Crystallization and Melting Behaviors of Discrete Butyolactone–Caprolactone Alternative Co-Oligomer: The Effect of End Groups

Abstract

Discrete oligomers are ideal candidates for the investigation of the crystallization behaviors of polymers since the molecular weight distribution and the precision of molecular structures play a crucial role in the crystallization behaviors of polymers. We precisely synthesize discrete alternative co-oligomers (o(γ-BL-alt-ε-CL)s) with different end groups based on ε-caprolactone (ε-CL) and γ-butyrolactone (γ-BL) as monomers using an iterative exponential growth (IEG) strategy and systematically study the crystallization and melting behaviors of the o(γ-BL-alt-ε-CL)s with precise monomer sequence. The roles that the end group plays in the crystallization and melting of co-oligomers are highlighted. The o(γ-BL-alt-ε-CL)s with different end groups (tert-butyldiphenylsilyl, benzoyl, acetyl) crystallize in an extended-chain conformation. Observation on the decrease of the crystallization rate of co-oligomers with the increase of the size of the end groups is associated with the slow dynamics or slow relaxation of co-oligomer chains with the large end group. The melting–recrystallization during the heating process for the o(γ-BL-alt-ε-CL)s with small end group is attributed primarily to the reduced steric hindrance effect. For the o(γ-BL-alt-ε-CL)s with large end groups, the rearrangement of co-oligomer chains is substantially hindered by steric effects, which lead to a significant suppression of the melting–recrystallization.