Covalent organic frameworks (COFs)
are a class of crystalline porous
materials with well-defined π arrays and ordered channels, which
can be predesigned with a topology diagram and prepared via a polycondensation
reaction. Over the past decade, various types of π building
units with different functional groups have been developed. Among
them, aldehyde is one of the most widely used monomers that form COFs
with azine, hydrazine, imine, squaranine, and CC linkages.
In contrast, its closest analogue, i.e., ketone, despite its broad
structural diversity, has not yet been investigated for the design
and synthesis of COFs. Herein we report the first examples of ketazine-linked
COFs by developing ketones as monomers to enable polycondensation
with hydrazine under solvothermal conditions. We observed that a careful
screening of reaction conditions including solvent, catalyst, concentration,
reaction temperature, and reaction time leads to the finding of optimal
polymerization systems to produce highly crystalline and porous ketazine-linked
COFs. Surprisingly, the ketazine linkage enables π conjugation
between knot and linker sites and renders the resultant materials
able to emit a strong blue fluorescence, highlighting the π
electronic features of this new family of COFs. Our findings of ketones
as monomers and ketazine as linkage bring unprecedented structures,
functions, and applications to the field of COFs.