The chiral PCp-substituted phosphaferrocene 7 was prepared from the dimeric
iron carbonyl complex [PCpFe(Co)(2)](2) (5) and t-butylphosphole (PCp=pine
ne-fused cyclopentadienyl). In 7, the PCp ligand is coordinated to the iron
atom via its exO-side as shown by X-ray crystallography. Formylation of th
e sandwich complex 7 leads to a mixture of the diastereomeric aldehydes 10a
,b in an approximate ratio of 2:1. As a side-product of the synthesis of 7,
the homoleptic ferrocene (PCp)(2)Fe (8) was obtained by a ring ligand tran
sfer reaction. Complex 8 is formed as a single C-2-symmetrical isomer. (C)
1999 Published by Elsevier Science Ltd. All rights reserved.