A robust ultra-microporous cationic aluminum-based metal-organic framework with a flexible tetra-carboxylate linker

Abstract

Al-based cationic metal-organic frameworks (MOFs) are uncommon. Here, we report a cationic Al-MOF, MIP-213(Al) ([Al₁₈(μ₂-OH)₂₄(OH₂)₁₂(mdip)₆]6Cl·6H₂O) constructed from flexible tetra-carboxylate ligand (5,5'-Methylenediisophthalic acid; H₄mdip). Its crystal structure was determined by the combination of three-dimensional electron diffraction (3DED) and high-resolution powder X-ray diffraction. The structure is built from infinite corner-sharing chains of AlO₄(OH)₂ and AlO₂(OH)₃(H₂O) octahedra forming an 18-membered rings honeycomb lattice, similar to that of MIL-96(Al), a scarce Al-polycarboxylate defective MOF. Despite sharing these structural similarities, MIP-213(Al), unlike MIL-96(Al), lacks the isolated μ₃-oxo-bridged Al-clusters. This leads to an ordered defective cationic framework whose charge is balanced by Cl^- sandwiched between two Al-trimers at the corner of the honeycomb, showing strong interaction with terminal H₂O coordinated to the Al-trimers. The overall structure is endowed by a narrow quasi-1D channel of dimension ~4.7 Å. The Cl^- in the framework restrains the accessibility of the channels, while the MOF selectively adsorbs CO₂ over N₂ and possesses high hydrolytic stability.

Aluminium-based cationic metal–organic frameworks remain rare, yet offer opportunities for unusual framework structures and material properties. Here, a robust ultra-microporous cationic metal–organic framework based on aluminium building units and flexible tetracarboxylic acid linkers is reported, and three-dimensional electron diffraction combined with high-resolution powder X-ray diffraction show that the material comprises an ordered defective cationic framework with narrow quasi-1D channels.