Selective oxidative synthesis of meso-beta fused porphyrin dimers

Bradley J. Brennan, Jaro Arero, Paul A. Liddell, Thomas Moore, Ana Moore, Devens Gust

Research output: Contribution to journalArticlepeer-review

12 Scopus citations


An efficient route to meso-β doubly connected fused porphyrin dimers was developed. Synthesis of the dimers incorporated two successive C-C bond-forming steps selectively coupling unsubstituted meso-and β-positions. Using Cu(BF4)2 as an oxidant in nitromethane solvent, the radical coupling of Cu(II)-porphyrins occurred in high yield and without side-products, allowing chromatography-free purification. Efficient demetalation of the product yielded free-base derivatives and the possibility to incorporate other metals into the macrocycles. The absorption and electrochemical properties vary with the inserted metal, showing broad UV-visible-NIR absorption and multiple one-electron oxidations/reductions in a relatively narrow electrochemical window.

Original languageEnglish (US)
Pages (from-to)247-251
Number of pages5
JournalJournal of Porphyrins and Phthalocyanines
Issue number4
StatePublished - Apr 2013


  • copper
  • dimer
  • porphyrin
  • radical coupling
  • synthesis

ASJC Scopus subject areas

  • Chemistry(all)


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