Covalent Linking of Coordination-Organized Slipped Cofacial Porphyrin Dimers

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Coordination-organized porphyrin dimers of 5,15-bis[2-(allyloxycarbonyl)ethyl]- and bis[3-(allyloxy)propyl]-20-(1-methyl-2-imidazolyl)porphyrinatozinc were covalently linked by an intramolecular olefin metathesis reaction in excellent yields (93–98%). It was found that the yields of the intramolecular metathesis reaction depended strongly on the molecular length of the substituent at the 5 and 15 positions. Introducing longer 3-(allyloxycarbonyl)propyl and 4-(allyloxycarbonyl)butyl substituents decreased sharply the yields of the covalent linking reaction to 26% and 16%, respectively. The covalently linked dimers maintained their coordination structures even when dissolved in as polar a solvent as pyridine.

収録刊行物

  • Bulletin of the Chemical Society of Japan

    Bulletin of the Chemical Society of Japan 77(2), 365-374, 2004-02-15

    The Chemical Society of Japan

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各種コード

  • NII論文ID(NAID)
    10012095174
  • NII書誌ID(NCID)
    AA00580132
  • 本文言語コード
    ENG
  • 資料種別
    ART
  • ISSN
    00092673
  • NDL 記事登録ID
    6845656
  • NDL 雑誌分類
    ZP1(科学技術--化学・化学工業)
  • NDL 請求記号
    Z53-B35
  • データ提供元
    CJP書誌  NDL  J-STAGE 
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