Conformational analysis of calix[n] arenes with chiral substituents by using circular dichroism

Atsushi Ikeda, Takeshi Nagasaki, Seiji Shinkai

研究成果: Contribution to journalArticle査読

40 被引用数 (Scopus)

抄録

Calix [n] arenes (n= 4 and 6) bearing chiral substituents (R*) on the lower rim (1n) or on the upper rim (4n) were synthesized. The isomers derived from 14 were conformationally immobile and showed different circular dichroism (CD) spectra. In the 1H NMR spectra the proton signals in R* shifted to higher magnetic field when the lower rim is sterically crowded and in the CD spectra a strong CD band appeared. Therefore, the change in the CD spectra is rationalized in terms of R*…π interactions. In contrast, compound 44 was not conformationally immobilized and the CD spectra changed in response to the metal binding to the methoxy oxygens arranged on the lower rim. The specific metal interaction enabled the metal binding event to be detected by the CD technique.

本文言語英語
ページ(範囲)699-710
ページ数12
ジャーナルJournal of Physical Organic Chemistry
5
10
DOI
出版ステータス出版済み - 10 1992

All Science Journal Classification (ASJC) codes

  • 物理化学および理論化学
  • 有機化学

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