Immobilization of Fe, Mn and Co tetraphenylporphyrin complexes in MCM-41 and their catalytic activity in cyclohexene oxidation reaction by hydrogen peroxide

Detalhes bibliográficos
Autor(a) principal: Costa, Andréia A.
Data de Publicação: 2008
Outros Autores: Ghesti, Grace F., Macedo, Julio L. de, Braga, Valdeilson Souza, Santos, Marcello M., Dias, José Alves, Dias, Sílvia Cláudia Loureiro
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFBA
Texto Completo: http://www.repositorio.ufba.br/ri/handle/ri/6350
Resumo: Acesso restrito: Texto completo. p. 149-157
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spelling Costa, Andréia A.Ghesti, Grace F.Macedo, Julio L. deBraga, Valdeilson SouzaSantos, Marcello M.Dias, José AlvesDias, Sílvia Cláudia LoureiroCosta, Andréia A.Ghesti, Grace F.Macedo, Julio L. deBraga, Valdeilson SouzaSantos, Marcello M.Dias, José AlvesDias, Sílvia Cláudia Loureiro2012-07-05T19:33:29Z20081381-1169http://www.repositorio.ufba.br/ri/handle/ri/6350v. 282, n. 1-2Acesso restrito: Texto completo. p. 149-157Metalloporphyrin catalysts are able to carry out selective oxidation of organic substrates with several oxidizing agents. Recently, mesoporous materials have been studied as supports because they present high specific surface area, better dispersion and regeneration properties. This work presents the results of synthesis, characterization and application of three metalloporphyrin catalysts (FeTPPCl, MnTPPCl and CoTPP, where TPP = tetraphenylporphyrin) anchored on MCM-41, in the reaction of cyclohexene oxidation with hydrogen peroxide. A modified sol–gel preparation was chosen for the synthesis of the MCM-41 mesoporous material, as well as the anchoring was followed by Soxhlet extraction to ensure strong adsorption of the complex. The supported materials were much more stable than pure metalloporphyrins. The synthesized catalysts were characterized by UV–vis, FTIR, XRD, ICP-AES, 29Si MAS-NMR and thermal analysis, before and after incorporation. Evidence of the metalloporphyrin immobilization was confirmed by elemental analysis and their activity in the oxidation reaction. FeTPPCl/MCM-41 showed higher conversion than CoTPP/MCM-41 and MnTPPCl/MCM-41. However, MnTPPCl/MCM-41 even in low concentration on the support showed a good conversion for the direct oxidation of cyclohexene with the highest turnover number (1.54×105). All catalysts showed similar selectivity that favors allylic oxidation products over epoxidation. No leaching of the metalloporphyrins was observed after the reaction.Submitted by JURANDI DE SOUZA SILVA (jssufba@hotmail.com) on 2012-07-05T19:33:29Z No. of bitstreams: 1 1-s2.0-S1381116907007121-main.pdf: 1303552 bytes, checksum: 9007caa5c8625b13c65cecaf3009aa97 (MD5)Made available in DSpace on 2012-07-05T19:33:29Z (GMT). No. of bitstreams: 1 1-s2.0-S1381116907007121-main.pdf: 1303552 bytes, checksum: 9007caa5c8625b13c65cecaf3009aa97 (MD5) Previous issue date: 2008ttp://dx.doi.org/10.1016/j.molcata.2007.12.024reponame:Repositório Institucional da UFBAinstname:Universidade Federal da Bahia (UFBA)instacron:UFBAMetalloporphyrinsMolecular sievesMCM-41Cyclohexene oxidationHydrogen peroxideImmobilization of Fe, Mn and Co tetraphenylporphyrin complexes in MCM-41 and their catalytic activity in cyclohexene oxidation reaction by hydrogen peroxideJournal of Molecular Catalysis A-Chemicalinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article10000-01-01enginfo:eu-repo/semantics/openAccessORIGINAL1-s2.0-S1381116907007121-main.pdf1-s2.0-S1381116907007121-main.pdfapplication/pdf1303552https://repositorio.ufba.br/bitstream/ri/6350/1/1-s2.0-S1381116907007121-main.pdf9007caa5c8625b13c65cecaf3009aa97MD51LICENSElicense.txtlicense.txttext/plain1762https://repositorio.ufba.br/bitstream/ri/6350/2/license.txt1b89a9a0548218172d7c829f87a0eab9MD52TEXT1-s2.0-S1381116907007121-main.pdf.txt1-s2.0-S1381116907007121-main.pdf.txtExtracted texttext/plain31152https://repositorio.ufba.br/bitstream/ri/6350/3/1-s2.0-S1381116907007121-main.pdf.txtaea050f8417ae1009ffaa8514729b73eMD53ri/63502022-07-05 14:03:50.802oai:repositorio.ufba.br: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Repositório InstitucionalPUBhttp://192.188.11.11:8080/oai/requestopendoar:19322022-07-05T17:03:50Repositório Institucional da UFBA - Universidade Federal da Bahia (UFBA)false
dc.title.pt_BR.fl_str_mv Immobilization of Fe, Mn and Co tetraphenylporphyrin complexes in MCM-41 and their catalytic activity in cyclohexene oxidation reaction by hydrogen peroxide
dc.title.alternative.pt_BR.fl_str_mv Journal of Molecular Catalysis A-Chemical
title Immobilization of Fe, Mn and Co tetraphenylporphyrin complexes in MCM-41 and their catalytic activity in cyclohexene oxidation reaction by hydrogen peroxide
spellingShingle Immobilization of Fe, Mn and Co tetraphenylporphyrin complexes in MCM-41 and their catalytic activity in cyclohexene oxidation reaction by hydrogen peroxide
Costa, Andréia A.
Metalloporphyrins
Molecular sieves
MCM-41
Cyclohexene oxidation
Hydrogen peroxide
title_short Immobilization of Fe, Mn and Co tetraphenylporphyrin complexes in MCM-41 and their catalytic activity in cyclohexene oxidation reaction by hydrogen peroxide
title_full Immobilization of Fe, Mn and Co tetraphenylporphyrin complexes in MCM-41 and their catalytic activity in cyclohexene oxidation reaction by hydrogen peroxide
title_fullStr Immobilization of Fe, Mn and Co tetraphenylporphyrin complexes in MCM-41 and their catalytic activity in cyclohexene oxidation reaction by hydrogen peroxide
title_full_unstemmed Immobilization of Fe, Mn and Co tetraphenylporphyrin complexes in MCM-41 and their catalytic activity in cyclohexene oxidation reaction by hydrogen peroxide
title_sort Immobilization of Fe, Mn and Co tetraphenylporphyrin complexes in MCM-41 and their catalytic activity in cyclohexene oxidation reaction by hydrogen peroxide
author Costa, Andréia A.
author_facet Costa, Andréia A.
Ghesti, Grace F.
Macedo, Julio L. de
Braga, Valdeilson Souza
Santos, Marcello M.
Dias, José Alves
Dias, Sílvia Cláudia Loureiro
author_role author
author2 Ghesti, Grace F.
Macedo, Julio L. de
Braga, Valdeilson Souza
Santos, Marcello M.
Dias, José Alves
Dias, Sílvia Cláudia Loureiro
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Costa, Andréia A.
Ghesti, Grace F.
Macedo, Julio L. de
Braga, Valdeilson Souza
Santos, Marcello M.
Dias, José Alves
Dias, Sílvia Cláudia Loureiro
Costa, Andréia A.
Ghesti, Grace F.
Macedo, Julio L. de
Braga, Valdeilson Souza
Santos, Marcello M.
Dias, José Alves
Dias, Sílvia Cláudia Loureiro
dc.subject.por.fl_str_mv Metalloporphyrins
Molecular sieves
MCM-41
Cyclohexene oxidation
Hydrogen peroxide
topic Metalloporphyrins
Molecular sieves
MCM-41
Cyclohexene oxidation
Hydrogen peroxide
description Acesso restrito: Texto completo. p. 149-157
publishDate 2008
dc.date.issued.fl_str_mv 2008
dc.date.accessioned.fl_str_mv 2012-07-05T19:33:29Z
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://www.repositorio.ufba.br/ri/handle/ri/6350
dc.identifier.issn.none.fl_str_mv 1381-1169
dc.identifier.number.pt_BR.fl_str_mv v. 282, n. 1-2
identifier_str_mv 1381-1169
v. 282, n. 1-2
url http://www.repositorio.ufba.br/ri/handle/ri/6350
dc.language.iso.fl_str_mv eng
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