Two Solvent-Induced In(III)-Based Metal-Organic Frameworks with Controllable Topology Performing High-Efficiency Separation of C 2 H 2 /CH 4 and CO 2 /CH 4 .

For pure acetylene manufacturing and natural gas purification, the development of porous materials displaying highly selective C 2 H 2 /CH 4 and CO 2 /CH 4 separation is greatly important but remains a major challenge. In this work, a plausible strategy involving solvent-induced effects and using the flexibility of the ligand conformation to make two In(III) metal-organic frameworks (MOFs) is developed, showing topological diversity and different stability. The X-shaped tetracarboxylic ligand H 4 TPTA ([1,1':3',1″-terphenyl]-4,4',4″,6'-tetracarboxylic acid) was selected to construct two new heteroid In MOFs, namely, {[CH 3 NH 3 ][In(TPTA)]·2(NMF)} (MOF 1) and {[In 2 (TPTA)(OH) 2 ]·2(H 2 O)·(DMF)} (MOF 2). MOF 1 is a (4, 4)-connected net showing a pts topology with a large channel that is not conducive to fine gas separation. By contrast, with the reduction of SBU from uninucleated In to an {In-OH-In} n chain, MOF 2 has a (4, 6)-connected net with the fsc topology with an ∼5 Å suitable micropore to confine matching small gas. The permanent porosity of MOF 2 leads to the preferential adsorption of C 2 H 2 over CO 2 with superior C 2 H 2 /CH 4 (332.3) and CO 2 /CH 4 (31.2) separation selectivities. Meanwhile, the cycling dynamic breakthrough experiments showed that the high-purity C 2 H 2 (>99.8%) capture capacities of MOF 2 were >1.92 mmol g -1 from a binary C 2 H 2 /CH 4 mixture, and its separation factor reached 10.