http://www.cnr.it/ontology/cnr/individuo/prodotto/ID51166
Further EPR-spin trapping studies of the photoinitiating activity of Irgacure 369 (Articolo in rivista)
- Type
- Label
- Further EPR-spin trapping studies of the photoinitiating activity of Irgacure 369 (Articolo in rivista) (literal)
- Anno
- 2008-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.eurpolymj.2008.06.043 (literal)
- Alternative label
aA. Alberti, aMassimo Benaglia, aDante Macciantelli, bStefano Rossetti, bMarco Scoponi (2008)
Further EPR-spin trapping studies of the photoinitiating activity of Irgacure 369
in European Polymer Journal
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- aA. Alberti, aMassimo Benaglia, aDante Macciantelli, bStefano Rossetti, bMarco Scoponi (literal)
- Pagina inizio
- Pagina fine
- 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
- a ISOF-CNR, Area della Ricerca, Via P. Gobetti 101, 40129 Bologna, Italy
b ISOF-CNR, Sez. di Ferrara, Via Borsari 46, 44100 Ferrara, Italy (literal)
- Titolo
- Further EPR-spin trapping studies of the photoinitiating activity of Irgacure 369 (literal)
- Abstract
- The radicals formed upon visible light irradiation of the photoinitiator 2-benzyl-2-dimeth-ylamino -40-morpholinobutyrophenone (Irgacure 369), 1, were investigated by means of EPR spectroscopy coupled with the spin trapping technique both in the absence and in the presence of a monomer. The results suggest a dual behavior of 1 that may act both as a Type I and a Type II photoinitiator. From experimen ts carried out in the presence of 2-ethoxythioxanth one (Pila 124), 2 , an additive commonly used in combination w ith 1 as sensitizer, it is inferred that 2 mainly acts via hydrogen abstraction from 1 . (literal)
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- Autore CNR
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