Polypyrrole films react with thiols to give covalently substituted, reduced
polymers. The extent of reaction and the depth to which the thiol penetrat
es depends upon the time the film is exposed to the thiol solution. The ele
ctrical conductivity of the derivatized chains is permanently destroyed dur
ing this process, but if the reaction is limited to the film surface, the b
ulk polymer remains electroactive. When a halobenzene- or haloacridinethiol
is used, it is possible to use palladium catalyzed coupling chemistry to a
ttach porphyrins to the surface anchor.