Kajita Toru, Leasure Robert M., Devenney Martin, Friesen Duane, Meyer Thomas J.
Kenan Laboratories of Chemistry, The University of North Carolina at Chapel Hill, Venable Hall, CB# 3290, Chapel Hill, North Carolina 27599-3290.
Inorg Chem. 1998 Sep 21;37(19):4782-4794. doi: 10.1021/ic971279w.
The polymer poly[4-(2-aminoethyl)styrene], prepared by living anionic polymerization, has been derivatized by amide coupling to Ru(II)(vbpy)(2)(4-CO(2)H-4'-CH(3)bpy) (vbpy is 4-vinyl-4'-methyl-2,2'-bipyridine; 4-CO(2)H-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 similar films of polyRu(II)(vbpy)(3)(2): (1) the macromeric films are considerably rougher, apparently having open, local microporous structures; (2) they undergo comparable rates of intrafilm charge transfer; and (3) they have shortened metal-to-ligand charge transfer (MLCT) excited state lifetimes, apparently due to quenching by film-based trap sites. Stable films of a mixed polymer have also been prepared by sequential addition of Ru(II)(bpy)(2)(4-CO(2)H-4'-CH(3)bpy) and then the vbpy derivative.
通过活性阴离子聚合制备的聚合物聚[4-(2-氨基乙基)苯乙烯],已通过酰胺偶联衍生化为Ru(II)(vbpy)(2)(4-CO₂H-4'-CH₃bpy)(vbpy为4-乙烯基-4'-甲基-2,2'-联吡啶;4-CO₂H-4'-CH₃bpy为4-甲基-2,2'-联吡啶-4'-羧酸)。所得的“大分子单体”可通过还原电聚合在多种电极材料上进行电聚合。与聚Ru(II)(vbpy)(3)(2)的类似薄膜相比:(1) 大分子薄膜粗糙度明显更高,显然具有开放的局部微孔结构;(2) 它们经历相当的膜内电荷转移速率;(3) 它们的金属到配体电荷转移(MLCT)激发态寿命缩短,显然是由于基于薄膜的陷阱位点的猝灭。通过依次加入Ru(II)(bpy)(2)(4-CO₂H-4'-CH₃bpy)然后加入vbpy衍生物,也制备了混合聚合物的稳定薄膜。