Abstract
The polymorphic self-correction from a metastable phase to a stable one often occurs and plays crucial roles in synthesizing robust hydrogen-bonded organic frameworks (HOFs). However, identifying metastable phases and understanding the self-correcting mechanisms is a challenging venture due to their intrinsic instability. Here, we for the first time introduce 1,8-naphtholactam (Np) as a hydrogen-bonding synthon positioned on the periphery of a bicarbazole to create a versatile molecular unit for 3D HOFs. The as-synthesized NCU-HOF1, analyzed by single-crystal X-ray diffraction (SCXRD), is found to be metastable. It exhibits an 11-fold interpenetrated dia topology with a quarter of the Np units exhibiting monomeric N-H⋯O interactions between adjacent Np link sites, which readily self-correct upon desolvation to form fully dimeric ones. Consequently, the resultant NCU-HOF1a becomes highly robust in polar solvents, strong acid or alkaline aqueous solutions, and has permanent porosity with contracted cavities for selective adsorption and efficient "turn-up" fluorescent sensing of C(2)H(4) gas. This work not only debuts a new hydrogen-bonding synthon but offers more insights into investigating solid-state dynamics in metastable HOFs.