摘要:
The reaction of [W(CO)(5){C(NEt2)Ph}] (3) with [PdClR(SMe2)](2) (R = Me, Ph) occurs with transfer of carbene and carbonyl groups to give [PdCl{C(O)R)} {C(NEt2)Ph}](2) (R = Me, 4; R = Ph, 5). When the reaction is monitored for R = Me, only [PdCl(COMe)(SMe2)](2) and the final carbene 4 are observed, suggesting that the transfer and insertion of the carbonyl group are faster than the carbene transmetalation. Although CO insertion into M-X bonds is thermodynamically excluded in many systems (e.g., in M-halogen and M-C6F5 bonds), this study warns of the fact that CO is easily available when [M(CO)(5)(carbene)] complexes are used as carbene sources, whether for stoichiometric or for catalytic reactions. This CO could react with the intermediates or the products in these reactions.