Zhi-Yuan Gu

Zirconium-Metalloporphyrin PCN-222: Mesoporous Metal–Organic Frameworks with Ultrahigh Stability as Biomimetic Catalysts†

In nature, metalloporphyrins are well known for performing many biological functions in aqueous media, such as light harvesting, oxygen transportation, and catalysis. Heme, the iron–porphyrin derivative, is the cofactor for many enzyme/ protein families, including peroxidases, cytochromes, hemoglobins, and myoglobins. Using synthetic systems to mimic natural enzymes with high catalytic activity and substrate selectivity has been a sought-after goal in the last decade. Direct application of a heme as an oxidation catalyst in aqueous solution is usually challenging due to the formation of catalytically inactive dimers and catalyst self-destruction in the oxidizing reaction media. One promising approach is to load heme on supports, such as zeolites, clays, nanoparticles, hydrogels, or carbon materials, a practice which inevitably dilutes the density of active sites. An alternative approach is to protect the heme center by modifying the porphyrin to produce dendrimers or molecular crystals, which is a synthetically demanding method. Herein, we propose a unique strategy employing heme-like active centers as structural motifs for the assembly of highly stable porous materials, which should possess well-defined mesochannels and ultrahigh stability in aqueous solution. Metal-organic frameworks (MOFs) are a new class of crystalline porous materials with fascinating structures and intriguing properties, such as permanent porosity, high surface area, and uniform open cavities. The availability of various building blocks consisting of metals and organic linkers makes it possible to construct MOFs with unique properties for diverse applications. However, these desirable features of MOFs have rarely been applied to an enzymatic mimic, especially for catalysis in an aqueous medium, despite the fact that the assembly of ligands bearing high-density active sites into 3D frameworks may provide an ideal system to both enhance the catalytic activity and protect the cofactors. One of the main reasons is the lack of water-stable MOFs containing redox-active metal centers. Furthermore, most MOFs are microporous (pore size< 2 nm). Although they are suitable for gas storage, the small pore size slows down diffusion and limits the access of large substrate molecules to the active sites inside a MOF. Therefore, MOFs with mesopores, accessible redox sites, and ultrahigh stability, especially in aqueous media, are indispensible for any successful biomimetic attempt. Herein we have employed Fe-TCPP (TCPP= tetrakis(4carboxyphenyl)porphyrin) as a heme-like ligand and chosen highly stable Zr6 clusters as nodes for the assembly of stable Zr-MOFs. With carefully selected starting materials, we have successfully constructed a 3D heme-like MOF, designated as PCN-222(Fe) (Figure 1; PCN= porous coordination net-

Metal-organic frameworks for analytical chemistry: from sample collection to chromatographic separation.

In modern analytical chemistry researchers pursue novel materials to meet analytical challenges such as improvements in sensitivity, selectivity, and detection limit. Metal-organic frameworks (MOFs) are an emerging class of microporous materials, and their unusual properties such as high surface area, good thermal stability, uniform structured nanoscale cavities, and the availability of in-pore functionality and outer-surface modification are attractive for diverse analytical applications. This Account summarizes our research on the analytical applications of MOFs ranging from sampling to chromatographic separation. MOFs have been either directly used or engineered to meet the demands of various analytical applications. Bulk MOFs with microsized crystals are convenient sorbents for direct application to in-field sampling and solid-phase extraction. Quartz tubes packed with MOF-5 have shown excellent stability, adsorption efficiency, and reproducibility for in-field sampling and trapping of atmospheric formaldehyde. The 2D copper(II) isonicotinate packed microcolumn has demonstrated large enhancement factors and good shape- and size-selectivity when applied to on-line solid-phase extraction of polycyclic aromatic hydrocarbons in water samples. We have explored the molecular sieving effect of MOFs for the efficient enrichment of peptides with simultaneous exclusion of proteins from biological fluids. These results show promise for the future of MOFs in peptidomics research. Moreover, nanosized MOFs and engineered thin films of MOFs are promising materials as novel coatings for solid-phase microextraction. We have developed an in situ hydrothermal growth approach to fabricate thin films of MOF-199 on etched stainless steel wire for solid-phase microextraction of volatile benzene homologues with large enhancement factors and wide linearity. Their high thermal stability and easy-to-engineer nanocrystals make MOFs attractive as new stationary phases to fabricate MOF-coated capillaries for high-resolution gas chromatography (GC). We have explored a dynamic coating approach to fabricate a MOF-coated capillary for the GC separation of important raw chemicals and persistent organic pollutants with high resolution and excellent selectivity. We have combined a MOF-coated fiber for solid-phase microextraction with a MOF-coated capillary for GC separation, which provides an effective MOF-based tandem molecular sieve platform for selective microextraction and high-resolution GC separation of target analytes in complex samples. Microsized MOFs with good solvent stability are attractive stationary phases for high-performance liquid chromatography (HPLC). These materials have shown high resolution and good selectivity and reproducibility in both the normal-phase HPLC separation of fullerenes and substituted aromatics on MIL-101 packed columns and position isomers on a MIL-53(Al) packed column and the reversed-phase HPLC separation of a wide range of analytes from nonpolar to polar and acidic to basic solutes. Despite the above achievements, further exploration of MOFs in analytical chemistry is needed. Especially, analytical application-oriented engineering of MOFs is imperative for specific applications.

Construction of Ultrastable Porphyrin Zr Metal–Organic Frameworks through Linker Elimination

A series of highly stable MOFs with 3-D nanochannels, namely PCN-224 (no metal, Ni, Co, Fe), have been assembled with six-connected Zr6 cluster and metalloporphyrins by a linker-elimination strategy. The PCN-224 series not only exhibits the highest BET surface area (2600 m(2)/g) among all the reported porphyrinic MOFs but also remains intact in pH = 0 to pH = 11 aqueous solution. Remarkably, PCN-224(Co) exhibits high catalytic activity for the CO2/propylene oxide coupling reaction and can be used as a recoverable heterogeneous catalyst.

An Exceptionally Stable, Porphyrinic Zr Metal–Organic Framework Exhibiting pH-Dependent Fluorescence

A reaction between a Zr(IV) salt and a porphyrinic tetracarboxylic acid leads to a metal-organic framework (MOF) with two types of open channels, representing a MOF featuring a (4,8)-connected sqc net. The MOF remains intact in both boiling water and aqueous solutions with pH ranging from 1 to 11, a remarkably extensive pH range that a MOF can sustain. Given its exceptional stability and pH-dependent fluorescent intensity, the MOF can potentially be applied in fluorescent pH sensing.

Metal–Organic Framework MIL-101 for High-Resolution Gas-Chromatographic Separation of Xylene Isomers and Ethylbenzene†

Metal–organic frameworks (MOFs) have received great attention because of their fascinating structures and intriguing applications in hydrogen storage, gas separation, catalysis, chiral separation, sensing, and imaging. Recently, MOFs such as MOF-508, MIL-47, and MIL53 have been shown to be promising as stationary phases for gas chromatography (GC) and liquid chromatography. 11] All these pioneering works on the utilization of MOFs as stationary phases in chromatography were performed on packed columns. However, packed columns usually result in low resolution as a result of peak broadening, which impairs the separation efficiency of MOFs. Moreover, gram-scale MOFs are needed for packed columns, leading to high-cost applications of MOFs as stationary phases in chromatographic separation. In contrast, capillary columns, either wall-coated open tubular (WCOT) columns or porous layer open tube (PLOT) columns, involve a thin film of MOFs coated on their inner walls, and thus improve the resolving power of MOFs and reduce the amount of MOFs required for GC applications. However, to the best of our knowledge, no work on the utilization of MOFs as stationary phases for high-resolution capillary GC separation has been reported so far. Herein we show the first fabrication of the MOF-coated capillary column for high-resolution GC separation. For a proof-of-concept demonstration, we choose MIL-101 as the stationary phase and xylene isomers and ethylbenzene (EB) as the targets for separation. Xylene isomers and EB are important raw chemicals in industry; in particular, p-xylene is used in the manufacture of terephthalic acid for the polyester industry. The separation and detection of individual xylene isomers and EB are also of environmental concern, and of great practical interest in air monitoring and blood analysis. For these reasons, numerous stationary phases have been developed for GC separation of xylene isomers and EB, for example, 7,8benzoquinoline, tetrachlorophthalate, 1,8-diaminonaphthalene, modified organo-clays Bentone-34, liquid-crystalline compounds, b-cyclodextrin derivatives, poly(ethylene glycol), and MIL-47. However, long analysis time (27–90 min) or temperature programming is often needed. MIL-101 is a chromium terephthalate MOF with coordinatively unsaturated sites (CUS). We utilized MIL-101 as the stationary phase because of its high surface area, large pores (2.9–3.4 nm), accessible CUS, and excellent chemical and thermal stability, which make it an attractive candidate for isomer separation. However, MIL-101 has never been explored as the stationary phase for chromatographic separation before, even though the tiny crystal size characteristic of MIL-101 is beneficial to the fabrication of MIL-101 coated capillary columns by a dynamic coating method. In this work, we prepared the MIL-101 coated capillary column and achieved a baseline separation of p-xylene, oxylene, m-xylene, and EB on the fabricated MOF coated capillary column by GC within 1.6 min without the need for temperature programming (Figure 1).

Zeolitic imidazolate framework-8 nanocrystal coated capillary for molecular sieving of branched alkanes from linear alkanes along with high-resolution chromatographic separation of linear alkanes.

A zeolitic imidazolate framework-8 (ZIF-8) nanocrystal coated capillary is shown not only to have a strong ability to sieve branched alkanes from linear alkane isomers owing to the narrow pore windows but also to offer excellent features for high-resolution gas chromatographic separation of linear alkanes due to van der Waals interaction between linear alkanes and the hydrophobic inner surfaces of the micropores. This makes the ZIF-8 coated capillary very promising for the specific adsorption and separation of alkanes in complicated matrices.

In Situ Hydrothermal Growth of Metal−Organic Framework 199 Films on Stainless Steel Fibers for Solid-Phase Microextraction of Gaseous Benzene Homologues

Metal-organic frameworks (MOFs) have received great attention due to their fascinating structures and intriguing potential applications in various fields. Herein, we report the first example of the utilization of MOFs for solid-phase microextraction (SPME). MOF-199 with unique pores and open metal sites (Lewis acid sites) was employed as the coating for SPME fiber to extract volatile and harmful benzene homologues. The SPME fiber was fabricated by in situ hydrothermal growth of thin MOF-199 films on etched stainless steel wire. The MOF-199-coated fiber not only offered large enhancement factors from 19,613 (benzene) to 110,860 (p-xylene), but also exhibited wide linearity with 3 orders of magnitude for the tested benzene homologues. The limits of detection for the benzene homologues were 8.3-23.3 ng L(-1). The relative standard deviation (RSD) for six replicate extractions using one SPME fiber ranged from 2.0% to 7.7%. The fiber-to-fiber reproducibility for three parallel prepared fibers was 3.5%-9.4% (RSD). Indoor air samples were analyzed for the benzene homologues using the SPME with the MOF-199-coated fiber in combination with gas chromatography-flame ionization detection. The recoveries for the spiked benzene homologues in the collected indoor air samples were in the range of 87%-106%. The high affinity of the MOF-199-coated fiber to benzene homologues resulted from the combined effects of the large surface area and the unique porous structure of the MOF-199, the pi-pi interactions of the aromatic rings of the analytes with the framework 1,3,5-benzenetricarboxylic acid molecules, and the pi-complexation of the electron-rich analytes to the Lewis acid sites in the pores of MOF-199.

Metal–Organic-Framework-Based Tandem Molecular Sieves as a Dual Platform for Selective Microextraction and High-Resolution Gas Chromatographic Separation of n-Alkanes in Complex Matrixes

Metal-organic frameworks (MOFs) were employed to design tandem molecular sieves as a dual platform for selective solid-phase microextraction (SPME) and high-resolution gas chromatographic (GC) separation of target analytes in complex matrixes. An elegant combination of a ZIF-8-coated fiber for SPME with a ZIF-8-coated capillary for GC allows selective extraction and separation of n-alkanes from complex matrixes such as petroleum-based fuel and biological fluids. The proposed tandem ZIF-8 molecular sieves not only offered good enhancement factors from 235 (hexane) to 1212 (nonane), but also exhibited wide linearity with 3 orders of magnitude for the tested linear alkanes. The limits of detection for the linear alkanes ranged from 0.46 ng L(-1) (nonane) to 1.06 ng L(-1)(hexane). The relative standard deviations of retention time, peak area, peak height, and half peak width for five replicate determinations of the tested n-alkanes at 30 ng L(-1) were 0.02-0.26%, 1.9-8.6%, 1.4-6.0%, and 1.3-7.2%, respectively. The developed tandem ZIF-8 molecular sieves were further used for the determination of linear alkanes in petroleum-based fuel and human serum. The large diversity in structure and pore size allows various combinations of MOFs for designing an MOF-based tandem molecular sieve platform to achieve different selectivities in extraction and chromatographic separation and to solve headache problems in complex real sample analysis.

Rigidifying fluorescent linkers by metal-organic framework formation for fluorescence blue shift and quantum yield enhancement.

We demonstrate that rigidifying the structure of fluorescent linkers by structurally constraining them in metal-organic frameworks (MOFs) to control their conformation effectively tunes the fluorescence energy and enhances the quantum yield. Thus, a new tetraphenylethylene-based zirconium MOF exhibits a deep-blue fluorescent emission at 470 nm with a unity quantum yield (99.9 ± 0.5%) under Ar, representing ca. 3600 cm(-1) blue shift and doubled radiative decay efficiency vs the linker precursor. An anomalous increase in the fluorescence lifetime and relative intensity takes place upon heating the solid MOF from cryogenic to ambient temperatures. The origin of these unusual photoluminescence properties is attributed to twisted linker conformation, intramolecular hindrance, and framework rigidity.

Metal–Organic Frameworks as Biomimetic Catalysts

In this Minireview, we have summarized the recent progress of biomimetic catalysis in the field of metal‐organic frameworks (MOFs) with a focus on the implantation of biomimetic active sites into a stable MOF. In addition, the potential of creating highly selective catalytic pockets and diffusion‐favored hierarchical structures in MOFs has also been explored. Furthermore, we have highlighted the achievements of MOF catalysts in the applications as mimics of peroxidase, cytochromes P450, hemoglobin, and photosynthetic systems.