酰肼
吸附
化学
共价键
联氨(抗抑郁剂)
联动装置(软件)
相对湿度
组合化学
有机化学
色谱法
吸附
生物化学
热力学
基因
物理
作者
Ha L. Nguyen,Cornelius Gropp,Anna Möckel,Nikita Hanikel,Alicia Lund,Omar M. Yaghi
标识
DOI:10.26434/chemrxiv-2022-2swtc
摘要
We report a retrosynthetic strategy and its implementation to making covalent organic frameworks (COFs) with irreversible hydrazide and diazole (oxadiazole and thiadiozole) linkages. This involved the synthesis of a series of 2D and 3D hydrazine-linked frameworks, followed by their oxidation and dehydrative cyclization. Each linkage synthesis and functional group transformation—hydrazine, hydrazide, oxadiazole, and thiadia-zole—was evidenced by 15N multi-CP-MAS NMR. In addition, the isothermal water uptake profiles of these frameworks were studied, leading to the discovery that one hydrazide-linked COF is suitable for water harvest-ing from air in arid conditions. These COFs displayed characteristic S-shaped water sorption profiles, a steep pore-filling step below 18% relative humidity at 25 °C, and a total uptake capacity of 0.45 g g–1 at P/Psat = 0.95. In addition, a total of ten 2D and 3D structures with various such linkages were studies for their affinity to water. We found that even small changes made on the molecular level can lead to major differences in the water isotherm profiles and therefore pointing to the utility of water sorption analysis as a complementary analytical tool to study linkage transformations.
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