Nanopores of a Covalent Organic Framework: A Customizable Vessel for Organocatalysis

[Image: see text] Covalent organic frameworks (COFs) as crystalline polymers possess ordered nanochannels. When their channels are adorned with catalytically active functional groups, their highly insoluble and fluffy powder texture makes them apt heterogeneous catalysts that can be dispersed in a range of solvents and heated to high temperatures (80–180 °C). This would mean very high catalyst density, facile active-site access, and easy separation leading to high isolated yields. Different approaches have been devised to anchor or disperse the catalytic sites into the nanospaces offered by the COF pores. Such engineered COFs have been investigated as catalysts for many organic transformation reactions. These range from Suzuki–Miyaura coupling, Heck coupling, Knoevenagel condensation, Michael addition, alkene epoxidation, CO(2) utilization, and more complex biomimetic catalysis. Such catalysts employ COF as a “passive” support that merely docks catalytically active inorganic clusters, or in other cases, the COF itself participates as an “active” support by altering the electronics of the inorganic catalytic sites through the redox activity of its framework. Even more, catalytic organic pockets or metal complexes have been directly tethered to COF walls to make them behave like single-site organocatalysts. Here, we have listed most COF-based organic transformations by categorizing them as metal-free non-noble-metal@COF and noble-metal@COF. The initial part of this review highlights the advantages of COFs as a component of a heterogeneous catalyst, while the latter part discusses all of the current literature on this topic.