Tuning the Surface Activity of Gemini Amphiphile by the Host–Guest Interaction of Cucurbit[7]uril

This research is aimed to develop an effective supramolecular route for tuning the surface activity of the surfactant. To this end, cationic gemini amphiphiles and cucurbit[7]­uril (CB[7]) were complexed in water, and each hydrophobic chain of the gemini amphiphiles was bound with a CB[7]. The steric hindrance of CB[7] prevented the two hydrophobic chains from getting closed to each other, leading a significant change of surface activity. Before supramolecular complexation, the surface activity of the gemini amphiphile is relatively high, which can generate the foams easily. However, the foam generated by gemini amphiphile can be destructed by adding CB[7], suggesting that the suface activity is lowed after the supramolecular complexation. The surface activity can recover after adding 1-adamantanamine hydrochloride, which has a stronger ability to bind CB[7]. Therefore, a controllable foaming and defoaming process can be realized. It is highly anticipated that supramolecular chemistry for tuning amphiphilicity of surfactants may find application in the fields that fast foaming and defoaming are needed

An Amylase-Responsive Bolaform Supra-Amphiphile

An amylase-responsive bolaform supra-amphiphile was constructed by the complexation between β-cyclodextrin and a bolaform covalent amphiphile on the basis of host–guest interaction. The bolaform covalent amphiphile could self-assemble in solution, forming sheet-like aggregates and displaying weak fluorescence because of aggregation-induced quenching. The addition of β-cyclodextrin led to the formation of the bolaform supra-amphiphile, prohibiting the aggregation of the bolaform covalent amphiphile and accompanying with the significant recovery of fluorescence. Upon the addition of α-amylase, with the degradation β-cyclodextrin, the fluorescence of the supra-amphiphile would quench gradually and significantly, and the quenching rate linearly correlated to the concentration of α-amylase. This study enriches the field of supra-amphiphiles on the basis of noncovalent interactions, and moreover, it may provide a facile way to estimate the activity of α-amylase

Controllable Supramolecular Polymerization Promoted by Host-Enhanced Photodimerization

In this letter, we report a new method of controllable supramolecular polymerization, taking advantage of host-enhanced photodimerization. The low-molecular-weight supramolecular oligomers were formed by noncovalent complexation between cucurbit[8]­urils (CB[8]) and the bifunctional monomers (DBN) with Brooker’s merocyanine moiety (MOED) on either end. Interestingly, when irradiated with UV light, the supramolecular oligomers could transform into supramolecular polymers with high molecular weight. The molecular weight of supramolecular polymers could be controlled by varying the irradiation time. It is highly anticipated that this work can enrich the methods on the modulation of supramolecular polymerization