The molecular structures of UO2(salophen)L (L = DMF, DMSO) and a uranyl-salophen complex without any unidentate ligands (L) in solid and solution were investigated using single-crystal X-ray analysis and IR, H-1 NMR, and UV-visible absorption spectroscopies. As a result, it was found that the uranyl-salophen complex without L is a racemic dimeric complex, [UO2(salophen)](2), in which the UO2(salophen) fragments are held together by bridging between one of the phenoxide oxygen atoms in salophen and the uranium in the other UO2(salophen) unit. Furthermore, it was spectrophotometrically demonstrated that [UO2(salophen)](2) retains its dimeric structure even in the noncoordinating solvents such as CH2Cl2 and CHCl3 and is in equilibrium with UO2(salophen)L {2UO(2)(salophen)L -><- [UO2(salophen)](2) + 2L}. The equilibrium constants and thermodynamic parameters of this equilibrium were evaluated from UV-visible absorption and H-1 NMR spectral changes; log K-dim = -2.51 +/- 0.01 for L = DMF and solvent = CH2Cl2, log K-dim = -1.68 +/- 0.02 for L = DMF and solvent = CHCl3, log K-dim = -4.23 +/-0.01 for L = DMSO and solvent = CH2Cl2, and log K-dim = -3.03 +/- 0.02 for L = DMSO and solvent = CHCl3. The kinetics of L-exchange reactions in UO2(salophen)L and enantiomer exchange of [UO2(salophen)](2) in noncoordinating solvents were also studied using NMR line-broadening method. As a consequence, it was suggested that the DMF-exchange reaction in UO2(salophen)DMF proceeds through two pathways (dissociative and associative paths) and that the predominant path of DMSO exchange in UO2(salophen)DMSO is the dissociative one. A sliding motion of the UO2(salophen) fragments was considered to be reasonable for the enantiomer-exchange mechanism of [UO2(salophen)](2). On the basis of the kinetic information for UO2(salophen)L and [UO2(salophen)](2), reaction mechanisms including the L-exchange reaction in UO2(salophen)L, the formation of [UO2(salophen)](2) from UO2(salophen)L, and the enantiomer exchange of [UO2(salophen)](2) are proposed.