Herein, we introduce pnictogen bonding interaction into polymer networks for the design and modulation of dynamic macromolecular materials. Several types of polymeric pnictogen-bonding networks with graded interaction strengths were constructed to explore the structure–property relationship. Comprehensive investigations revealed that strengthening the pnictogen bonding significantly enhances the topological stability of the resulting materials. In contrast, analogous hydrogen-bonded networks did not exhibit comparable mechanical reinforcement. Moreover, the pnictogen-bonding networks endow the materials with tunable self-healing capability, allowing not only spontaneous healing at room temperature and thermally triggered healing on demand, but also effective healing in aqueous environments. This represents the first exploration of self-healing behavior driven by pnictogen bonding in polymeric materials. Mechanistic insights into the role of pnictogen bonding in polymer networks were elucidated through NMR titration of donor–acceptor polymer pairs, comparative self-assembly behavior, and cocrystal structures of small-molecule analogues. The incorporation of pnictogen bonding interaction into polymer networks provides a robust and versatile platform for engineering high-performance dynamic polymeric materials.