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donglijieÒø³æ (³õÈëÎÄ̳)
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Conventional and Unconventional MetalOrganic Frameworks Based
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The class of materials known as metalorganic frameworks, or MOFs, is the subject of an enormous amount of current research. The other reviews in this issue serve as testament to this fact. The defining character of these compounds is their porosity, which can be tuned by changing the geometry and size of the carboxylic acid ligands. In the early years of this research, carboxylate-based MOFs were designed to have ever-greater surface areas, resulting in the astonishing increase from 600 to >5000 m2/g.16 In addition, interest was keyed toward very large uptake of certain gases such as hydrogen, methane, and carbon dioxide and the possibility of a range of potential gas separations. The number of reported MOFs has skyrocketed as researchers have explored the vast number of possible combinations of ligand design, transition metals, coligands, and structuredirecting agents. Many investigators were fascinated by the idea that one could use a set of principles to define structures that would be porous. However, although many papers claim to have created porous products, the structural data is insufficient. One must have a sorption isotherm to prove the extent of porosity. Carboxylate-based MOFs have been shown to have remarkably high surface area and uniform pore size distribution, but their lack of stability in air and water poses a significant problem if they are to be used in industrial or commercial applications. Divalent metal carboxylates are subject to hydrolysis and usuallyquite soluble in acid solution. It should be pointed out that other types of MOFs, such as those based on pyrazolate ligands, can be much more robust.7 Phosphonates form stronger bonds than carboxylates do with metal atoms, so it is natural that investigators should try to prepare phosphonate-based MOFs. From our own experience, monovalent metal phosphonates are highly soluble, even though they may crystallize as supramolecular structures. As the valence of the metal increases, the solubility decreases. Divalent metal phosphonates are soluble enough that single crystals can be obtained by hydrothermal or solvothermal techniques, whereas trivalent and tetravalent metal phosphonates are rarely crystalline as they are highly insoluble and tend to precipitate as poorly ordered layered materials. The tetravalent metal phosphonates are insoluble even in strong acid solution. Phosphonates have three oxygen atoms capable of bonding to metals. They can also coordinate metals when they are in any state of protonation. This results in many possible modes of cocoordination and myriad different arrangements that the structures can take, many of which are not porous and therefore not MOFs. The majority of metal phosphonate compounds are not MOFs, and although there are a number of instances where phosphonate- based MOFs have been prepared, they were generally not by design. The interested reader is directed to a recently released book for more information. |
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