Polysulfones carrying benzoyl(difluoromethylenephosphonic acid) side chains were prepared and investigated for use as proton‐conducting fuel‐cell membranes. In the first step, polysulfones were lithiated and reacted with methyl iodobenzoates to prepare p ‐ and o ‐iodobenzoyl polysulfones. Next, the phosphonated polysulfones were prepared via CuBr‐mediated cross‐coupling reactions between the iodinated polymer and [(diethoxyphosphinyl)difluoromethyl]zinc bromide. Finally, dealkylation with bromotrimethylsilane afforded highly acidic CF 2 PO 3 H 2 derivatives. The replacement of the iodine atoms by CF 2 PO 3 Et 2 units was almost quantitative in the case of o ‐iodobenzoyl polysulfone. Membranes based on ionomers having 0.90 mmol of phosphonic acid units/g of dry polymer took up 6 wt % water when immersed at room temperature, and conductivities up to 5 mS cm −1 at 100 °C were recorded. This level of conductivity was comparable to that reached by a membrane based on a sulfonated polysulfone having 0.86 mmol of sulfonic acid/g of dry polymer. Thermogravimetry revealed that the arylCF 2 PO 3 H 2 arrangement decomposed at approximately 230 °C via cleavage of the CP bond.
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Lafitte et al. (2006) studied this question.
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