Chirality organization of aniline oligomers through hydrogen bonds of amino acid moieties

J Org Chem. 2010 Nov 19;75(22):7909-12. doi: 10.1021/jo100853b. Epub 2010 Oct 19.

Abstract

Aniline oligomers bearing amino acid moieties were designed by the introduction of L/D-Ala-OMe into aniline oligomers to induce chirality organization of the π-conjugated aniline oligomer moieties, wherein the formation of intramolecular hydrogen bonds was demonstrated to play an important role to regulate the aniline oligomer moieties conformationally.

MeSH terms

  • Amino Acids / chemistry*
  • Aniline Compounds / chemical synthesis
  • Aniline Compounds / chemistry*
  • Crystallography, X-Ray
  • Hydrogen Bonding
  • Molecular Conformation
  • Oligopeptides / chemistry*
  • Stereoisomerism

Substances

  • Amino Acids
  • Aniline Compounds
  • Oligopeptides
  • aniline