Surfactant ruthenium complexes are attracting attention as potential photoinduced electron-transfer reagents, especially for possible light energy storage schemes. The ester derivatives i(bpy)2RuH[bpy(COORi)(COOR2)]|2+ (where bpy = 2,2'-bipyridine, the carboxy substituents are in the 4,4' positions, and Rt = R2 = CigH37 (I); R3 = C18H37, R2 = H (111); and Ri = C18H37, R2 = C2H5 (IV)) have been prepared and characterized. The alkaline hydrolysis of I to octadecanol and 11 (Rt = R2 = H), with III as an intermediate product, proceeds more rapidly in monolayers and in 50% aqueous THE than does that of the water-soluble analogue V (R¡ = R2 = C2H3) in aqueous solution. Both the surface pressure-area characteristics and luminescence of monolayers of the surfactant compounds spread on aqueous subphases depends strongly on dissolved anions; even traces of strongly interacting anions such as perchlorate lead to condensation of the films, while luminescence is ~20-fold more intense in the presence of perchlorate as compared with chloride. When the monolayers are transferred to glass slides, the pretreatment of the glass affects the extent of dark ester hydrolysis. Prolonged photolysis of monolayer assemblies on glass in contact with water leads to a slow (quantum yield, ~5 X 10-6) nonhydrolytic degradation of the complex, but to no detectable water dissociation (quantum yield for H2 production, <1 X 10-4).