http://www.cnr.it/ontology/cnr/individuo/prodotto/ID40602
Defined Chitosan-based networks by C-6-Azide-alkyne \"click\" reaction (Articolo in rivista)
- Type
- Label
- Defined Chitosan-based networks by C-6-Azide-alkyne \"click\" reaction (Articolo in rivista) (literal)
- Anno
- 2010-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.reactfunctpolym.2010.01.004 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Zampano, Giovanni; Bertoldo, Monica; Ciardelli Francesco (literal)
- Pagina inizio
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- PolyLab-INFM-CNR
Dipartimento di Chimica e Chimica Industriale, Università di Pisa (literal)
- Titolo
- Defined Chitosan-based networks by C-6-Azide-alkyne \"click\" reaction (literal)
- Abstract
- Chitosan was converted to its NH2-protected derivative by reacting with phthalic anhydride and then selectively functionalized with an azido group in C-6 position. Two different procedures were employed. The first was a one-pot procedure and the second was a two steps reaction through the tosylated intermediate. Both methods resulted in an effective functionalization of chitosan with azido groups. For the two before mentioned procedures, the functionalization degree was estimated by elemental analysis as number of azido groups per pyranoside ring and was 0.28 mol/mol and 0.26 mol/mol, respectively. The azido-functionalized derivatives underwent further modification by Cu(I) catalyzed dipolar cycloaddition with mono- or di-alkynes. The reaction with phenylacetylene produced soluble derivatives that were fully characterized at molecular level by FT-IR and NMR spectroscopies, elemental analysis and size exclusion chromatography (SEC). Crosslinked derivatives were obtained by reactions with 1,7-octadiyne or 1,4-diethynylbenzene and subsequently deprotected to restore the free amino groups. These last systems
showed selective swellability in acid medium. (literal)
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