Controlling the Degree of Interpenetration in Chiral Three-Dimensional Covalent Organic Frameworks via Steric Tuning

Abstract

Network interpenetration plays a crucial role in functionalizing porous framework materials. However, controlling the degree of interpenetration in covalent organic frameworks (COFs) to influence their pore sizes, shapes, and functionalities still remains a significant challenge. Here, we demonstrate a steric tuning strategy to control the degree of COF interpenetration and modulate their physicochemical properties. By imine condensations of 1,1′-bi-2naphthol-derived tetraaldehydes bearing different alkyl substituents with the monomer tetra(p-aminophenyl)-methane, we synthesized and characterized a family of two-component and three-component chiral COFs with different interpenetrated dia networks. The alkyl groups are periodically appended on the pore walls, and their types/contents that can be synthetically tuned control the interpenetration degree of COFs by minimizing repulsive interactions between the alkyl groups. Specifically, the COF with −OH groups adopts an interpenetrated dia-c5 topology, those with −OMe/−OEt groups take an interpenetrated dia-c4 topology, whereas those with the bulky −O n Pr/− O n Bu groups exhibit a noninterpenetrated dia-c1 topology. The multivariate COFs with both −OH and −O n Bu groups display either a noninterpenetrated or dia-c5 topology, depending on the proportion of −O n Bu groups. The extent of interpenetration in COFs significantly affects their porosity, thermal stability, and chemical stability, resulting in varying selective performances in the adsorption and separation of dyes and asymmetric catalysis. This work highlights the potential of using steric hindrance to tune and control interpenetration, porosity, stability, and functionalities of COFs materials, broadening the range of their applications.