Multiple conformational changes of β-tetraphenyl meso- hexakis(pentafluorophenyl) substituted [26] and [28]hexaphyrins(1.1.1.1.1.1)

Taro Koide, Katsuyuki Youfu, Shohei Saito, Atsuhiro Osuka

研究成果: ジャーナルへの寄稿 › 記事

46 引用 (Scopus)

抄録

β-Tetraphenyl meso-hexakis(pentafluorophenyl) substituted [26]hexaphyrin 3 is conformationally flexible between rectangular and figure-of-eight shapes and its two-electron reduced [28]hexaphyrin 4 takes figure-of-eight conformations, which are changed, upon protonation, to twisted conformations with distinct Möbius aromaticity.

元の言語英語
ページ（範囲）6047-6049
ページ数3
ジャーナルChemical Communications
発行部数40
DOI
出版物ステータス出版済み - 12 1 2009

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Conformations
Protonation
Electrons

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • Chemistry(all)
  • Surfaces, Coatings and Films
  • Metals and Alloys
  • Materials Chemistry

これを引用

Multiple conformational changes of β-tetraphenyl meso- hexakis(pentafluorophenyl) substituted [26] and [28]hexaphyrins(1.1.1.1.1.1). / Koide, Taro; Youfu, Katsuyuki; Saito, Shohei; Osuka, Atsuhiro.

：: Chemical Communications, 番号 40, 01.12.2009, p. 6047-6049.

研究成果: ジャーナルへの寄稿 › 記事

Koide, T, Youfu, K, Saito, S & Osuka, A 2009, 'Multiple conformational changes of β-tetraphenyl meso- hexakis(pentafluorophenyl) substituted [26] and [28]hexaphyrins(1.1.1.1.1.1)', Chemical Communications, 番号 40, pp. 6047-6049. https://doi.org/10.1039/b910167e
Koide T, Youfu K, Saito S, Osuka A. Multiple conformational changes of β-tetraphenyl meso- hexakis(pentafluorophenyl) substituted [26] and [28]hexaphyrins(1.1.1.1.1.1). Chemical Communications. 2009 12 1;(40):6047-6049. https://doi.org/10.1039/b910167e
Koide, Taro ; Youfu, Katsuyuki ; Saito, Shohei ; Osuka, Atsuhiro. / Multiple conformational changes of β-tetraphenyl meso- hexakis(pentafluorophenyl) substituted [26] and [28]hexaphyrins(1.1.1.1.1.1). ：: Chemical Communications. 2009 ; 番号 40. pp. 6047-6049.
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abstract = "β-Tetraphenyl meso-hexakis(pentafluorophenyl) substituted [26]hexaphyrin 3 is conformationally flexible between rectangular and figure-of-eight shapes and its two-electron reduced [28]hexaphyrin 4 takes figure-of-eight conformations, which are changed, upon protonation, to twisted conformations with distinct M{\"o}bius aromaticity.",
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