2009
DOI: 10.1021/ja906302t
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Multiroute Synthesis of Porous Anionic Frameworks and Size-Tunable Extraframework Organic Cation-Controlled Gas Sorption Properties

Abstract: Under diverse and dramatically different chemical environments, including organic solvents, an ionic liquid, and a deep eutectic solvent, a series of porous anionic framework materials that contain size-tunable, ion-exchangeable extraframework organic cations have been prepared. Even though a large fraction of the pore space is occupied with charge-balancing cations, some of these materials exhibit a very high gas uptake capacity (e.g., 70.6 cm(3)/g for CO(2) at 1 atm and 273 K), suggesting that the charged an… Show more

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Cited by 244 publications
(131 citation statements)
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“…MOFs have emerged as promising materials for the selective capture and utilization of CO2.To date, research efforts have focused on generating open metal sites or incorporating ligands functionalized with Lewis basic groups; both strategies have shown to be promising for the selective capture of CO2 over other gasses such as N2 (flue gas) or CH4 (natural gas). [1,20,28,[175][176][177][178][179][180][181][182][183] Bio-ligands can be decorated with multiple groups which can be incorporated into bio-MOFs which can be promising candidates for the selective capture of CO2.…”
Section: Co2 Capturementioning
confidence: 99%
“…MOFs have emerged as promising materials for the selective capture and utilization of CO2.To date, research efforts have focused on generating open metal sites or incorporating ligands functionalized with Lewis basic groups; both strategies have shown to be promising for the selective capture of CO2 over other gasses such as N2 (flue gas) or CH4 (natural gas). [1,20,28,[175][176][177][178][179][180][181][182][183] Bio-ligands can be decorated with multiple groups which can be incorporated into bio-MOFs which can be promising candidates for the selective capture of CO2.…”
Section: Co2 Capturementioning
confidence: 99%
“…The pores within porous MOFs, particularly those within isoreticular MOFs whose structures are pre-determined by the coordination geometries of the secondary building blocks, can be systematically modified by changing the organic bridging linkers and controlling the framework interpenetration [2][3][4][5] . Furthermore, the pore surfaces of porous MOFs can be functionalized by the immobilization of different recognition sites, such as open metal sites, Lewis basic/acidic sites and chiral pockets, to direct the recognition of small molecules [6][7][8][9][10][11][12][13][14] . Systematically tuning micropores can achieve size-specific encapsulation of small gas molecules, and immobilization of functional sites enables varying substrate interactions: microporous MOF materials have emerged as promising microporous media for the recognition and separation of small molecules [15][16][17][18][19][20][21][22][23][24][25][26][27][28][29][30][31][32] .…”
mentioning
confidence: 99%
“…This is among the highest reported CO 2 uptakes for any MOPs at 298 K and slightly higher than the alcohol-functionalized phenolic resin network POF1B (2.14 mmol g −1 ) [36]. Amines are important functional groups that are usually used to enhance the isosteric heat, selectivity, and uptake capacity of CO 2 in the materials [37,38]. However, only few MOPs containing -NH 2 groups have been synthesized [39].…”
Section: Hypercrosslinked Organic Polymersmentioning
confidence: 84%