R.G. Influence of Intramolecular Hydrogen Bonding on Electronic De‐excitation in Amidophenylbenzotriazoles. J. Chem. Phys., 1965, 43(4), 1410-1414. DOI:https://doi.org/10.1063/1.1696934.

18. Begunov R.S., Khlopotinin A.I., Lobanova L.V., Vorontsov S.M., Savina L.I., Danilova A.S. New UV absorbers based on N-(2-aminoaryl)benzotriazoles. ChemChemTech, 2024, 67(11), 86-94. DOI:https://doi.org/10.6060/ivkkt.20246711.7070. EDN: https://elibrary.ru/WYPDNK

19. Khlopotinin A.I. Sintez, funkcionalizacija i svojstva N-(2-aminoaril)benzotriazolov, dis. kand. him. nauk. M., 2026, 137 s. (in Russian).

20. Begunov R.S., Orlov V.Yu., Kopeikin V.V. Vliyanie prirody rastvoritelya na orientatsiyu monovosstanovleniya odnozameshchennykh 2,4-dinitrobenzolov. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol., 1998, 41(5), 9-11 (in Russian)

21. Rusanov A.L., Komarova L.G., Prigozhina M.P., Begunov R.S., Yakovleva Y.S. Benzophenone-type unsymmetrical substituted aromatic diamines and organosoluble polyimides therefrom. High Perform. Polym., 2009, 21(6), 729-743. DOI:https://doi.org/10.1177/0954008308099187 EDN: https://elibrary.ru/YVILSH

22. Begunov R.S., Valyaeva A.N., Bashkirova A.A., Belomoina N.M., Bulycheva E.G. An effective synthesis of polynuclear tetraamines, monomers for polyheteroarylenes. Russ. Chem. Bull., 2018, 67(6), 1072-1077. DOI:https://doi.org/10.1007/s11172-018-2182-8 EDN: https://elibrary.ru/YBRLDF

23. Bogdanova D.M., Savina L.I. Begunov R.S. Synthesis and functionalization of pyrido[1,2-a]benzimidazole amino derivatives. From Chemistry Towards Technology Step-By-Step, 2022, 3(4), 80-87 [online]. Available at: http://chemintech.ru/index.php/tor/2022-3-4 (accessed 23.07.2026) DOI: https://doi.org/10.52957/27821900_2022_04_80

24. Neese F. Software update: The ORCA program system –Version 5.0. Wiley Interdiscip. Rev. Comput. Mol. Sci., 2022, 12(5), e1606. DOI:https://doi.org/10.1002/wcms.1606 EDN: https://elibrary.ru/YAMDOJ

25. Grimme S., Hansen A., Ehlert S., Mewes J.-M. r2SCAN-3c: A “Swiss army knife” composite electronic structure method. J. Chem. Phys., 2021, 154(6), 064103. DOI:https://doi.org/10.1063/5.0040021 EDN: https://elibrary.ru/MHTRWP

26. Stephens P.J., Devlin F.J., Chabalowski C.F., Frisch M.J. Ab initio calculation of vibrational absorption and circular dichroism spectra using density functional force fields. J. Phys. Chem., 1994, 98(45), 11623-11627. DOI:https://doi.org/10.1021/j100096a001 EDN: https://elibrary.ru/SQFWJT

27. Lee C., Yang W., Parr R.G. Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density. Phys. Rev. B., 1988, 37(2), 785-789. DOI:https://doi.org/10.1103/PhysRevB.37.785

28. Weigend F., Ahlrichs R. Balanced basis sets of split valence, triple zeta valence and quadruple zeta valence quality for H to Rn: Design and assessment of accuracy. Phys. Chem. Chem. Phys., 2005, 7(18), 3297-3305. DOI:https://doi.org/10.1039/b508541a

29. Grimme S., Antony J., Ehrlich S., Krieg H. A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu. J. Chem. Phys., 2010, 132(15), 154104. DOI:https://doi.org/10.1063/1.3382344 EDN: https://elibrary.ru/NAHYOL

30. Barone V., Cossi M. Quantum calculation of molecular energies and energy gradients in solution by a conductor solvent model. J. Phys. Chem. A., 1998, 102(11), 1995-2001. DOI:https://doi.org/10.1021/jp9716997

31. Chemcraft – graphical software for visualization of quantum chemistry computations. Version 1.8, build 682. https://www.chemcraftprog.com