Exploring the Performance Improvement for CO Chemical Fixation in Zn/ZnMg-MOFs.

Inorg Chem

Inner Mongolia Key Lab of Carbon Nanomaterials, Nano Innovation Institute (NII), College of Chemistry and Materials Science, Inner Mongolia Minzu University (IMUN), Tongliao 028000, Inner Mongolia, People's Republic of China.

Published: February 2024

AI Article Synopsis

  • A new 3D zinc-based metal-organic framework (MOF) was created using a unique organosilicon-based linker, which provides multiple -COO sites for zinc immobilization and features irregular channels and a large surface area for potential catalytic use.
  • The framework was further modified by adding magnesium to form a bimetallic MOF (ZnMg-), which showed improved catalytic performance over the original zinc framework in specific reactions.
  • Experiments and theoretical analyses suggested that the presence of bimetallic active sites in ZnMg- enhances the chemical fixation of epoxides and CO, leading to effective production of cyclic carbonates.

Article Abstract

A new 3D zinc-based metal-organic framework {[ZnL(DMF)(HO)(OH)]·5DMF} () (HL = 5,5',5″-(methylsilanetriyl) triisophthalic acid) was constructed with an organosilicon-based linker, where HL is a tetrahedral structure furnished with rich -COO chelating sites for Zn(II) immobilization. Compound exhibited two types of irregular one-dimensional channels and a three-dimensional skeleton with large specific surface area, making it a promising catalytic platform. Moreover, by incorporation of the second metal ion into the inorganic node of framework , isomorphic bimetallic MOF ZnMg- was successfully synthesized. ZnMg- demonstrated enhanced catalytic activity compared to under identical conditions. Contrast experiments and theoretical calculations indicate that bimetallic active sites play a facilitating role in the chemical fixation of epoxides and CO. It indicated that efficient chemical fixation of CO to cyclic carbonates was obtained over isomorphic MOF catalysts and ZnMg-.

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http://dx.doi.org/10.1021/acs.inorgchem.3c03744DOI Listing

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