論文

査読有り
2018年

Supramolecular chiroptical switching of helical-sense preferences through the two-way intramolecular transmission of a single chiral source

Organic and Biomolecular Chemistry
  • Ryo Katoono
  • ,
  • Keiichi Kusaka
  • ,
  • Yuki Tanaka
  • ,
  • Kenshu Fujiwara
  • ,
  • Takanori Suzuki

16
7
開始ページ
1167
終了ページ
1171
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1039/c7ob03057f
出版者・発行元
Royal Society of Chemistry

© The Royal Society of Chemistry 2018. We demonstrate a chiroptical switching system with a simple molecule. The molecule contains a pair of chromophores of diphenylacetylene that are linked with a diyne bond and arranged to exert exciton coupling in helically folded forms with (M)- or (P)-helicity. A tertiary amide group is attached to each end of the looped molecule. The amide carbonyls were used to capture a ditopic hydrogen-bonding guest. A chiral auxiliary group on the amide nitrogen acted as a chiral handle to control the helical-sense preference of dynamic helical forms of the loop. The helical-sense preference is brought about by an intramolecular transmission of point chirality associated with the loop. The preferred sense was switched upon complexation with an achiral additive through the formation of hydrogen bonds. In both states, before and after complexation, the helical-sense preferences were controlled through two-way transmission of the single chiral source.

リンク情報
DOI
https://doi.org/10.1039/c7ob03057f
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/29376181
Scopus
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85042141354&origin=inward
Scopus Citedby
https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85042141354&origin=inward
ID情報
  • DOI : 10.1039/c7ob03057f
  • ISSN : 1477-0520
  • PubMed ID : 29376181
  • SCOPUS ID : 85042141354

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