Ether-free polyfluorenes tethered with quinuclidinium cations as hydroxide exchange membranes

We report on aryl ether-free 2,7-diphenylfluorene-based copolymers tethered with quinuclidinium (Qui) cations via hexyl spacers, prepared through superacid catalyzed Friedel-Crafts polycondensation and quaternization reactions. The 2,7-diphenylfluorene monomers were synthesised by Suzuki coupling and were employed to increase polymer backbone stiffness. Corresponding copolymers and anion-exchange membranes (AEMs) tethered with piperidinium (Pip) and trimethylalkyl ammonium (TMA) cations were prepared as reference materials. At a given water content, the AEM functionalized with Qui cations was the most efficient hydroxide conductor and its OH- conductivity reached 100 mS cm(-1) at 80 degrees C at an ion exchange capacity of 2.0 mequiv. g(-1). Moreover, this membrane showed the highest thermal and alkaline stability in the series. H-1 NMR analysis of AEMs stored in 2 M aq. NaOH at 90 degrees C over 672 h revealed the complete absence of any ring-opening beta-elimination in the bicyclic cage-like Qui structure, and less than 2% beta-elimination in the hexyl spacer. In contrast, the Pip cations were found to degrade via beta-elimination in both the monocyclic ring structure and the hexyl spacer. Results on the Pip-modified AEM implied that a beta-hydrogen in the linear alkyl spacer chain was approximately 4 times more vulnerable to elimination than a beta-hydrogen in the 6-membered ring. In addition, all the cations degraded via substitution reactions to some degree, and the total loss of Qui, Pip and TMA cations over the period was estimated to be 4, 12 and 9%, respectively. The overall findings demonstrate that the combination of aryl ether-free backbone polymers and Qui cations results in durable and high-performance AEMs suitable for use in alkaline electrochemical energy conversion and storage devices.