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. Author manuscript; available in PMC: 2021 Feb 10.
Published in final edited form as: Angew Chem Int Ed Engl. 2020 Jan 16;59(7):2784–2792. doi: 10.1002/anie.201913297

Figure 2. Synthesis and characterization of s-Gel.

Figure 2.

(a) Synthesis and schematic representation of s-Gel. DMF = N,N-dimethylformamide. (b) UV-vis spectrum of s-Gel (black line) showing the red-shifting of λmax to 724 nm compared to copper acetate (red line). This red shift is indicative of the formation of Cu-m-BDC paddlewheel complexes. (c) SAXS/WAXS curve depicting the spacing between Cu24L24 MOCs within s-Gel as well as the form factor of MOC junctions. (d) Frequency sweep rheology curve for s-Gel (5.3 wt. %) swollen to equilibrium in DMF. (e) Stress relaxation data for s-Gel. The red line corresponds to fitting of the data using the Kohlrausch stretched exponential model, which provide the characteristic relaxation time τ. Inset: Image of s-Gel cut into several pieces (left). Placing the mashed sample in a mold and applying pressure leads to complete healing (right).