| Literature DB >> 32079395 |
Xing Li1, Jingsi Qiao2, See Wee Chee3,4, Hai-Sen Xu1, Xiaoxu Zhao5, Hwa Seob Choi1, Wei Yu1, Su Ying Quek2,3, Utkur Mirsaidov3,4, Kian Ping Loh1,2.
Abstract
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.Entities:
Year: 2020 PMID: 32079395 DOI: 10.1021/jacs.0c00553
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419