Abstract
In a previous paper, it has been reported about the formation of catechol di-, tri- and tetramers within an oxidative polymerization catalyzed by synthetic water-soluble iron-porphyrin as an efficient alternative to bio-labile natural peroxidase. It has also been demonstrated the occurrence of both C-C and C-O-C coupling mechanisms. However, since the coupling products were determined by mass spectroscopy, the exact bonding position could not have been precisely ascertained for the C-C bonded isomeric dimers that are the dominant products of catechol oligomerization. Therefore, here isolation and characterization of catechol isomeric dimers, obtained by oxidative coupling under the catalysis of a synthetic iron-porphyrin, have been done by NMR spectroscopy
Lingua originale | English |
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pagine (da-a) | 737-743 |
Numero di pagine | 7 |
Rivista | Biomacromolecules |
Volume | 8 |
Stato di pubblicazione | Published - 2007 |
All Science Journal Classification (ASJC) codes
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- ???subjectarea.asjc.2500.2502???
- ???subjectarea.asjc.2500.2507???
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