Study of a bifuran vs. bithiophene unit for the rational design of π-conjugated systems. What have we learned?

Ori Gidron, Neta Varsano, Linda J.W. Shimon, Gregory Leitus, Michael Bendikov

Research output: Contribution to journalArticlepeer-review

Abstract

A comparative study of two structural isomers highlights the advantages of bifuran vs. bithiophene units in conjugated systems, such as higher fluorescence, solubility, and increased stability of the oxidized species. Importantly, we have found that the small bifuran unit bestows the advantages found in longer oligofurans, and should be considered in the rational design of π-conjugated systems.

Original languageEnglish
Pages (from-to)6256-6258
Number of pages3
JournalChemical Communications
Volume49
Issue number56
DOIs
StatePublished - 18 Jun 2013

All Science Journal Classification (ASJC) codes

  • Electronic, Optical and Magnetic Materials
  • General Chemistry
  • Ceramics and Composites
  • Metals and Alloys
  • Materials Chemistry
  • Surfaces, Coatings and Films
  • Catalysis

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