The effect of varying the bidentate ligand upon the reaction of unconj
ugated dienes with. (R2P(CH2)(n)PR2)Fe-0 species has been investigated
. Depending upon the nature of the substituents at phosphorus and upon
the length of the hydrocarbon chain joining the phosphorus atoms, eit
her (eta(2):eta(2)-diene)Fe(R2P(CH2)(n)PR2) or (eta(5)-dienyl)Fe(R2P(C
H2)(n)PR2)H species are formed. Extended Huckel MO-calculations have b
een used to assess the importance of electronic factors in influencing
the course of reaction, and it can be shown that distortion of the te
trahedral geometry of the (diene)Fe species causes a destabilization.