http://www.cnr.it/ontology/cnr/individuo/prodotto/ID194522
Fluorescent Polyolefins by Free Radical Post-Reactor Modification with Functional Nitroxides (Articolo in rivista)
- Type
- Label
- Fluorescent Polyolefins by Free Radical Post-Reactor Modification with Functional Nitroxides (Articolo in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.reactfunctpolym.2012.06.021 (literal)
- Alternative label
Cicogna, Francesca; Coiai, Serena; Pinzino, Calogero; Ciardelli, Francesco; Passaglia, Elisa (2012)
Fluorescent Polyolefins by Free Radical Post-Reactor Modification with Functional Nitroxides
in Reactive & functional polymers (Print); Elsevier, Oxford (Regno Unito)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Cicogna, Francesca; Coiai, Serena; Pinzino, Calogero; Ciardelli, Francesco; Passaglia, Elisa (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
- CNR-ICCOM UOS Pisa, Area della Ricerca CNR, via G. Moruzzi 1, 56124 Pisa, Italy (literal)
- Titolo
- Fluorescent Polyolefins by Free Radical Post-Reactor Modification with Functional Nitroxides (literal)
- Abstract
- The 4-(1-naphthoate)-2,2,6,6-tetramethylpiperidine-1-oxyl (NfO-TEMPO) has been synthesized and successfully
grafted in the melt onto a random poly(ethylene-co-1-ottene) copolymer. Functionalized polyolefins
have been prepared by coupling reaction between NfO-TEMPO free radicals and macroradicals
which have been formed by H-abstraction induced by the presence of a peroxide. In order to deepen
insight into the functionalization mechanism, the reaction has been investigated by Electron Paramagnetic
Resonance (EPR). EPR spectra collected during the reaction run, have evidenced the decrease of
TEMPO signal as a consequence of temperature increasing. This decrease has been attributed to the formation
of a covalent bond between macroradicals and nitroxide free radical. The resulting functionalized
polyolefins, PO-g-(NfO-TEMPO), have been characterized by FT-IR and 1H NMR which has allowed to
evaluate their functionalization degree, whereas UV-Vis and fluorescence spectroscopy have been used
to investigate their optical properties. The comparison with low molecular weight model compounds,
has allowed to state that our methodology can be conveniently adopted to prepare fluorescent polyolefins
where the optical properties of the chromophore has been completely transferred to polymer backbone
both in solution and in the condensed phase. (literal)
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