Brassinne Jérémy, Gohy Jean-François, Fustin Charles-André
Institute of Condensed Matter and Nanosciences (IMCN), Division of Bio and Soft Matter (BSMA), Université catholique de Louvain, Place L. Pasteur 1, 1348 Louvain-la-Neuve, Belgium.
ACS Macro Lett. 2016 Dec 20;5(12):1364-1368. doi: 10.1021/acsmacrolett.6b00831. Epub 2016 Nov 28.
One of the first examples of supramolecular gels presenting independent dual dynamics is built through a combination of hydrophobic and metal-ligand interactions. The associating building block consists in a water-soluble linear polymer terminated by a short hydrophobic sticker at one end, and a coordinating moiety at the other end. The distinct supramolecular nature of these noninterfering binding motifs allows the dynamics of the hydrogels to be finely tuned in an orthogonal fashion by the application of specific stimuli. Precisely, the solvent-induced plasticization of the hydrophobic associations and the acid-promoted dissociation of the metal-ligand complexes are used to control the network dynamics. By opposition to classically encountered binary gel-sol responses, we demonstrate that the stimuli-induced transition in material properties can be gradual, provided that the material structure is well designed and strong enough.
呈现独立双动态的超分子凝胶的首批示例之一是通过疏水相互作用和金属-配体相互作用的组合构建而成的。缔合结构单元由一种水溶性线性聚合物组成,该聚合物一端由短疏水链段封端,另一端由配位部分封端。这些互不干扰的结合基序独特的超分子性质使得通过施加特定刺激以正交方式对水凝胶的动态进行精细调节成为可能。具体而言,疏水缔合的溶剂诱导增塑作用以及金属-配体络合物的酸促进解离作用被用于控制网络动态。与经典的二元凝胶-溶胶响应不同,我们证明,只要材料结构设计良好且足够坚固,刺激诱导的材料性质转变可以是渐进的。