The first nine-membered triphosphorus macrocycles based on an o-benzobis(et
hane-1,2-diyl) core have been prepared in high yield by the coupling of 1,2
-diphosphinobenzene with trivinylphosphine on a cationic (eta(5)-pentamethy
lcylopentadienyl)iron(II) template. Hydrogenation of the vinyl function fol
lowed by alkylation of the secondary phosphines gives the coordinated triet
hyl macrocycle, which has been structurally characterized.