cis-Trihydrogen cyclotriphosphazenates—acidic anions in strongly basic media

G.T. Lawson, F. Rivals, M. Tascher, Chacko Jacob, J.F. Bickley, Alexander Steiner

Chemical Communications · 2000 · 31 citations · 5 references

Concepts

Abstract

Exclusively cis-protonation occurs at axial N-atoms of chair shaped P3N9 ring cores in the protolysis of the lithium salt of hexaanionic cyclotriphosphazenate [(CyN)6P3N3]6− with three equivalents of butan-1-ol and cis-deprotonation takes place at the hexaprotic cyclotriphosphazene (PhNH)6P3N3 with three equivalents of BunLi, respectively, yielding both times lithium salts of cis-trihydrogen cyclotriphosphazenates [(RNH)3(RN)3P3N3]3− .

References

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