P. Godillot et al., DIRECT CHEMICAL FUNCTIONALIZATION OF AS-GROWN ELECTROACTIVE POLYPYRROLE FILM CONTAINING LEAVING GROUPS, Synthetic metals, 83(2), 1996, pp. 117-123
A synthetic route for the functionalization of polypyrrole is describe
d, which involves a direct chemical modification of as-grown polymer f
ilms containing labile groups, such as N-hydroxysuccinimide (NHS). Pyr
role is first substituted at the 3-position with NHS, and further elec
trochemically polymerized into a film of poly [3-NHS pyrrole]. A direc
t chemical substitution of the easily leaving group NHS by another fun
ctional group is then carried out on the polymer film. beta-Ferrocene
ethylamine has been chosen as electrochemical probe, and the experimen
tal conditions for substitution have been analyzed. Based on the ferro
cene electroactivity, results show that substitution occurs with 100%
yield on all the bulk of the polymer film, allowing the deposition of
10(-6) mol cm(-2) of electroactive ferrocene linked to polypyrrole. Th
is new approach toward the functionalization of polyheterocycles opens
the way for an easy realization of elaborate electroactive architectu
res, involving fragile and expensive chemical or biochemicals groups,
such as oligonucleotides, enzymes or hormones showing recognition prop
erties.