“…A convenient approach used to introduce phosphonic acid groups along a polymer chain consists in the chemical-modification of high molecular weight pre-existing polymers. In this respect, different aromatic and heterocyclic polymer structures have been investigated, such as (poly(phosphazene)s [11][12][13][14] , poly(oxadiazoles)s [15] , poly(paraphenylene)s [16] , poly(benzimidazole) [17] , poly(diimidazopyridine)s [18] and the most extensively studied poly(aryl ether)s. Phosphonic acid groups can be incorporated by different chemical reactions (Arbusov or Michaelis-Arbusov reaction [19] , lithiation and direct phosphonation [20] , reaction with a phosphonate containing reactant [21] or a iodobenzoyl reactant [22] , by nickel-catalyzed [23,24] or palladium catalysed phosphonation [25][26][27] , N-alkylation [28] or even by polymerization of vinylphosphonic side-chains [29] ….). However, due to harsh reaction conditions (long reaction times, high temperature and low yields), such post-modifications usually induce some undesirable chain breaking or cross-linking.…”