Synthesis of C60(OH)18-20 in aqueous alkaline solution under O2-atmosphere

Detalhes bibliográficos
Autor(a) principal: Alves,Gustavo Catão
Data de Publicação: 2006
Outros Autores: Ladeira,Luiz Orlando, Righi,Ariete, Krambrock,Klaus, Calado,Hállen Daniel, Gil,Rossimiriam Pereira de Freitas, Pinheiro,Maurício Veloso B.
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=S0103-50532006000600017
Resumo: In this work we report on an alternative synthesis of water-soluble fullerenes known as fullerols, aiming for biomedical applications. The synthesis is based on a process in which polyethylene glycol (PEG400) is used as phase-transfer catalyst between fullerene/benzene and aqueous NaOH solutions. The polyhydroxylation of the fullerenes occurs in the NaOH solution under a continuous flow of O2 to enhance the reaction yield. The resulting compound was characterized with infrared spectroscopy, nuclear magnetic resonance, thermo-gravimetric analysis and optical absorption. The formation of C60(OH)18-20 in high yields was confirmed.
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spelling Synthesis of C60(OH)18-20 in aqueous alkaline solution under O2-atmospherefullerenefullerolpolyhydroxylationFTIRNMRTGIn this work we report on an alternative synthesis of water-soluble fullerenes known as fullerols, aiming for biomedical applications. The synthesis is based on a process in which polyethylene glycol (PEG400) is used as phase-transfer catalyst between fullerene/benzene and aqueous NaOH solutions. The polyhydroxylation of the fullerenes occurs in the NaOH solution under a continuous flow of O2 to enhance the reaction yield. The resulting compound was characterized with infrared spectroscopy, nuclear magnetic resonance, thermo-gravimetric analysis and optical absorption. The formation of C60(OH)18-20 in high yields was confirmed.Sociedade Brasileira de Química2006-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000600017Journal of the Brazilian Chemical Society v.17 n.6 2006reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532006000600017info:eu-repo/semantics/openAccessAlves,Gustavo CatãoLadeira,Luiz OrlandoRighi,ArieteKrambrock,KlausCalado,Hállen DanielGil,Rossimiriam Pereira de FreitasPinheiro,Maurício Veloso B.eng2006-11-29T00:00:00Zoai:scielo:S0103-50532006000600017Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2006-11-29T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Synthesis of C60(OH)18-20 in aqueous alkaline solution under O2-atmosphere
title Synthesis of C60(OH)18-20 in aqueous alkaline solution under O2-atmosphere
spellingShingle Synthesis of C60(OH)18-20 in aqueous alkaline solution under O2-atmosphere
Alves,Gustavo Catão
fullerene
fullerol
polyhydroxylation
FTIR
NMR
TG
title_short Synthesis of C60(OH)18-20 in aqueous alkaline solution under O2-atmosphere
title_full Synthesis of C60(OH)18-20 in aqueous alkaline solution under O2-atmosphere
title_fullStr Synthesis of C60(OH)18-20 in aqueous alkaline solution under O2-atmosphere
title_full_unstemmed Synthesis of C60(OH)18-20 in aqueous alkaline solution under O2-atmosphere
title_sort Synthesis of C60(OH)18-20 in aqueous alkaline solution under O2-atmosphere
author Alves,Gustavo Catão
author_facet Alves,Gustavo Catão
Ladeira,Luiz Orlando
Righi,Ariete
Krambrock,Klaus
Calado,Hállen Daniel
Gil,Rossimiriam Pereira de Freitas
Pinheiro,Maurício Veloso B.
author_role author
author2 Ladeira,Luiz Orlando
Righi,Ariete
Krambrock,Klaus
Calado,Hállen Daniel
Gil,Rossimiriam Pereira de Freitas
Pinheiro,Maurício Veloso B.
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Alves,Gustavo Catão
Ladeira,Luiz Orlando
Righi,Ariete
Krambrock,Klaus
Calado,Hállen Daniel
Gil,Rossimiriam Pereira de Freitas
Pinheiro,Maurício Veloso B.
dc.subject.por.fl_str_mv fullerene
fullerol
polyhydroxylation
FTIR
NMR
TG
topic fullerene
fullerol
polyhydroxylation
FTIR
NMR
TG
description In this work we report on an alternative synthesis of water-soluble fullerenes known as fullerols, aiming for biomedical applications. The synthesis is based on a process in which polyethylene glycol (PEG400) is used as phase-transfer catalyst between fullerene/benzene and aqueous NaOH solutions. The polyhydroxylation of the fullerenes occurs in the NaOH solution under a continuous flow of O2 to enhance the reaction yield. The resulting compound was characterized with infrared spectroscopy, nuclear magnetic resonance, thermo-gravimetric analysis and optical absorption. The formation of C60(OH)18-20 in high yields was confirmed.
publishDate 2006
dc.date.none.fl_str_mv 2006-10-01
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=S0103-50532006000600017
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000600017
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532006000600017
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.17 n.6 2006
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
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