Synthesis and Structures of a Series of Bulky “Rind-Br” Based on a Rigid Fused-Ring <i>s</i>-Hydrindacene Skeleton

  • Tsukasa Matsuo
    Functional Elemento-Organic Chemistry Unit, RIKEN Advanced Science Institute
  • Katsunori Suzuki
    Functional Elemento-Organic Chemistry Unit, RIKEN Advanced Science Institute
  • Tomohide Fukawa
    Functional Elemento-Organic Chemistry Unit, RIKEN Advanced Science Institute
  • Baolin Li
    Functional Elemento-Organic Chemistry Unit, RIKEN Advanced Science Institute
  • Mikinao Ito
    Functional Elemento-Organic Chemistry Unit, RIKEN Advanced Science Institute
  • Yoshiaki Shoji
    Functional Elemento-Organic Chemistry Unit, RIKEN Advanced Science Institute
  • Takashi Otani
    Functional Elemento-Organic Chemistry Unit, RIKEN Advanced Science Institute
  • Liangchun Li
    Functional Elemento-Organic Chemistry Unit, RIKEN Advanced Science Institute
  • Megumi Kobayashi
    Functional Elemento-Organic Chemistry Unit, RIKEN Advanced Science Institute
  • Makoto Hachiya
    Functional Elemento-Organic Chemistry Unit, RIKEN Advanced Science Institute
  • Yoshiyuki Tahara
    Functional Elemento-Organic Chemistry Unit, RIKEN Advanced Science Institute
  • Daisuke Hashizume
    Advanced Technology Support Division, RIKEN Advanced Science Institute
  • Takeo Fukunaga
    Advanced Technology Support Division, RIKEN Advanced Science Institute
  • Aiko Fukazawa
    International Research Center for Elements Science (IRCELS), Institute for Chemical Research, Kyoto University
  • Yongming Li
    International Research Center for Elements Science (IRCELS), Institute for Chemical Research, Kyoto University
  • Hayato Tsuji
    International Research Center for Elements Science (IRCELS), Institute for Chemical Research, Kyoto University
  • Kohei Tamao
    Functional Elemento-Organic Chemistry Unit, RIKEN Advanced Science Institute

抄録

<jats:title>Abstract</jats:title> <jats:p>A series of octa-R-substituted bromo-s-hydrindacenes, “Rind-Br,” have been synthesized by a sequence of the Lewis acid catalyzed intramolecular Friedel–Crafts reaction, bromination and vice versa. Their structural features and physical properties depend on the eight R-substituents at the four benzylic positions on the s-hydrindacenyl skeleton. The molecular structures of the Rind-Br have been confirmed by X-ray crystallography, indicating the unique structural diversities of the bulky Rind groups.</jats:p>

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