Isomeric Oligo(Phenylenevinylene)‐Based Covalent Organic Frameworks with Different Orientation of Imine Bonds and Distinct Photocatalytic Activities. (22nd December 2022)

• Record Type: Journal Article
• Authors: Dong, Wenbo; Qin, Zhiying; Wang, Kuixing; Xiao, Yueyuan; Liu, Xiangyang; Ren, Shijie; Li, Longyu
• Is Part Of: Angewandte Chemie. Volume 135:Number 5(2023)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-12-22
• Subjects: Covalent Organic Framework -- Imine Bond -- Isomerism -- Phenylenevinylene -- Photocatalytic Hydrogen Evolution; Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.202216073
• Languages: English
• ISSNs: 0044-8249

Abstract

Abstract: Imine‐linked covalent organic frameworks (COFs) have been extensively studied in photocatalysis because of their easy synthesis and excellent crystallinity. The effect of imine‐bond orientation on the photocatalytic properties of COFs, however, is still rarely studied. Herein, we report two novel COFs with different orientations of imine bonds using oligo(phenylenevinylene) moieties. The COFs showed similar structures but great differences in their photoelectric properties. COF‐932 demonstrated a superior hydrogen evolution performance compared to COF‐923 when triethanolamine was used as the sacrificial agent. Interestingly, the use of ascorbic acid led to the protonation of the COFs, further altering the direction of electron transfer. The photocatalytic performances were increased to 23.4 and 0.73 mmol g −1 h −1 for protonated COF‐923 and COF‐932, respectively. This study provides a clear strategy for the design of imine‐linked COF‐based photocatalysts and advances the development of COFs. Abstract : Two isomeric imine‐linked covalent organic frameworks (COFs) with different orientations of their imine bonds were prepared by the introduction of oligo(phenylenevinylene) moieties through a Schiff‐base condensation reaction. The effects of the different orientation of imine bonds on the photoelectric properties of the COFs were evaluated through photocatalytic hydrogen evolution reactions.