TY - JOUR
T1 - Strain-stiffening in dynamic supramolecular fiber networks
AU - Fernández-Castaño Romera, Marcos
AU - Lou, Xianwen
AU - Schill, Jurgen
AU - ter Huurne, Gijs
AU - Fransen, Peter Paul K.H.
AU - Voets, Ilja K.
AU - Storm, Cornelis
AU - Sijbesma, Rint P.
PY - 2018/12/19
Y1 - 2018/12/19
N2 - The cytoskeleton is a highly adaptive network of filamentous proteins capable of stiffening under stress even as it dynamically assembles and disassembles with time constants of minutes. Synthetic materials that combine reversibility and strain-stiffening properties remain elusive. Here, strain-stiffening hydrogels that have dynamic fibrous polymers as their main structural components are reported. The fibers form via self-assembly of bolaamphiphiles (BA) in water and have a well-defined cross-section of 9 to 10 molecules. Fiber length recovery after sonication, H/D exchange experiments, and rheology confirm the dynamic nature of the fibers. Cross-linking of the fibers yields strain-stiffening, self-healing hydrogels that closely mimic the mechanics of biological networks, with mechanical properties that can be modulated by chemical modification of the components. Comparison of the supramolecular networks with covalently fixated networks shows that the noncovalent nature of the fibers limits the maximum stress that fibers can bear and, hence, limits the range of stiffening.
AB - The cytoskeleton is a highly adaptive network of filamentous proteins capable of stiffening under stress even as it dynamically assembles and disassembles with time constants of minutes. Synthetic materials that combine reversibility and strain-stiffening properties remain elusive. Here, strain-stiffening hydrogels that have dynamic fibrous polymers as their main structural components are reported. The fibers form via self-assembly of bolaamphiphiles (BA) in water and have a well-defined cross-section of 9 to 10 molecules. Fiber length recovery after sonication, H/D exchange experiments, and rheology confirm the dynamic nature of the fibers. Cross-linking of the fibers yields strain-stiffening, self-healing hydrogels that closely mimic the mechanics of biological networks, with mechanical properties that can be modulated by chemical modification of the components. Comparison of the supramolecular networks with covalently fixated networks shows that the noncovalent nature of the fibers limits the maximum stress that fibers can bear and, hence, limits the range of stiffening.
UR - http://www.scopus.com/inward/record.url?scp=85058546646&partnerID=8YFLogxK
U2 - 10.1021/jacs.8b09289
DO - 10.1021/jacs.8b09289
M3 - Article
C2 - 30465604
AN - SCOPUS:85058546646
SN - 0002-7863
VL - 140
SP - 17547
EP - 17555
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 50
ER -