Reactions of H3PO4 forming polymers. Apparently simple reactions leading to sophisticated structures and applications

Abstract Natural phosphorus containing polymers play crucial role in living organisms. The precursor for polymeric phosphates is phosphoric acid (H 3 PO 4 ), although chemical or enzymatic routes to these polymers are based on phosphoric acid derivatives rather than the free acid. In this review mostly reactions of H 3 PO 4 and its precursors, leading to oligomeric or polymeric poly(alkylene phosphates) are described, based mainly on the authors’ work, since attempts to prepare the corresponding polymers using H 3 PO 4 have been originated and conducted in our group. These results are compared with the work of other authors using the anhydride of H 3 PO 4 (P 4 O 10 ). Thus, as an example, phosphorylation of monomethyl ether of poly(ethylene glycol) is described in detail showing that the pure monoester free of any side products can be prepared using either H 3 PO 4 or its dimer (pyrophosphoric acid). Further discussion is related to reactions of H 3 PO 4 and preformed pyrophosphoric acid with di- or trifunctional alcohols or diepoxides. Polycondensation with ethylene glycol, glycerol as well as polyaddition with several diepoxy monomers lead to highly branched polymeric products, converted eventually into polymeric gels. The hydrolytic stability of poly(alkylene phosphates) and the hydrolysis rates of tri-, di-, and monoesters are discussed. For example, gels may be partially hydrolyzed, due to the much higher hydrolysis rate of triesters (branching points in gels) than di- and monoesters. Some applications of poly(alkylene phosphates) (e.g., as liquid membranes or polymer–inorganic hybrids) are described, stressing that simple phosphorylation products of ethylene glycol or glycerol could be advantageously compared in formation of hybrids with more sophisticated dihydrophilic block copolymers.