The emergence of visible-light photocatalytic frameworks provides a sustainable technology for dealing with CO2 greenhouse gas. Herein, the solvothermal reaction of copper(I) cyclic trinuclear complex (Cu-CTC) with 2,5-dihydroxyterephthalaldehyde (2,5-DHTA) or 3,3'-dihydroxy-[1,1'-biphenyl]-4,4'-dicarbaldehyde (3,3'-DHBDA) led to two crystalline hcb topological copper(I)-organic frameworks USTB-48 and USTB-49, respectively. The post-cobaltization of 2-(benzylideneamino)phenol units in these two frameworks, providing the active catalytic centers in obtained USTB-48(Co) and USTB-49(Co) for photocatalysis of CO2 reduction. The parent frameworks and post-modificated species have been thoroughly characterized through powder X-ray diffraction analysis and various spectroscopies. The combination of trinuclear copper units and single cobalt centers is able to achieve the CO generation rate up to ca. 8451 μmol·g-1·h-1 and 96% selectivity for USTB-48(Co).
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