Linker Engineering toward Tunable Emission Behavior of Porous Interpenetrated Zr-Organic Frameworks.

Conjugated molecules with donor-acceptor-donor (D-A-D) moieties have garnered significant attention for their ability to form luminescent metal-organic frameworks (LMOFs). D-A-D molecules feature tunable bandgaps, which can be varied systematically to control the fluorescence wavelength of LMOFs. In this study, we prepared and characterized the fluorescence properties of two porous interpenetrated Zr-organic frameworks (PIZOFs) constructed using 4,4'-(benzo[][1,2,5]selenadiazole-4,7-diylbis(ethyne-2,1-diyl))dibenzoic acid () or 4,4'-(benzo[][1,2,5]thiadiazole-4,7-diylbis(ethyne-2,1-diyl))dibenzoic acid () as linkers. The corresponding MOFs are denoted as and , respectively. Through our investigation, we explored the correlation between the structure of the frameworks and their respective optical properties. Our findings revealed that there are distinct differences in the fluorescence properties of the two PIZOFs. Specifically, the fluorescence of is red-shifted from that characteristic of the corresponding linker, . By contrast, the fluorescence of is substantially blue-shifted from that of linker . The emission of mixed-linker MOFs is explored by combining or with structurally analogous, but nonfluorescent linker, 4,4'-((perfluoro-1,4-phenylene)bis(ethyne-2,1-diyl))dibenzoic acid (. Based on steady-state and time-resolved photoluminescence experiments, as well as confocal fluorescence microscopy combined with fluorescence lifetime imaging (FILM), we demonstrated that linker engineering is an effective method to tune the emission behavior of LMOFs.