Diaqua-β-octaferrocenyltetraphenylporphyrin: a multiredox-active and air-stable 16π non-aromatic species
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Updated: Jan 31, 2026

Quantitative and Qualitative Method for Sphingomyelin by LC-MS Using Two Stable Isotopically Labeled Sphingomyelin Species
Published on: May 7, 2018
Rasha K Al-Shewiki1, Marcus Korb1, Alexander Hildebrandt1
1Chemnitz University of Technology, Inorganic Chemistry, Strasse der Nationen 62, 09111 Chemnitz, Germany. tobias.rueffer@chemie.tu-chemnitz.de.
Abstract:
Herein the synthesis and properties of the first β-octaferrocenyltetraphenylporphyrin, {TPPFc8(H2O)2}, in its extraordinary stable and non-aromatic 16π form are reported, showing seven separate reversible redox events. As oxidation progresses, the neighbouring ferrocenyls of the pyrrole subunits display moderate electronic coupling, while electron transfer along the 16π porphyrin cycle was, due to its non-aromatic nature, not observed.
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