Salt/current-triggered stabilization of β-cyclodextrins encapsulated host-guest low-molecular-weight gels
The stability of supramolecular gel fabricated by β-cyclodextrins/phenylboronic acid gelator inclusion complexes was significantly enhanced by inorganic/organic salts or current with significant variations in morphology and rheological properties. [Display omitted] Host-guest supramolecular gels wer...
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Veröffentlicht in: | Chinese chemical letters 2020-02, Vol.31 (2), p.369-372 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The stability of supramolecular gel fabricated by β-cyclodextrins/phenylboronic acid gelator inclusion complexes was significantly enhanced by inorganic/organic salts or current with significant variations in morphology and rheological properties.
[Display omitted]
Host-guest supramolecular gels were developed via the self-assembly of inclusion complexes (ICs) of β-cyclodextrins/phenylboronic acid gelator (PBA). Salts and current were involved in the self-assembly to stabilize the host-guest gels. The stability of the gels was greatly improved after salts were added. The stable time of gels was extended from 2.5 h to 120 h with the addition of NH4NO3 at the concentration of 2.5 × 10−2 g/mL. The morphology of the gel was affected by the concentrations of NH4NO3. SEM images revealed that the gels were three-dimensional nanofibrous networks, the sizes of fibers decreased with decreasing NH4NO3 concentrations, which affected the stability of gels, further proved by the rheological properties of gels. More stable gels were obtained with current stimulation, the stable time of the gel was increased from 2.5 h to 55 h with current by adding NaBF4. The current also exhibited significant influence on the aggregation as the voltage varied (0–500 mV) with a constant concentration of salts. The result showed the self-assembly process of host-guest gel could be well controlled via the addition of salts and current to desired morphology and stability. |
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ISSN: | 1001-8417 1878-5964 |
DOI: | 10.1016/j.cclet.2019.07.048 |