Tetramesityl porphinato rhodium(III) methoxide ((TMP)Rh-OCH3) binds with methanol in benzene to form a 1:1 methanol complex ((TMP)Rh-OCH3(CH3OH)) (1). Dynamic processes are observed to occur for the rhodium(III) methoxide methanol complex (1) that involve both hydrogen and methanol exchange. Hydrogen exchange between coordinated methanol and methoxide through methanol in solution results in an interchange of the environments for the non-equivalent porphyrin faces that contain methoxide and methanol ligands. Interchange of the environments of the coordinated methanol and methoxide sites in 1 produces interchange of the inequivalent mesityl o-CH3 groups, but methanol ligand exchange occurs on one face of the porphyrin and the mesityl o-CH3 groups remain inequivalent. Rate constants for dynamic processes are evaluated by full line shape analysis for the H-1 NMR of the mesityl o-CH3 and high field methyl resonances of coordinated methanol and methoxide groups in 1. The rate constant for interchange of the inequivalent porphyrin faces is associated with hydrogen exchange between 1 and methanol in solution and is observed to increase regularly with the increase in the mole fraction of methanol. The rate constant for methanol ligand exchange between 1 and the solution varies with the solution composition and fluctuates in a manner that parallels the change in the activation energy for methanol diffusion which is a consequence of solution non-ideality from hydrogen bonded clusters.