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Synthesis and Properties of Asymmetrically Substituted Mn(III)-Nitro-Phenylporphyrins

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Abstract

Mn(III)-5-(4-nitrophenyl)-10,15,20-triphenylporphyrin and Mn(III)-5,10,15-tri(4-nitrophenyl)-20-phenylporphyrin were synthesized by complex formation reactions of the specified porphyrins and by metal exchange of Cd porphyrin complexes with MnCl2 in dimethylformamide. The products were identified by mass spectrometry and UV-Vis, IR, and 1H NMR spectroscopy. Partial reduction of Mn(III) to Mn(II) takes place upon dissolution of manganese(III) complexes in DMF. The addition of solid NaOH to a solution in DMF or ethanolamine gives unstable Mn(II) porphyrins. The photochemical stability and oxidative degradation of Mn(III) porphyrins were studied in chloroform and in a chloroform–hydrogen peroxide mixture. The metal exchange reaction between asymmetrically substituted Cd(II) porphyrins and MnCl2 in DMF was studied. The kinetic parameters of the reaction were calculated. The influence of substituents and the nature of the salt on the kinetic parameters of the metal exchange reaction was identified.

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ACKNOWLEDGMENTS

This study was performed using the research equipment of the Center for Collective Use “Upper Volga Regional Center for Physicochemical Research.”

Funding

The study was supported by the Ministry of Science and Higher Education of the Russian Federation (Project no. 075-15-2021-579).

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Authors and Affiliations

  1. Krestov Institute of Solution Chemistry Russian Academy of Sciences, 153040, Ivanovo, Russia

    N. V. Chizhova, S. V. Zvezdina, A. E. Likhonina & N. Zh. Mamardashvili

  2. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991, Moscow, Russia

    O. I. Koifman

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  1. N. V. Chizhova
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  2. S. V. Zvezdina
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  3. A. E. Likhonina
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  4. N. Zh. Mamardashvili
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  5. O. I. Koifman
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Correspondence to N. Zh. Mamardashvili.

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Translated by Z. Svitanko

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Chizhova, N.V., Zvezdina, S.V., Likhonina, A.E. et al. Synthesis and Properties of Asymmetrically Substituted Mn(III)-Nitro-Phenylporphyrins. Russ. J. Inorg. Chem. (2024). https://doi.org/10.1134/S0036023623602775

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