Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/201831
Type: Artigo de periódico
Title: Esi(+)-ms And Gc-ms Study Of The Hydrolysis Of N-azobenzyl Derivatives Of Chitosan.
Author: Pereira, Fernanda S
Nascimento, Heliara D L
Magalhães, Alviclér
Peter, Martin G
Bataglion, Giovana Anceski
Eberlin, Marcos N
González, Eduardo R P
Abstract: New N-p-chloro-, N-p-bromo-, and N-p-nitrophenylazobenzylchitosan derivatives, as well as the corresponding azophenyl and azophenyl-p-sulfonic acids, were synthesized by coupling N-benzylvchitosan with aryl diazonium salts. The synthesized molecules were analyzed by UV-Vis, FT-IR, 1H-NMR and 15N-NMR spectroscopy. The capacity of copper chelation by these materials was studied by AAS. Chitosan and the derivatives were subjected to hydrolysis and the products were analyzed by ESI(+)-MS and GC-MS, confirming the formation of N-benzyl chitosan. Furthermore, the MS results indicate that a nucleophilic aromatic substitution (SnAr) reaction occurs under hydrolysis conditions, yielding chloroaniline from N-p-bromo-, and N-p-nitrophenylazo-benzylchitosan as well as bromoaniline from N-p-chloro-, and N-p-nitrophenylazobenzyl-chitosan.
Rights: aberto
Identifier DOI: 10.3390/molecules191117604
Address: http://www.ncbi.nlm.nih.gov/pubmed/25361424
Date Issue: 2014
Appears in Collections:Unicamp - Artigos e Outros Documentos

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