A new Ru-II complex, [Ru(fpbpymH)(2)]Cl-2 (1), in which fpbpymH = [5-(trifluoromethyl)pyrazol-3-yl](2,2'-bipyrid-6-yl)methane, was prepared by the treatment of [Ru(DMSO)(4)Cl-2] with 2 equiv of the terdentate chelate fpbpymH in refluxing ethanol. A single-crystal X-ray diffraction study of 1 revealed a distorted octahedral Ru-II framework, showing strong N-H center dot center dot center dot Cl hydrogen bonding between the fpbpymH ligand and Cl anions. In the presence of Na2CO3, the methylene linkers of chelates in 1 underwent stepwise oxygenation, forming the charge-neutral complexes [Ru(fpbpym)(fpbpyk)] (2) and [Ru(fpbpyk)(2)] (3) [fpbpykH = [5-(trifluoromethyl)pyrazol-3-yl](2,2'-bipydd-6-yl) ketone] in sequence. The respective charge-neutral Os-II complex [Os(fpbpyk)(2)] (4) was also isolated by the treatment of OsCl3 center dot 3H(2)O with 2 equiv of the terdentate chelate fpbpymH, Electrochemical analysis indicated that the introduction of the electron-withdrawing ketone group in 2-4 increased the metal-based oxidation potential in sequence. For the photophysical properties, complexes 1-4 are essentially nonluminescent in solution (e.g., CH2Cl2 or MeOH) at room temperature, but all exhibit 600-1100 nm phosphorescence with moderate intensity for the powdery, solid sample at room temperature. The trend in terms of the emission peak wave ength of 1 (666 nm) < 3 (795 nm) < 2 (810 nm) < 4 (994 nm) among titled complexes is in agreement with the corresponding onset of absorption spectra as well as the time-dependent density functional theory calculation of 1 < 3 < 2 < 4.