Solubilization of phenol derivatives in polymer micelles formed by cationic block copolymer
Author
dc.contributor.author
Fuentes, Irma
Author
dc.contributor.author
Silva, Patricio
Author
dc.contributor.author
Martínez Concha, Francisco
Author
dc.contributor.author
Olea, Andrés F.
Admission date
dc.date.accessioned
2018-04-03T21:07:38Z
Available date
dc.date.available
2018-04-03T21:07:38Z
Publication date
dc.date.issued
2017
Cita de ítem
dc.identifier.citation
Journal of Nanomaterials Volume 2017, Article ID 7187324, 8 pages
es_ES
Identifier
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10.1155/2017/7187324
Identifier
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https://repositorio.uchile.cl/handle/2250/147142
Abstract
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The aggregation of cationic block copolymers formed by polystyrene (PS) and poly(ethyl-4-vinylpyridine) (PS-b-PE4VP) was studied in aqueous solution. Diblock copolymers of PS and poly(4-vinylpyridine) were synthesized by sequential anionic polymerization using BuLi as initiator. Subsequently, the 4-vinylpyridine units were quaternized with ethyl bromide to obtain cationic PS-b-PE4VP block copolymers with different quaternization degree. The self-aggregation of cationic block copolymers was studied by fluorescence probing, whereas the morphology and size of polymer micelles were determined by transmission electronic microscopy. Results indicate that spherical micelles with sizes lower than 100 nm were formed, whereas their micropolarity decreases with increasing quaternization degree. The partition of phenols between the micellar and aqueous phase was studied by using the pseudo-phase model, and the results show that the partition coefficients increase with increasing length of the side alkyl chain and are larger for star micelles. These results are discussed in terms of three-region model.