Covalent organic frameworks (COFs) are a class of porous polymers that enable the atomically precise incorporation of organic units into periodic structures, creating highly ordered π-columnar arrays and one-dimensional open channels. One significant structural feature is that they can be predesigned at both primary and high-order structure levels. COFs have emerged as a platform for materials design and functional explorations. However, their low stability has been impeded any practical implementations.
The newly explored hexagonal two-dimensional layered COF.
Hong Xu, a Ph. D graduate of SOKENDAI (The Graduate University for Advanced Studies; now a postdoctoral researcher in Cornell university) at the Institute for Molecular Science, National Institutes of National Sciences, and his colleagues challenged for the design and synthesis of stable, crystalline, porous, covalent organic frameworks. They focused on the imine-linked COFs that formed hexagonal two-dimensional layered architectures. By incorporating electron-donating groups to the phenyl rings of imine linkages, they found that the polarization of imine bonds were softened; this electronic effect reduces the repulsion between layers and strengthens the interlayer interactions to reinforce the stability of the resulting COFs.
The newly explored COFs are stable in various organic solvents, water (25 and 100 °C), strong acid (aqueous HCl solution, 12 M) and strong base (aqueous NaOH solution, 14 M). Upon dispersion in these solvents for seven days, the crystallinity and porosity of the COFs were retained. Such a robust COF has not been developed and the stable COFs provide a platform for functional exploration.
In this work, they further developed chiral organocatalytic functions based on these stable COFs. By incorporating chiral catalytic sites into the pore walls of the COFs, the group developed a series of chiral COFs in which the content organocatalytic sites on the walls can be precisely tuned. By virtue of insolubility of COF skeletons, the chiral COFs serve as heterogeneous catalysts for the asymmetric Michael reactions.
These catalysts exhibited greatly enhanced catalytic activity and high enantioselectivity, and most importantly, they catalyzed the reactions in water under ambient conditions. These COF catalysts are easily separated from the reaction systems through simple filtration and can be cycle used for many times. The development of heterogeneous organocatalysts would greatly reduce the cost of chemical transformations and open a way to practical application. Their findings were published in Nature Chemistry on the 21st of September 2015.
Hong Xu said "Stability of COFs is a central issue before any applications. The finding of the electron-donating effects on the stabilization of COFs is a serendipity. This work demonstrates very well the interesting point of COFs in a way how chemistry plays a key role in materials science.".
Associate Prof. Donglin Jiang, the team leader of this research group commented "One of the most challenging issues in the field of COFs is the combination of stability, crystallinity and porosity. This study would accelerate the functional explorations and applications of COFs".
The Jiang laboratory in Institute of Molecular Science, National Institutes of National Sciences has been long involved in this filed and is pioneering the design, synthesis and functional exploration of COFs. Recently, a series of novel reactions and functions, including triangular topology and double stage reaction (Nature Communication 2015, 6, 7786; Scientific Reports in press), CO
2 adsorption and separation (J. Am. Chem. Soc. 2015, 137, 7079; Angew. Chem. Int. Ed. 2015, 54, 2986), energy storage (Scientific Reports 2015, 5, 8225; Angew. Chem. Int. Ed. 2015, 54, 6814), photoresponsibility (Angew. Chem. Int. Ed. 2015, 54, 8704) and photoinduced charge separation (J. Am. Chem. Soc. 2015, 137, 7817), have been successfully disclosed.