meso-aryl-substituted [26]hexaphyrin(1.1.0.1.1.0) and [38]nonaphyrin(1.1.0. 1.1.0.1.1.0) from oxidative coupling of a tripyrrane

Soji Shimizu, Ryuichiro Taniguchi, Atsuhiro Osuka

Research output: Contribution to journalArticle

48 Citations (Scopus)

Abstract

(Figure Presented) Acid-specific conformational changes: Protonation of meso-aryl-substituted rubyrin 1 with HCl or CF3CO2H causes different conformational changes, as revealed by specific shifts in the UV/Vis absorption bands relative to those of the free-base form (Cl-: blue shift; CF3CO2-: red shift). The distinct counteranion-dependent color changes upon addition of the acids to the "anion sensor" 1 are easily detected.

Original languageEnglish
Pages (from-to)2225-2229
Number of pages5
JournalAngewandte Chemie - International Edition
Volume44
Issue number15
DOIs
Publication statusPublished - Apr 8 2005
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Chemistry(all)

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