Micellar effects and analytical applications of nitro substitution in 4-Nitro-N-alkyl-1,8-naphthalimide by cysteine derivatives

The aromatic nucleophilic substitution reactions of the nitro group of 4-Nitro-N-alkyl-1,8-naphthalimides by thiolate anions produce fluorescent derivatives and their rates are strongly accelerated by micelles of hexadecyltrimethylammonium chloride even at low pH. Acceleration factors of this reacti...

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Detalles Bibliográficos
Autores principales: Martins, V.S., Triboni, E.R., Bonilha, J.B.S., Gonçalves, L.M., Mortara, L., Carvalho, L.A.C., Manda, B.R., Lacerda, C.D., Meotti, F.C., Politi, M.J., Chaimovich, H., Cuccovia, I.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502353/
https://www.ncbi.nlm.nih.gov/pubmed/32995623
http://dx.doi.org/10.1016/j.heliyon.2020.e04938

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502353/
https://www.ncbi.nlm.nih.gov/pubmed/32995623
http://dx.doi.org/10.1016/j.heliyon.2020.e04938

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