Abstract

We synthesized a series of rigid ladder-type diamines from readily available bromoanilines and norbornadiene in one step using facile catalytic arene–norbornene annulation (CANAL). Polycondensation of CANAL ladder diamines with 4,4′-(hexafluoroisopropylidene)diphthalic anhydride led to a series of microporous polyimides with different degrees of rotational freedom around the imide linkages. CANAL-PIs exhibited good solubility in a wide range of organic solvents, high thermal stability with decomposition temperature above 450 °C, high Brunauer–Emmett–Teller surface areas of ∼200–530 m2 g–1, and abundant micropore volume with variable pore size distributions. Mechanically robust membranes can be easily formed from CANAL-PIs and gave high gas permeabilities and moderate gas-pair selectivities. CANAL-PIs had higher permeability than and similar permselectivity to analogous PIs synthesized from Troger’s base and carbocyclic Troger’s base diamines under identical test conditions. CANAL-PIs also exhibited relati...

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call