TY - JOUR
T1 - Highly Entangled Hydrogels by Photoiniferter-Mediated Polymerization
AU - Irvine, Gavin
AU - Myronidis, Konstantinos
AU - Pinto, Fulvio
AU - Kopec, Maciek
PY - 2025/2/21
Y1 - 2025/2/21
N2 - We report the synthesis of ultra-high molecular weight (UHMW) poly(N,N-dimethylacrylamide) (PDMAm) hydrogels with extremely low crosslinking densities by trithiocarbonate photoiniferter-mediated reversible deactivation radical polymerization (RDRP). Fixing the photoiniferter to crosslinker ratio and gradually increasing the targeted degree of polymerization (DPtarget) allowed for simultaneous control over the crosslinking density and the average molecular weight (Mn) of the primary chains, both below and above the critical molecular weight of entanglement (Mc). Interestingly, a plateau in storage moduli (G’) was observed for UHMW PDMAm hydrogels with a sufficiently high DPtarget (>5,000), indicating a transition to the entanglement-dominated regime, with no contribution from crosslinks to the overall modulus, thus indicating the formation of highly entangled hydrogels. These hydrogels exhibit enhanced properties such as high toughness and resistance to swelling despite their vanishingly small crosslinking densities. Furthermore, even when equipped with cleavable crosslinkers, the UHMW PDMAm hydrogels resist degradation due to dense entanglements which act as transient crosslinks preventing the gels from swelling, while sparse covalent crosslinks help to maintain their structural integrity and avoid chain disentanglement. This approach allows simple synthesis of elastic and tough hydrogels with a well-defined structure and tuneable contributions from both crosslinks and entanglements.
AB - We report the synthesis of ultra-high molecular weight (UHMW) poly(N,N-dimethylacrylamide) (PDMAm) hydrogels with extremely low crosslinking densities by trithiocarbonate photoiniferter-mediated reversible deactivation radical polymerization (RDRP). Fixing the photoiniferter to crosslinker ratio and gradually increasing the targeted degree of polymerization (DPtarget) allowed for simultaneous control over the crosslinking density and the average molecular weight (Mn) of the primary chains, both below and above the critical molecular weight of entanglement (Mc). Interestingly, a plateau in storage moduli (G’) was observed for UHMW PDMAm hydrogels with a sufficiently high DPtarget (>5,000), indicating a transition to the entanglement-dominated regime, with no contribution from crosslinks to the overall modulus, thus indicating the formation of highly entangled hydrogels. These hydrogels exhibit enhanced properties such as high toughness and resistance to swelling despite their vanishingly small crosslinking densities. Furthermore, even when equipped with cleavable crosslinkers, the UHMW PDMAm hydrogels resist degradation due to dense entanglements which act as transient crosslinks preventing the gels from swelling, while sparse covalent crosslinks help to maintain their structural integrity and avoid chain disentanglement. This approach allows simple synthesis of elastic and tough hydrogels with a well-defined structure and tuneable contributions from both crosslinks and entanglements.
KW - entanglements
KW - hydrogels
KW - polymer networks
KW - RAFT
KW - rheology
UR - http://www.scopus.com/inward/record.url?scp=85218276051&partnerID=8YFLogxK
U2 - 10.1002/anie.202421970
DO - 10.1002/anie.202421970
M3 - Article
AN - SCOPUS:85218276051
SN - 1433-7851
JO - Angewandte Chemie International Edition
JF - Angewandte Chemie International Edition
M1 - e202421970
ER -