ABSTRACT
Although a series of studies have introduced noncovalent branched networks to enhance the properties of polyisoprene (PIP) based on a structural mimic of NR, it is still a challenge to reveal the relationship between properties of modified PIP and the aggregation behaviors of end groups. Herein, the two quadruple hydrogen bonding motifs 2-ureido-4-1[H]-pyrimidinones (UPy) and α-alanine tetrapeptide (4A) were introduced into the end of model PIP polymers. Branched networks of terminal groups were prepared by self-assembly of quadruple hydrogen bonding motifs, thereby elucidating the key role of the terminal structures in the PIP chain. Previous work has demonstrated that the branched network intensifies the entanglement between polymer chains, resulting in higher modulus and shear viscosity of the branched polymers than the linear polymers. Because of the stable aggregation of 4A, the mechanical properties of PIP-4A are superior to those of PIP-UPy. Rheological analysis and two-dimensional Fourier transform infrared spectroscopy collaboratively demonstrate that PIP-UPy and PIP-4A both exhibit two-step dissociation processes. These results expand our understanding of the role of the aggregation structures of PIP terminals and provide insight into the generic design of mechanically strong rubber.