Nucleophilic Addition of Thiol to Peripheral C=C Bonds of Tetraaryltetracyanoporphyrazine Macrocycle
- Authors: Lyubova T.S1, Lermontova S.A1, Klapshina L.G1, Ladilina E.Y.1
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Affiliations:
- G.A. Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences
- Issue: Vol 93, No 2 (2023)
- Pages: 246-252
- Section: Articles
- URL: https://cardiosomatics.ru/0044-460X/article/view/667106
- DOI: https://doi.org/10.31857/S0044460X23020105
- EDN: https://elibrary.ru/QBSVNN
- ID: 667106
Cite item
Abstract
An irreversible addition reaction of benzylmercaptan to the macrocycle of the cyanoarylporphyrazine family (Ar = p -MeOPh and Nph) was established for the first time. The reaction proceeds along the polarized peripheral semi-isolated double bonds of the macrocycle and takes place under mild conditions. Mass spectrometry and 1H NMR spectroscopy confirm the composition and structure of the products.
About the authors
T. S Lyubova
G.A. Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences
S. A Lermontova
G.A. Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences
L. G Klapshina
G.A. Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences
E. Yu. Ladilina
G.A. Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences
Email: eladilina@gmail.ru
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