Innentitelbild: Hexaphyrin Fused to Two Anthracenes (Angew. Chem. 39/2012)

Authors

  • Koji Naoda,

    1. Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo-ku, Kyoto 606-8502 (Japan)
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  • Hirotaka Mori,

    1. Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo-ku, Kyoto 606-8502 (Japan)
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  • Dr. Naoki Aratani,

    1. Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo-ku, Kyoto 606-8502 (Japan)
    2. PRESTO (Japan) Science and Technology Agency (Japan)
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  • Byung Sun Lee,

    1. Spectroscopy Laboratory for Functional π-Electronic Systems and Department of Chemistry, Yonsei University, Seoul 120-749 (Korea)
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  • Prof. Dr. Dongho Kim,

    Corresponding author
    1. Spectroscopy Laboratory for Functional π-Electronic Systems and Department of Chemistry, Yonsei University, Seoul 120-749 (Korea)
    • Spectroscopy Laboratory for Functional π-Electronic Systems and Department of Chemistry, Yonsei University, Seoul 120-749 (Korea)
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  • Prof. Dr. Atsuhiro Osuka

    Corresponding author
    1. Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo-ku, Kyoto 606-8502 (Japan)
    • Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo-ku, Kyoto 606-8502 (Japan)
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Abstract

original image

π-expandierte Porphyrinoide in denen aromatische Strukturteile an den Porphyrinring kondensiert sind, rücken zunehmend in den Blickpunkt. In ihrer Zuschrift auf S. 9994 ff. berichten D. Kim, A. Osuka et al. über die Bildung eines Hexaphyrins, das mit zwei Anthracenylsubstituenten oxidativ kondensiert wurde. Das rechteckige konjugierte System verleiht dem kondensierten Hexaphyrin eine bemerkenswerte rotverschobene und eine ungewöhnlich scharfe Q-Banden-ähnliche Absorption bei 1467nm. (Photos: kyoto-design.jp)

Cartoon 1.

Ancillary

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