Elaborating boron dipyrromethene dyes with conjugated polyaromatic frameworks

Raymond Ziessel, Thomas Bura, Jean-Hubert Olivier

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

New difluoro-bora-diaza-s-indacenes were synthesized from tetramethyl derivatives following a sequence of reactions including Knoevenagel condensation, selective cross-coupling reactions in order to extend the delocalization pathway. The introduction of flexible chains bearing a terminal ester or based on polyethylene glycol insure a good solubility and import polarity which facilitates the purification procedures. Many polyaromatic subunits (pyrene, perylene, anthracene, naphtalene, ferrocene) were fused to the main central core of the Bodipy.

Original languageEnglish (US)
Pages (from-to)2304-2310
Number of pages7
JournalSynlett
Issue number15
DOIs
StatePublished - Sep 16 2010
Externally publishedYes

Fingerprint

Bearings (structural)
Perylene
Boron
Purification
Condensation
Esters
Coloring Agents
Solubility
Derivatives
pyrene
ferrocene
dipyrromethene
anthracene

Keywords

  • anthracene
  • Bodipy
  • ferrocene
  • palladium
  • perylene
  • pyrene
  • vinyl

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Elaborating boron dipyrromethene dyes with conjugated polyaromatic frameworks. / Ziessel, Raymond; Bura, Thomas; Olivier, Jean-Hubert.

In: Synlett, No. 15, 16.09.2010, p. 2304-2310.

Research output: Contribution to journalArticle

Ziessel, Raymond ; Bura, Thomas ; Olivier, Jean-Hubert. / Elaborating boron dipyrromethene dyes with conjugated polyaromatic frameworks. In: Synlett. 2010 ; No. 15. pp. 2304-2310.
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