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      Hierarchical assemblies of molecular frameworks—MOF-on-MOF epitaxial heterostructures

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      Nano Research
      Springer Science and Business Media LLC

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          Abstract

          Functional, porous metal-organic frameworks (MOFs) have attracted much attention as a very flexible class of crystalline, porous materials. For more advanced applications that exploit photophysical properties, the fabrication of hierarchical assemblies, including the creation of MOF/MOF heterointerfaces, is important. For the manufacturing of superstructures with length scales well beyond that of the MOF pore size, layer-by-layer (lbl) methods are particularly attractive. These allow the isoreticular approach to be extended to superstructures with micrometer length scales, a range that is not accessible using conventional MOF design. The lbl approach further substantially extends the compositional diversity in MOFs. At the same time, the favorable elastic properties of MOFs allow for heteroepitaxial growth, even in the case of lattice misfits as large as 20%. While the MOF-on-MOF approach to designing multicomponent superstructures with synergistic multifunctionality can also be realized with sophisticated solvothermal synthesis schemes, the lbl (or liquid-phase epitaxy) approach carries substantial advantages, in particular when it comes to the integration of such MOF superstructures into optical or electronic devices. While the structure vertical to the substrate can be adjusted using the lbl method, photolithographic methods can be used for lateral structuring. In this review, we will discuss the lbl liquid-phase epitaxy approach to growing surface-anchored MOF thins films (SURMOFs) as well as other relevant one-pot synthesis methods for constructing such hierarchically designed structures and their emerging applications.

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          Functional Porous Coordination Polymers

          The chemistry of the coordination polymers has in recent years advanced extensively, affording various architectures, which are constructed from a variety of molecular building blocks with different interactions between them. The next challenge is the chemical and physical functionalization of these architectures, through the porous properties of the frameworks. This review concentrates on three aspects of coordination polymers: 1). the use of crystal engineering to construct porous frameworks from connectors and linkers ("nanospace engineering"), 2). characterizing and cataloging the porous properties by functions for storage, exchange, separation, etc., and 3). the next generation of porous functions based on dynamic crystal transformations caused by guest molecules or physical stimuli. Our aim is to present the state of the art chemistry and physics of and in the micropores of porous coordination polymers.
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            Systematic design of pore size and functionality in isoreticular MOFs and their application in methane storage.

            A strategy based on reticulating metal ions and organic carboxylate links into extended networks has been advanced to a point that allowed the design of porous structures in which pore size and functionality could be varied systematically. Metal-organic framework (MOF-5), a prototype of a new class of porous materials and one that is constructed from octahedral Zn-O-C clusters and benzene links, was used to demonstrate that its three-dimensional porous system can be functionalized with the organic groups -Br, -NH2, -OC3H7, -OC5H11, -C2H4, and -C4H4 and that its pore size can be expanded with the long molecular struts biphenyl, tetrahydropyrene, pyrene, and terphenyl. We synthesized an isoreticular series (one that has the same framework topology) of 16 highly crystalline materials whose open space represented up to 91.1% of the crystal volume, as well as homogeneous periodic pores that can be incrementally varied from 3.8 to 28.8 angstroms. One member of this series exhibited a high capacity for methane storage (240 cubic centimeters at standard temperature and pressure per gram at 36 atmospheres and ambient temperature), and others the lowest densities (0.41 to 0.21 gram per cubic centimeter) for a crystalline material at room temperature.
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              Metal-organic frameworks: functional luminescent and photonic materials for sensing applications.

              Metal-organic frameworks (MOFs) or porous coordination polymers (PCPs) are open, crystalline supramolecular coordination architectures with porous facets. These chemically tailorable framework materials are the subject of intense and expansive research, and are particularly relevant in the fields of sensory materials and device engineering. As the subfield of MOF-based sensing has developed, many diverse chemical functionalities have been carefully and rationally implanted into the coordination nanospace of MOF materials. MOFs with widely varied fluorometric sensing properties have been developed using the design principles of crystal engineering and structure-property correlations, resulting in a large and rapidly growing body of literature. This work has led to advancements in a number of crucial sensing domains, including biomolecules, environmental toxins, explosives, ionic species, and many others. Furthermore, new classes of MOF sensory materials utilizing advanced signal transduction by devices based on MOF photonic crystals and thin films have been developed. This comprehensive review summarizes the topical developments in the field of luminescent MOF and MOF-based photonic crystals/thin film sensory materials.
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                Author and article information

                Journal
                Nano Research
                Nano Res.
                Springer Science and Business Media LLC
                1998-0124
                1998-0000
                February 2021
                July 20 2020
                February 2021
                : 14
                : 2
                : 355-368
                Article
                10.1007/s12274-020-2953-z
                43233950-d783-4df5-bd5f-44c0a8903639
                © 2021

                https://creativecommons.org/licenses/by/4.0

                https://creativecommons.org/licenses/by/4.0

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