Xue Miaomiao, Zhang Lei, Li Xiao-Xin, Chen Zihao, Kang Fangyuan, Wang Xiang, Dong Qiang, Wang Xin, Lee Chun-Sing, Lan Ya-Qian, Zhang Qichun
Department of Materials Science and Engineering, City University of Hong Kong, Tat Chee Avenue 83, Kowloon, Hong Kong SAR, P. R. China.
School of Chemistry, South China Normal University, Guangzhou, 510006, P. R. China.
Nat Commun. 2024 Nov 20;15(1):10026. doi: 10.1038/s41467-024-54235-9.
Understanding precise structures of two-/three- dimensional (2D/3D) covalent organic polymers (COPs) through single-crystal X-ray diffraction (SCXRD) analysis is important. However, how to grow high-quality single crystals for 2D/3D COPs is of challenge due to poor reversibility and difficult self-correction of covalent bonds. In addition, the success of introducing tellurium into the backbone to construct 2D/3D COPs and obtaining their single crystals is rare. Here, utilizing the strategy that a heavy element (e.g., tellurium) can form dynamic linkages with a self-correction function, we develop a fast and universal method for growing large-sized single crystals (up to 500 µm) for 2D/3D COPs, especially for 2D COPs. Three 2D COPs and one 3D COP are harvested through dynamic -Te-O-P- bonds in two days, with structures clearly uncovered via the SCXRD analysis. These 2D/3D COPs also show promising photocatalytic activities (nearly 100% selectivity and 100% yield) in superoxide anion radical-mediated coupling of (arylmethyl)amines.
通过单晶X射线衍射(SCXRD)分析来了解二维/三维(2D/3D)共价有机聚合物(COPs)的精确结构很重要。然而,由于共价键的可逆性差和自校正困难,如何生长高质量的2D/3D COPs单晶具有挑战性。此外,将碲引入主链以构建2D/3D COPs并获得其单晶的成功案例很少。在此,利用重元素(如碲)可形成具有自校正功能的动态键合这一策略,我们开发了一种快速且通用的方法来生长用于2D/3D COPs的大尺寸单晶(高达500 µm),特别是用于2D COPs。通过动态-Te-O-P-键在两天内收获了三种2D COPs和一种3D COP,其结构通过SCXRD分析清晰地揭示出来。这些2D/3D COPs在超氧阴离子自由基介导的(芳基甲基)胺偶联反应中也表现出有前景的光催化活性(近100%的选择性和100%的产率)。