Synthesis of ferrocenyl porphyrins via suzuki coupling and their photophysical properties

Muntaz Abu Bakar, Natalia N. Sergeeva, Thomas Juillard, Mathias O. Senge

Research output: Contribution to journalArticle

35 Citations (Scopus)

Abstract

In order to improve the synthetic access to ferrocene porphyrin type electron transfer compounds, meso-ferrocenyl-appended porphyrins and bisporphyrins were prepared using Suzuki coupling reactions of borylated porphyrins with appropriate ferrocene precursors. The fluorescence lifetimes of all ferrocene porphyrin compounds are between 7.4 and 10.3 ns.

Original languageEnglish
Pages (from-to)3225-3228
Number of pages4
JournalOrganometallics
Volume30
Issue number11
DOIs
Publication statusPublished - 17 May 2011
Externally publishedYes

Fingerprint

Porphyrins
porphyrins
synthesis
electron transfer
Fluorescence
life (durability)
fluorescence
Electrons
ferrocene

ASJC Scopus subject areas

  • Organic Chemistry
  • Physical and Theoretical Chemistry
  • Inorganic Chemistry

Cite this

Synthesis of ferrocenyl porphyrins via suzuki coupling and their photophysical properties. / Abu Bakar, Muntaz; Sergeeva, Natalia N.; Juillard, Thomas; Senge, Mathias O.

In: Organometallics, Vol. 30, No. 11, 17.05.2011, p. 3225-3228.

Research output: Contribution to journalArticle

Abu Bakar, Muntaz ; Sergeeva, Natalia N. ; Juillard, Thomas ; Senge, Mathias O. / Synthesis of ferrocenyl porphyrins via suzuki coupling and their photophysical properties. In: Organometallics. 2011 ; Vol. 30, No. 11. pp. 3225-3228.
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