<p>Quasi-one-dimensional covalent organic frameworks have emerged as promising platforms for photochemical energy conversion due to their low density of basal sites, abundant edge sites, and dual-chain-like structure. However, the development of quasi-one-dimensional covalent organic frameworks in photocatalysis is still highly hindered by their limited linkage chemistry. Herein, we report an enaminone-linked quasi-one-dimensional covalent organic framework. The polar enaminone bonds together with dual-chain-like structure endow enaminone-linked quasi-one-dimensional covalent organic framework with broad light adsorption and effective excitonic dissociation abilities. Significantly, a high CO yield of 3045 μmol g^-1 with approximately 100% selectivity was achieved in a 24 h reaction under gas-solid conditions. More interestingly, the hydrogen atom on nitrogen site in enaminone bond could assist in the activation of CO₂ molecule via hydrogen-bond interaction. This interaction leads to the strongest adsorption ability for CO₂ and the lowest energy barrier for the rate-determining step during CO₂ reduction over enaminone-linked quasi-one-dimensional covalent organic framework compared to those over mixture-linked quasi-one-dimensional covalent organic framework and imine-linked quasi-one-dimensional covalent organic framework counterparts. All of these factors directly contribute to the enhanced activity of enaminone-linked quasi-one-dimensional covalent organic framework in the photocatalytic CO₂ reduction to CO.</p>