Synthesis and Structures of Triple-Decker Complexes with a Bridging Tetramethylcyclopentadienyl Ligand
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文摘
New triple-decker complexes with bridging tetramethylcyclopentadienyl ligands were synthesized by the reaction of electrophilic metal fragments with octamethylferrocene, Cp鈥?sub>2Fe (Cp鈥?= C5Me4H). The reaction of coordinatively unsaturated ruthenium cations [(C5R5)Ru]+ (R = H, CH3) with Cp鈥?sub>2Fe afforded purple-colored heterometallic triple-decker complexes [(C5R5)Ru(渭-Cp鈥?FeCp鈥瞉+ by direct electrophilic addition. Surprisingly, the analogous reaction with the coordinatively unsaturated manganese cation [Mn(CO)3]+ and Cp鈥?sub>2Fe produced a blue homometallic triple-decker complex, [Cp鈥睩e(渭-Cp鈥?FeCp鈥瞉+, by ring abstraction and subsequent addition of the newly generated cation [Cp鈥睩e]+ to an equivalent of Cp鈥?sub>2Fe. Three air-stable triple-decker complexes, [Cp鈥睩e(渭-Cp鈥?FeCp鈥瞉+ (2), [CpRu(渭-Cp鈥?FeCp鈥瞉+ (3), and [Cp*Ru(渭-Cp鈥?FeCp鈥瞉+ (4), have been characterized by NMR spectroscopy, elemental analysis, and single-crystal X-ray diffraction.

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