In order to gain insight into the electrochemical and conformational properties of the prototypical high polymeric poly(ferrocenylsilane), poly(ferrocenyldimethylsilane) [Fe(eta-C5H4)(2)SiMe(2)](n) 6, three series of oligo(ferrocenylsilanes) R-fc-[SiMe(2)-fc](n-1)-R’ (fc = Fe(eta-C5H4)(2)) 7(2)-7(9) (R = R’ = H), 8(2)-8(7) (R = H and R’ = SiMe(3)), and 9(2)-9(7) (R = R’ = SiMe(3)) have been prepared and studied (the subscript n in the oligomer refers to the number of ferrocene units present). These species were prepared via the anionic ring-opening oligomerization of the silicon-bridged [1]ferrocenophane Fe(eta-C5H4)(2)SiMe(2) 5. Initiation with ferrocenyllithium FcLi (Fc = Fe(eta-C5H5)(eta-C5H4)) followed by quenching with H2O or SiMe(3)Cl afforded H-fc-[SiMe2-fc](n-1)-H (7(2-9)) or H-fc-[SiMe(2)-fc](n-1)-SiMe(3) (8(2-7)), respectively. Initiation with the dilithioferrocene complex fcLi . 2/3TMEDA followed by quenching with H2O or SiMe(3)Cl similarly afforded the oligomers H-fc-[SiMe(2)-fc](n-1)-H (7(2-9)) or alternatively the bis(silyl)-capped species Me(3)Si-fc-[SiMe(2)-fc](n-1)-SiMe(3) (9(2-7)), respectively. The individual molecular compounds of these three series of oligomers 7(2)-7(9), 8(2)-8(7), and 9(2)-9(7) were isolated in pure form from the oligomeric mixtures by column chromatography and these were structurally characterized by H-1, C-13, and Si-29 NMR spectroscopy, mass spectrometry, and in selected cases by elemental analysis. The structure of the linear pentamer 7(5) has also been-determined by single crystal X-ray diffraction. The central portion of this species possesses a trans planar zigzag conformation in the solid state and appears to be a valuable model for the analogous conformation of the high polymer 6 in crystalline domains. The electrochemical behavior of each pure oligomer was studied by cyclic and differential pulse voltammetry and was found to depend on whether an odd or an even number of ferrocene units were present.