A-βcyclodextrin/siloxane hybrid polymer: synthesis, characterization and inclusion complexes

Detalhes bibliográficos
Autor(a) principal: Abbehausen,Camilla
Data de Publicação: 2010
Outros Autores: Formiga,André L. B., Sabadini,Edvaldo, Yoshida,Inez V. P.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010001000011
Resumo: A hybrid polymer derived from siloxane and β-cyclodextrin (β-CD) was obtained by reaction of β-CD with g-isocyanatopropyltriethoxysilane (IPTS), followed by hydrolysis/condensation reactions, generating a β-CD-modified polysilsesquioxane resin (PSS-β-CD). PSS-β-CD hybrid was characterized by infrared spectroscopy and 13C and 29Si nuclear magnetic resonance. This hybrid was typically amorphous and thermally stable up to 180 ºC. PSS-β-CD was able to form films and its morphology was evaluated by scanning electron microscopy. The capability of β-CD grafted in the hybrid polymer to form inclusion complex was evaluated by the formation of a β-CD-phenolphthalein complex using UV-Vis spectroscopy. Even without changes in pH, the red form of phenolphthalein converts to the colorless one when PSS-β-CD is immersed in the solution. Theoretical calculations (AM1 and DFT methods) show that the complex is formed through the inclusion of the phenolate ring into β-CD cavity, favoring the colorless form of phenolphthalein by more than 15 kcal mol-1.
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spelling A-βcyclodextrin/siloxane hybrid polymer: synthesis, characterization and inclusion complexescyclodextrinpolysiloxanespolysilsesquioxanesinclusion complexesA hybrid polymer derived from siloxane and β-cyclodextrin (β-CD) was obtained by reaction of β-CD with g-isocyanatopropyltriethoxysilane (IPTS), followed by hydrolysis/condensation reactions, generating a β-CD-modified polysilsesquioxane resin (PSS-β-CD). PSS-β-CD hybrid was characterized by infrared spectroscopy and 13C and 29Si nuclear magnetic resonance. This hybrid was typically amorphous and thermally stable up to 180 ºC. PSS-β-CD was able to form films and its morphology was evaluated by scanning electron microscopy. The capability of β-CD grafted in the hybrid polymer to form inclusion complex was evaluated by the formation of a β-CD-phenolphthalein complex using UV-Vis spectroscopy. Even without changes in pH, the red form of phenolphthalein converts to the colorless one when PSS-β-CD is immersed in the solution. Theoretical calculations (AM1 and DFT methods) show that the complex is formed through the inclusion of the phenolate ring into β-CD cavity, favoring the colorless form of phenolphthalein by more than 15 kcal mol-1.Sociedade Brasileira de Química2010-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010001000011Journal of the Brazilian Chemical Society v.21 n.10 2010reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532010001000011info:eu-repo/semantics/openAccessAbbehausen,CamillaFormiga,André L. B.Sabadini,EdvaldoYoshida,Inez V. P.eng2010-12-01T00:00:00Zoai:scielo:S0103-50532010001000011Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2010-12-01T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv A-βcyclodextrin/siloxane hybrid polymer: synthesis, characterization and inclusion complexes
title A-βcyclodextrin/siloxane hybrid polymer: synthesis, characterization and inclusion complexes
spellingShingle A-βcyclodextrin/siloxane hybrid polymer: synthesis, characterization and inclusion complexes
Abbehausen,Camilla
cyclodextrin
polysiloxanes
polysilsesquioxanes
inclusion complexes
title_short A-βcyclodextrin/siloxane hybrid polymer: synthesis, characterization and inclusion complexes
title_full A-βcyclodextrin/siloxane hybrid polymer: synthesis, characterization and inclusion complexes
title_fullStr A-βcyclodextrin/siloxane hybrid polymer: synthesis, characterization and inclusion complexes
title_full_unstemmed A-βcyclodextrin/siloxane hybrid polymer: synthesis, characterization and inclusion complexes
title_sort A-βcyclodextrin/siloxane hybrid polymer: synthesis, characterization and inclusion complexes
author Abbehausen,Camilla
author_facet Abbehausen,Camilla
Formiga,André L. B.
Sabadini,Edvaldo
Yoshida,Inez V. P.
author_role author
author2 Formiga,André L. B.
Sabadini,Edvaldo
Yoshida,Inez V. P.
author2_role author
author
author
dc.contributor.author.fl_str_mv Abbehausen,Camilla
Formiga,André L. B.
Sabadini,Edvaldo
Yoshida,Inez V. P.
dc.subject.por.fl_str_mv cyclodextrin
polysiloxanes
polysilsesquioxanes
inclusion complexes
topic cyclodextrin
polysiloxanes
polysilsesquioxanes
inclusion complexes
description A hybrid polymer derived from siloxane and β-cyclodextrin (β-CD) was obtained by reaction of β-CD with g-isocyanatopropyltriethoxysilane (IPTS), followed by hydrolysis/condensation reactions, generating a β-CD-modified polysilsesquioxane resin (PSS-β-CD). PSS-β-CD hybrid was characterized by infrared spectroscopy and 13C and 29Si nuclear magnetic resonance. This hybrid was typically amorphous and thermally stable up to 180 ºC. PSS-β-CD was able to form films and its morphology was evaluated by scanning electron microscopy. The capability of β-CD grafted in the hybrid polymer to form inclusion complex was evaluated by the formation of a β-CD-phenolphthalein complex using UV-Vis spectroscopy. Even without changes in pH, the red form of phenolphthalein converts to the colorless one when PSS-β-CD is immersed in the solution. Theoretical calculations (AM1 and DFT methods) show that the complex is formed through the inclusion of the phenolate ring into β-CD cavity, favoring the colorless form of phenolphthalein by more than 15 kcal mol-1.
publishDate 2010
dc.date.none.fl_str_mv 2010-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010001000011
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010001000011
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532010001000011
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.21 n.10 2010
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
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institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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