成核
聚合
共价键
溶解度
纳米技术
材料科学
化学工程
相(物质)
化学物理
化学
聚合物
有机化学
工程类
作者
Christoph Gruber,Laura Frey,Roman Guntermann,Dana D. Medina,Emiliano Cortés
出处
期刊:Nature
[Springer Nature]
日期:2024-06-05
卷期号:630 (8018): 872-877
被引量:3
标识
DOI:10.1038/s41586-024-07483-0
摘要
Abstract Covalent organic frameworks (COFs) are a functional material class able to harness, convert and store energy. However, after almost 20 years of research, there are no coherent prediction rules for their synthesis conditions. This is partly because of an incomplete picture of nucleation and growth at the early stages of formation. Here we use the optical technique interferometric scattering microscopy (iSCAT) 1–3 for in operando studies of COF polymerization and framework formation. We observe liquid–liquid phase separation, pointing to the existence of structured solvents in the form of surfactant-free (micro)emulsions in conventional COF synthesis. Our findings show that the role of solvents extends beyond solubility to being kinetic modulators by compartmentation of reactants and catalyst. Taking advantage of these observations, we develop a synthesis protocol for COFs using room temperature instead of elevated temperatures. This work connects framework synthesis with liquid phase diagrams and thereby enables an active design of the reaction environment, emphasizing that visualization of chemical reactions by means of light-scattering-based techniques can be a powerful approach for advancing rational materials synthesis.
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