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Alkali Ion Exchanged Nafion as a Confining Medium for Photochemical Reactions

Arumugam, Selvanathan ; Kaanumalle, Lakshmi S. ; Ramamurthy, V.

Photochemistry and photobiology, 2006-01, Vol.82 (1), p.139-145 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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  • Título:
    Alkali Ion Exchanged Nafion as a Confining Medium for Photochemical Reactions
  • Autor: Arumugam, Selvanathan ; Kaanumalle, Lakshmi S. ; Ramamurthy, V.
  • Assuntos: J. C. (Tito) Scaiano Honorary Issue
  • É parte de: Photochemistry and photobiology, 2006-01, Vol.82 (1), p.139-145
  • Notas: ArticleID:PHP139
    ark:/67375/WNG-DXTNPF8D-6
    istex:7C7A4D1C12039D0DAF8746D1CCB6328AE9FC5FD1
    This paper is part of a special issue dedicated to Professor J. C. (Tito) Scaiano on the occasion of his 60th birthday.
    ObjectType-Article-1
    SourceType-Scholarly Journals-1
    ObjectType-Feature-2
    content type line 23
  • Descrição: Methanol-swollen Nafion beads were used as microreactors to control the photochemical reaction pathways. Product selectivity in three unimolecular reactions, namely, the photo-Fries rearrangement of naphthyl esters, Norrish Type I reaction of 1-phenyl-3-p-tolyl-propan-2-one and Norrish Type I and Type II reactions of benzoin alkyl ethers were examined. The influence of cations over the photodimerization of acenaphthylene and cross-photodimerization between acenaphthylene and N-benzyl maleimide included within Nafion were also examined. The photochemical behaviors of the above substrates were significantly altered within Nafion compared with their solution photochemistry. Of particular interest, the product distributions were found to depend on the counter cations of Nafion.
  • Editor: Oxford, UK: Blackwell Publishing Ltd
  • Idioma: Inglês

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