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The Chemistry and Applications of Metal-Organic Frameworks

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TLDR
Metal-organic frameworks are porous materials that have potential for applications such as gas storage and separation, as well as catalysis, and methods are being developed for making nanocrystals and supercrystals of MOFs for their incorporation into devices.
Abstract
Crystalline metal-organic frameworks (MOFs) are formed by reticular synthesis, which creates strong bonds between inorganic and organic units. Careful selection of MOF constituents can yield crystals of ultrahigh porosity and high thermal and chemical stability. These characteristics allow the interior of MOFs to be chemically altered for use in gas separation, gas storage, and catalysis, among other applications. The precision commonly exercised in their chemical modification and the ability to expand their metrics without changing the underlying topology have not been achieved with other solids. MOFs whose chemical composition and shape of building units can be multiply varied within a particular structure already exist and may lead to materials that offer a synergistic combination of properties.

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Citations
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Journal ArticleDOI

In Situ Fabrication of Highly Luminescent Bifunctional Amino Acid Crosslinked 2D/3D NH3C4H9COO(CH3NH3PbBr3)n Perovskite Films

TL;DR: In this article, a crosslinked 2D/3D NH3C4H9COO(CH3NH3) nPbnBr3n perovskite planar films with controllable quantum confine via bifunctional amino acid crosslinkage is reported.
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When CuAAC 'Click Chemistry' goes heterogeneous

TL;DR: In this article, the authors present a review of various reliable heterogeneous methods, alternative to the commonly used Meldal-Sharpless method for click chemistry, including those involving flow chemistry, and that they could be applied to a variety of compounds, solving some problems faced by more conventional methods.
Journal ArticleDOI

Metal-Organic Framework Membranes: Recent Development in the Synthesis Strategies and their Application in Oil-Water Separation

TL;DR: In this article, the authors classified the synthesis strategies of pure MOF membranes and MOF-based mixed matrix membranes and provided theoretical basis and technical guidance for realizing the large-scale application of MOF membrane in the field of oil-water separation.
Journal ArticleDOI

Robust Metal-Triazolate Frameworks for CO2 Capture from Flue Gas.

TL;DR: The best performing MOF in this series features low regeneration energy, high CO2 capture utility under hu-mid conditions, and decent cycling performance for mimic flue gas.
Journal ArticleDOI

Engineering of Pore Geometry for Ultrahigh Capacity Methane Storage in Mesoporous Metal–Organic Frameworks

TL;DR: It is illustrated that the fine-tuned mesoporosity is critical in further improving the deliverable capacities at ultrahigh pressure.
References
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Journal ArticleDOI

Reticular synthesis and the design of new materials

TL;DR: This work has shown that highly porous frameworks held together by strong metal–oxygen–carbon bonds and with exceptionally large surface area and capacity for gas storage have been prepared and their pore metrics systematically varied and functionalized.
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Metal–organic framework materials as catalysts

TL;DR: A critical review of the emerging field of MOF-based catalysis is presented and examples of catalysis by homogeneous catalysts incorporated as framework struts or cavity modifiers are presented.
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Systematic Design of Pore Size and Functionality in Isoreticular MOFs and Their Application in Methane Storage

TL;DR: 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 and can be expanded with the long molecular struts biphenyl, tetrahydropyrene, pyrene, and terphenyl.
Journal ArticleDOI

Design and synthesis of an exceptionally stable and highly porous metal-organic framework

TL;DR: In this article, an organic dicarboxylate linker is used in a reaction that gives supertetrahedron clusters when capped with monocarboxyates.
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