Atropisomers of meso-conjugated uracyl porphyrin derivatives and their assembling structures

Satoshi Arai, Daisuke Niwa, Hiroyuki Nishide, Shinji Takeoka*

*この研究の対応する著者

研究成果: Article査読

14 被引用数 (Scopus)

抄録

(Chemical Equation Presented) We have synthesized a 5,15 meso-substituted methyluracyl porphyrin derivative bearing 6-methyluracyl units directly at the meso positions. The atropisomerization was regulated by steric replusion between the methyl substituents. When the atropisomers were mixed with alkylated melamine as a complementary hydrogen-bonding unit, the hydrogen-bonded assemblies were analyzed by diffusion-ordered spectroscopy (DOSY) in solution, which clarified that the αα isomer formed a face-to-face dimer, whereas the αβ isomer took a zigzag structure.

本文言語English
ページ(範囲)17-20
ページ数4
ジャーナルOrganic Letters
9
1
DOI
出版ステータスPublished - 2007 1月 4

ASJC Scopus subject areas

  • 生化学
  • 物理化学および理論化学
  • 有機化学

フィンガープリント

「Atropisomers of meso-conjugated uracyl porphyrin derivatives and their assembling structures」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。

引用スタイル