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      Removal and safe reuse of highly toxic allyl alcohol using a highly selective photo-sensitive metal–organic framework

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          Abstract

          By means of a MOF platform and photo-assistant adsorption technique, the removal and reuse of highly toxic allyl alcohol can be achieved. This is mainly based on a reversible asymmetric [2 + 2] cycloaddition inside a MOF.

          Abstract

          Herein, we report a facile and green approach to remove, convert and even release highly toxic allyl alcohol inside a MOF. The MOF used here, namely ECIT-20, barely adsorbs allyl alcohol under ambient conditions, whereas a sharp increase up to 90 mg g −1 (1.03 mol mol −1) under UV (297 nm) irradiation is observed, giving an ultra-big photo-switching behavior of more than 19 times. Thermogravimetric analysis, infrared spectroscopy, and 1H MAS plus 13C CPMAS solid-state NMR spectroscopy showed that a host–guest photochemical [2 + 2] reaction followed by the formation of asymmetric cyclobutanes is responsible for this unique photo-switching behavior towards allyl alcohol. The final conversion capability by means of ECIT-20 from allyl alcohol to asymmetric cyclobutanes is estimated to be 0.5 mol mol −1, which agrees well with both the structural features and the results from density functional theory (DFT) calculations. Moreover, the reuse of this MOF material is also facile and even after four cycles, excellent photo-switching performance towards allyl alcohol could be well maintained. This indicates that the highly promising material of ECIT-20 is suitable for the green removal and safe reuse of highly toxic allyl alcohol.

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          Most cited references42

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          Cooperative insertion of CO2 in diamine-appended metal-organic frameworks.

          The process of carbon capture and sequestration has been proposed as a method of mitigating the build-up of greenhouse gases in the atmosphere. If implemented, the cost of electricity generated by a fossil fuel-burning power plant would rise substantially, owing to the expense of removing CO2 from the effluent stream. There is therefore an urgent need for more efficient gas separation technologies, such as those potentially offered by advanced solid adsorbents. Here we show that diamine-appended metal-organic frameworks can behave as 'phase-change' adsorbents, with unusual step-shaped CO2 adsorption isotherms that shift markedly with temperature. Results from spectroscopic, diffraction and computational studies show that the origin of the sharp adsorption step is an unprecedented cooperative process in which, above a metal-dependent threshold pressure, CO2 molecules insert into metal-amine bonds, inducing a reorganization of the amines into well-ordered chains of ammonium carbamate. As a consequence, large CO2 separation capacities can be achieved with small temperature swings, and regeneration energies appreciably lower than achievable with state-of-the-art aqueous amine solutions become feasible. The results provide a mechanistic framework for designing highly efficient adsorbents for removing CO2 from various gas mixtures, and yield insights into the conservation of Mg(2+) within the ribulose-1,5-bisphosphate carboxylase/oxygenase family of enzymes.
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            Evaluating metal–organic frameworks for natural gas storage

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              Highly controlled acetylene accommodation in a metal–organic microporous material

              Metal-organic microporous materials (MOMs) have attracted wide scientific attention owing to their unusual structure and properties, as well as commercial interest due to their potential applications in storage, separation and heterogeneous catalysis. One of the advantages of MOMs compared to other microporous materials, such as activated carbons, is their ability to exhibit a variety of pore surface properties such as hydrophilicity and chirality, as a result of the controlled incorporation of organic functional groups into the pore walls. This capability means that the pore surfaces of MOMs could be designed to adsorb specific molecules; but few design strategies for the adsorption of small molecules have been established so far. Here we report high levels of selective sorption of acetylene molecules as compared to a very similar molecule, carbon dioxide, onto the functionalized surface of a MOM. The acetylene molecules are held at a periodic distance from one another by hydrogen bonding between two non-coordinated oxygen atoms in the nanoscale pore wall of the MOM and the two hydrogen atoms of the acetylene molecule. This permits the stable storage of acetylene at a density 200 times the safe compression limit of free acetylene at room temperature.
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                Author and article information

                Journal
                GRCHFJ
                Green Chemistry
                Green Chem.
                Royal Society of Chemistry (RSC)
                1463-9262
                1463-9270
                2016
                2016
                : 18
                : 7
                : 2047-2055
                Affiliations
                [1 ]School of Biology
                [2 ]Chemistry and Material Science
                [3 ]East China University of Technology
                [4 ]Nanchang
                [5 ]China
                [6 ]State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics
                [7 ]Wuhan Institute of Physics and Mathematics
                [8 ]The Chinese Academy of Sciences
                [9 ]Wuhan 430071
                Article
                10.1039/C5GC02182K
                3197fd57-a3c2-4452-900c-043e50c8cf48
                © 2016
                History

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