The profound impact of the central metal on the morphological properties of metalloporphyrins bearing 3,4,5-tri((S)-dihydrocitronellyloxy)phenyl groups at the diagonal meso-positions is disclosed. Systematic comparison of the free-base porphyrin 1H 2 with metalloporphyrins 1Ms incorporating Ni(II), Cu(II), and Zn(II) as the central metal found the counterintuitive antifreezing effect of the central metal; 1H 2 crystallizes immediately after the removal of the solvent, while the central metal retards nucleation. We interpret that the miscibility of the elastic alkyl chains and the porphyrin segment is crucial in imparting fluidity to 1M and smooth nucleation in the context of classical nucleation theory, while the full rationalization of the thermal behaviors requires the existence of the nuclei precursor according to the two-step nucleation model. The morphological behaviors of 1Ms are highly susceptible to only marginal differences in the chemical structure, presumably due to the relatively large discrete size of the porphyrin ring, approximately 1 nm. The somewhat counterintuitive antifreezing effect of the central metal is interpreted to arise from the increased viscosity due to the enhanced molecular interactions.