A Smart Metal–Organic Framework Nanomaterial for Lung Targeting

Despite high morbidity and mortality associated with lung diseases, addressing drugs towards lung tissue remains a pending task. Particle lung filtration has been proposed for passive lung targeting and drug delivery. However, toxicity issues derived from the long‐term presence of the particles must be overcome. By exploiting some of the ignored properties of nanosized metal–organic frameworks it is possible to achieve impressive antitumoral effects on experimental lung tumors, even without the need to engineer the surface of the material. In fact, it was discovered that, based on unique pH‐responsiveness and reversible aggregation behaviors, nanoMOF was capable of targeting lung tissue. At the neutral pH of the blood, the nanoMOFs form aggregates with the adequate size to be retained in lung capillaries. Within 24 h they then disaggregate and release their drug payload. This phenomenon was compatible with lung tissue physiology.     

Formation of Ultrathin,Continuous Metal–Organic Framework Membranes on Flexible Polymer Substrates

Metal–organic framework (MOF) materials have an enormous potential in separation applications, but to realize their potential as semipermeable membranes they need to be assembled into thin continuous macroscopic films for fabrication into devices. By using a facile immersion technique, we prepared ultrathin, continuous zeolitic imidazolate framework (ZIF‐8) membranes on titania‐functionalized porous polymeric supports. The coherent ZIF‐8 layer was surprisingly flexible and adhered well to the support, and the composite membrane could sustain bending and elongation. The membranes exhibited molecular sieving behavior, close to the theoretical permeability of ZIF‐8, with hydrogen permeance up to 201×10⁻⁷ mol m⁻² s⁻¹ Pa⁻¹ and an ideal H₂/CO₂ selectivity of 7:1. This approach offers significant opportunities to exploit the unique properties of MOFs in the fabrication of separation and sensing devices.     

NiII Coordination to an Al‐Based Metal–Organic Framework Made from 2‐Aminoterephthalate for Photocatalytic Overall Water Splitting

The aluminum‐based metal–organic framework (MOF) made from 2‐aminoterephthalate is a photocatalyst for oxygen evolution. This MOF can be modified by incorporating Ni²⁺ cations into the pores through coordination to the amino groups, and the resulting MOF is an efficient photocatalyst for overall water splitting.     

A Metal–Organic Framework Based Methane Nano‐trap for the Capture of Coal‐Mine Methane

As a major greenhouse gas, methane, which is directly vented from the coal‐mine to the atmosphere, has not yet drawn sufficient attention. To address this problem, we report a methane nano‐trap that features oppositely adjacent open metal sites and dense alkyl groups in a metal–organic framework (MOF). The alkyl MOF‐based methane nano‐trap exhibits a record‐high methane uptake and CH₄/N₂ selectivity at 298 K and 1 bar. The methane molecules trapped within the alkyl MOF were crystalographically identified by single‐crystal X‐ray diffraction experiments, which in combination with molecular simulation studies unveiled the methane adsorption mechanism within the MOF‐based nano‐trap. The IAST calculations and the breakthrough experiments revealed that the alkyl MOF‐based methane nano‐trap is a new benchmark for CH₄/N₂ separation, thereby providing a new perspective for capturing methane from coal‐mine methane to recover fuel and reduce greenhouse gas emissions.     

Mixed‐Metal MOFs: Unique Opportunities in Metal–Organic Framework (MOF) Functionality and Design

Mixed‐metal metal–organic frameworks (MM‐MOFs) can be considered to be those MOFs having two different metals anywhere in the structure. Herein we summarize the various strategies for the preparation of MM‐MOFs and some of their applications in adsorption, gas separation, and catalysis. It is shown that compared to homometallic MOFs, MM‐MOFs bring about the opportunity to take advantage of the complexity and the synergism derived from the presence of different metal ions in the structure of MOFs. This is reflected in a superior performance and even stability of MM‐MOFs respect to related single‐metal MOFs. Emphasis is made on the use of MM‐MOFs as catalysts for tandem reactions.     

An Americium‐Containing Metal–Organic Framework: A Platform for Studying Transplutonium Elements

The synthesis, structure, and spectroscopic characterization of the first transplutonium metal–organic framework (MOF) is described. The preparation and structure of Am‐GWMOF‐6, [Am₂(C₆H₈O₄)₃(H₂O)₂][(C₁₀H₈N₂)], is analogous to that of the isostructural trivalent lanthanide‐only containing material GWMOF‐6. The presented MOF architecture is used as a platform to probe Am³⁺ coordination chemistry and guest‐enhanced luminescent emission, whereas the framework itself provides a means to monitor the effects of self‐irradiation upon crystallinity over time. Presented here is a discussion of these properties and the opportunities that MOFs provide in the structural and spectroscopic study of actinides.     

Pressure‐Induced Multiphoton Excited Fluorochromic Metal–Organic Frameworks for Improving MPEF Properties

In multiphoton excited fluorescence (MPEF), high‐energy upconversion emission is obtained from low‐energy excitation by absorbance of two or more photons simultaneously. In a pressure‐induced fluorochromic process, the emission energy is switched by outer pressure stimuli. Now, five metal–organic frameworks containing the same ligand with simultaneous multiphoton absorption and pressure‐induced fluorochromic attributes were studied. One‐, two‐, and three‐photon excited fluorescence (1/2/3PEF) can be achieved in the frameworks, which exhibit pressure‐induced blue‐to‐yellow fluorochromism. The performances are closely dependent with the topologies, flexibilities, and packing states of the frameworks and chromophores therein. The multiphoton upconversion performance can be intensified by pressure‐related structural contraction. Over ten‐fold increment in the 2PA active cross‐section up to 2217 GM is achieved in pressed LIFM‐114 compared with the 210 GM for pristine sample at 780 nm.     

Selective Aerobic Oxidation of a Metal–Organic Framework Boosts Thermodynamic and Kinetic Propylene/Propane Selectivity

Efficient adsorptive separation of propylene/propane (C₃H₆/C₃H₈) is highly desired and challenging. Known strategies focus on either the thermodynamic or the kinetic mechanism. Here, we report an interesting reactivity of a metal–organic framework that improves thermodynamic and kinetic adsorption selectivity simultaneously. When the metal–organic framework is heated under oxygen flow, half of the soft methylene bridges of the organic ligands are selectively oxidized to form the more polar and rigid carbonyl bridges. Mixture breakthrough experiments showed drastic increase of C₃H₆/C₃H₈ selectivity from 1.5 to 15. For comparison, the C₃H₆/C₃H₈ selectivities of the best‐performing metal–organic frameworks Co‐MOF‐74 and KAUST‐7 were experimentally determined to be 6.5 and 12, respectively. Gas adsorption isotherms/kinetics, single‐crystal X‐ray diffraction, and computational simulations revealed that the oxidation gives additional guest recognition sites, which improve thermodynamic selectivity, and reduces the framework flexibility, which generate kinetic selectivity.     

Defect‐Rich Graphene Nanomesh Produced by Thermal Exfoliation of Metal–Organic Frameworks for the Oxygen Reduction Reaction

Although graphene nanomesh is an attractive 2D carbon material, general synthetic routes to produce functional graphene nanomesh in large‐scale are complex and tedious. Herein, we elaborately design a simple two‐step dimensional reduction strategy for exploring nitrogen‐doped graphene nanomesh by thermal exfoliation of crystal‐ and shape‐modified metal‐organic frameworks (MOFs). MOF nanoleaves with 2D rather than 3D crystal structure are used as the precursor, which are further thermally unraveled into nitrogen‐doped graphene nanomesh by using metal chlorides as the exfoliators and etching agent. The nitrogen‐doped graphene nanomesh has a unique ultrathin two‐dimensional morphology, high porosity, rich and accessible nitrogen‐doped active sites, and defective graphene edges, contributing to an unprecedented catalytic activity for the oxygen reduction reaction (ORR) in acid electrolytes. This approach is suitable for scalable production.     

Anodized Aluminum Oxide Templated Synthesis of Metal–Organic Frameworks Used as Membrane Reactors

The incorporation of metal–organic frameworks (MOFs) into membrane‐shaped architectures is of great importance for practical applications. The currently synthesized MOF‐based membranes show many disadvantages, such as poor compatibility, low dispersity, and instability, which severely limit their utility. Herein, we present a general, facile, and robust approach for the synthesis of MOF‐based composite membranes through the in situ growth of MOF plates in the channels of anodized aluminum oxide (AAO) membranes. After being used as catalysis reactors, they exhibit high catalytic performance and stability in the Knoevenagel condensation reaction. The high catalytic performance might be attributed to the intrinsic structure of MOF‐based composite membranes, which can remove the products from the reaction zone quickly, and prevent the aggregation and loss of catalysts during reaction and recycling process.     

Two‐Dimensional Metal–Organic Framework Nanosheets for Membrane‐Based Gas Separation

Metal–organic framework (MOF) nanosheets could serve as ideal building blocks of molecular sieve membranes owing to their structural diversity and minimized mass‐transfer barrier. To date, discovery of appropriate MOF nanosheets and facile fabrication of high performance MOF nanosheet‐based membranes remain as great challenges. A modified soft‐physical exfoliation method was used to disintegrate a lamellar amphiprotic MOF into nanosheets with a high aspect ratio. Consequently sub‐10 nm‐thick ultrathin membranes were successfully prepared, and these demonstrated a remarkable H₂/CO₂ separation performance, with a separation factor of up to 166 and H₂ permeance of up to 8×10⁻⁷ mol m⁻² s⁻¹ Pa⁻¹ at elevated testing temperatures owing to a well‐defined size‐exclusion effect. This nanosheet‐based membrane holds great promise as the next generation of ultrapermeable gas separation membrane.     

Evaporation‐Directed Crack‐Patterning of Metal–Organic Framework Colloidal Films and Their Application as Photonic Sensors

A straightforward crack‐patterning method is reported allowing the direct formation of periodic cracks in metal–organic framework (MOF) nanoparticle films during dip‐coating deposition. The crack propagation and periodicity can be easily tailored by controlling the evaporation front and the withdrawal speed. Several MOF‐patterned films can be fabricated on large surfaces and on several substrates (flat, curved or flexible) including the inner surface of a tube, not achievable by other lithographic techniques. We demonstrate that the periodic cracked arrays diffract light and, due to the MOF sorption properties, photonic vapor sensors are fabricated. A new concept of “in‐tube”, MOF‐based diffraction grating sensors is proposed with outstanding sensitivity that can be easily tuned “on‐demand” as function of the desired detection range.     

Engineering Donor–Acceptor Heterostructure Metal–Organic Framework Crystals for Photonic Logic Computation

Photonic materials use photons as information carriers and offer the potential for unprecedented applications in optical and optoelectronic devices. In this study, we introduce a new strategy for photonic materials using metal–organic frameworks (MOFs) as the host for the rational construction of donor–acceptor (D–A) heterostructure crystals. We have engineered a rich library of heterostructure crystals using the MOF NKU‐111 as a host. NKU‐111 is based upon an electron‐deficient tridentate ligand (acceptor) that can bind to various electron‐rich guests (donors). The resulting heterocrystals exhibit spatially segregated multi‐color emission resulting from the guest‐dependent charge‐transfer (CT) emission. Spatially effective mono‐directional energy transfer results from tuning the energy gradient between adjacent domains through the selection of donor guest molecules, which suggests potential applications in integrated optical circuit devices, for example, photonic diodes, on‐chip signal processing, optical logic gates.     

Polymer Composite Membrane with Penetrating ZIF‐7 Sheets Displays High Hydrogen Permselectivity

Oriented and penetrating molecular sieving membranes display enhanced separation performance. A polyimide (PI) solution containing highly dispersed ZIF‐7(III) sheets in CHCl₃ was deposited on a glass side and subjected to flat‐scraping with a membrane fabricator. In this way we developed a novel oriented and penetrating ZIF‐7@PI mixed matrix membrane (MMM) with 50 wt. % ZIF‐7 loading. Because the height of the ZIF‐7 sheets (5 μm) is higher than the film thickness, every ZIF‐7 sheet penetrates both surfaces of the polyimide film. Since the ZIF‐7 channels are the dominant pathway for gas permeation, the ZIF‐7@PI MMM displays a high molecular sieve performance for the separation of H₂ (0.29 nm) from larger gas molecules. At 100 °C and 2 bar, the mixture separation factors of H₂/CO₂ and H₂/CH₄ are 91.5 and 128.4, with a high H₂ permeance of about 3.0×10^?7 mol m^?2 s^?1 Pa^?1, which is promising for hydrogen separation by molecular sieving.     

Nanocrystal/Metal–Organic Framework Hybrids as Electrocatalytic Platforms for CO2 Conversion

The tunable chemistry linked to the organic/inorganic components in colloidal nanocrystals (NCs) and metal–organic frameworks (MOFs) offers a rich playground to advance the fundamental understanding of materials design for various applications. Herein, we combine these two classes of materials by synthesizing NC/MOF hybrids comprising Ag NCs that are in intimate contact with Al‐PMOF ([Al₂(OH)₂(TCPP)]) (tetrakis(4‐carboxyphenyl)porphyrin (TCPP)), to form Ag@Al‐PMOF. In our hybrids, the NCs are embedded in the MOF while still preserving electrical contact with a conductive substrate. This key feature allows the investigation of the Ag@Al‐PMOFs as electrocatalysts for the CO₂ reduction reaction (CO₂RR). We show that the pristine interface between the NCs and the MOFs accounts for electronic changes in the Ag, which suppress the hydrogen evolution reaction (HER) and promote the CO₂RR. We also demonstrate a minor contribution of mass‐transfer effects imposed by the porous MOF layer under the chosen testing conditions. Furthermore, we find an increased morphological stability of the Ag NCs when combined with the Al‐PMOF. The synthesis method is general and applicable to other metal NCs, thus revealing a new way to think about rationally tailored electrocatalytic materials to steer selectivity and improve stability.     

A Surfactant‐Free and Scalable General Strategy for Synthesizing Ultrathin Two‐Dimensional Metal–Organic Framework Nanosheets for the Oxygen Evolution Reaction

Metal–organic framework (MOFs) two‐dimensional (2D) nanosheets have many coordinatively unsaturated metal sites that act as active centres for catalysis. To date, limited numbers of 2D MOFs nanosheets can be obtained through top‐down or bottom‐up synthesis strategies. Herein, we report a 2D oxide sacrifice approach (2dOSA) to facilely synthesize ultrathin MOF‐74 and BTC MOF nanosheets with a flexible combination of metal sites, which cannot be obtained through the delamination of their bulk counterparts (top‐down) or the conventional solvothermal method (bottom‐up). The ultrathin iron–cobalt MOF‐74 nanosheets prepared are only 2.6 nm thick. The sample enriched with surface coordinatively unsaturated metal sites, exhibits a significantly higher oxygen evolution reaction reactivity than bulk FeCo MOF‐74 particles and the state‐of‐the‐art MOF catalyst. It is believed that this 2dOSA could provide a new and simple way to synthesize various ultrathin MOF nanosheets for wide applications.     

Stereoselectively Assembled Metal–Organic Framework (MOF) Host for Catalytic Synthesis of Carbon Hybrids for Alkaline‐Metal‐Ion Batteries

Cost‐effective metal‐based nanostructured hybrids have been widely dedicated to potential energy storage and conversion applications. Herein, we develop a facile methodology for the synthesis of precise carbon‐confined hybrid nanostructures by stereoselective assembly accompanied by catalytic pyrolysis. Polyacrylonitrile fiber films favors not only metal‐polymer coordination, but also oriented assembly to ensure the well‐defined nanostructure of the carbon hybrids. During chemical vapor deposition (CVD), cobalt‐nanoparticle‐catalyzed growth of carbon‐nanotube branches driven by organic molecules (e.g. melamine) delivers hierarchical carbon hybrids. The resulting carbon hybrids exhibit outstanding electrochemical performance for metal‐ion batteries, for example, a high specific capacity of 680 mAh g^?1 after 320 cycles (Li‐storage) and 220 mAh g^?1 after 500 cycles (Na‐storage) without decay.     

Molecular Pivot‐Hinge Installation to Evolve Topology in Rare‐Earth Metal–Organic Frameworks

Linker desymmetrization has been witnessed as a powerful design strategy for the discovery of highly connected metal–organic frameworks (MOFs) with unprecedented topologies. Herein, we introduce molecular pivot‐hinge installation as a linker desymmetrization strategy to evolve the topology of highly connected rare‐earth (RE) MOFs, where a pivot group is placed in the center of a linker similar to a hinge. By tuning the composition of pivot groups and steric hindrances of the substituents on various linker rotamers, MOFs with various topologies can be obtained. The combination of L‐SO₂ with C_2v symmetry and 12‐connected RE₉ clusters leads to the formation of a fascinating (4,12)‐c dfs new topology. Interestingly, when replacing L‐SO₂ with a tetrahedra linker L‐O, the stacking behaviors of RE‐organic layers switch from an eclipsed mode to a staggered stacking mode, leading to the discovery of an intriguing hjz topology. Additionally, the combination of the RE cluster and a linker [(L‐(CH₃)₆)] with more bulky groups gives rise to a flu topology with a new 8‐c inorganic cluster. The diversity of these RE‐MOFs was further enhanced through post‐synthetic installation of linkers with various functional groups. Functionalization of each linker with acidic and basic units in the mesoporous RE‐based PCN‐905‐SO₂ allows for efficient cascade catalytic transformation within the functionalized channels.