Targeted Synthesis of Isomeric Naphthalene‐Based 2D Kagome Covalent Organic Frameworks

Abstract

AbstractTargeted synthesis of kagome (kgm) topologic 2D covalent organic frameworks remains challenging, presumably due to the severe dependence on building units and synthetic conditions. Herein, two isomeric “two‐in‐one” monomers with different lengths of substituted arms based on naphthalene core (p‐Naph andm‐Naph) are elaborately designed and utilized for the defined synthesis of isomerickgmNaph‐COFs. The two isomeric frameworks exhibit splendid crystallinity and showcase the same chemical composition and topologic structure with, however, different pore channels. Interestingly, C60is able to uniformly be encapsulated into the triangle channels ofm‐Naph‐COF via in situ incorporation method, while not the isomericp‐Naph‐COF, likely due to the different pore structures of the two isomeric COFs. The resulting stable C60@m‐Naph‐COF composite exhibits much higher photoconductivity than them‐Naph‐COF owing to charge transfer between the conjugated skeletons and C60guests.