Immobilised porphyrins in monoterpene photooxidations

Detalhes bibliográficos
Autor(a) principal: Ribeiro, Sónia M.
Data de Publicação: 2008
Outros Autores: Serra, Arménio C., Gonsalves, A. M. d'A. Rocha
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/5007
https://doi.org/10.1016/j.jcat.2008.04.001
Resumo: Porphyrins were covalently linked to modified Merrifield polymers by chlorosulphonation activation of the porphyrin nucleus. These supported porphyrins were used as photosensitizers to promote singlet oxygen oxidation of monoterpenes with an efficiency that depends on porphyrin structure and the spacer used to link it to the polymer structure. The performance of these photosensitizers was studied. Citronellol and [alpha]-terpinene gave the expected singlet oxygen ene addition products. [alpha]-Pinene and [beta]-pinene also gave products from non-ene reactions, which is explained by the existence of an alternative radical pathway.
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spelling Immobilised porphyrins in monoterpene photooxidationsPolymer-supported porphyrinsSinglet oxygenMonoterpene oxidationPorphyrins were covalently linked to modified Merrifield polymers by chlorosulphonation activation of the porphyrin nucleus. These supported porphyrins were used as photosensitizers to promote singlet oxygen oxidation of monoterpenes with an efficiency that depends on porphyrin structure and the spacer used to link it to the polymer structure. The performance of these photosensitizers was studied. Citronellol and [alpha]-terpinene gave the expected singlet oxygen ene addition products. [alpha]-Pinene and [beta]-pinene also gave products from non-ene reactions, which is explained by the existence of an alternative radical pathway.http://www.sciencedirect.com/science/article/B6WHJ-4SG556B-1/1/0455044852b08c2b9832fda1d11113532008info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttp://hdl.handle.net/10316/5007http://hdl.handle.net/10316/5007https://doi.org/10.1016/j.jcat.2008.04.001engJournal of Catalysis. 256:2 (2008) 331-337Ribeiro, Sónia M.Serra, Arménio C.Gonsalves, A. M. d'A. Rochainfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2021-09-02T11:09:08Zoai:estudogeral.uc.pt:10316/5007Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:35.367296Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Immobilised porphyrins in monoterpene photooxidations
title Immobilised porphyrins in monoterpene photooxidations
spellingShingle Immobilised porphyrins in monoterpene photooxidations
Ribeiro, Sónia M.
Polymer-supported porphyrins
Singlet oxygen
Monoterpene oxidation
title_short Immobilised porphyrins in monoterpene photooxidations
title_full Immobilised porphyrins in monoterpene photooxidations
title_fullStr Immobilised porphyrins in monoterpene photooxidations
title_full_unstemmed Immobilised porphyrins in monoterpene photooxidations
title_sort Immobilised porphyrins in monoterpene photooxidations
author Ribeiro, Sónia M.
author_facet Ribeiro, Sónia M.
Serra, Arménio C.
Gonsalves, A. M. d'A. Rocha
author_role author
author2 Serra, Arménio C.
Gonsalves, A. M. d'A. Rocha
author2_role author
author
dc.contributor.author.fl_str_mv Ribeiro, Sónia M.
Serra, Arménio C.
Gonsalves, A. M. d'A. Rocha
dc.subject.por.fl_str_mv Polymer-supported porphyrins
Singlet oxygen
Monoterpene oxidation
topic Polymer-supported porphyrins
Singlet oxygen
Monoterpene oxidation
description Porphyrins were covalently linked to modified Merrifield polymers by chlorosulphonation activation of the porphyrin nucleus. These supported porphyrins were used as photosensitizers to promote singlet oxygen oxidation of monoterpenes with an efficiency that depends on porphyrin structure and the spacer used to link it to the polymer structure. The performance of these photosensitizers was studied. Citronellol and [alpha]-terpinene gave the expected singlet oxygen ene addition products. [alpha]-Pinene and [beta]-pinene also gave products from non-ene reactions, which is explained by the existence of an alternative radical pathway.
publishDate 2008
dc.date.none.fl_str_mv 2008
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/5007
http://hdl.handle.net/10316/5007
https://doi.org/10.1016/j.jcat.2008.04.001
url http://hdl.handle.net/10316/5007
https://doi.org/10.1016/j.jcat.2008.04.001
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Catalysis. 256:2 (2008) 331-337
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eu_rights_str_mv openAccess
dc.format.none.fl_str_mv aplication/PDF
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