From analysis and refinement by the LAOCOON III program of the 220-'H spectrum of 52'-biquinoline, recorded as a saturated solution in carbon disdphide, most derived chemical shifts and coupling constants are close to corresponding values in quinoline. However, H-3 is at 1.5ppm lower field in 2,2'-biquinoline than in quinoliie and the orfho-coupling "434) in the heterocyclic ring is 0.5 Hz larger in 2,2'-biquinoline than in quinoline; fairly free rotation about the 2,2' bond is inferred.