Exploiting substituent effects for the synthesis of a photooxidatively resistant heptacene derivative.

Academic Article

Abstract

  • Substituent effects have been exploited to produce an unusually persistent heptacene derivative. In total, four new heptacene derivatives with varying levels of photooxidative resistance (1 < 2 < 3 < 4) have been synthesized. A combination of p-(t-butyl)thiophenyl substituents at positions 7 and 16 (i.e., arylthio substituents attached to the most reactive ring) and o-dimethylphenyl substituents at positions 5, 9, 14, and 18 (i.e., steric resistance on neighboring rings) make heptacene derivative 4 especially resistant to photooxidation. It persists for weeks as a solid, for 1-2 days in solution if shielded from light, and for several hours in solution when directly exposed to both light and air. Heptacene derivative 4 has been fully characterized. It possesses a small HOMO-LUMO gap of 1.37 eV.
  • Authors

  • Kaur, Irvinder
  • Stein, Nathan N
  • Kopreski, Ryan P
  • Miller, Glen
  • Status

    Publication Date

  • March 18, 2009
  • Has Subject Area

    Keywords

  • Antimicrobial Resistance
  • Digital Object Identifier (doi)

    Pubmed Id

  • 19243093
  • Start Page

  • 3424
  • End Page

  • 3425
  • Volume

  • 131
  • Issue

  • 10