Metal-organic frameworks (MOFs) with the Zr 6 O 4 (OH) 4 secondary building unit (SBU) have been of particular interest for potential commercial and industrial uses because they can be easily tailored and are reported to be chemically and thermally stable. However, we show that there are significant changes in chemical and thermal stability of Zr 6 O 4 (OH) 4 MOFs with the incorporation of different organic linkers. As the number of aromatic rings is increased from one to two in 1,4-benzene dicarboxylate (UiO-66, ZrMOF-BDC) and 4,4 0 -biphenyl dicarboxylate (UiO-67, ZrMOF-BPDC), the Zr 6 O 4 (OH) 4 SBU becomes more susceptible to chemical degradation by water and hydrochloric acid. Furthermore, as the linker is replaced with 2,2 0 -bipyridine-5,5 0 -dicarboxylate (ZrMOF-BIPY) the chemical stability decreases further as the MOF is susceptible to chemical breakdown by protic chemicals such as methanol and isopropanol. The results reported here bring into question the superior structural stability of the UiO-67 analogs as reported by others. Furthermore, the degradation mechanisms proposed here may be applied to other classes of MOFs containing aromatic dicarboxylate organic linkers, in order to predict their structural stability upon exposure to solvents.

The rational design of metal-organic frameworks (MOFs) with structural stability in the presence of humid conditions is critical to the commercialization of this class of materials. However, the systematic water stability studies required to develop design criteria for the construction of water-stable MOFs are still scarce. In this work, we show that by varying the functional groups on the 1,4-benzenedicarboxylic acid (BDC) linker of DMOF [Zn(BDC)(DABCO)(0.5)], we can systematically tune the kinetic water stability of this isostructural, pillared family of MOFs. To illustrate this concept, we have performed water adsorption studies on four novel, methyl-functionalized DMOF variations along with a number of already reported functionalized analogues containing polar (fluorine) and nonpolar (methyl) functional groups on the BDC ligand. These results are distinctly different from previous reports where the apparent water stability is improved through the inclusion of functional groups such as -CH(3), -C(2)H(5), and -CF(3) which only serve to prevent significant amounts of water from adsorbing into the pores. In this study, we present the first demonstration of tuning the inherent kinetic stability of MOF structures in the presence of large amounts of adsorbed water. Notably, we demonstrate that while the parent DMOF structure is unstable, the DMOF variation containing the tetramethyl BDC ligand remains fully stable after adsorbing large amounts of water vapor during cyclic water adsorption cycles. These trends cannot be rationalized in terms of hydrophobicity alone; experimental water isotherms show that MOFs containing the same number of methyl groups per unit cell will have different kinetic stabilities and that the precise placements of the methyl groups on the BDC ligand are therefore critically important in determining their stability in the presence of water. We present the water adsorption isotherms, PXRD (powder X-ray diffraction) patterns, and BET surface areas before and after water exposure to illustrate these trends. Furthermore, we shed light on the important distinction between kinetic and thermodynamic stability in MOFs. Molecular simulations are also used to provide insight into the structural characteristics governing these trends in kinetic water stability.

No abstract

The practical use of metal-organic frameworks (MOFs) in applications ranging from adsorption separations to controlled storage and release hinges on their stability in humid or aqueous environments. The sensitivity of certain MOFs under humid conditions is well-known, but systematic studies of water adsorption properties of MOFs are lacking. This information is critical for developing design criteria for directing future synthesis efforts. The goal of this work is to understand the influence of the extent of Zn-O bond shielding on the relative stabilities of MOFs belonging to same family of isostructural, noncatenated pillared MOFs [Zn(L)(DABCO)(0.5)], where L is the functionalized BDC (1,4-benzenedicarboxylic acid) linker. The different extent of Zn-O bond shielding is provided by incorporating a broad range of functional groups on the BDC ligand. The resulting MOFs have varying surface areas, pore sizes, and pore volumes. Stability is assessed through water vapor adsorption isotherms combined with powder X-ray diffraction (PXRD) experiments and surface area analyses. Our study demonstrates that integration of polar functional groups (e.g., nitro, bromo, chloro, hydroxy, etc.) on the dicarboxylate linker renders these MOFs water unstable compared to the parent MOF as these polar functional groups have a negative shielding effect; i.e., they facilitate hydrolysis of the Zn-O bond. On the other hand, placing nonpolar groups (e.g., methyl) on the BDC ligand results in structurally robust MOFs because the Zn-O bond is effectively shielded from attack by water molecules. Therefore, the anthracene- and tetramethyl-BDC MOFs do not lose crystallinity or surface area after water exposure, in spite of the large amount of water adsorption due to capillary condensation at ∼20% relative humidity (RH). This has been observed rarely in the MOF literature. The results of this work show that by ligand functionalization it is possible to adjust the water stability of a pillared MOF in both the positive and negative directions and, thus, provide an important step toward understanding the water adsorption behavior of MOFs.

No abstract