This paper reports the effects of linker length on electron propagation through ferrocene moieties covalently anchored onto insulator-based cylindrical nanopores derived from a cylinder-forming polystyrene-poly(methylmethacrylate) diblock copolymer. These nanopores (24 nm in diameter, 30 nm long) aligned perpendicular to an underlying gold electrode were modified via esterification of their surface COOH groups with OH-terminated ferrocene derivatives having different alkyl linkers (FcCO(CH2)(n)OH; n = 2, 5, 15). Cyclic voltammograms were measured in 0.1 M NaBF4 at different scan rates to assess the efficiency of electron propagation through the ferrocene moieties. The redox peaks of the anchored ferrocenes were observed at nanoporous films decorated with FcCO(CH2)(15)OH and FcCO(CH2)(5)OH, but not at those with FcCO(CH2)(2)OH. Importantly, the higher electron propagation efficiency was observed in the use of the longer linker, as shown by the apparent diffusion coefficients (ca. 10(-12) cm(2)/s for n = 15; ca. 10(-13) cm(2)/s for n = 5; no electron propagation for n = 2). The observed electron propagation resulted from electron hopping across relatively large spacing that was controlled by the motion of anchored redox sites (bounded diffusion). The longer linker led to the larger physical displacement range of anchored ferrocene moieties, facilitating the approach of the adjacent ferrocene moieties within a distance required for electron self-exchange reaction. The linker-based control of redox-involved electron propagation on nanostructured, insulating surfaces will provide a mean:; for designing novel molecular electronics and electrochemical sensors.