A straightforward strategy toward large BN-embedded π-systems: synthesis, structure, and optoelectronic properties of extended BN heterosuperbenzenes

J Am Chem Soc. 2014 Mar 12;136(10):3764-7. doi: 10.1021/ja500117z. Epub 2014 Mar 4.

Abstract

A straightforward strategy has been used to construct large BN-embedded π-systems simply from azaacenes. BN heterosuperbenzene derivatives, the largest BN heteroaromatics to date, have been synthesized in three steps. The molecules exhibit curved π-surfaces, showing two different conformations which are self-organized into a sandwich structure and further packed into a π-stacking column. The assembled microribbons exhibit good charge transport properties and photoconductivity, representing an important step toward the optoelectronic applications of BN-embedded aromatics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aza Compounds / chemistry
  • Chemistry Techniques, Synthetic / economics
  • Chemistry Techniques, Synthetic / methods
  • Equipment Design
  • Models, Molecular
  • Molecular Conformation
  • Polycyclic Aromatic Hydrocarbons / chemical synthesis
  • Polycyclic Aromatic Hydrocarbons / chemistry*
  • Transistors, Electronic

Substances

  • Aza Compounds
  • Polycyclic Aromatic Hydrocarbons
  • heterosuperbenzene