The polymer poly[4-(2-aminoethyl)styrene], prepared by living anionic
polymerization, has been derivatized by amide coupling to [Ru-II(vbpy)
(2)(4-CO2H-4'-CH(3)bpy)](2+) (vbpy is 4-vinyl-4'-methyl-2,2'-bipyridin
e; 4-CO2H-4'-CH(3)bpy is 4-methyl-2,2'-bipyridine-4'-carboxylic acid).
The resulting ''macromer'' can be electropolymerized on a variety of
electrode materials by reductive electropolymerization. Compared to si
milar films of poly[Ru-II(vbpy)(3)](PF6)(2): (1) the macromeric films
are considerably rougher, apparently having open, local microporous st
ructures; (2) they undergo comparable rates of intrafilm charge transf
er, and (3) they have shortened metal-to-ligand charge transfer (MLCT)
excited state lifetimes, apparently due to quenching by film-based tr
ap sites. Stable films of a mixed polymer have also been prepared by s
equential addition of [Ru-II(bpy)(2)(4 -CO2H-4'-CH(3)bpy)](2+) and the
n the vbpy derivative.