堆积
超分子化学
超分子聚合物
非共价相互作用
接受者
聚合物
单体
分子
阳离子聚合
氢键
化学
水溶液
光催化
材料科学
光化学
高分子化学
有机化学
催化作用
物理
凝聚态物理
作者
Zhao Gao,Lulu Shi,Fei Yan,Yifei Han,Wei Yuan,Wei Tian
标识
DOI:10.1002/anie.202302274
摘要
Two-dimensional (2D) organic polymers have recently received considerable interest, especially those whose architectures are held together via supramolecular engineering. However, current approaches toward supramolecular 2D structures usually suffer from mutual interference of noncovalent interactions and lack of intrinsic functions. Herein, we report well-regulated 2D supramolecular polymers (2DSPs) through an aromatics-selective recognition strategy of cation-π and donor-acceptor (D-A) motifs, which are derived from C4 -symmetric cationic monomers and electron-withdrawing molecules. By subtly designing the strength and direction of noncovalent driving forces, the mutual interference between cation-π and D-A interactions is effectively avoided, enabling the construction of 2DSPs in aqueous solution. On this basis, the resultant 2DSPs possess boosted photocatalytic hydrogen evolution activity at a rate of 600 μmol g-1 h-1 , which is mainly ascribed to the specific stacking mode of cation-π/D-A motifs and the ordered 2D structures.
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