Hydrogen-bonding-induced chirality organization and stabilization of redox species of polyaniline-unit molecules by introduction of amino acid pendant groups.
Chem Asian J
; 6(12): 3206-13, 2011 Dec 02.
Article
en En
| MEDLINE
| ID: mdl-21954093
ABSTRACT
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.
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Aminoácidos
/
Compuestos de Anilina
Idioma:
En
Revista:
Chem Asian J
Año:
2011
Tipo del documento:
Article
País de afiliación:
Japón