This article deals with a class of ruthenium-BIAN-derived complexes, [RuII(tpm)(R-BIAN)Cl]ClO4 (tpm = tris(1-pyrazolyl)methane, R-BIAN = bis(arylimino)acenaphthene, R = 4-OMe ([1a]ClO4), 4-F ([1b]ClO4), 4-Cl ([1c]ClO4), 4-NO2 ([1d]ClO4)) and [RuII(tpm)(OMe-BIAN)H2O]2+ ([3a](ClO4)2). The R-BIAN framework with R = H, however, leads to the selective formation of partially hydrolyzed BIAO ([N-(phenyl)imino]acenapthenone)-derived complex [RuII(tpm)(BIAO)Cl]ClO4 ([2]ClO4). The redox-sensitive bond parameters involving -N=C-C=N- or -Ni=C-C=O of BIAN or BIAO in the crystals of representative [1a]ClO4, [3a](PF6)2, or [2]ClO4 establish its unreduced form. The chloro derivatives 1a+-1d+ and 2+ exhibit one oxidation and successive reduction processes in CH3CN within the potential limit of ±2.0 V versus SCE, and the redox potentials follow the order 1a+ < 1b+ < 1c+ < 1d+ ≈ 2+. The electronic structural aspects of 1an-1dn and 2n (n = +2, +1, 0, -1, -2, -3) have been assessed by UV-vis and EPR spectroelectrochemistry, DFT-calculated MO compositions, and Mulliken spin density distributions in paramagnetic intermediate states which reveal metal-based (RuII → RuIII) oxidation and primarily BIAN- or BIAO-based successive reduction processes. The aqua complex 3a2+ undergoes two proton-coupled redox processes at 0.56 and 0.85 V versus SCE in phosphate buffer (pH 7) corresponding to {RuII-H2O}/{RuIII-OH} and {RuIII-OH}/{RuIV=O}, respectively. The chloro (1a+-1d+) and aqua (3a2+) derivatives are found to be equally active in functioning as efficient precatalysts toward the epoxidation of a wide variety of alkenes in the presence of PhI(OAc)2 as oxidant in CH2Cl2 at 298 K, though the analogous 2+ remains virtually inactive. The detailed experimental analysis with the representative precatalyst 1a+ suggests the involvement of the active {RuIV=O} species in the catalytic cycle, and the reaction proceeds through the radical mechanism, as also supported by the DFT calculations. © 2015 American Chemical Society.