http://www.cnr.it/ontology/cnr/individuo/prodotto/ID313427
Towards controlled cationic polymer growth from inorganic oxide defects: Directing the mechanism of polystyrene grafting from g-irradiated silica (Articolo in rivista)
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- Label
- Towards controlled cationic polymer growth from inorganic oxide defects: Directing the mechanism of polystyrene grafting from g-irradiated silica (Articolo in rivista) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.polymer.2014.08.041 (literal)
- Alternative label
F. D'Acunzo , P. Gentili , G. Masci , O. Ursini (2014)
Towards controlled cationic polymer growth from inorganic oxide defects: Directing the mechanism of polystyrene grafting from g-irradiated silica
in Polymer (Amsterdam. Online); Elsevier, Amsterdam (Paesi Bassi)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- F. D'Acunzo , P. Gentili , G. Masci , O. Ursini (literal)
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- http://dx.doi.org/10.1016/j.polymer.2014.08.041 (literal)
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- ISI Web of Science (WOS) (literal)
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- Scopus (literal)
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- Institute of Chemical Methodologies, CNR, Via Salaria Km. 29.300 00015 Monterotondo Rome, Italy
Department of Chemistry, Sapienza University of Rome, Piazzale Aldo Moro 5, 00185 Rome, Italy (literal)
- Titolo
- Towards controlled cationic polymer growth from inorganic oxide defects: Directing the mechanism of polystyrene grafting from g-irradiated silica (literal)
- Abstract
- Most studies on surface-initiated controlled polymerizations for the synthesis of polymeric covalent
organic-inorganic hybrid materials focus on chemical methods requiring specific modifications of the
inorganic substrate. Few mechanistically-aware approaches have been undertaken towards exploiting
the reactivity of defects induced by physical techniques such as ionizing radiations or UVeVis light.
Within this framework, we take grafted polymerization of styrene from g-irradiated silica as a mechanistic
testing ground where para- and diamagnetic silica defects are present, and polymerization proceeds
through both radical and cationic mechanisms, resulting in a bimodal molecular weight
distribution. We show that these mechanistic intricacies can be sorted out by resorting to the chemical
arsenal developed in the last decades for controlled polymerizations. Specifically, we obtained a silicapolystyrene
grafted material by cationic grafting from at 30 ?C, a unimodal molecular weight distribution,
and a relatively high molecular weight (Mn ¼ 7.4 kDa) with a PDI of 1.68. (literal)
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