Postsynthetically Modified Alkoxide‐Exchanged Ni2(OR)2BTDD: Synergistic Interactions of CO2 with Open Metal Sites and Functional Groups

Through fine-tuned post-synthetic modifications, the bridging ligands of Ni₂Cl₂BTDD were selectively replaced by various alkoxide groups while retaining open metal sites. Alkoxide-exchanged MOFs showed synergistic CO₂ uptake aided by multiple interactions with open metal sites and ligands.

Abstract

Postsynthetic modifications (PSMs) of metal–organic frameworks (MOFs) play a crucial role in enhancing material performance through open metal site (OMS) functionalization or ligand exchange. However, a significant challenge persists in preserving open metal sites during ligand exchange, as these sites are inherently bound by incoming ligands. In this study, for the first time, we introduced alkoxides by exchanging bridging chloride in Ni₂Cl₂BTDD (BTDD=bis (1H-1,2,3,–triazolo [4,5-b],–[4′,5′-i]) dibenzo[1,4]dioxin) through PSM. Rietveld refinement of synchrotron X-ray diffraction data indicated that the alkoxide oxygen atom bridges Ni(II) centers while the OMSs of the MOF are preserved. Due to the synergy of the existing OMS and introduced functional group, the alkoxide-exchanged MOFs showed CO₂ uptakes superior to the pristine MOF. Remarkably, the tert-butoxide-substituted Ni_T exhibited a nearly threefold and twofold increase in CO₂ uptake compared to Ni₂Cl₂BTDD at 0.15 and 1 bar, respectively, as well as high water stability relative to the other exchanged frameworks. Furthermore, the Grand Canonical Monte Carlo simulations for Ni_T suggested that CO₂ interacts with the OMS and the surrounding methyl groups of tert-butoxide groups, which is responsible for the enhanced CO₂ capacity. This work provides a facile and unique synthetic strategy for realizing a desirable OMS-incorporating MOF platform through bridging ligand exchange.

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