“…11,18,19 Particular emphasis was placed on aromatic polymer backbones due to the inherent thermochemical resilience associated with sp 2 linkages (aryl-aryl and aryl-heteroatom) compared to labile sp 3 -based linkages (methylene and methenyl) found in early sulfonated polystyrene research. 20,21 Diverse synthetic strategies not limited by perfluorinated reagents led to numerous classes of proton-conducting sulfonated polyarylenes with differing backbone architectures: poly(arylene ether ketone)s, 11,22,14 poly(arylene ether sulfone)s, 11,22,23,24 poly(benzimidazole)s, 11,14,25 poly(arylene sulfone sulfide)s, 26,18,27,28 , and poly(phenylene)s. 29,30,31,32 A persistent criticism of hydrocarbon-based polymer membranes, however, is that they lack the oxidative stability of their PFSA counterparts; research into 4 | P a g e hydrocarbon-based PEMS eventually dwindled, caused in-part by the emerging interest and available funding for the discovery of anion exchange membranes.…”