Abstract New fluorochromic materials that reversibly change their emission properties in response to their environment are of interest for the development of sensors and light‐emitting materials. A new design of Eu‐containing polymer hydrogels showing fast self‐healing and tunable fluorochromic properties in response to five different stimuli, including pH, temperature, metal ions, sonication, and force, is reported. The polymer hydrogels are fabricated using Eu–iminodiacetate (IDA) coordination in a hydrophilic poly(N,N‐dimethylacrylamide) matrix. Dynamic metal–ligand coordination allows reversible formation and disruption of hydrogel networks under various stimuli which makes hydrogels self‐healable and injectable. Such hydrogels show interesting switchable ON/OFF luminescence along with the sol–gel transition through the reversible formation and dissociation of Eu–IDA complexes upon various stimuli. It is demonstrated that Eu‐containing hydrogels display fast and reversible mechanochromic response as well in hydrogels having interpenetrating polymer network. Those multistimuli responsive fluorochromic hydrogels illustrate a new pathway to make smart optical materials, particularly for biological sensors where multistimuli response is required.
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Controlled Delivery and Photopatterning of Mechanical Properties in Polysaccharide Hydrogels Using Vanadium Coordination and Photochemistry
Incorporation of the transition metal ion V(V) into hydrogels has been used to impart photoresponsive behavior, which was used to tune materials properties during light irradiation. The photoreaction in QHE-cellulose/agarose hydrogels coordinated with vanadium was evidenced by a clear color change of yellow to blue through a green intermediate. This color change was attributed to the reduction of V(V) to V(IV) as described in our previous work. A concomitant oxidative breakdown of the polysaccharide chain was noticeable upon the reduction of V(V) with a decrease in stiffness (G′) of the hydrogel material. This reduction of the metal ion and breakdown of polysaccharide chain induced irreversible changes in the microstructure of the hydrogel, enabling the controlled delivery of V(IV) and/or encapsulated cargo. Scanning electron microscopy studies showed an increase in pore sizes and guest cavity formation during irradiation. In addition to the significant drop in mechanical properties like storage and loss modulus in the gel materials, a viscosity drop in the polymer solution was observed through irradiation, indicating breakdown of the polysaccharide chain. A photomask can be used to create discrete patterns on these materials upon irradiation
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- Award ID(s):
- 1653892
- PAR ID:
- 10401730
- Date Published:
- Journal Name:
- ACS Applied Bio Materials
- Volume:
- 5
- Issue:
- 10
- ISSN:
- 2576-6422
- Page Range / eLocation ID:
- 4827
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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