Hydrogen Bonding Regulated Flexibility and Disorder in Hydrazone-Linked Covalent Organic Frameworks

Covalent organic framework (COF) chemistry is experiencing unprecedented development in recent decades. The current studies on COF chemistry are mainly focused on the discovery of novel covalent linkages, new topological structures, synthetic methodologies, and potential applications. However, despite the fact that noncovalent interactions are ubiquitous in COF chemistry, relatively little attention has been given to the role of noncovalent bonds on COF structures and their properties. In this work, a series of hydrazone-linked COFs involving noncovalent hydrogen bonds have been constructed, where the hydrogen-bonding interaction plays critical roles in the COF crystallinity and structures. The regulation of structural flexibility, the reversible transition between order and disorder, and the variety of host–guest interactions have been demonstrated in succession for the first time in COFs. The results obtained by the hydrogen-bonding-regulated strategy may also be extendable to other noncovalent interactions, such as π–π interactions, metal coordination interactions, Lewis acid–base interactions, etc. These findings will inspire future developments in the design, synthesis, structural regulation, and applications of COFs by manipulating noncovalent interactions.