Synthesis of an organic-soluble π-conjugated [3]rotaxane via rotation of glucopyranose units in permethylated β-cyclodextrin

نویسندگان

  • Jun Terao
  • Yohei Konoshima
  • Akitoshi Matono
  • Hiroshi Masai
  • Tetsuaki Fujihara
  • Yasushi Tsuji
چکیده

We synthesized symmetrically insulated oligo(para-phenylene) and oligothiophene with a pseudo-linked [3]rotaxane structure by full rotation of glucopyranose units via a flipping (tumbling) mechanism in the π-conjugated guest having two permethylated β-cyclodextrin units at both ends. We also succeeded in the synthesis of an organic-soluble fixed [3]rotaxane by a cross-coupling or complexation reaction of thus formed pseudo linked [3]rotaxane. Oligo(para-phenylene), oligothiophene, and porphyrin derivatives were used as π-conjugated guests with stopper groups.

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عنوان ژورنال:

دوره 10  شماره 

صفحات  -

تاریخ انتشار 2014