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Metal-ligand complexation and clustering in mussel-inspired side-chain functionalized supramolecular hydrogels
Byssus threads of mussels have high resistance against abrasion in wave-swept habitats because of their outer cuticle, which is rich in amino acid dopa complexes with Fe 3+ ions. This stems from the transient nature of metal-ligand complexes that creates extra relaxation mechanisms. Inspired by this...
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Published in: | Soft matter 2022-09, Vol.18 (36), p.6836-6847 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Byssus threads of mussels have high resistance against abrasion in wave-swept habitats because of their outer cuticle, which is rich in amino acid dopa complexes with Fe
3+
ions. This stems from the transient nature of metal-ligand complexes that creates extra relaxation mechanisms. Inspired by this concept, in this work, supramolecular hydrogels based on poly(acrylic acid) functionalized with nitrocatechol groups are synthesized. Polymer chains are physically crosslinked
via
nitrocatechol-Fe
3+
complexes. The hydrogels have different polymer volume fractions as well as different nitrocatechol : Fe
3+
molar ratios. The strength of the supramolecular crosslinks strongly depends on the pH of the medium. The dynamics of these hydrogels are studied by stress relaxation experiments followed by calculation of the relaxation time spectrum. Generally, samples have three relaxation modes, including dissociation of distinct metal-ligand complexes, reptation of sticky polymer chains, and disengagement of network segments from supramolecular aggregates and clusters. Such clusters hinder the terminal relaxation and potentially increase the stability of supramolecular hydrogels.
Mussel-inspired side-chain functionalized supramolecular hydrogels based on nitrocatechol-Fe
3+
physical complexations reveal three relaxation modes whose lifetime varies six orders of magnitudes from 0.1 s to 9.8 × 10
4
s. |
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ISSN: | 1744-683X 1744-6848 |
DOI: | 10.1039/d2sm00666a |