Treatment of zirconacyclopentadienes with two equiv of iodine in THF i
n the presence of 1.0 equiv of CuCl gave diiododienes in good to high
yields without formation of monoiododienes. This is in sharp contrast
to the case without CuCl which afforded monoiododienes as major produc
ts. For zirconacyclopentenes. CuCl was also effective but the use of I
Cl was more practical. When zirconacyclopentenes were treated with 2 e
quiv of ICl, only diiodination products were formed. Preparation of si
lacyclopentadienes or spiro compounds using the diidodienes was demons
trated. (C) 1997 Elsevier Science Ltd.