Molecular Dynamics Simulations of Ideal Living Polymerization: Terminal Model and Kinetic Aspects

• Published in: The Journal of Physical Chemistry B Vol. 127; no. 35; pp. 7624 - 7635
• Main Author: Li, Wei
• Format: Journal Article
• Language: English
• Published: American Chemical Society 29.08.2023; American Chemical Society (ACS)
• Subjects: B: Soft Matter, Fluid Interfaces, Colloids, Polymers, and Glassy Materials; mass transfer; molecular dynamics; molecular weight; polymerization; polymers; probability; reaction kinetics
• DOI: 10.1021/acs.jpcb.3c03126
• ISSN: 1520-6106; 1520-5207

Living polymerization is an important synthetic approach to achieving precise control of synthesized polymers, which is crucial for their applications. The molecular weight distribution (MWD) prescribes the macroscopic properties of polymers and hence is a key feature to characterize polymerization. In this work, we present a systematic molecular dynamics simulation study of ideal living polymerization in bulk and surface-initiated systems based on a terminal stochastic reaction model. The evolution of polymer dispersity and MWD along with the polymerization process is examined. We demonstrate that MWD is generally well captured by the Schulz–Zimm distribution for bulk and surface-initiated systems with low grafting densities. However, as the grafting density in the surface-initiated case increases, heterogeneity in chain growth emerges due to the kinetic trapping of reactive sites, which causes the starving of short chains and the thriving of minority long chains such that a shoulder region shows up in MWD. This effect can be enhanced by kinetic compressing induced by polymerization. In addition, the interplay of bonding reaction kinetics and other kinetic properties (e.g., mass transfer and polymer relaxation) is further explored, alongside the influences of bonding probability and reactant concentration. We expect that this investigation will aid in our understanding of typical kinetic aspects of living polymerization.