'Click' synthesis and redox properties of triazolyl cobalticinium dendrimers.
Inorg Chem
; 52(11): 6685-93, 2013 Jun 03.
Article
em En
| MEDLINE
| ID: mdl-23692324
ABSTRACT
The derivatization of macromolecules with redox-stable groups is a challenge for molecular electronics applications. The large majority of redox-derivatized macromolecules involve ferrocenes, and there are only a few reports with cobalticinium. We report here the first click derivatization of macromolecules with the cobalticinium redox group using ethynylcobalticinium hexafluorophosphate, 1. Cu(I) catalysis was used for these selective click metallodendrimer syntheses starting from 1 and providing the tripodal dendron 3 that contains three 1,2,3-triazolylcobalticinium termini and a phenol focal point and the dendrimers of generations 0, 1, and 2 containing 9, 27, and 81 triazolylcobalticinium units for the dendrimers 4, 5, and 6, respectively. Atomic force microscopy (AFM) statistical studies provided the progression of height upon increase of dendrimer generation. Cyclic voltammetry studies in MeCN and dimethylformamide (DMF) show the solvent-dependent reversibility of the Co(III/II) wave (18e/19e) and generation dependent reversibility of the Co(II/I) (19e/20e) wave in DMF. The H2PO4(-) anion is only recognized by the largest metallodendrimer 6 by a significant cathodic shift of the Co(III/II) wave.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Compostos Organometálicos
/
Triazóis
/
Cobalto
/
Dendrímeros
Idioma:
En
Revista:
Inorg Chem
Ano de publicação:
2013
Tipo de documento:
Article
País de afiliação:
França