Self-healing gels triggered by ultrasound with color-tunable emission based on ion recognition.

Herein, O-substituted terpyridine motif was used as both rigid fluorescent π core and ion binding site, in order to construct an novel amphiphilic organogelator TEC containing cholesterol unit. We demonstrated a ultrasound induced reversible sol-gel transition approach driven by adjusted non covalent interactions and the resulted gels showed self-healing properties and tunable emission color when incorporating inorganic ions into the gel matrices. By heating-cooling process, the gel transformed to sol again. Simultaneously, the vesicle-tube morphology transition controlled by sonication and heating-cooling was also observed, together with aggregation induced emission enhancement (AIE) property of the gel. The results suggested that ultrasound promoted the J aggregations of terpyridine motifs and enhanced the hydrogen bonding interactions of TEC molecules, leading to the gelation process.