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Highlights: The progress of metal–organic frameworks (MOFs) in capturing and separating F-gases is highlighted. The molecular mechanisms of adsorption and separation are classified and analyzed. Toolboxes of MOFs structural design for fluorinated gases separation are provided. Fluorinated gases (F-gases) play a vital role in the chemical industry and in the fields of air conditioning, refrigeration, health care, and organic synthesis. However, the direct emission of waste gases containing F-gases into the atmosphere contributes to greenhouse effects and generates toxic substances. Developing porous materials for the energy-efficient capture, separation, and recovery of F-gases is highly desired. Recently, as a highly designable porous adsorbents, metal–organic frameworks (MOFs) exhibit excellent selective sorption performance toward F-gases, especially for the recognition and separation of different F-gases with highly similar properties, showing their great potential in F-gases control and recovery. In this review, we discuss the capture and separation of F-gases and their azeotropic, near-azeotropic, and isomeric mixtures in various application scenarios by MOFs, specifically classify and analyze molecular interaction between F-gases and MOFs, and interpret the mechanisms underlying their high performance regarding both adsorption capacity and selectivity, providing a repertoire for future materials design. Challenges faced in the transformation research roadmap of MOFs adsorbent separation technologies toward F-gases are also discussed, and areas for future research endeavors are highlighted. [ABSTRACT FROM AUTHOR]

To solve the energy crisis and environmental issues, it is essential to create effective and sustainable energy conversion and storage technologies. Traditional materials for energy conversion and storage however have several drawbacks, such as poor energy density and inadequate efficiency. The advantages of MOF-based materials, such as pristine MOFs, also known as porous coordination polymers, MOF composites, and their derivatives, over traditional materials, have been thoroughly investigated. These advantages stem from their high specific surface area, highly adjustable structure, and multifunctional nature. MOFs are promising porous materials for energy storage and conversion technologies, according to research on their many applications. Moreover, MOFs have served as sacrificial materials for the synthesis of different nanostructures for energy applications and as support substrates for metals, metal oxides, semiconductors, and complexes. One of the most intriguing characteristics of MOFs is their porosity, which permits space on the micro- and meso-scales, revealing and limiting their functions. The main goals of MOF research are to create high-porosity MOFs and develop more efficient activation techniques to preserve and access their pore space. This paper examines the porosity tunable mixed and hybrid MOF, pore architecture, physical and chemical properties of tunable MOF, pore conditions, market size of MOF, and the latest development of MOFs as precursors for the synthesis of different nanostructures and their potential uses. [ABSTRACT FROM AUTHOR]

Extracting water directly from the atmosphere seems to be a perfect way to solve the water scarcity facing 2 billion people; however, traditional Atmospheric Water Harvesting (AWH) lacks the ability to adsorb water molecules in an arid climate. Porous materials are capable of assisting water adsorption; however, currently, only certain customizable Metal–Organic Frameworks (MOFs) are able to meet the standard of adsorbing water molecules at low humidity and releasing water at low temperatures at certain times that can realize assisted AWH's practical and energy-efficient use (Energy consumption < 5kWh/L-water). From this perspective, we offer a concise review of the advancements in enhanced AWH technologies, delve into the attributes of appropriate MOFs, and offer insights into the potential and future directions of MOFs–AWH. In conclusion, we underscore that that the development of designable MOFs holds the key to the widespread practical implementation of AWH, promising the availability of affordable clean water anywhere in the world. [ABSTRACT FROM AUTHOR]

Metal-organic frameworks (MOFs) are a class of porous materials that are of topical interest for their utility in water-related applications. Nevertheless, molecular-level insight into water-MOF interactions and MOF hydrolytic reactivity remains understudied. Herein, we report two hydrolytic pathways leading to either structural stability or framework decomposition of a MOF (ZnMOF-1). The two distinct ZnMOF-1 water reaction pathways are linked to the diffusion rate of incorporated guest dimethylformamide (DMF) molecules: slow diffusion of DMF triggers evolution of the initial MOF into a water-stable MOF product exhibiting enhanced water adsorption, while fast exchange of DMF with water leads to decomposition. The starting MOF, three intermediates from the water reaction pathways and the final stable MOF have been characterized. The documentation of two distinct pathways counters the stereotype that water exposure always leads to destruction or degradation of water-sensitive MOFs, and demonstrates that water-stable MOFs with improved adsorption properties can be prepared via controlled solvent-triggered structural rearrangement. Interactions between metal-organic frameworks (MOFs) and water are difficult to predict. Here, the authors report a Zn MOF follows two pathways upon water exposure. Characterization of both routes has revealed insights for future rational design. [ABSTRACT FROM AUTHOR]

Highlights: The effects of the size structure and stability of metal–organic frameworks (MOFs) on proton conduction are comprehensively summarized. Advanced strategies for constructing proton conduction MOFs are critically discussed. Challenges and opportunities for the development of novel proton-conducting MOFs are further outlined. Proton-conducting materials have attracted considerable interest because of their extensive application in energy storage and conversion devices. Among them, metal–organic frameworks (MOFs) present tremendous development potential and possibilities for constructing novel advanced proton conductors due to their special advantages in crystallinity, designability, and porosity. In particular, several special design strategies for the structure of MOFs have opened new doors for the advancement of MOF proton conductors, such as charged network construction, ligand functionalization, metal-center manipulation, defective engineering, guest molecule incorporation, and pore-space manipulation. With the implementation of these strategies, proton-conducting MOFs have developed significantly and profoundly within the last decade. Therefore, in this review, we critically discuss and analyze the fundamental principles, design strategies, and implementation methods targeted at improving the proton conductivity of MOFs through representative examples. Besides, the structural features, the proton conduction mechanism and the behavior of MOFs are discussed thoroughly and meticulously. Future endeavors are also proposed to address the challenges of proton-conducting MOFs in practical research. We sincerely expect that this review will bring guidance and inspiration for the design of proton-conducting MOFs and further motivate the research enthusiasm for novel proton-conducting materials. [ABSTRACT FROM AUTHOR]

Emissions of volatile organic compounds (VOCs) such as benzene, toluene, xylene, styrene, hexane, tetrachloroethylene, acetone, acetaldehyde, formaldehyde, isopropanol, etc., increase dramatically with accelerated industrialization and economic growth. Most VOCs cause serious environmental pollution and threaten human health due to their toxic and carcinogenic nature. Adsorption on porous materials is considered one of the most promising technologies for VOC removal due to its cost-effectiveness, operational flexibility, and low energy consumption. This review aims to provide a comprehensive understanding of VOC adsorption on various porous adsorbents and indicate future research directions in this field. It is focused on (i) the molecular characterization of structures, polarity, and boiling points of VOCs, (ii) the adsorption mechanisms and adsorption interactions in the physical, chemical, and competitive adsorption of VOCs on adsorbents, and (iii) the favorable characteristics of materials for VOCs adsorption. Porous adsorbents that would play an important role in the removal of benzene and other VOCs are presented in detail, including carbon-based materials (activated carbons, active carbon fibers, ordered mesoporous carbons, and graphene-based materials), metal-organic frameworks, covalent organic frameworks, zeolites, and siliceous adsorbents. Finally, the challenges and prospects related to the removal of VOCs via adsorption are pointed out. [ABSTRACT FROM AUTHOR]

Covalent organic frameworks (COFs) are new porous organic materials made of organic building blocks precisely constructed by strong covalent bonds. These new materials feature tunable structure, permanent porosity, high crystallinity, high specific surface area, and excellent stability, which enable COFs to be used in many applications. Linkage chemistry is a key factor in the synthesis of COFs and the control of their physicochemical properties. The boroxine, boronate‐ester, imine, hydrazone, imide, and C=C linkages have been widely used in the construction of COFs. Among the various linkages, imine has become the most important linkage for the COFs due to the easy formation of imine linkage with structural and functional diversity. Over the past decade, imine‐linked COFs have made significant progress and become an indispensable part of various applications of COFs. Here, we aim to provide a comprehensive review of the research progress in the field of imine‐linked COFs, especially the advances in topology design and COF powder and film preparation, and their important advances in gas adsorption, catalysis, and optoelectronic devices. Finally, we discuss the challenges in the design, synthesis, and application of imine‐linked COFs, and present our views on the further development of imine‐linked COFs. [ABSTRACT FROM AUTHOR]

Flexibility has been pursued enthusiastically in the field of porous crystals for enhancing their adsorption and separation performances. However, flexibility has never been observed among porous crystals sustained thoroughly by van der Waals interactions since flexible motions readily lead to the collapse of the porous architecture. Here we report a van der Waals crystal featuring conformational flexibility as well as permanent microporosity. The single-crystal structure and its structural transition in response to the adsorption of water molecules were unambiguously disclosed by means of electron and X-ray crystal structure analyses. The peripheral aromatic rings of the constituent molecule rotated as increasing the ambient humidity, while the connectivity of the pores was maintained throughout the structural transition. The transformative pores allowed the guest water molecules to move exceedingly quickly through the pores with a time constant of 490 μs. We demonstrated that the quick release of water induced by photothermal heating induced a significant upward bending of a film set above the crystalline powder compared to conventional porous materials. This finding contributes to the future crystal engineering based on van der Waals interactions rather than cohesive bonds. Flexibility in porous crystals can enhance their adsorption and separation performances, however, achieving flexibility in porous crystals sustained solely through van der Waals interactions is challenging given that flexible motions typically lead to framework collapse. Here, the authors present a van der Waals crystal that features both conformational flexibility and permanent microporosity [ABSTRACT FROM AUTHOR]

Metal-organic frameworks (MOFs) are crystalline materials characterized by their porous structures, formed through coordination bonding between metal ions/clusters and multidentate organic linkers. MOFs have emerged as a significant class of materials with applications in energy storage, CO2 adsorption, and catalysis. This study serves as a brief introduction to the currently available synthesis methods of MOFs, aimed at acquainting beginners in the field of chemical engineering with the ongoing developments in MOF research. The discussed synthesis methods encompass traditional solvothermal/hydrothermal approaches, microwave synthesis of MOFs, one-pot synthesis, MOF nanocomposites, isothermal synthesis, and fluid-fluid synthesis. Notably, the MOF/NH2/Fe3O4 combination exhibited enhanced adsorption capacity of 618 mg/g and retained an efficiency of over 90 %. This study displays a valuable technique for designing functional MOF hybrid composites. By combining MOFs with specific materials, numerous advantages can be achieved in the newly created compounds (MOF composites), including synergistic effects beneficial in catalytic applications, and overcoming the challenges associated with using bare MOFs. [ABSTRACT FROM AUTHOR]

Metal-organic frameworks (MOFs) are highly attractive porous materials with applications spanning the fields of chemistry, physics, biology, and engineering. Their exceptional porosity and structural flexibility have led to widespread use in catalysis, separation, biomedicine, and electrochemistry. Currently, most MOFs are synthesized under equilibrium liquid-phase reaction conditions. Here we show a general and versatile non-equilibrium flame aerosol synthesis of MOFs, in which rapid kinetics of MOF formation yields two distinct classes of MOFs, nano-crystalline MOFs and amorphous MOFs. A key advantage of this far-from-equilibrium synthesis is integration of different metal cations within a single MOF phase, even when this is thermodynamically unfavorable. This can, for example, produce single-atom catalysts and bimetallic MOFs of arbitrary metal pairs. Moreover, we demonstrate that dopant metals (e.g., Pt, Pd) can be exsolved from the MOF framework by reduction, forming nanoclusters anchored on the MOF. A prototypical example of such a material exhibited outstanding performance as a CO oxidation catalyst. This general synthesis route opens new opportunities in MOF design and applications across diverse fields and is inherently scalable for continuous production at industrial scales. Metal-organic frameworks (MOFs) are typically synthesized in equilibrium liquid-phase reactions. Here, the authors have developed and present a general non-equilibrium flame aerosol method to produce nanocrystal, amorphous, and bi-metallic MOFs. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks (MOFs) have seen rapid expansion in the scientific community during the last two decades. This type of crystalline material has a great degree of structural and functional tunability not found in other porous materials such as activated carbons, and zeolites. Numerous MOFs have demonstrated themselves to be viable options in a variety of sectors due to their larger surface area, enormous pore size, crystalline structure, and tunability. MOFs are ideal candidate materials to resolve many everlasting societal issues about energy and environmental sustainability and beyond due to their structural modularity (e.g., use of different metals, post-synthetic modifications, reticular chemistry, etc.) and exceptionally controlled porosity. MOFs are indispensable across numerous applications, particularly in the removal of contaminants and emerging micropollutants from wastewater. MOFs enable a wide range of multifaceted applications by catalyzing various reactions for increasing adsorption capacity, sensing, drug delivery, and water disinfection, and thus making major contributions in several fields. This review focuses on the basics of MOFs, their classification and structural features, types, various synthetic methods, characterization, factors affecting and the applications of MOF and its nanocomposites towards a wide range of applications including, drug delivery, catalysis, adsorption, biosensing and killing/inactivation of a wide range of microorganisms including fungi, bacteria, and viruses. In conclusion, knowing MOF synthesis including green synthesis, characterization, influencing parameters, and applications is essential to capitalizing on their special qualities and expanding its application across a range of industries, ultimately resulting in creative responses to urgent global issues. [ABSTRACT FROM AUTHOR]

Quantum materials and metal‐organic framework (MOFs) materials describe two attractive research areas in physics and chemistry. Yet, with very few exceptions, these fields have been developed with little overlap. This review aims to summarize these efforts and outline the huge potential of considering MOFs as quantum materials, called quantum MOFs. Quantum MOFs exhibit macroscopic quantum states over wide energy and lengths scales. Examples are topological materials and superconductors, to name but a few. In contrast to conventional quantum materials, MOFs exhibit promising unconventional degrees of freedom such as buckling, interpenetration, porosity, and rotations, stimulating the design of novel quantum phases of matter. [ABSTRACT FROM AUTHOR]

The modern healthcare system strives to provide patients with more comfortable and less invasive experiences, focusing on noninvasive and painless diagnostic and treatment methods. A key priority is the early diagnosis of life-threatening diseases, which can significantly improve patient outcomes by enabling treatment at earlier stages. While most patients must undergo diagnostic procedures before beginning treatment, many existing methods are invasive, time-consuming, and inconvenient. To address these challenges, electrochemical-based wearable and point-of-care (PoC) sensing devices have emerged, playing a crucial role in the noninvasive, continuous, periodic, and remote monitoring of key biomarkers. Due to their numerous advantages, several wearable and PoC devices have been developed. In this focused review, we explore the advancements in metal–organic frameworks (MOFs)-based wearable and PoC devices. MOFs are porous crystalline materials that are cost-effective, biocompatible, and can be synthesized sustainably on a large scale, making them promising candidates for sensor development. However, research on MOF-based wearable and PoC sensors remains limited, and no comprehensive review has yet to synthesize the existing knowledge in this area. This review aims to fill that gap by emphasizing the design of materials, fabrication methodologies, sensing mechanisms, device construction, and real-world applicability of these sensors. Additionally, we underscore the importance and potential of MOF-based wearable and PoC sensors for advancing healthcare technologies. In conclusion, this review sheds light on the current state of the art, the challenges faced, and the opportunities ahead in MOF-based wearable and PoC sensing technologies. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks (MOFs) are a class of porous materials based on the strong coordinated bonds between inorganic secondary building units (SBUs) and organic linkers to form high-porosity periodic structures. MOFs with tunable pore size, shape, and catalysis active sites recently sparked recognition interest for the design and synthesis of catalysts with the capability to decompose aromatic-based VOCs. In this review, we introduce our viewpoints for the design and synthesis of better MOF-based photocatalysts including (i) methods to enhance the interaction of aromatic-based VOCs with MOFs by controlling micropore size, tuning Lewis acidity of the metal SBUs and/or using linkers bearing electron withdrawal groups; (ii) methods to enhance adsorption/diffusion by synthesizing hierarchical MOFs through defect control, reticular structural design and/or employing the xerogel monoliths to exploit the mesopore between particles for enhancing the adsorption/diffusion; (iii) methods to optimize the band gap by selecting appropriate building block and/or doping with exotic components. Alongside that, design principles and strategies for the development of MOF-based catalysts for thermal decomposition of aromatic-based VOCs are also provided such as (i) the need to improve the thermal stability at high temperature together with a slit pore architecture connected by small windows to prevent the aggregation of active components; and (ii) methods to control the distribution and type of active components in the MOFs' matrix to alter their catalysis performance. We expect our discussion and viewpoints on the design and synthesis of MOFs and MOF-based composites to inspire researchers to design better and more efficient systems for aromatic-based VOC decomposition. [ABSTRACT FROM AUTHOR]

In the present work, we report a "two-in-one" strategy to construct single-linker-based pillar-layered metal–organic frameworks (PL-MOFs) guided by reticular chemistry via an in situ "one-pot" approach. Two carboxyl groups and one pyridine group are integrated into one molecular skeleton to form bifunctional organic linkers via the reaction of pyridine-containing aldehyde and bicarboxylate-containing o-phenylenediamine. During the synthesis of organic linkers, two zinc-based PL-MOFs, non-interpenetrated HIAM-3016-op and two-fold interpenetrated HIAM-3017-op, can be simultaneously constructed. The different interpenetrations for these two PL-MOFs can be attributed to the increased length of the pyridine-containing moiety. HIAM-3017-op can be utilized for Cr2O72− detection with excellent sensitivity and selectivity. The present work not only provides a novel insight to design and prepare PL-MOFs with specific structures guided by reticular chemistry, but also indicates the universality of the in situ "one-pot" strategy to construct porous materials. [ABSTRACT FROM AUTHOR]

The field of carborane research has witnessed continuous development, leading to the construction and development of a diverse range of crystalline porous materials for various applications. Moreover, innovative synthetic approaches are expanding in this field. Since the first report of carborane-based crystalline porous materials (CCPMs) in 2007, the synthesis of carborane ligands, particularly through innovative methods, has consistently posed a significant challenge in discovering new structures of CCPMs. This paper provides a comprehensive summary of recent advances in various synthetic approaches for CCPMs, along with their applications in different domains. The primary challenges and future opportunities are expected to stimulate further multidisciplinary development in the field of CCPMs. [ABSTRACT FROM AUTHOR]

Resolving the detailed structures of metal organic frameworks is of great significance for understanding their structure-property relation. Real-space imaging methods could exhibit superiority in revealing not only the local structure but also the bulk symmetry of these complex porous materials, compared to reciprocal-space diffraction methods, despite the technical challenges. Here we apply a low-dose imaging technique to clearly resolve the atomic structures of building units in a metal-organic framework, MIL-125. An unexpected node structure is discovered by directly imaging the rotation of Ti-O nodes, different from the unrotated structure predicted by previous X-ray diffraction. The imaged structure and symmetry can be confirmed by the structural simulations and energy calculations. Then, the distribution of node rotation from the edge to the center of a MIL-125 particle is revealed by the image analysis of Ti-O rotation. The related defects and surface terminations in MIL-125 are also investigated in the real-space images. These results not only unraveled the node symmetry in MIL-125 with atomic resolution but also inspired further studies on discovering more unpredicted structural changes in other porous materials by real-space imaging methods. Resolving the structures of MOFs is significant for understanding their structure-property relation. Here, authors apply a low-dose imaging technique to resolve the atomic structures of building units in MOF MIL-125. A low-symmetry structure of MIL-125 is discovered by directly imaging the rotated Ti-O nodes, different from the unrotated one predicted in previous works. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks (MOFs), as novel porous crystalline materials with high porosity and a large specific surface area, have been increasingly utilized for CO2 adsorption. Machine learning (ML) combined with molecular simulations is used to identify MOFs with high CO2 adsorption capacity from millions of MOF structures. In this study, 23 structural and molecular features and 765 calculated features were proposed for the ML model and trained on a hypothetical MOF dataset for CO2 adsorption at different pressures. The calculated features improved the prediction accuracy of the ML model by 15%–20% and revealed its interpretability, consistent with the analysis of the interaction potential. Subsequently, the importance of the relevant features was ranked at different pressures. Regardless of the pressure, the molecular structure and pore size were the most critical factors. van der Waals force-related descriptors gained more competitive advantages at low pressures, whereas electrical-field-related descriptors gradually dominated at high pressures. Overall, this study provides a novel perspective to guide the initial high-throughput screening of MOFs as high-performance CO2 adsorption materials. [ABSTRACT FROM AUTHOR]

Artificial olfaction, also known as an electronic nose, is a gas identification device that replicates the human olfactory organ. This system integrates sensor arrays to detect gases, data acquisition for signal processing, and data analysis for precise identification, enabling it to assess gases both qualitatively and quantitatively in complex settings. This article provides a brief overview of the research progress in electronic nose technology, which is divided into three main elements, focusing on gas-sensitive materials, electronic nose applications, and data analysis methods. Furthermore, the review explores both traditional MOS materials and the newer porous materials like MOFs for gas sensors, summarizing the applications of electronic noses across diverse fields including disease diagnosis, environmental monitoring, food safety, and agricultural production. Additionally, it covers electronic nose pattern recognition and signal drift suppression algorithms. Ultimately, the summary identifies challenges faced by current systems and offers innovative solutions for future advancements. Overall, this endeavor forges a solid foundation and establishes a conceptual framework for ongoing research in the field. [ABSTRACT FROM AUTHOR]

Zeolites exhibit significant potential as porous materials for selective carbon dioxide (CO2) capture, leveraging their distinctive adsorption properties. However, the presence of moisture (H2O) and sulfur dioxide (SO2) in flue gas streams can significantly affect the efficiency of CO2 capture. This study investigates the CO2 adsorption characteristics of zeolites FAU 5A and LTA 13X, revealing the competitive adsorption mechanism between H2O(g), SO2, and CO2. The zeolites exhibit CO2 adsorption capacities of 93.19 mg/g and 95.80 mg/g for 5A and 13X, respectively, and demonstrate good regeneration potential. Metal cations correlated positively with CO2 adsorption. H2O(g), SO2, and CO2 exhibit a competitive adsorption relationship, with H2O(g) having the highest adsorption capacity, followed by SO2 and CO2. Additionally, the synergistic effect of SO2 and H2O(g) on CO2 adsorption is elucidated. These findings provide valuable insights into the competitive adsorption behavior of moisture and SO2 for CO2 capture using zeolites LTA 5A and FAU 13X, contributing to the development of more efficient CO2 capture processes and the design of tailored adsorbents for industrial applications. [ABSTRACT FROM AUTHOR]

Nanoporous materials, such as metal-organic frameworks (MOFs), are renowned for their high selectivity as gas adsorbents due to their specific surface area, nanoporosity, and active surface chemistry. A significant challenge for their widespread application is reduced gas uptake in wet conditions, attributed to competitive adsorption between gas and water. Recent studies of gas adsorption in wet materials have typically used small amounts of powdered porous materials (in the milligram range) within very small reactors (1–5 mL). This leaves a gap in knowledge about gas adsorption behaviors in larger reactors and with increased MOF sample sizes (to the gram scale). Additionally, there has been a notable absence of experimental research on MOFs heavily saturated with water. In this study, we aimed to fill the gaps in our understanding of gas adsorption in wet conditions by measuring CH4 adsorption in MOFs. To do this, we used larger MOF samples (in grams) and a large-volume reactor. Our selection of commercially available MOFs, including HKUST-1, ZIF-8, MOF-303, and activated carbon, was based on their widespread application, available previous research, and differences in hydrophobicity. Using a volumetric approach, we measured high-pressure isotherms (at T = 274.15 K) to compare the moles of gas adsorbed under both dry and wet conditions across different MOFs and weights. The experimental results indicate that water decreases total CH4 adsorption in MOFs, with a more pronounced decrease in hydrophilic MOFs compared to hydrophobic ones at lower pressures. However, hydrophilic MOFs exhibited stepped isotherms at higher pressures, suggesting water converts to hydrate, positively impacting total gas uptake. In contrast, the hydrophobic ZIF-8 did not promote hydrate formation due to particle aggregation in the presence of water, leading to a loss of surface area and surface charge. This study highlights the additional challenges associated with hydrate-MOF synergy when experiments are scaled up and larger sample sizes are used. Future studies should consider using monolith or pellet forms of MOFs to address the limitations of powdered MOFs in scale-up studies. [ABSTRACT FROM AUTHOR]

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In recent years, due to the rapid growth of mankind's demand for energy, harmful gases (SOx) produced by the combustion of sulfur-containing compounds in fuel oil have caused serious problems to the ecological environment and human health. Therefore, in order to solve this hidden danger from the source, countries around the world have created increasingly strict standards for the sulfur content in fuel. Adsorption desulfurization technology has attracted wide attention due to its advantages of energy saving and low operating cost. This paper reviewed the latest research progress on various porous adsorption materials. The future challenges and research directions of adsorption materials to meet the needs of clean fuels are proposed. [ABSTRACT FROM AUTHOR]

Access to clean drinking water is a basic requirement, and eliminating pollutants from wastewater is important for saving water ecosystems. The porous structure and surface characteristics of metal–organic frameworks (MOFs) can function as a perfect scaffold for removing toxic compounds from wastewater. Porphyrins are promising building blocks for constructing MOFs. Porphyrin-based metal–organic frameworks (P-MOFs) have been fabricated using porphyrin ligands, metal clusters, or ions. These materials can harvest light from a wide region of the solar spectrum, and their framework morphology and physicochemical properties can be controlled by changing their peripheral subunits or metal ions. These porous crystalline materials have generated interest because of their distinctive characteristics, including large permanent porosity, interesting surface morphology, broad conformational diversity, high photostability, and semiconducting nature. This article discusses the recent progress and usefulness of P-MOFs. The fabrication procedures of P-MOFs are discussed, followed by the adsorptive and photocatalytic removal of contaminants from wastewater. The relationships between the geometries of P-MOFs and their light-harvesting and charge-transfer mechanisms for the photocatalytic degradation of pollutants are highlighted. Finally, some future perspectives and obstacles in the photodegradation usage of P-MOFs are discussed, along with feasible research directions to standardize efficient photocatalysts for improved photodegradation for water treatment. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks (MOFs) are porous materials assembled using metal and organic linkers, showing a high specific surface area and a tunable pore size. Large portions of metal open sites in MOFs can be exposed to electrolyte ions, meaning they have high potential to be used as electrode materials in energy storage devices such as supercapacitors. Also, they can be easily converted into porous metal oxides by heat treatment. In this study, we obtained high energy storage performance by preparing electrode materials through applying heat treatment to manganese MOFs (Mn-MOFs) under air. The chemical and structural properties of synthesized and thermally treated Mn-MOFs were measured by Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). The surface area and porosity were investigated by nitrogen adsorption/desorption isotherms. The electrochemical properties were studied by cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) using a three-electrode cell. It was found that Mn-MOF electrodes that underwent heat treatment at 400 °C under air consisted of Mn2O3 with high specific surface area and porosity. They also showed a superior specific capacitance of 214.0 F g−1 and an energy density value of 29.7 Wh kg−1 (at 0.1 A g−1) compared to non-treated Mn-MOFs. [ABSTRACT FROM AUTHOR]

Unavoidably, the expansion of industry causes the release of numerous heavy metals, radionuclides, and organic pollutants into the environment. Due to these pollutants, the extremely toxic, highly carcinogenic chemicals provide a serious risk to people and aquatic life. Wastewater pollutants must be removed to safeguard the ecology. A huge specific surface area, multiple binding sites, a plethora of functional groups, variable pore size, and simplicity of surface modification are just a few advantages of porous materials. They are considered viable candidate materials for the efficient and selective removal of contaminants from aqueous solutions in a range of difficult circumstances due to their benefits. This work reviews the characteristics, methods of functionalization, and ways of modification of many novel porous materials in recent years. The use of these porous materials in the treatment of wastewater was examined. The development potential of porous materials is finally summed up. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks (MOFs) represent the largest class of materials among crystalline porous materials ever developed, and have attracted attention as core materials for separation technology. Their extremely uniform pore aperture and nearly unlimited structural and chemical characteristics have attracted great interest and promise for applying MOFs to adsorptive and membrane-based separations. This paper reviews the recent research into and development of MOF membranes for gas separation. Strategies for polycrystalline membranes and mixed-matrix membranes are discussed, with a focus on separation systems involving hydrocarbon separation, CO2 capture, and H2 purification. Challenges to and opportunities for the industrial deployment of MOF membranes are also discussed, providing guidance for the design and fabrication of future high-performance membranes. The contributions of the underlying mechanism to separation performance and adopted strategies and membrane-processing technologies for breaking the selectivity/permeability trade-off are discussed. [ABSTRACT FROM AUTHOR]

Due to their large surface area and pore volume, three-dimensional covalent organic frameworks (3D COFs) have emerged as competitive porous materials. However, structural dynamic behavior, often observed in imine-linked 3D COFs, could potentially unlock their potential application in gas storage. Herein, we showed how a pre-locked linker strategy introduces breaking dynamic behavior in 3D COFs. A predesigned planar linker-based 3,8-diamino-6-phenylphenanthridine (DPP) was prepared to produce non-dynamic 3D JUC-595, as the benzylideneamine moiety in DPP locked the linker flexibility and restricted the molecular bond rotation of the imine linkages. Upon solvent inclusion and release, the PXRD profile of JUC-595 remained intake, while JUC-594 with a flexible benzidine linker experienced crystal transformation due to framework contraction–expansion. As a result, the activated JUC-595 achieved higher surface areas (754 m2 g−1) than that of JUC-594 (548 m2 g−1). Furthermore, improved CO2 and CH4 storages were also seen in JUC-595 compared with JUC-594. Impressively, JUC-595 recorded a high normalized H2 storage capacity that surpassed other reported high-surface area 3D COFs. This works shows important insights on manipulating the structural properties of 3D COF to tune gas storage performance. [ABSTRACT FROM AUTHOR]

Cancer remains a major global health challenge, necessitating the development of innovative treatment strategies. This review focuses on the functionalization of porous nanoparticles for combination therapy, a promising approach to enhance cancer treatment efficacy while mitigating the limitations associated with conventional methods. Combination therapy, integrating multiple treatment modalities such as chemotherapy, phototherapy, immunotherapy, and others, has emerged as an effective strategy to address the shortcomings of individual treatments. The unique properties of mesoporous silica nanoparticles (MSN) and other porous materials, like nanoparticles coated with mesoporous silica (NP@MS), metal–organic frameworks (MOF), mesoporous platinum nanoparticles (mesoPt), and carbon dots (CDs), are being explored for drug solubility, bioavailability, targeted delivery, and controlled drug release. Recent advancements in the functionalization of mesoporous nanoparticles with ligands, biomaterials, and polymers are reviewed here, highlighting their role in enhancing the efficacy of combination therapy. Various research has demonstrated the effectiveness of these nanoparticles in co-delivering drugs and photosensitizers, achieving targeted delivery, and responding to multiple stimuli for controlled drug release. This review introduces the synthesis and functionalization methods of these porous nanoparticles, along with their applications in combination therapy. [ABSTRACT FROM AUTHOR]

Metal-organic frameworks (MOFs) are an incredibly diverse group of highly porous hybrid materials, which are interesting for a wide range of possible applications. For a meaningful theoretical description of many of their properties accurate and computationally highly efficient methods are in high demand. These would avoid compromises regarding either the quality of modelling results or the level of complexity of the calculated properties. With the advent of machine learning approaches, it is now possible to generate such approaches with relatively little human effort. Here, we build on existing types of machine-learned force fields belonging to the moment-tensor and kernel-based potential families to develop a recipe for their efficient parametrization. This yields exceptionally accurate and computationally highly efficient force fields. The parametrization relies on reference configurations generated during molecular dynamics based, active learning runs. The performance of the potentials is benchmarked for a representative selection of commonly studied MOFs revealing a close to DFT accuracy in predicting forces and structural parameters for a set of validation structures. The same applies to elastic constants and phonon band structures. Additionally, for MOF-5 the thermal conductivity is obtained with full quantitative agreement to single-crystal experiments. All this is possible while maintaining a very high degree of computational efficiency. The exceptional accuracy of the parameterized force field potentials combined with their computational efficiency has the potential of lifting the computational modelling of MOFs to the next level. [ABSTRACT FROM AUTHOR]

Metal-organic frameworks (MOFs) are a novel category of porous crystalline materials with an exceptionally high surface area and adjustable pore structure. They possess a designable composition and can be easily functionalized with different units. Porphyrins with conjugated tetrapyrrole macrocyclic structures can absorb light from ultraviolet to visible light regions, and their structures and properties can be facilely regulated by altering their peripheral groups or central metal ions. Porphyrin-based MOFs constructed from porphyrin ligands and metal nodes combine the unique features of porphyrins and MOFs as well as overcoming their respective limitations. This paper reviewed the design and construction, light absorption and charge transfer pathways, and strategy for improving the photocatalytic performance of porphyrin-based MOFs, and highlighted the recent progress in the field of CO2 reduction, hydrogen evolution, organic synthesis, organic pollutant removal, and nitrogen fixation. The intrinsic relationships between the structure and the property of porphyrin-based MOFs received special attention, especially the relationships between the arrangements of porphyrin ligands and metal nods and the charge transfer mechanism. We attempted to provide more valuable information for the design and construction of advanced photocatalysts in the future. Finally, the challenges and future perspectives of the porphyrin-based MOFs are also discussed. [ABSTRACT FROM AUTHOR]

Covalent organic frameworks (COFs) represent an important class of crystalline porous materials with designable structures and functions. The interconnected organic monomers, featuring pre-designed symmetries and connectivities, dictate the structures of COFs, endowing them with high thermal and chemical stability, large surface area, and tunable micropores. Furthermore, by utilizing pre-functionalization or post-synthetic functionalization strategies, COFs can acquire multifunctionalities, leading to their versatile applications in gas separation/storage, catalysis, and optoelectronic devices. Our review provides a comprehensive account of the latest advancements in the principles, methods, and techniques for structural design and determination of COFs. These cutting-edge approaches enable the rational design and precise elucidation of COF structures, addressing fundamental physicochemical challenges associated with host–guest interactions, topological transformations, network interpenetration, and defect-mediated catalysis. [ABSTRACT FROM AUTHOR]

The metal–organic framework (MOF) is a kind of porous material with lattice materials. Due to its large surface area and structural diversity, it has made great progress in the fields of batteries, capacitors, electrocatalysis, etc. Conductive MOF (c-MOF) increases the conductivity based on the original advantages of the MOF, which is more suitable for the development of batteries, capacitors, electrocatalysis, and other fields. This review summarizes the preparation of c-MOF and the research progress of conductive MOFs in the field of electrochemical energy storage and conversion. [ABSTRACT FROM AUTHOR]

Mismanagement of plastic waste results in its ubiquitous presence in the environment. Despite being durable and persistent materials, plastics are reduced by weathering phenomena into debris with a particle size down to nanometers. The fate and ecotoxicological effects of these solid micropollutants are not fully understood yet, but they are raising increasing concerns for the environment and people's health. Even if different current technologies have the potential to remove plastic particles, the efficiency of these processes is modest, especially for nanoparticles. Metal-organic frameworks (MOFs) are crystalline nano-porous materials with unique properties, have unique properties, such as strong coordination bonds, large and robustus porous structures, high accessible surface areas and adsorption capacity, which make them suitable adsorbent materials for micropollutants. This review examines the preliminary results reported in literature indicating that MOFs are promising adsorbents for the removal of plastic particles from water, especially when MOFs are integrated in porous composite materials or membranes, where they are able to assure high removal efficiency, superior water flux and antifouling properties, even in the presence of other dissolved co-pollutants. Moreover, a recent trend for the alternative preparation of MOFs starting from plastic waste, especially polyethylene terephthalate, as a sustainable source of organic linkers is also reviewed, as it represents a promising route for mitigating the impact of the costs deriving from the widescale MOFs production and application. This connubial between MOFs and plastic has the potential to contribute at implementing a more effective waste management and the circular economy principles in the polymer life cycle. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks (MOFs) and zeolitic imidazolate frameworks (ZIFs) are promising porous materials for adsorption and storage of greenhouse gases, especially CO2. In this study, guided by the CO2 phase diagram, we explore the adsorption behavior of solid CO2 loaded with ZIF-8 framework by heating the sample under high pressures, resulting in a drastic improvement in the CO2 uptake. The behavior of CO2 under simultaneous high temperature (T) and pressure (P) conditions is directly monitored by in situ FTIR spectroscopy. The remarkable enhancement in CO2 adsorption capability observed can be attributed to the synergetic effect of high T and P: high temperature greatly enhances the transport property of solid CO2 by facilitating its diffusion into the framework; high pressure effectively modifies the pore size and shape via changing the linker orientation and creating new adsorption sites within ZIF-8. Our study thus provides important new insights into the tunability and enhancement of CO2 adsorptive capability in MOFs/ZIFs using pressure and temperature combined as a synergetic approach. [ABSTRACT FROM AUTHOR]

The ordered porous frameworks like MOFs and COFs are generally constructed using the monomers through distinctive metal-coordinated and covalent linkages. Meanwhile, the inter-structural transition between each class of these porous materials is an under-explored research area. However, such altered frameworks are expected to have exciting features compared to their pristine versions. Herein, we have demonstrated a chemical-induction phase-engineering strategy to transform a two-dimensional conjugated Cu-based SA-MOF (Cu-Tp) into 2D-COFs (Cu-TpCOFs). The structural phase transition offered in-situ pore size engineering from 1.1 nm to 1.5–2.0 nm. Moreover, the Cu-TpCOFs showed uniform and low percentage-doped (~ 1–1.5%) metal distribution and improved crystallinity, porosity, and stability compared to the parent Cu-Tp MOF. The construction of a framework from another framework with new linkages opens interesting opportunities for phase-engineering. [ABSTRACT FROM AUTHOR]

Physisorption relying on crystalline porous materials offers prospective avenues for sustainable separation processes, greenhouse gas capture, and energy storage. However, the lack of end-to-end deep learning model for adsorption prediction confines the rapid and precise screen of crystalline porous materials. Here, we present DeepSorption, a spatial atom interaction learning network that realizes accurate, fast, and direct structure-adsorption prediction with only information of atomic coordinate and chemical element types. The breakthrough in prediction is attributed to the awareness of global structure and local spatial atom interactions endowed by the developed Matformer, which provides the intuitive visualization of atomic-level thinking and executing trajectory in crystalline porous materials prediction. Complete adsorption curves prediction could be performed using DeepSorption with a higher accuracy than Grand canonical Monte Carlo simulation and other machine learning models, a 20-35% decline in the mean absolute error compared to graph neural network CGCNN and machine learning models based on descriptors. Since the established direct associations between raw structure and target functions are based on the understanding of the fundamental chemistry of interatomic interactions, the deep learning network is rationally universal in predicting the different physicochemical properties of various crystalline materials. Accurate end-to-end deep learning models for adsorption prediction in porous materials would help its discovery. Here, the authors present DeepSorption, a spatial atom interaction learning network to predict structure-adsorption from atomic coordinates and chemical element types. [ABSTRACT FROM AUTHOR]

Metal-organic frameworks (MOFs) are among the most appealing porous materials with a wide range of surface chemistry, high pore structure, high specific surface area and various functionalities. They have found extensive use in a variety of industries. The handling and processing of their properties, however, continue to be quite difficult, which limits the use of MOFs. The most plentiful and environmentally friendly biopolymer in the world is cellulose, and by combining cellulose with MOFs, it is possible to create engineered materials with a variety of hitherto unachievable qualities. This is an excellent way to increase the usage of MOFs in functional materials. This review describes the synthesis of cellulose MOFs composites, mainly MOFs and cellulose compounded in aqueous solution, with two synthetic strategies: in-situ and ex-situ synthesis. By completing further post-processing procedures, the aqueous mixture of MOFs and cellulose can be further processed into four different types of composites, including powders, films, aerogels and hydrogels. We also highlight the use of MOF cellulose composites for antibacterial and drug delivery in nanomedicine. The primary present restrictions on MOF cellulose composites are also reviewed, as well as possible future research directions. [ABSTRACT FROM AUTHOR]

Methane and carbon dioxide are the main contributors to global warming, with the methane effect being 25 times more powerful than carbon dioxide. Although the sources of methane are diverse, it is a very volatile and explosive gas. One way to store the energy content of methane is through its conversion to methanol. Methanol is a liquid under ambient conditions, easy to transport, and, apart from its use as an energy source, it is a chemical platform that can serve as a starting material for the production of various higher-value products. Accordingly, the transformation of methane to methanol has been extensively studied in the literature, using traditional catalysts as different types of zeolites. However, in the last few years, a new generation of catalysts has emerged to carry out this transformation with higher conversion and selectivity, and more importantly, under mild temperature and pressure conditions. These new catalysts typically involve the use of a highly porous supporting material such as zeolite, or more recently, metal-organic frameworks (MOFs) and graphene, and metallic nanoparticles or a combination of different types of nanoparticles that are the core of the catalytic process. In this review, recent advances in the porous supports for nanoparticles used for methane oxidation to methanol under mild conditions are discussed. [ABSTRACT FROM AUTHOR]

As a flexible porous material, the amorphous behavior of zeolitic imidazolate framework‐8 (ZIF‐8) has garnered considerable interest. However, the association between its strain behavior and topology has not yet been exhaustively studied computationally. We perform molecular dynamic simulations on both ZIF‐8 and its topological silicate isomer sodalite (SOD) to investigate the pressure‐induced development of the mid‐ and short‐range structures. We find that both ZIF‐8 and SOD undergo two successive transformations. The first is the amorphization process, which is characterized by the breakdown of the mid‐range structure without a significant change in the elastic modulus. The other type of densification involves a change in the short‐range structure, during which the mechanical properties are improved as the short‐range disorder increases. [ABSTRACT FROM AUTHOR]

Over the past two decades, covalent organic frameworks (COFs) have become the most widely studied porous crystalline materials. Their specific physical and chemical properties are determined by the arrangement of atoms (crystal structure). Therefore, the determination of their structure is arguably the most important characterization step for COFs. Although single-crystal X-ray diffraction is the most widely used method for structure determination, confirmation of the structure of COFs is limited to lattice fringes in transmission electron microscopy (TEM) because of their small crystal size (nanocrystals) or poor crystal quality. At present, many two-dimensional COFs (2D-COFs) have clear powder X-ray diffraction (PXRD) patterns, but specific lattice fringes are not available for all 2D-COFs. This severely hinders the development of the COF field. Here, we discovered the lattice shrinkage behavior of COFs under electron beam irradiation by comparing the lattice fringes of 2D-COFs under different conditions. By comparing the lattice fringes of a 1,3,5-tris-(4-aminophenyl)triazine-1,3,5-tris-(4-formylphenyl)triazine covalent organic framework (TAPT-TFPT COF) at room temperature and under liquid nitrogen freezing conditions, we found that the lattice fringes are in good agreement with the PXRD and the theoretical values of the COF (2.213 nm) under freezing conditions. However, the lattice fringe spacing is only 1.656 nm at room temperature. The discovery not only provides new insights into the TEM characterization of COFs, but also further expands the range of crystalline COF materials. [ABSTRACT FROM AUTHOR]

The term "organic and inorganic composite porous materials" refers to metal–organic frameworks. Due to their low density and high porosity, MOFs have an enormous surface area that can be used to store and aggregate many molecules. The pore size may work as a grid to segregate molecules. Changing the materials' inherent characteristics is advantageous because MOFs are porous. Over the past 10 years, several hybrid MOFs containing polymer compounds, carbon-based substances, metal nanoparticles, metal oxides of metal, & biomolecules have been reported for use in various applications. Electronic components, detectors, storage of energy, separation of gases, capacitors, medication delivery, and environmental remediation have all been made using MOFs. The initial part of this review has been devoted to discussing the extraordinary qualities, distinctive architectural orientation, & contemporary uses of MOFs as well as their permeability, equilibrium, and additional determining elements. Additionally, several methods & processes used in the creation & development of MOFs are discussed, including solvothermal, electrochemical, mechanochemical, ultrasonication, & microwave approaches. Various approaches have been used to generate various dimensional MOFs like OD, 1D, etc. & their combined substances were additionally provided, in demand to comprehend the methodical viability of MOFs in generating novel goods. The opportunities for MOFs in the future, as well as the problems still to be solved, research gaps, and potential solutions, have all been discussed. These include the improved design of experiments, mathematical models, simulated approaches, and conceptual notions. [ABSTRACT FROM AUTHOR]

The development of novel sample preparation media plays a crucial role in pharmaceutical analysis. To facilitate the extraction and enrichment of pharmaceutical molecules in complex samples, various functionalized materials have been developed and prepared as adsorbents. Recently, some functionalized porous organic materials have become adsorbents for pharmaceutical analysis due to their unique properties of adsorption and recognition. These advanced porous organic materials, combined with consequent analytical techniques, have been successfully used for pharmaceutical analysis in complex samples such as environmental and biological samples. This review encapsulates the progress of advanced porous materials for pharmaceutical analysis including pesticides, antibiotics, chiral drugs, and other compounds in the past decade. In addition, we also address the limitations and future trends of these porous organic materials in pharmaceutical analysis. [ABSTRACT FROM AUTHOR]

Until reaching climate neutrality by attaining the EU 2050 level, the current levels of CO2 must be mitigated through the research and development of resilient technologies. This research explored potential approaches to lower CO2 emissions resulting from combustion fossil fuels in power plant furnaces. Different nanomaterials (MOFs versus silica nanoparticles) were used in this context to compare their effectiveness to mitigate GHG emissions. Porous materials known as metal–organic frameworks (MOFs) are frequently employed in sustainable CO2 management for selective adsorption and separation. Understanding the underlying mechanism is difficult due to their textural characteristics, the presence of functional groups and the variation in technological parameters (temperature and pressure) during CO2-selective adsorption. A silica-based nanomaterial was also employed in comparison. To systematically map CO2 adsorption as a function of the textural and compositional features of the nanomaterials and the process parameters set to a column-reactor system (CRS), 160 data points were collected for the current investigation. Different scenarios, as a function of P (bar) or as a function of T (K), were designed based on assumptions, 1 and 5 vs. 1–10 (bar) and 313.15 and 373.15 vs. 313.15–423.15 (K), where the regression analyses through Pearson coefficients of 0.92–0.95, coefficients of determination of 0.87–0.90 and p-values < 0.05, on predictive and on-site laboratory data, confirmed the performances of the CRS. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks (MOFs) are a class of crystalline porous materials with outstanding physical and chemical properties that make them suitable candidates in many fields, such as catalysis, sensing, energy production, and drug delivery. By combining MOFs with polymeric substrates, advanced functional materials are devised with excellent potential for biomedical applications. In this research, Zeolitic Imidazolate Framework 8 (ZIF-8), a zinc-based MOF, was selected together with cellulose, an almost inexhaustible polymeric raw material produced by nature, to prepare cellulose/ZIF-8 composite flat sheets via an in-situ growing single-step method in aqueous media. The composite materials were characterized by several techniques (IR, XRD, SEM, TGA, ICP, and BET) and their antibacterial activity as well as their biocompatibility in a mammalian model system were investigated. The cellulose/ZIF-8 samples remarkably inhibited the growth of Gram-positive and Gram-negative reference strains, and, notably, they proved to be effective against clinical isolates of Staphylococcus epidermidis and Pseudomonas aeruginosa presenting different antibiotic resistance profiles. As these pathogens are of primary importance in skin diseases and in the delayed healing of wounds, and the cellulose/ZIF-8 composites met the requirements of biological safety, the herein materials reveal a great potential for use as gauze pads in the management of wound infections. [ABSTRACT FROM AUTHOR]

Covalent Organic Frameworks (COFs) are a newly emerged class of porous materials consisting of organic building blocks linked by strong covalent bonds. The physical and chemical properties of COFs, i.e., modularity, porosity, well-developed specific surface area, crystallinity, and chemical-thermal stability, make them a good application material, especially in the aspects of adsorption and gas separation. The organic compositions of their building blocks also render them with biocompatible properties; therefore, they also have potential in biomedical applications. Depending on the symmetry of the building blocks, COF materials form two-dimensional (2D COF) or three-dimensional (3D COF) crystal structures. 3D COF structures have a higher specific surface area, they are much lighter due to their low density, and they have a larger volume than 2D COF crystals, but, unlike the latter, 3D COF crystals are less frequently obtained and studied. Selecting and obtaining suitable building blocks to form a stable 3D COF crystal structure is challenging and therefore of interest to the chemical community. Triptycene, due to its 3D structure, is a versatile building block for the synthesis of 3D COFs. Polymeric materials containing triptycene fragments show good thermal stability parameters and have a very well-developed surface area. They often tend to be characterized by more than one type of porosity and exhibit impressive gas adsorption properties. The introduction of a triptycene backbone into the structure of 3D COFs is a relatively new procedure, the results of which only began to be published in 2020. Triptycene-based 3D COFs show interesting physicochemical properties, i.e., high physical stability and high specific surface area. In addition, they have variable porosities with different pore diameters, capable of adsorbing both gases and large biological molecules. These promising parameters, guaranteed by the addition of a triptycene backbone to the 3D structure of COFs, may create new opportunities for the application of such materials in many industrial and biomedical areas. This review aims to draw attention to the symmetry of the building blocks used for COF synthesis. In particular, we discussed triptycene as a building block for the synthesis of 3D COFs and we present the latest results in this area. [ABSTRACT FROM AUTHOR]

Functionalizing porous materials with capping agents generates hybrid materials with enhanced properties, while the challenge is how to improve the selectivity and maintain the porosity of the parent framework. Herein, we developed a "Cage-on-MOF" strategy to tune the recognition and catalytic properties of MOFs without impairing their porosity. Two types of porous coordination cages (PCCs) of opposite charges containing secondary binding groups were developed to coordinatively functionalize two distinct porous MOFs, namely MOF@PCC nanocomposites. We demonstrated that the surface-capped PCCs can act as "modulators" to effectively tune the surface charge, stability, and adsorption behavior of different host MOF particles. More importantly, the MOF@PCCs can serve as selective heterogeneous catalysts for condensation reactions to achieve reversed product selectivity and excellent recyclability. This work sets the foundation for using molecular cages as porous surface-capping agents to functionalize and manipulate another porous material, without affecting the intrinsic properties of the parent framework. Functionalising porous materials is a route to enhancing properties of hybrid materials. Here authors present a "Cage-on-MOF" strategy to modify the surface of mesoporous MOFs by using molecular cages to achieve selective dyes adsorption behavior and heterogeneous catalysis. [ABSTRACT FROM AUTHOR]

Zeolitic imidazolate frameworks (ZIFs) are an important subclass of metal–organic frameworks (MOFs). Recently, we reported a new kind of MOF, namely tetrahedral imidazolate frameworks with auxiliary ligands (TIF-Ax), by adding linear ligands (Hint) into the zinc–imidazolate system. Introducing linear ligands into the M2+-imidazolate system overcomes the limitation of imidazole derivatives. Thanks to the synergistic effect of two different types of ligands, a series of new TIF-Ax with interesting topologies and a special pore environment has been reported, and they have attracted extensive attention in gas adsorption, separation, catalysis, heavy metal ion capture, and so on. In this review, we give a comprehensive overview of TIF-Ax, including their synthesis methods, structural diversity, and multi-field applications. Finally, we also discuss the challenges and perspectives of the rational design and syntheses of new TIF-Ax from the aspects of their composition, solvent, and template. This review provides deep insight into TIF-Ax and a reference for scholars with backgrounds of porous materials, gas separation, and catalysis. [ABSTRACT FROM AUTHOR]

Over the last ten years, there has been a growing interest in metal–organic frameworks (MOFs), which are a unique category of porous materials that combine organic and inorganic components. MOFs have garnered significant attention due to their highly favorable characteristics, such as environmentally friendly nature, enhanced surface area and pore volume, hierarchical arrangements, and adjustable properties, as well as their versatile applications in fields such as chemical engineering, materials science, and the environmental and biomedical sectors. This article centers on examining the advancements in using MOFs for environmental remediation purposes. Additionally, it discusses the latest developments in employing MOFs as potential tools for disease diagnosis and drug delivery across various ailments, including cancer, diabetes, neurological disorders, and ocular diseases. Firstly, a concise overview of MOF evolution and the synthetic techniques employed for creating MOFs are provided, presenting their advantages and limitations. Subsequently, the challenges, potential avenues, and perspectives for future advancements in the utilization of MOFs in the respective application domains are addressed. Lastly, a comprehensive comparison of the materials presently employed in these applications is conducted. [ABSTRACT FROM AUTHOR]

Nanoscopic materials have demonstrated a versatile role in almost every emerging field of research. Nanomaterials have come to be one of the most important fields of advanced research today due to its controllable particle size in the nanoscale range, capacity to adopt diverse forms and morphologies, high surface area, and involvement of transition and non-transition metals. With the introduction of porosity, nanomaterials have become a more promising candidate than their bulk counterparts in catalysis, biomedicine, drug delivery, and other areas. This review intends to compile a self-contained set of papers related to new synthesis methods and versatile applications of porous nanomaterials that can give a realistic picture of current state-of-the-art research, especially for catalysis and sensor area. Especially, we cover various surface functionalization strategies by improving accessibility and mass transfer limitation of catalytic applications for wide variety of materials, including organic and inorganic materials (metals/metal oxides) with covalent porous organic (COFs) and inorganic (silica/carbon) frameworks, constituting solid backgrounds on porous materials. [ABSTRACT FROM AUTHOR]