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Facile syntheses of quater-, penta-, and sexipyrroles

  • Jonathan L. Sessler*
  • , Apolonio Aguilar
  • , David Sanchez-Garcia
  • , Daniel Seidel
  • , Thomas Köhler
  • , Forrest Arp
  • , Vincent M. Lynch
  • *Corresponding author for this work

Research output: Indexed journal article Articlepeer-review

41 Citations (Scopus)

Abstract

(Chemical Equation Presented) α,α-Linked oligopyrroles are attractive precursors for both expanded porphyrin and conducting polymer chemistry. We demonstrate facile methods for synthesizing quater-, penta-, and sexipyrroles from more readily available bi- and terpyrrole intermediates. These products demonstrate stability in their brightly colored oxidized forms, while reduction using borohydride reagents gives the corresponding all-pyrrole oligomers, which oxidize readily in air. The oxidized quater- and sexipyrroles were characterized by single-crystal X-ray diffraction analysis.

Original languageEnglish
Pages (from-to)1887-1890
Number of pages4
JournalOrganic Letters
Volume7
Issue number10
DOIs
Publication statusPublished - 12 May 2005
Externally publishedYes

Keywords

  • Expanded porphyrin
  • Polypyrrole
  • Pyrrole

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