To study the effect of a stable radical on the photophysical properties of a phosphorescent Pt(II) coordination framework and the intramolecular magnetic interaction between radical ligands in the N<^>N Pt(II) bisacetylide complexes, we prepared a series of N<^>N Pt(II) bis(acetylide) complexes with oxoverdazyl radical acetylide ligands. The linker between the Pt(II) center and the spin carrier was systematically varied, to probe the effect on the sign and magnitude of the spin exchange interactions between the radical ligands and photophysical properties. The complexes were studied with steady-state and femtosecond/nanosecond transient absorption spectroscopy, continuous-wave electron paramagnetic resonance (EPR) spectroscopy, and density functional theory (DFT) computations. The transient absorption spectral studies show that the doublet excited state of the radicals are short-lived (tau(D) approximate to 2 ps) and nonfluorescent. Moreover, the intrinsic long-lived triplet excited state (tau(T) = 1.2 mu s) of the Pt(II) coordination center was efficiently quenched by the radical (tau(T) = 6.9 ps for one representative radical Pt(II) complex). The intramolecular magnetic interaction between the radical ligands through the diamagnetic Pt(II) atom was studied with temperature-dependent EPR spectroscopy; antiferromagnetic exchange interaction (-J S1S2, J = -5.4 +/- 0.1 cm(-1)) for the complex with the shortest radicalradical distance through bridge fragments was observed. DFT computations give similar results for the sign and magnitude of the J values. For complexes with larger inter-radical distance, however, very weak coupling between the radical ligands was observed (vertical bar J vertical bar < 0.7 cm(-1)). Our results are useful for the study of the effect of a radical on the photophysical properties of the phosphorescent transition-metal complexes.