Photoinitiated Olefin Epoxidation with Molecular Oxygen, Sensitized by Free Base Porphyrins and Promoted by Hexacarbonylmolybdenum in Homogeneous Solution (Articolo in rivista)

Type
Label
  • Photoinitiated Olefin Epoxidation with Molecular Oxygen, Sensitized by Free Base Porphyrins and Promoted by Hexacarbonylmolybdenum in Homogeneous Solution (Articolo in rivista) (literal)
Anno
  • 2002-01-01T00:00:00+01:00 (literal)
Alternative label
  • Campestrini S., Tonellato U. (2002)
    Photoinitiated Olefin Epoxidation with Molecular Oxygen, Sensitized by Free Base Porphyrins and Promoted by Hexacarbonylmolybdenum in Homogeneous Solution
    in European journal of organic chemistry (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Campestrini S., Tonellato U. (literal)
Pagina inizio
  • 3827 (literal)
Pagina fine
  • 3832 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Titolo
  • Photoinitiated Olefin Epoxidation with Molecular Oxygen, Sensitized by Free Base Porphyrins and Promoted by Hexacarbonylmolybdenum in Homogeneous Solution (literal)
Abstract
  • The photooxidation of various olefins in homogeneous solution under an oxygen atmosphere, by use of visible light, a dye sensitizer, and an oxygen-transfer catalyst, has been investigated. The oxygen transfer from molecular oxygen to olefin involves the following steps: i) photoinduced singlet-oxygen formation, ii) alkyl hydroperoxide formation through the ene reaction, iii) the intermediacy of a reactive molybdenum peroxide, and iv) olefin epoxidation of the remaining substrate or of a second olefin. Among the various sensitizers and catalysts tested, the electron- deficient free base porphyrin 5,10,15,20-tetrakis(2',6'-dichlorophenyl)- beta-octabromoporphyrin and hexacarbonylmolybdenum showed the best performances in terms of robustness and activity. Under suitable conditions, complete olefin conversion may be obtained by adoption of molar ratios of sensitizer/catalyst/substrate of 1:50:2000, with the formation of the corresponding epoxide in up to 38% yield, which corresponds to 77% of the theoretical maximum. Quite interestingly, olefins reluctant to undergo ene reactions may be epoxidized in the presence of a second sacrificial olefin, yielding the corresponding epoxides with up to 80% total selectivity. (literal)
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