Imaging Science and Photochemistry ›› 1994, Vol. 12 ›› Issue (4): 289-294.DOI: 10.7517/j.issn.1674-0475.1994.04.289

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A STUDY ON FLUORESCENCE QUENCHING OF9-CYANOANTHRACENE BY NITRONE COMPOUNDS

DIAO LI, WU SHI-KANG   

  1. Institue of Photographic Chemistry, Academia Sinica, Beijing 100101, P. R. China
  • Received:1993-08-30 Revised:1993-12-06 Online:1994-11-20 Published:1994-11-20

Abstract: Through the observation on the quenching process of the nitrone/9-cyanoanthracenesystem.it was found that the process may have different mechanism, including electrontransfer, energy transfer, and competitive absorption etc.α, N-diphenyl nitrone quenchesthe fluorescence of 9-CNA through the electron transfer mechanism, Which forms ionradicals of quencher and sensitizer respectively.But the nitrone positive ion radical neverleads to the cyclization reaction.The results also show that the 1,3-dipolar structure is the most important moiety forquencher.When the cyclization takes place, the product, oxaziridine Which is without 1,3-dipolar structure, loses the quenching ability.So, if the quenched system is directlyexposed to light, the fluorescence will recover.

Key words: nitrone, sensitizer, photo cyclization reaction, electron transfer