反平行(数学)
堆积
化学
共价键
氢键
分子内力
纳米技术
拓扑(电路)
结晶学
分子
立体化学
材料科学
有机化学
物理
磁场
组合数学
量子力学
数学
作者
Xing Li,Jingsi Qiao,See Wee Chee,Hai‐Sen Xu,Xiaoxu Zhao,Hwa Seob Choi,Wei Yu,Su Ying Quek,Utkur Mirsaidov,Kian Ping Loh
摘要
Covalent organic frameworks are an emerging class of porous crystalline organic materials that can be designed and synthesized from the bottom up. Despite progress made in synthesizing COFs of diverse topologies, the synthesis methods are often tedious and unscalable, hampering practical applications. Herein, we demonstrate a scalable, robust method of producing highly crystalline acylhydrazone two-dimensional (2D) COFs with diversified structures (six examples) under open and stirred conditions, with growth typically completed in only 30 min. Our strategy involves selecting molecular building blocks that have bond dipole moments with spatial orientations that favor antiparallel stacking and whose structure allows the restriction of intramolecular bond rotation (RIR) via intra- and interlayer hydrogen bonding. This method is widely applicable for hydrazide linkers containing various side-chain functionalities and topicities. By this strategy, the gram-scale synthesis of two highly crystalline COFs (up to 1.4 g yield) was obtained in a one-pot reaction within 30 min.
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