摘要： The investigation of intermolecular hydrogen bonding between the luminescent polypyrene covalent organic framework and formaldehyde (PPy-COF-HCHO) was carried out with the density functional theory and time-dependent density functional theory. The strengthening of the photoexcited hydrogen bond C = O—H–C was verified via geometric structures, electronic transition energies, binding energies, UV-Vis and infrared spectra comparison in both ground state and excited state of the PPy-COF’s truncated representative fragment. From the frontier molecular orbitals examination, natural population analysis, and plotted electron density difference map demonstrated that the strengthened hydrogen bond facilitated the rearrangement of electron density between H-donor and H-acceptor moieties which should account for charge transfer and ultimate fluorescence quenching. Interestingly, the energy gap between excited state and triplet state of the hydrogen-bonded complex showed the possibility of the intersystem crossing. The MOMAP programme further confirmed the quenching process because there was a lower fluorescent rate constant for the donor–acceptor PPy-COF-HCHO complex compared to free PPy-COF fragment. Results above significantly highlighted the high sensitivity of the PPy-COF towards organic analyte, i.e. the formaldehyde and can be employed as a sensor.