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  • Title: Silver Nanoparticle-Functionalized Postsynthetically Modified Thiol MOF UiO-66-NH-SH for Efficient CO2 Fixation.
    Author: Patra R, Sarma D.
    Journal: ACS Appl Mater Interfaces; 2024 Feb 28; 16(8):10196-10210. PubMed ID: 38359330.
    Abstract:
    Thiols are essential functional groups imparting unique properties, such as reactivity and selectivity, to many vital enzymes and biomolecules. The integration of electronically soft thiol groups within metal-organic frameworks (MOFs) yields elevated reactivity and a pronounced affinity for soft metal ions. However, the scarcity of thiol-based ligands and synthetic challenges hinder the advancement of thiol-based MOFs. To bypass the difficulties of synthesizing thiol MOFs by a direct reaction between thiol-based ligands and corresponding metal salts, postsynthetic modification (PSM) of MOFs is an efficient strategy to introduce thiol functionality. Herein, we have introduced Ag nanoparticles in postsynthetically modified thiol MOFs UiO-66-NH-SH (1) (synthesized by reaction between UiO-66-NH2 and thioglycolic acid) and UiO-66-NH-SH (2) (synthesized by reaction between UiO-66-NH2 and 3-mercaptopropionic acid) to synthesize a series of heterogeneous catalysts for CO2 fixation. Catalysts Cat 1-2 and Cat 3 - 4 were synthesized from UiO-66-NH-SH (1) and UiO-66-NH-SH (2), respectively, by using varying concentrations of silver (AgNO3). Catalyst Ag@UiO-66-NH-SH (1) (Ag = 3.45%; namely Cat 2) shows the highest efficiency for the catalytic conversion of propargylic alcohol and terminal epoxide to the corresponding cyclic carbonates. Finally, a rationalized reaction mechanism is proposed by correlating our results with the current literature. This work presents a viable strategy to utilize the thiol functionality of MOFs (avoiding the complexities associated with synthesizing thiol MOFs directly from thiol ligands) as a platform for introducing catalytically active metal centers and applying them as a heterogeneous catalyst for CO2 fixation reactions.
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