SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS

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New graft copolymers were synthesized from the free radical polymerization of N-isopropylacrylamide (NIPAAm) and 2-methyl-2-oxazoline (MM) macromonomers initiated by 2,2'-azobisisobutyronitrile in dimethylformamide. The macromonomers, with polymerization degrees 31 and 62, were synthesized by r...

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Detalles Bibliográficos
Autores: Rueda, Juan Carlos, Paola Palacios, Ana María
Formato: artículo
Fecha de Publicación:2021
Institución:Sociedad Química del Perú
Repositorio:Revista de la Sociedad Química del Perú
Lenguaje:español
OAI Identifier:oai:rsqp.revistas.sqperu.org.pe:article/336
Enlace del recurso:http://revistas.sqperu.org.pe/index.php/revistasqperu/article/view/336
Nivel de acceso:acceso abierto
Materia:Graft copolymers
NIPAAm
thermoresponsive
macromonomer
polyoxazolines
Copolímero de injerto
termosensibilidad
macromonómero
polioxazolinas
id REVSQP_3caa01a04fe93a39d487ae1f697b0a92
oai_identifier_str oai:rsqp.revistas.sqperu.org.pe:article/336
network_acronym_str REVSQP
network_name_str Revista de la Sociedad Química del Perú
repository_id_str
dc.title.none.fl_str_mv SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS
SÍNTESIS Y CARACTERIZACIÓN DE NUEVOS COPOLÍMEROS DE INJERTO TERMOSENSIBLES A PARTIR DE N-ISOPROPILACRILAMIDA Y MACROMONÓMEROS DE 2-METIL-2-OXAZOLINA
title SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS
spellingShingle SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS
Rueda, Juan Carlos
Graft copolymers
NIPAAm
thermoresponsive
macromonomer
polyoxazolines
Copolímero de injerto
NIPAAm
termosensibilidad
macromonómero
polioxazolinas
title_short SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS
title_full SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS
title_fullStr SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS
title_full_unstemmed SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS
title_sort SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERS
dc.creator.none.fl_str_mv Rueda, Juan Carlos
Paola Palacios, Ana María
author Rueda, Juan Carlos
author_facet Rueda, Juan Carlos
Paola Palacios, Ana María
author_role author
author2 Paola Palacios, Ana María
author2_role author
dc.subject.none.fl_str_mv Graft copolymers
NIPAAm
thermoresponsive
macromonomer
polyoxazolines
Copolímero de injerto
NIPAAm
termosensibilidad
macromonómero
polioxazolinas
topic Graft copolymers
NIPAAm
thermoresponsive
macromonomer
polyoxazolines
Copolímero de injerto
NIPAAm
termosensibilidad
macromonómero
polioxazolinas
description New graft copolymers were synthesized from the free radical polymerization of N-isopropylacrylamide (NIPAAm) and 2-methyl-2-oxazoline (MM) macromonomers initiated by 2,2'-azobisisobutyronitrile in dimethylformamide. The macromonomers, with polymerization degrees 31 and 62, were synthesized by ring-opening cationic polymerization of 2-methyl-2-oxazoline initiated by chloromethylstyrene in the presence of sodium iodide. The grafted macromonomers and copolymers were characterized by proton nuclear magnetic resonance spectrometry (1H-RMN) and the conformational transition temperature was determined by turbidimetric measurements and 1H-RMN spectroscopy. The NIPAAm / MM molar ratio in the copolymer, determined by 1H-RMN, was higher than in the feed to the reactor due to the higher reactivity of the NIPAAm due to its greater diffusivity in the reacting medium due to its lower molecular weight. The conformational transition temperature (LCST) of the graft copolymers ranged from 33 to 38 °C and the intensity of the same was a function of the molar ratio of NIPAAm / macromonomer within the graft copolymer. The value of the LCST increased, and at the same time its intensity decreased, as the NIPAAm / MM molar ratio decreased in the copolymer. The LCST also decreased even more in intensity as the degree of polymerization of the macromonomer increased. From the LCST temperature, the graft copolymers with a relatively high content of MM could form micelles or molecular aggregates type "core-shell" in aqueous solution, which would be formed by a core with collapsed segments of polyNIPAAm and a shell formed of hydrophilic polymethyloxazoline chains, which partially prevent an intermolecular collapse of these aggregates.
publishDate 2021
dc.date.none.fl_str_mv 2021-11-01
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Text
texto
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://revistas.sqperu.org.pe/index.php/revistasqperu/article/view/336
10.37761/rsqp.v87i2.336
url http://revistas.sqperu.org.pe/index.php/revistasqperu/article/view/336
identifier_str_mv 10.37761/rsqp.v87i2.336
dc.language.none.fl_str_mv spa
language spa
dc.relation.none.fl_str_mv http://revistas.sqperu.org.pe/index.php/revistasqperu/article/view/336/307
dc.rights.none.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.coverage.none.fl_str_mv 2021
2021
dc.publisher.none.fl_str_mv Sociedad Química del Perú
publisher.none.fl_str_mv Sociedad Química del Perú
dc.source.none.fl_str_mv Revista de la Sociedad Química del Perú; Vol. 87 Núm. 2 (2021): Revista de la Sociedad Química del Perú; 163-179
Journal of the Chemical Society of Peru; Vol. 87 No. 2 (2021): Journal of Sociedad Química del Perú; 163-179
2309-8740
1810-634X
10.37761/rsqp.v87i2
reponame:Revista de la Sociedad Química del Perú
instname:Sociedad Química del Perú
instacron:SQP
instname_str Sociedad Química del Perú
instacron_str SQP
institution SQP
reponame_str Revista de la Sociedad Química del Perú
collection Revista de la Sociedad Química del Perú
repository.name.fl_str_mv
repository.mail.fl_str_mv
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spelling SYNTHESIS AND CHARACTERIZATION OF NEW THERMOSENSITIVE GRAFT COPOLYMERS FROM N-ISOPROPYLACRYLAMIDE AND 2-METHYL-2-OXAZOLINE MACROMONOMERSSÍNTESIS Y CARACTERIZACIÓN DE NUEVOS COPOLÍMEROS DE INJERTO TERMOSENSIBLES A PARTIR DE N-ISOPROPILACRILAMIDA Y MACROMONÓMEROS DE 2-METIL-2-OXAZOLINARueda, Juan CarlosPaola Palacios, Ana MaríaGraft copolymersNIPAAmthermoresponsivemacromonomerpolyoxazolinesCopolímero de injertoNIPAAmtermosensibilidadmacromonómeropolioxazolinasNew graft copolymers were synthesized from the free radical polymerization of N-isopropylacrylamide (NIPAAm) and 2-methyl-2-oxazoline (MM) macromonomers initiated by 2,2'-azobisisobutyronitrile in dimethylformamide. The macromonomers, with polymerization degrees 31 and 62, were synthesized by ring-opening cationic polymerization of 2-methyl-2-oxazoline initiated by chloromethylstyrene in the presence of sodium iodide. The grafted macromonomers and copolymers were characterized by proton nuclear magnetic resonance spectrometry (1H-RMN) and the conformational transition temperature was determined by turbidimetric measurements and 1H-RMN spectroscopy. The NIPAAm / MM molar ratio in the copolymer, determined by 1H-RMN, was higher than in the feed to the reactor due to the higher reactivity of the NIPAAm due to its greater diffusivity in the reacting medium due to its lower molecular weight. The conformational transition temperature (LCST) of the graft copolymers ranged from 33 to 38 °C and the intensity of the same was a function of the molar ratio of NIPAAm / macromonomer within the graft copolymer. The value of the LCST increased, and at the same time its intensity decreased, as the NIPAAm / MM molar ratio decreased in the copolymer. The LCST also decreased even more in intensity as the degree of polymerization of the macromonomer increased. From the LCST temperature, the graft copolymers with a relatively high content of MM could form micelles or molecular aggregates type "core-shell" in aqueous solution, which would be formed by a core with collapsed segments of polyNIPAAm and a shell formed of hydrophilic polymethyloxazoline chains, which partially prevent an intermolecular collapse of these aggregates.Fueron sintetizados nuevos copolímeros injertados a partir de la polimerización por radicales libres de N-isopropilacrilamida (NIPAAm) y macromonómeros de 2-metil-2-oxazolina (MM) iniciada por el 2,2´-azobisisobutironitrilo en dimetilformamida. Los macromonómeros, de grados de polimerización 31 y 62, fueron sintetizados mediante la polimerización catiónica por apertura de anillo de 2-metil-2-oxazolina iniciada por el clorometilestireno en presencia de ioduro de sodio. Los macromonómeros y copolímeros injertados fueron caracterizados por espectrometría de resonancia magnética nuclear de protones (1H-RMN) y la temperatura de transición conformacional fue determinada mediante mediciones turbidimétricas yespectroscopía 1H-RMN.La razón molar NIPAAm/MM en el copolímero, determinada por 1H-RMN, fue mayor que en la alimentación al reactor debido a la mayor reactividad del NIPAAm por su mayor difusividad en el medio reaccionante debido a su menor peso molecular. La temperatura de transición conformacional (LCST) de los copolímeros injertados estuvo en el rango de 33 a 38 °C y la intensidad de la misma fue función de la razón molar de NIPAAm/ macromonómero dentro del copolímero injertado. Se incrementó el valor de la LCST, y al mismo tiempo disminuyó su intensidad, al disminuir la razón molar NIPAAm/MM en el copolímero. La LCST también disminuyó aún más en intensidad al aumentar el grado de polimerización del macromonómero. A partir de la temperatura LCST, los copolímeros injertados con un relativamente alto contenido de MM podrían formar micelas o agregados moleculares tipo “core-shell” en solución acuosa, que estarían formados por un núcleo con segmentos colapsados de poliNIPAAm y una corona formada de cadenas hidrofílicas de polimetiloxazolina, las cuales impiden parcialmente un colapso intermolecular de estos agregados.Sociedad Química del Perú2021-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionTexttextoapplication/pdfhttp://revistas.sqperu.org.pe/index.php/revistasqperu/article/view/33610.37761/rsqp.v87i2.336Revista de la Sociedad Química del Perú; Vol. 87 Núm. 2 (2021): Revista de la Sociedad Química del Perú; 163-179Journal of the Chemical Society of Peru; Vol. 87 No. 2 (2021): Journal of Sociedad Química del Perú; 163-1792309-87401810-634X10.37761/rsqp.v87i2reponame:Revista de la Sociedad Química del Perúinstname:Sociedad Química del Perúinstacron:SQPspahttp://revistas.sqperu.org.pe/index.php/revistasqperu/article/view/336/30720212021https://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessoai:rsqp.revistas.sqperu.org.pe:article/3362022-01-13T23:43:34Z
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