TY - JOUR
T1 - Controlling primary chain dispersity in network polymers
T2 - elucidating the effect of dispersity on degradation
AU - Shimizu, Takanori
AU - Whitfield, Richard
AU - Jones, Glen R.
AU - Raji, Ibrahim O.
AU - Konkolewicz, Dominik
AU - Truong, Nghia P.
AU - Anastasaki, Athina
N1 - Funding Information:
A. A. gratefully acknowledges ETH Zurich (Switzerland) and the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme (DEPO: Grant no. 949219) for financial support. T. S. acknowledges Mitsubishi Chemical Corporation for generous support. N. P. T. acknowledges the award of a DECRA Fellowship from the ARC (DE180100076).
Publisher Copyright:
© 2023 The Royal Society of Chemistry
PY - 2023/12/14
Y1 - 2023/12/14
N2 - Although dispersity has been demonstrated to be instrumental in determining many polymer properties, current synthetic strategies predominantly focus on tailoring the dispersity of linear polymers. In contrast, controlling the primary chain dispersity in network polymers is much more challenging, in part due to the complex nature of the reactions, which has limited the exploration of properties and applications. Here, a one-step method to prepare networks with precisely tuned primary chain dispersity is presented. By using an acid-switchable chain transfer agent and a degradable crosslinker in PET-RAFT polymerization, the in situ crosslinking of the propagating polymer chains was achieved in a quantitative manner. The incorporation of a degradable crosslinker, not only enables the accurate quantification of the various primary chain dispersities, post-synthesis, but also allows the investigation and comparison of their respective degradation profiles. Notably, the highest dispersity networks resulted in a 40% increase in degradation time when compared to their lower dispersity analogues, demonstrating that primary chain dispersity has a substantial impact on the network degradation rate. Our experimental findings were further supported by simulations, which emphasized the importance of higher molecular weight polymer chains, found within the high dispersity materials, in extending the lifetime of the network. This methodology presents a new and promising avenue to precisely tune primary chain dispersity within networks and demonstrates that polymer dispersity is an important parameter to consider when designing degradable materials.
AB - Although dispersity has been demonstrated to be instrumental in determining many polymer properties, current synthetic strategies predominantly focus on tailoring the dispersity of linear polymers. In contrast, controlling the primary chain dispersity in network polymers is much more challenging, in part due to the complex nature of the reactions, which has limited the exploration of properties and applications. Here, a one-step method to prepare networks with precisely tuned primary chain dispersity is presented. By using an acid-switchable chain transfer agent and a degradable crosslinker in PET-RAFT polymerization, the in situ crosslinking of the propagating polymer chains was achieved in a quantitative manner. The incorporation of a degradable crosslinker, not only enables the accurate quantification of the various primary chain dispersities, post-synthesis, but also allows the investigation and comparison of their respective degradation profiles. Notably, the highest dispersity networks resulted in a 40% increase in degradation time when compared to their lower dispersity analogues, demonstrating that primary chain dispersity has a substantial impact on the network degradation rate. Our experimental findings were further supported by simulations, which emphasized the importance of higher molecular weight polymer chains, found within the high dispersity materials, in extending the lifetime of the network. This methodology presents a new and promising avenue to precisely tune primary chain dispersity within networks and demonstrates that polymer dispersity is an important parameter to consider when designing degradable materials.
UR - http://www.scopus.com/inward/record.url?scp=85178267392&partnerID=8YFLogxK
U2 - 10.1039/d3sc05203f
DO - 10.1039/d3sc05203f
M3 - Article
AN - SCOPUS:85178267392
SN - 2041-6520
VL - 14
SP - 13419
EP - 13428
JO - Chemical Science
JF - Chemical Science
IS - 46
ER -