Reticular Design Research Articles

Encoding ordered structural complexity to covalent organic frameworks

Installing different chemical entities onto crystalline frameworks with well-defined spatial distributions represents a viable approach to achieve ordered and complex synthetic materials. Herein, a covalent organic framework (COF-305) is constructed from tetrakis(4-aminophenyl)methane and 2,3-dimethoxyterephthalaldehyde, which has the largest unit cell and asymmetric unit among known COFs. The ordered complexity of COF-305 is embodied by nine different stereoisomers of its constituents showing specific sequences on topologically equivalent sites, which can be attributed to its building blocks deviating from their intrinsically preferred simple packing geometries in their molecular crystals to adapt to the framework formation. The insight provided by COF-305 supplements the principle of covalent reticular design from the perspective of non-covalent interactions and opens opportunities for pursuing complex chemical sequences in molecular frameworks.

Reticular design and alkyne bridge engineering in donor–π–acceptor type conjugated microporous polymers for boosting photocatalytic hydrogen evolution

Through the successful application of Suzuki and Sonogashira coupling reactions, we have synthesized Py–TPA and Py–TB–TPA CMPs, demonstrating impressive hydrogen evolution rates (HER) of 3633 and 16 700 μmol g−1 h−1, respectively.

Insight into the Isoreticularity of Li-MOFs for the Design of Low-Density Solid and Quasi-Solid Electrolytes.

Isoreticularity in metal organic frameworks (MOFs) allows the design of the framework structure and tailoring the pore aperture at the molecular level. The optimal pore volume, long-range order of framework expansion, and crystallite size (grain size) could enable improving Li-ion conduction, thereby providing a unique opportunity to design high-performance solid and quasi-solid electrolytes. However, definitive understanding of the pore aperture, framework expansion, and crystallite size on the Li-ion conduction and its mechanism in MOFs remains at the exploratory stage. Among the different MOF subfamilies, Li-MOFs created by the isoreticular framework expansion using dicarboxylates of benzene, naphthalene, and biphenyl building blocks emerge as low-density porous solids with exceptional thermal stability to study the solid-state Li+ transport mechanisms. Herein, we report the subtle effect of the isoreticularity in Li-MOFs on the performance of solid and quasi-solid-state Li+ conduction, providing new insight into Li+ transport mechanisms in MOFs for the first time. Our experimental and computational results show that the reticular design on an isostructural extended framework structure with the optimal pore aperture and crystallite size can influence the Li+ conductivity, exhibiting comparable ionic conductivities to solid polymer electrolytes at room temperature. Aligning with the computational studies, our experimental absorption spectral traces of solid electrolytes prepared by encapsulating lithium salt (LiClO4) and the plasticizer (ethylene carbonate) with Li-MOFs confirm the participation of the free and bound states of Li+ in a pore filling-driven ion conduction mechanism. We postulate that porous channels of Li-MOFs aid free Li+ to move through the pores via a vehicle-type mechanism, in which the pore-filled plasticizer acts as a carrier for mobile Li+ while the framework's functional sites transport the bound state of Li+ via an ion hopping mechanism from one crystallite site to another. Our computational studies performed on the Li+ conduction pathway validated the postulated pore filling mechanism and confirmed the involvement of bridging complexes, formed by binding Li+ onto the framework's functional sites as well as to the pore-filled ethylene carbonates. The Li+ diffusion energy barrier profiles along with the respective conformational changes during the diffusion of Li+ in solid electrolytes prepared from Li-BDC MOF and Li-NDC MOF strongly support the cooperative movement of Li+ ions via ion hopping along the framework's edges and vehicle-type transfer, involving the pore-filled plasticizer. Our findings suggest that cooperative function of the optimal pore volume, framework expansion, and crystallite size play a unique role in Li-ion conduction, thereby providing design guidelines for the low-density solid and quasi-solid electrolytes.

Intrinsic disorder in metal–organic frameworks: an untapped resource for reticular design

Intrinsic disorder in metal–organic frameworks: an untapped resource for reticular design

Monolithic Titanium Alkoxide Networks for Lithium-Ion Conductive All-Solid-State Electrolytes.

Reticular chemistry provides opportunities to design solid-state electrolytes (SSEs) with modular tunability. However, SSEs based on modularly designed crystalline metal-organic frameworks (MOFs) often require liquid electrolytes for interfacial contact. Monolithic glassy MOFs can have liquid processability and uniform lithium conduction, which is promising for the reticular design of SSE without liquid electrolytes. Here, we develop a generalizable strategy for the modular design of noncrystalline SSEs based on a bottom-up synthesis of glassy MOFs. We demonstrate such a strategy by linking polyethylene glycol (PEG) struts and nanosized titanium-oxo clusters into network structures termed titanium alkoxide networks (TANs). The modular design allows the incorporation of PEG linkers with different molecular weights, which give optimal chain flexibility for high ionic conductivity, and the reticular coordinative network provides a controlled degree of cross-linking that gives adequate mechanical strength. This research shows the power of reticular design in noncrystalline molecular framework materials for SSEs.

Reticular Design of Precise Linker Installation into a Zirconium Metal–Organic Framework to Reinforce Hydrolytic Stability

Reticular chemistry allows for the rational assembly of metal-organic frameworks (MOFs) with designed structures and desirable functionalities for advanced applications. However, it remains challenging to construct multi-component MOFs with unprecedented complexity and control through insertion of secondary or ternary linkers. Herein, we demonstrate that a Zr-based MOF, NU-600 with a (4,6)-connected she topology, has been judiciously selected to employ a linker installation strategy to precisely insert two linear linkers with different lengths into two crystallographically distinct pockets in a one-pot, de novo reaction. We reveal that the hydrolytic stability of these linker-inserted MOFs can be remarkably reinforced by increasing the Zr6 node connectivity, while maintaining comparable water uptake capacity and pore-filling pressure as the pristine NU-600. Furthermore, introducing hydrophilic -OH groups into the linear linker backbones to construct multivariate MOFs can effectively shift the pore-filling step to lower partial pressures. This methodology demonstrates a powerful strategy to reinforce the structural stability of other MOF frameworks by increasing the connectivity of metal nodes, capable of encouraging developments in fundamental sciences and practical applications.

Water Sorption Evolution Enabled by Reticular Construction of Zirconium Metal-Organic Frameworks Based on a Unique [2.2]Paracyclophane Scaffold.

Water vapor sorption by metal-organic frameworks (MOFs) has gathered significant interest because of its prominent potential in many applications such as moisture harvesting, dehumidification, heat pump regulation, and hydrolysis catalysis. However, the reticular design and exploration of robust and high-performing Zr-MOFs for such purposes remains a sought-after endeavor. In this work, we present the deployment of reticular chemistry to target a series of robust Zr-MOFs based on a unique [2.2]paracyclophane (PCP) scaffold. The ease of functionalization of PCP enables the desired synthesis of three carboxylate linkers, one ditopic and two tetratopic, which further assemble into a total of five Zr-MOFs with distinct topological structures, i.e., a new 2D net (NU-700), fcu (NU-405), flu (NU-1800), she (NU-602), scu (NU-913). Notably, the water vapor sorption performances of all the Zr-MOFs are highly dependent on their framework topology and pore metric, in which NU-602 and NU-913 with uniform 1D channels exhibit S-shaped water sorption isotherms with a steep pore-filling step and high uptake capacities of 0.72 g g-1 at 70% relative humidity (RH) and 0.88 g g-1 at 60% RH, respectively. Moreover, NU-913 displays exceptionally high working capacity of 0.72 g g-1 in the range of 40-60% RH. Additionally, we demonstrate that the hydrolytic stability and water adsorption-desorption recyclability of NU-913 can be remarkably improved by capping the Zr6 nodes with the more hydrophobic agent, trifluoroacetic acid, making it a potential candidate for water sorption-based applications.

The Current Status of MOF and COF Applications.

The amalgamation of different disciplines is at the heart of reticular chemistry and has broadened the boundaries of chemistry by opening up an infinite space of chemical composition, structure, and material properties. Reticular design has enabled the precise prediction of crystalline framework structures, tunability of chemical composition, incorporation of various functionalities onto the framework backbone, and as a consequence, fine-tuning of metal-organic framework (MOF) and covalent organic framework (COF) properties beyond that of any other material class. Leveraging the unique properties of reticular materials has resulted in significant advances from both a fundamental and an applied perspective. Here, we wish to review the milestones in MOF and COF research and give a critical view on progress in their real-world applications. Finally, we briefly discuss the major challenges in the field that need to be addressed to pave the way for industrial applications.

Reticular design and crystal structure determination of covalent organic frameworks.

Reticular chemistry of covalent organic frameworks (COFs) deals with the linking of discrete organic molecular building units into extended structures adopting various topologies by strong covalent bonds. The past decade has witnessed a rapid development of COF chemistry in terms of both structural diversity and applications. From the structural perspective, irrespective of our subject of concern with regard to COFs, it is inevitable to take into account the structural aspects of COFs in all dimensions from 1D ribbons to 3D frameworks, for which understanding the concepts of reticular chemistry, based mainly on ‘reticular design’, will seemingly lead to unlimited ways of exploring the exquisiteness of this advanced class of porous, extended, and crystalline materials. A comprehensive discussion and understanding of reticular design, therefore, is of paramount importance so that everyone willing to research on COFs can interpret well and chemically correlate the geometrical structures of this subset of reticular materials and their practical applications. This article lies at the heart of using the conceptual basis of reticular chemistry for designing, modeling, and determination of novel infinite and crystalline structures. Especially, the structure determinations are described by means of chronological advances of discoveries and development of COFs whereby their crystal structures are elucidated by modeling through the topological approach, 3D electron diffraction, single-crystal X-ray diffraction, and powder X-ray diffraction techniques.

Thiazolo[5,4‐d]thiazole‐Based Donor–Acceptor Covalent Organic Framework for Sunlight‐Driven Hydrogen Evolution

Abstract2D covalent organic frameworks (COFs) could have well‐defined arrangements of photo‐ and electro‐active units that serve as electron or hole transport channels for solar energy harvesting and conversion, but their insufficient charge transfer and rapid charge recombination impede the sunlight‐driven photocatalytic performance. We report a new donor–acceptor (D–A) system, PyTz‐COF that was constructed from the electron‐rich pyrene (Py) and electron‐deficient thiazolo[5,4‐d]thiazole (Tz). With its bicontinuous heterojunction, PyTz‐COF demonstrated exceptional optoelectronic properties, photocatalytic ability in superoxide anion radical‐mediated coupling of (arylmethyl)amines and photoelectrochemical activity in sunlight‐driven hydrogen evolution. Remarkably, PyTz‐COF exhibited a photocurrent up to 100 μA cm−2 at 0.2 V vs. RHE and could reach a hydrogen evolution rate of 2072.4 μmol g−1 h−1. This work is paving the way for reticular design of highly efficient and highly active D–A systems for solar energy harvesting and conversion.

Thiazolo[5,4-d]thiazole-Based Donor-Acceptor Covalent Organic Framework for Sunlight-Driven Hydrogen Evolution.

2D covalent organic frameworks (COFs) could have well-defined arrangements of photo- and electro-active units that serve as electron or hole transport channels for solar energy harvesting and conversion, but their insufficient charge transfer and rapid charge recombination impede the sunlight-driven photocatalytic performance. We report a new donor-acceptor (D-A) system, PyTz-COF that was constructed from the electron-rich pyrene (Py) and electron-deficient thiazolo[5,4-d]thiazole (Tz). With its bicontinuous heterojunction, PyTz-COF demonstrated exceptional optoelectronic properties, photocatalytic ability in superoxide anion radical-mediated coupling of (arylmethyl)amines and photoelectrochemical activity in sunlight-driven hydrogen evolution. Remarkably, PyTz-COF exhibited a photocurrent up to 100 μA cm-2 at 0.2 V vs. RHE and could reach a hydrogen evolution rate of 2072.4 μmol g-1 h-1 . This work is paving the way for reticular design of highly efficient and highly active D-A systems for solar energy harvesting and conversion.

Reticular exploration of uranium-based metal—organic frameworks with hexacarboxylate building units

The rational reticular design of metal—organic frameworks (MOFs) from building units of known geometries is essential for enriching the diversity of MOF structures. Unexpected and intriguing structures, however, can also arise from subtle changes in the rigidity/length of organic linkers and/or synthetic conditions. Herein, we report three uranium-based MOF structures—i.e., NU-135X (X = 0, 1, 2)—synthesized from trigonal planar uranyl nodes and triptycene-based hexacarboxylate ligands with variable arm lengths. A new chiral 3,6-connected nuc net was observed in NU-1350, while the extended versions of the ligand led to 3-fold catenated MOFs (NU-1351 and NU-1352) with rare 3,6-connected cml-c3 nets. The differences in the topology of NU-1350 and NU-1351/NU-1352 could be attributed to the slight distortions of the shorter linker in the former from the ideal trigonal prism geometry to an octahedral geometry when coordinated to the trigonal planar uranyl nodes.

Surface-confined single-layer covalent organic frameworks: design, synthesis and application

Two-dimensional (2D) nanomaterials, such as graphene and single layer covalent organic frameworks (sCOFs) are being widely studied due to their unusual structure/property relationships. sCOFs typically feature atomic thickness, intrinsic nanoscale porosity and a crystalline lattice. Compared to other organic 2D materials, sCOFs exhibit major advantages including topological designation and constitutional tunability. This review describes the state of the art of surface-confined sCOFs, emphasizing reticular design, synthesis approaches, and key challenges related to improving quality and exploring applications.

Advances in ligand-unsupported argentophilic interactions in crystal engineering: an emerging platform for supramolecular architectures

Ligand-unsupported argentophilic interactions are described, emphasizing reticular design and recent developments in advanced synthetic strategies, and highlighting diverse interactions that are useful for the construction of unmitigated networks.

Exfoliation of Covalent Organic Frameworks into Few-Layer Redox-Active Nanosheets as Cathode Materials for Lithium-Ion Batteries.

Covalent organic frameworks (COFs) have attracted growing interest by virtue of their structural diversity and tunability. Herein, we present a novel approach for the development of organic rechargeable battery cathodes in which three distinct redox-active COFs were successfully prepared and delaminated into 2D few-layer nanosheets. Compared with the pristine COFs, the exfoliated COFs with shorter Li+ diffusion pathways allow a significant higher utilization efficiency of redox sites and faster kinetics for lithium storage. Unlike diffusion-controlled manners in the bulk COFs, the redox reactions in ECOFs are mainly dominated by charge transfer process. The capacity and potential are further engineered by reticular design of COFs without altering the underlying topology. Specifically, DAAQ-ECOF exhibits excellent rechargeability (98% capacity retention after 1800 cycles) and fast charge-discharge ability (74% retention at 500 mA g-1 as compared to at 20 mA g-1). DABQ-ECOF shows a specific capacity of 210 mA h g-1 and a voltage plateau of 2.8 V.

Tardigrades from Nahuel Huapi National Park (Argentina, South America) with descriptions of two new Macrobiotidae species.

In 31 samples of mosses and lichens collected in the Argentinean province of Río Negro, 657 tardigrades, 53 exuviae and 219 free-laid eggs were found. In total, 20 species were identified: Diphascon chilenense, Dip. mitrense, Echiniscus bigranulatus, Ech. corrugicaudatus, Ech. merokensis merokensis, Ech. testudo, Hebesuncus mollispinus, Hypsibius convergens, Macrobiotus cf. anderssoni, Mac. andinus, Mac. kazmierskii, Mac. patagonicus, Mesobiotus szeptyckii, Mes. pseudoblocki sp. nov., Milnesium argentinum, Mil. beatae, Mil. brachyungue, Mil. granulatum, Mopsechiniscus granulosus, Minibiotus pseudostellarus sp. nov. Of the two new species, Mesobiotus pseudoblocki sp. nov. is most similar to Mes. blocki, but it differs mainly by the lack of dentate lunules, smaller eggs and presence of reticular design on egg processes. Minibiotus pseudostellarus sp. nov. is most similar to Min. constellatus, Min. eichhorni, Min. sidereus or Min. vinciguerrae, but it differs from them by the presence of 'pseudo-star'-shaped pores in the dorsal cuticle instead of fully developed 'stars' and by other morphometric characters.

Experimental and Simulation Study of Complex Structure Well Pattern Optimization for Buried Hill Fractured Reservoirs

The use of a vertical well pattern results in productivity deficiency and poor development effect when developing buried hill reservoirs with complex properties. In this work, experiments are conducted to determine the best pattern for complex structure wells in buried hill reservoirs. Discretization is employed in an experimental method that uses unit cubic rocks with a size of 5 cm × 5 cm × 5 cm. The rocks are bonded in a spotty or reticular design to form a macroscopic model. Based on water flooding similarity criteria of fractured reservoir, an experimental model similar to a quarter of a five-spot unit in an actual reservoir is designed and manufactured. By selectively plugging wells in the model, various well patterns are established. Simulation results indicate that the vertical–vertical well pattern exhibits the fastest water breakthrough, fastest increase in water cut, and lowest recovery under the same pressure difference and well spacing. The horizontal–horizontal well pattern has the slowest water cut increase and the highest final oil recovery. For fishbone wells, this pattern facilitates an ideal development effect when the percolation direction is perpendicular to the plane determined by the mother bore and branch. When liquid rate, water cut, and recovery are considered, the horizontal–horizontal well pattern is recommended when conditions allow.

ChemInform Abstract: Fascinating Chemistry or Frustrating Unpredictability: Observations in Crystal Engineering of Metal‐Organic Frameworks

AbstractReview: 87 refs.

Fascinating chemistry or frustrating unpredictability: observations in crystal engineering of metal–organic frameworks

Reticular design is a highly attractive concept, but coordination chemistry around the tectonic units of metal–organic frameworks (MOFs) and additional interplay with anionic and solvent species provide for dazzling complexity that effectively rules out structure prediction. We can however study the chemistry around pre-existing clusters, and assemble novel materials correspondingly, using a priori information about the connectivity of an investigated metal cluster. Studies, often spectroscopic of nature, have in recent years solved many puzzles in MOF crystallization. The obtained knowledge opens new doors in crystal engineering, but more research on MOF coordination chemistry has to be carried out.

ChemInform Abstract: Covalent Organic Frameworks

AbstractReview: 64 refs.