“…5,6 The vast number of studies on AEMs based on different aromatic polymer backbones, including polyethers, polysulfones, polyphenylenes, polybenzimidazoles, etc., has shown that aryl ether links are sensitive to hydrolysis under alkaline conditions, especially if this reaction is activated by nearby electron-withdrawing groups such as sulfone links. [9][10][11][12][13][14][15][16][17][18][19][20] Hence, AEMs based on ether-free aromatic backbones, such as polyphenylenes, 9,[21][22][23] poly(arylene alkylene)s [24][25][26][27][28][29][30][31][32] and sterically protected polyimidazoliums, [33][34][35][36] as well as on aliphatic backbones such as poly(diallyldialkyl ammonium) 37 and polynorbornenes, 38,39 have shown excellent alkaline stability.…”