In this report we describe a very convenient synthetic method for the preparation in high yields and purity of cyclic [N3P3(OCH2CF3)6] and [N3P3(OC6H4R)6] (R = Br, CN, CHO, COC6H5, COCH3, H, OCH3), and polymeric [NP(OC6H4R)2]n (R = Br, CHO, COC6H5, H, But) phosphazenes from the direct reaction of the trimer [N3P3Cl6] or the high polymer [NPCl2]n and the alcohol HOCH2CF3 or the para‐substituted phenols HOC6H4R, using Cs2CO3 as proton abstractor and acetone or tetrahydrofuran as solvent.
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Carriedo et al. (1997) studied this question.
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