F. Yu. Vyalba, A. V. Ivantsova, K. A. Zhdanova, M. N. Usachev, M. A. Gradova, N. A. Bragina, “Synthesis of conjugates of 5,15-disubstituted aminoporphyrins and terpyridine derivatives with potential chelating properties”, Mendeleev Commun., 32:5 (2022), 675

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Mendeleev Communications, 2022, Volume 32, Issue 5, Pages 675–677
DOI: https://doi.org/10.1016/j.mencom.2022.09.036 (Mi mendc764)

This article is cited in 5 scientific papers (total in 5 papers)

Communications

Synthesis of conjugates of 5,15-disubstituted aminoporphyrins and terpyridine derivatives with potential chelating properties

F. Yu. Vyalba^a, A. V. Ivantsova^a, K. A. Zhdanova^a, M. N. Usachev^a, M. A. Gradova^b, N. A. Bragina^a

^a M.V. Lomonosov Institute of Fine Chemical Technologies, MIREA - Russian Technological University, Moscow, Russian Federation
^b N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation

Full-text PDF (285 kB) Citations (5)

DOI: https://doi.org/10.1016/j.mencom.2022.09.036

Graphic abstract: Synthesis of conjugates of 5,15-disubstituted aminoporphyrins and terpyridine derivatives with potential chelating properties

Abstract: meso-Arylporphyrin containing two external chelating 2,2':6',2'-terpyridine fragments and its zinc complex were synthesized. The key step comprised the amide bond formation between the porphyrin diamine derivative and 4'-(4-carboxyphenyl)-2,2':6',2'-terpyridine. The compounds obtained seem to be potent for photodynamic therapy and diagnosis.

Keywords: porphyrins, terpyridine, Zn complexes of porphyrins, photodiagnostics, photodynamic therapy, chelating groups.

Document Type: Article

Language: English

*Supplementary materials:*
		Supplementary_data_1.pdf	(1.3 Mb)

Citation: F. Yu. Vyalba, A. V. Ivantsova, K. A. Zhdanova, M. N. Usachev, M. A. Gradova, N. A. Bragina, “Synthesis of conjugates of 5,15-disubstituted aminoporphyrins and terpyridine derivatives with potential chelating properties”, Mendeleev Commun., 32:5 (2022), 675–677

Linking options:

https://www.mathnet.ru/eng/mendc764

https://www.mathnet.ru/eng/mendc/v32/i5/p675

This publication is cited in the following 5 articles:

Shang Wu, Penghui Zhang, Xin Sun, Jiankun Li, Ningning Wang, Xia Wang, Zhe Wang, Yanbin Wang, Quanlu Yang, “Synthesis of Quinolines Catalyzed by Bidentate Terpyridine Mn(I) Complex”, Applied Organom Chemis, 2024
E. S. Sorin, R. K. Baimuratova, V. V. Tkachev, A. N. Utenyshev, A. V. Kuzmin, G. I. Dzhardimalieva, “Structure and properties of the metal-containing monomer based on nickel acrylate and 4'-phenyl-2,2':6',2"-terpyridine for self-healing polymers”, Mendeleev Commun., 34:3 (2024), 382–384
Yu. S. Bortnevskaya, V. A. Malikova, N. Yu. Karpechenko, N. A. Bragina, K. A. Zhdanova, “The 'click' synthesis of new cytotoxic conjugate based on meso-arylporphyrin and Erlotinib”, Mendeleev Commun., 34:5 (2024), 685–687
Kseniya A. Zhdanova, Anastasia V. Ivantsova, Fedor Yu. Vyalba, Maxim N. Usachev, Margarita A. Gradova, Oleg V. Gradov, Natalia Yu. Karpechenko, Natal'ya A. Bragina, “Design of A3B-Porphyrin Conjugates with Terpyridine as Potential Theranostic Agents: Synthesis, Complexation with Fe(III), Gd(III), and Photodynamic Activity”, Pharmaceutics, 15:1 (2023), 269
Mikhail Grin, Petr Ostroverkhov, Nikita Suvorov, Sergey Tikhonov, Alexander Popov, Anastasia Shelyagina, Nikita Kirin, Artemiy Nichugovskiy, Maxim Usachev, Natalia Bragina, Ekaterina Plotnikova, Andrey Pankratov, “Potential agents for combined photodynamic and chemotherapy in oncology based on Pt(II) complexes and pyridine-containing natural chlorins”, J. Porphyrins Phthalocyanines, 27:01n04 (2023), 728

Citing articles in Google Scholar: Russian citations, English citations
Related articles in Google Scholar: Russian articles, English articles

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