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Protonation-triggered conformational changes to Möbius aromatic [32]heptaphyrins(1.1.1.1.1.1.1)

  • Shohei Saito
  • , Jae Yoon Shin
  • , Jong Min Lim
  • , Kil Suk Kim
  • , Dongho Kim
  • , Atsuhiro Osuka

Research output: Contribution to journalArticlepeer-review

134 Scopus citations

Abstract

Switching Aromaticity: Conformations of [32]heptaphyrins (1.1.1.1.1.1.1) are dependent upon meso-aryl substituents, solvents, temperature, and protonation. Particularly, protonation of meso-pentafluorophenyl-substituted [32]heptaphyrin triggers conformational changes to form twisted aromatic Möbius structures (see picture), even at room temperature. (Figure Presented).

Original languageEnglish
Pages (from-to)9657-9660
Number of pages4
JournalAngewandte Chemie - International Edition
Volume47
Issue number50
DOIs
StatePublished - 1 Dec 2008

Keywords

  • Aromaticity
  • Heptaphyrins
  • Möbius aromaticity
  • Porphyrinoids
  • Two-photon absorption

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