Gao Yiwei, Zhao Jie, Huang Zehuan, Ronson Tanya K, Zhao Fen, Wang Yue, Li Boyang, Feng Chenlu, Yu You, Cheng Yongliang, Yang Dong, Yang Xiao-Juan, Wu Biao
Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an, 710069, China.
School of Chemistry and Chemical Engineering, Xi'an University of Architecture and Technology, Xi'an, 710055, China.
Angew Chem Int Ed Engl. 2022 May 23;61(22):e202201793. doi: 10.1002/anie.202201793. Epub 2022 Apr 5.
The fabrication of anion-coordinated assemblies into functional soft materials remains a major challenge. To this end, four C -symmetric anion-binding ligands equipped with ortho-phenylene-bridged bis(urea) and amine or amide ends were designed, which generated A L triple helical architectures upon self-assembly with phosphate ions. Hierarchical intermolecular hydrogen bonds among the terminal amine/amide groups and urea moieties resulted in the formation of functional gels. The obtained gels were further applied for conductive adhesion between different surfaces, displaying excellent flexibility and selective wettability. The viscoelastic gels constructed from anion-coordinated assemblies described in this work represent the first example of a new class of anion-coordination-driven smart materials.
将阴离子配位组装体制备成功能性软材料仍然是一个重大挑战。为此,设计了四种具有邻亚苯基桥连双(脲)以及胺或酰胺端基的C对称阴离子结合配体,它们与磷酸根离子自组装时会形成AL三螺旋结构。末端胺/酰胺基团与脲部分之间的分级分子间氢键导致形成功能性凝胶。所获得的凝胶进一步应用于不同表面之间的导电粘附,表现出优异的柔韧性和选择性润湿性。由本文所述的阴离子配位组装体构建的粘弹性凝胶代表了一类新型阴离子配位驱动智能材料的首个实例。