Recent advancement in metal–organic framework: Synthesis, activation, functionalisation, and bulk production

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Abstract

Metal–organic framework (MOF) is an emerging hybrid material that possesses high surface area, narrow pore size distribution, and tuneable functionality. In recent years, MOF-based materials have been widely studied in various applications such as gas storage, gas separation, heterogeneous catalysis, and drug delivery. However, less emphasis has been placed on the fundamentals of MOF that are crucial to provide scientific knowledge for tailoring MOFs with desirable properties for commercial applications. This review discusses recent advancement in the MOF chemistry, in particular, synthesis, activation, functionalisation, and bulk production of MOFs. This review will be of great interest to the researchers and chemists actively involved in the field of MOFs production.

Abbreviations: BBR: Building block replacement; BDC: 1,4-benzenedicarboxylate; BET: Brunauer–Emmett–Teller; BTC: 1,3,5-benzenetricarboxylate; B _oc: Tert-butoxycarbonyl; Bpy: 4,4’-bipyridine; CFG: Carboxylic functional group; CTAB: Cetyltrimethylammoniumbromide; DABCO: 1,4-diazabicyclo[2.2.2]octane; DEF: N, N-diethylformamide; DMF: N, N-dimethylformamide; Dhybdc: 2,5-dihydroxy-1,4-benzenedicarboxylate; [EMIm]Br: 1-ethyl-3-methylimidazolium bromide; FIR: Fujian Institute of Research; H ₂BDC: 1,4-benzenedicarboxylic acid; H ₃BTC: 1,3,5-benzenetricarboxylic acid; H ₄TBAPy: 1,3,6,8-tetrakis( p-benzoic acid)pyrene; HKUST: Hong-Kong University of Science and Technology; ICP-MS: Inductively coupled plasma mass spectrometry; ILAG: Ion- and liquid-assisted grinding; Im: Imidazole ; IPA: Isophthalate; IRMOF: Isoreticular metal–organic framework; IUPAC: International Union of Pure and Applied Chemistry; LAG: Liquid-assisted grinding; LBL: Layer-by-layer; LIB: Lithium-ion battery; mesoMOF: Mesoporous metal–organic framework; MeIm: 2-methyimidazole; MIL: Matériaux de l'Institut Lavoisier; MixMOF: Mixed-linker metal–organic framework; MOF: Metal–organic framework; MTBS: Methyltributylammoniummethylsulfate; NH ₂BTC: 2-aminobenzene-1,3,5-tricarboxylate; NOTT: University of Nottingham; NU: Northwestern University ; PCD: Protection-complexation-deprotection; PCN: Porous coordination network; PCP: Porous coordination polymer; PIM: Polymer of intrinsic microporosity; PSD: Post-synthetic deprotection; PSM: Post-synthetic modification; PXRD: Powder X-ray diffraction; PyCHO: 2-pyridinecarboxaldehyde; RH: Relative humidity; SALE: Solvent-assisted linker exchange; SALI: Solvent-assisted ligand incorporation; scCO ₂: Supercritical carbon dioxide; STEM: Scanning transmission electron microscopy; STY: Space–time yield; TBHP: tert-butyl hydroperoxide; TMU: Tarbiat Modares University; UiO: Universitetet i Oslo; ZIF: Zeolitic imidazolate framework

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The chemistry and applications of metal-organic frameworks.

Hiroyasu Furukawa, Kyle E. Cordova, Michael O'Keeffe … (2013)

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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Functional Porous Coordination Polymers

Susumu Kitagawa, Ryo Kitaura, Shin-ichiro Noro (2004)

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.