Abstract

A class of porous organic polymers (POPs), which are constructed by aryl–aryl linkages, has the wholly conjugated organic frameworks that can post-transform into two-dimensional graphenal polymers by the intramolecular dehydrogenation. However, typical examples are difficultly defined on the molecular sizes, numbers, and distributions of graphene subunits within the networks, thereby giving rise to uncertainty in applications. Here we report a dehydrogenation fusion of polycyclic aromatic hydrocarbons (PAHs) into graphenal polymers under solvent-free and ionothermal conditions, by which 5,6,11,12,17,18-hexaazatrinaphthylene (HATNA) is linked on itself to expand along the coplanar direction. During the reaction, the catalyst AlCl3 solids turn into the molten media to homogenize the reaction system, and alter the molecular configuration and reactivity of HATNA units, resulting in the formation of self-segregated nanosheets with the neighboring layers of the weakened π–π interaction. Besides, the obtained fr...

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