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      Rapid microwave-assisted synthesis of hybrid zeolitic–imidazolate frameworks with mixed metals and mixed linkers

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          Abstract

          Herein we report a new microwave-assisted synthetic strategy to rapidly prepare hybrid zeolitic–imidazolate frameworks (ZIFs): ZIFs with mixed metal centers and/or mixed linkers.

          Abstract

          Herein we report a new microwave-assisted synthetic strategy to rapidly prepare hybrid zeolitic–imidazolate frameworks (ZIFs): ZIFs with mixed metal centers and/or mixed linkers. The microwave-based method significantly shortens synthesis time, produces a higher yield, substantially reduces the amounts of ligands, and eliminates the use of deprotonating agents. The X-ray diffraction pattern reveals that mixed metal CoZn–ZIF-8 ( i.e., ZIF-8 with both Co and Zn centers) maintains the sodalite (SOD) zeolitic topology from the ZIF-8 parent. Elemental mapping using energy-dispersive X-ray spectroscopy (EDS) and electronic/geometric information obtained from X-ray absorption spectroscopy (XAS) confirm the uniform distribution of tetrahedral Co and Zn metal centers within the same framework of the mixed-metal ZIF. The metal to nitrogen (M–N) stretching frequencies of IR bands were observed to be systematically blue-shifted as the Co/Zn ratio in the mixed metal ZIF increases. Furthermore, for the first time, a hybrid ZIF with both mixed metal centers (Co and Zn) and mixed linkers (2-methylimidazolate and benzimidazolate) was prepared through one-step microwave synthesis. Finally, mixed metal CoZn–ZIF-8 with a Co/Zn ratio of ∼1 was grown as membranes on porous α-Al 2O 3 supports, showing a higher propylene/propane separation factor (∼120) when compared to pure Zn–ZIF-8 membranes (∼63) prepared by a similar method.

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          Metal-organic framework materials as chemical sensors.

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            Dramatic tuning of carbon dioxide uptake via metal substitution in a coordination polymer with cylindrical pores.

            A series of four isostructural microporous coordination polymers (MCPs) differing in metal composition is demonstrated to exhibit exceptional uptake of CO2 at low pressures and ambient temperature. These conditions are particularly relevant for capture of flue gas from coal-fired power plants. A magnesium-based material is presented that is the highest surface area magnesium MCP yet reported and displays ultrahigh affinity based on heat of adsorption for CO2. This study demonstrates that physisorptive materials can achieve affinities and capacities competitive with amine sorbents while greatly reducing the energy cost associated with regeneration.
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              Rapid synthesis of zeolitic imidazolate framework-8 (ZIF-8) nanocrystals in an aqueous system

              We report here the first example of ZIF materials synthesized in aqueous solution. The synthesis was performed at room temperature and typically took several minutes compared to hours and days in non-aqueous conditions. The obtained product were ZIF-8 nanocrystals having size of ~85 nm and showed excellent thermal, hydrothermal and solvothermal stabilities.
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                Author and article information

                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2017
                2017
                : 5
                : 13
                : 6090-6099
                Affiliations
                [1 ]Artie McFerrin Department of Chemical Engineering
                [2 ]Texas A&M University
                [3 ]College Station
                [4 ]USA
                [5 ]Department of Chemistry
                [6 ]Kyungpook National University
                [7 ]Taegu 41566
                [8 ]Korea
                [9 ]Department of Applied Chemistry
                [10 ]Andong National University
                [11 ]Andong 36729
                [12 ]Department of Materials Science and Engineering
                Article
                10.1039/C6TA11170J
                3540bcc0-d6b4-4731-8809-a9f16c2fba72
                © 2017
                History

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