Modification at a boron unit: tuning electronic and optical properties of pi-conjugated acyclic anion receptors

Org Biomol Chem. 2010 Oct 7;8(19):4308-15. doi: 10.1039/c0ob00044b. Epub 2010 Jul 30.

Abstract

Substituents at the boron unit of dipyrrolyldiketone boron complexes as pi-conjugated acyclic anion receptors play crucial roles for the tuning of solid-state molecular assemblies, anion-binding behaviour and electronic and optical properties. In particular, emission quantum yields can be significantly tunable by boron substituents and pyrrole alpha-aryl moieties.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anions / chemistry*
  • Boron Compounds / chemistry*
  • Crystallography, X-Ray
  • Ketones / chemistry
  • Models, Molecular
  • Molecular Structure
  • Pyrroles / chemistry*
  • Spectrometry, Fluorescence
  • Spectrophotometry

Substances

  • Anions
  • Boron Compounds
  • Ketones
  • Pyrroles