Reaction of Corroles with Sarcosine and Paraformaldehyde: A New Facet of Corrole Chemistry
Autor: | Joana F. B. Barata, Paula S. S. Lacerda, Maria Graça P. M. S. Neves, José A. S. Cavaleiro, Catarina I. V. Ramos, Augusto C. Tomé, Paulo E. Abreu, Alberto A. C. C. Pais |
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Jazyk: | angličtina |
Rok vydání: | 2022 |
Předmět: | |
Zdroj: | International Journal of Molecular Sciences, Vol 23, Iss 21, p 13581 (2022) |
Druh dokumentu: | article |
ISSN: | 1422-0067 1661-6596 |
DOI: | 10.3390/ijms232113581 |
Popis: | Details on the unexpected formation of two new (dimethylamino)methyl corrole isomers from the reaction of 5,10,15-tris(pentafluorophenyl)corrolatogallium(III) with sarcosine and paraformaldehyde are presented. Semi-empirical calculations on possible mechanism pathways seem to indicate that the new compounds are probably formed through a Mannich-type reaction. The extension of the protocol to the free-base 5,10,15-tris(pentafluorophenyl)corrole afforded an unexpected new seven-membered ring corrole derivative, confirming the peculiar behavior of corroles towards known reactions when compared to the well-behaved porphyrin counterparts. |
Databáze: | Directory of Open Access Journals |
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