Partial Linker Substitution Strategy to Construct a Quaternary HKUST-like MOF for Efficient Acetylene Storage and Separation.

ACS Appl Mater Interfaces

Fujian Provincial Key Laboratory of Polymer Materials, College of Chemistry and Materials Science, Fujian Normal University, Fuzhou 350007, P. R. China.

Published: August 2022

AI Article Synopsis

  • - The study develops a new multicomponent metal-organic framework (MOF) by introducing a bifunctional ligand into the well-known HKUST-1 structure, enhancing its structure and functionality.
  • - This new MOF demonstrates excellent mechanical, water, and chemical stability across a range of pH levels, making it highly suitable for various applications.
  • - It shows remarkable capabilities for capturing methane (CH) from carbon monoxide (CO) mixtures, leveraging specific interactions between CH and the MOF's unique metallocycle clusters.

Article Abstract

Multicomponent metal-organic frameworks (MOFs) have received much attention as emerging materials capable of precisely programing exquisite structures and specific functions. Here, we applied a partial linker substitution strategy to compile an HKUST-1-like quaternary MOF by introducing a bifunctional ligand into the well-known HKUST-1 structure. , a new HKUST-like topology MOF, was assembled with paddlewheel [Cu(COO)], triangular metallocycle pyrazole cluster Cu(μ-OH) (NN) building blocks, and two distinct linkers. exhibited good mechanical stability, water stability, and chemical stability (pH = 3-12) in aqueous solutions. Moreover, the porous environments created by this multicomponent primitive endow with high CH storage and significantly selective separation performance of CH/CO. Dynamic breakthrough experiments and ideal adsorbed solution theory calculations further demonstrate that can selectively capture CH from CH/CO mixtures under ambient conditions. Based on grand canonical Monte Carlo simulations, the high CH separation performance of is attributed to the π-complex formed between the CH molecule and the trinuclear metallocycle clusters on the wall, which provides stronger affinity for CH recognition than the CO molecule.

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http://dx.doi.org/10.1021/acsami.2c10346DOI Listing

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