1352211-66-5Relevant articles and documents
Hydrogen-bonding-induced chirality organization and stabilization of redox species of polyaniline-unit molecules by introduction of amino acid pendant groups
Moriuchi, Toshiyuki,Ohmura, Satoshi D.,Morita, Kenji,Hirao, Toshikazu
, p. 3206 - 3213 (2012/02/13)
The chirality organization of polyaniline-unit molecules was achieved by the introduction of amino acid pendant groups through intramolecular hydrogen bonding, which plays an important role in the stabilization of the chirality-organized redox species. Another interesting feature of the synthesized polyaniline-unit molecules is the luminescent switching properties based on the redox states of the phenylenediamine moiety. Getting organized: The chirality organization of polyaniline-unit molecules was achieved by the introduction of pendant amino acid groups through intramolecular hydrogen bonding; these groups play an important role in the stabilization of the chirality-organized redox species.
