Photo-Ring-Opening Efficiency of 2,2-Diphenyl-2<i>H</i>-1-benzopyran Evaluated from Addition Reactivity of Amines to Its Ring-Opened Isomers

  • Sakuragi Masako
    Nanotechnology Research Institute, National Institute of Advanced Industrial Science and Technology
  • Kawanishi Yuji
    Nanotechnology Research Institute, National Institute of Advanced Industrial Science and Technology
  • Suzuki Yasuzo
    Nanotechnology Research Institute, National Institute of Advanced Industrial Science and Technology
  • Sakuragi Hirochika
    Department of Chemistry, University of Tsukuba

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  • Photo-Ring-Opening Efficiency of 2,2-Diphenyl-2H-1-benzopyran Evaluated from Addition Reactivity of Amines to Its Ring-Opened Isomers

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Irradiation of 2,2-diphenyl-2H-1-benzopyran (DPBP) in the presence of a primary or a secondary amine gave an addition product. With a large excess of amine, the apparent quantum yield for product formation reached 0.5. This value corresponds to a minimal quantum yield for formation of DPBP colored ring-opened forms.

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