Structures and reactivity of doubly-bridged dicyclopentadienyl dinuclear iron complexes

Abstract

The molecular structure of the doubly-bridged bis(cyclopentadienyl) diiron complex [(η5-C5H3)2(SiMe2)2]Fe2(CO)2(μ-CO)2 (1b) was determined, and compared with that of the other analogue [(η5-C5H3)2(CMe2)(SiMe2)]Fe2(CO)4 (1a). The former involves two bridging and two terminal carbonyls, and a normal Fe–Fe bond distance, while the latter contains all-terminal carbonyls and a longer than normal Fe–Fe bond distance. The possible reason for different coordination modes is discussed. Complexes (1a–b) react with I2 to give the corresponding diiodo products [(η5-C5H3)2(EMe2)(SiMe2)]Fe2(CO)4I2 (E=C, 2a; E=Si, 2b) and with phenylacetylene to give the bridging μ-CCHPh products [(η5-C5H3)2(EMe2)(SiMe2)]Fe2(CO)2(μ-CO)(μ-CCHPh) (3a–b). Reaction of 1a with Na/Hg, then with MeI yields the unexpected desilylated product [(η5-C5H4)2(CMe2)][Fe(CO)2Me]2 (5a). Reaction of 1b with LiBHEt3 affords the bridging methylene product [(η5-C5H3)2(SiMe2)2]Fe2(CO)2(μ-CO)(μ-CH2) (6b). The molecular structures of 2a and 3b were also determined by X-ray diffraction.