2022
DOI: 10.1039/d2tc01014c
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Supramolecular topology controlled self-healing conformal hydrogels for stable human–machine interfaces

Abstract: Soft materials (such as hydrogels) with good conformal capabilities and self-healing properties have shown considerable promise in the realms of human-machine interfaces. However, creating wearable hydrogels with excellent adhesion, mechanical...

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Cited by 21 publications
(19 citation statements)
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“…Moreover, the structure formula and corresponding 1 H NMR spectra are shown in Figure S3–S6. The characteristic signals appearing at 5.55–6.27 and 8.15–8.20 ppm for A-DMAPAM are attributed to the acryl group and the aromatic ring, respectively . This result was consistent with the structure in ATR-FTIR, indicating the successful reaction of the adhesive factor.…”
Section: Resultssupporting
confidence: 79%
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“…Moreover, the structure formula and corresponding 1 H NMR spectra are shown in Figure S3–S6. The characteristic signals appearing at 5.55–6.27 and 8.15–8.20 ppm for A-DMAPAM are attributed to the acryl group and the aromatic ring, respectively . This result was consistent with the structure in ATR-FTIR, indicating the successful reaction of the adhesive factor.…”
Section: Resultssupporting
confidence: 79%
“…Specifically, 2.7 g of adenine, 16.35 g of 1,2-dibromoethane, 100 mL of DMF, and 6.63 g of K 2 CO 3 were mixed, and the reaction was carried out at room temperature (RT) under N 2 protection for 48 h. The yellow solid A–Br was obtained by filtration and rotary evaporation. In Figure S5, the procedure for synthesizing the adhesive group (A-DMAPAM) was based on a previously reported work . The DMF mixture containing A–Br (1.5 g) and DMAPAM (1.45 g) was stirred at 80 °C under N 2 atmosphere for 10 h. The crude products were dissolved in methanol after rotary evaporation.…”
Section: Materials and Methodsmentioning
confidence: 99%
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