Magnetic field-affected reaction yield (MARY) spectroscopy is a spin chemistry technique for detecting short-lived radical ions. Having sensitivity to transient species with lifetimes as short as nanoseconds, MARY spectroscopy usually does not provide detailed information on their magnetic resonance parameters, except for simple systems with equivalent magnetic nuclei. In this work, the radical anions of two fluorinated diphenylacetylene derivatives with nonequivalent magnetic nuclei and unknown hyperfine coupling constants (A(HF)) were investigated by MARY spectroscopy. The MARY spectra were found to be resolved and have resonance lines in nonzero magnetic fields, which are determined by the A(HF) values. Simple relationships between the positions of resonance MARY lines and the A(HF) values were established from the analysis of the different Hamiltonian block contributions to the MARY spectrum. The obtained experimental A(HF) values are in agreement with the results of quantum chemical calculations at the density functional theory level.