Butane-1,4-diyl dications stabilized by steric factors: Electrochiroptical response systems based on reversible interconversion between dihydro[5]helicene-type electron acceptors and electron-donating 1,1′-binaphthyls

Eisuke Ohta, Hiroki Higuchi, Hidetoshi Kawai, Kenshu Fujiwara, Takanori Suzuki

研究成果: Contribution to journalArticle査読

28 被引用数 (Scopus)

抄録

Incorporation in the dihydro[5]helicene framework prevents deprotonation of the title dications by steric factors, thus allowing their isolation as deeply colored stable salts. Based on the reversible interconversion with the electron-donating binaphthylic diolefins, they constitute a new class of electrochromic systems, in which C-C bond making/breaking is accompanied by two-electron transfer. Optically pure (R)-binaphthylic donors are interconvertible with the 1,4-dications with the R,R-configuration. The very large molar ellipticity makes it possible for them to be used as electrochiroptical response systems, by which the electrochemical input is transduced into two spectral outputs, i.e. UV-Vis and circular dichroism. Structurally related push-pull-type bis(quinonemethide)s also exhibit a similar multi-output electrochemical response.

本文言語英語
ページ(範囲)3024-3031
ページ数8
ジャーナルOrganic and Biomolecular Chemistry
3
16
DOI
出版ステータス出版済み - 8 21 2005

All Science Journal Classification (ASJC) codes

  • 生化学
  • 物理化学および理論化学
  • 有機化学

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「Butane-1,4-diyl dications stabilized by steric factors: Electrochiroptical response systems based on reversible interconversion between dihydro[5]helicene-type electron acceptors and electron-donating 1,1′-binaphthyls」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

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