DSpace

RI UFBA >
Instituto de Química >
Artigos Publicados em Periódicos (Quimica) >

Please use this identifier to cite or link to this item: http://repositorio.ufba.br/ri/handle/ri/6350

Title: Immobilization of Fe, Mn and Co tetraphenylporphyrin complexes in MCM-41 and their catalytic activity in cyclohexene oxidation reaction by hydrogen peroxide
Other Titles: Journal of Molecular Catalysis A-Chemical
Authors: Costa, Andréia A.
Ghesti, Grace F.
Macedo, Julio L. de
Braga, Valdeilson Souza
Santos, Marcello M.
Dias, José Alves
Dias, Sílvia Cláudia Loureiro
Keywords: Metalloporphyrins;Molecular sieves;MCM-41;Cyclohexene oxidation;Hydrogen peroxide
Issue Date: 2008
Abstract: Metalloporphyrin 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.
Description: Acesso restrito: Texto completo. p. 149-157
URI: http://www.repositorio.ufba.br/ri/handle/ri/6350
ISSN: 1381-1169
Appears in Collections:Artigos Publicados em Periódicos (Quimica)

Files in This Item:

File Description SizeFormat
1-s2.0-S1381116907007121-main.pdf1.27 MBAdobe PDFView/Open
View Statistics

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

    Universidade Federal da Bahia

Contate-nos. Saiba mais sobre o RI/UFBA