A-βcyclodextrin/siloxane hybrid polymer: synthesis, characterization and inclusion complexes
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Outros Autores: | , , |
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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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 |
format |
article |
status_str |
publishedVersion |
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) |
instacron_str |
SBQ |
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 |
_version_ |
1750318171454177280 |