4.8 Article

Two-dimensional Supramolecular Polymers Based on Selectively Recognized Aromatic Cation-π and Donor-Acceptor Motifs for Photocatalytic Hydrogen Evolution

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202302274

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Anthracene; Aromatic Stacking; Molecular Recognition; Self-Assembly; Supramolecular Polymers

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We report the synthesis of well-regulated 2D supramolecular polymers (2DSPs) through an aromatics-selective recognition strategy. These polymers exhibit enhanced photocatalytic hydrogen evolution activity and ordered 2D structures.
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-pi and donor-acceptor (D-A) motifs, which are derived from C-4-symmetric cationic monomers and electron-withdrawing molecules. By subtly designing the strength and direction of noncovalent driving forces, the mutual interference between cation-pi 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 mu mol g(-1) h(-1), which is mainly ascribed to the specific stacking mode of cation-pi/D-A motifs and the ordered 2D structures.

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