Treatment of Me3NHF with I equiv of [(Me3Si)(2)C5H3](3)Ln or (C5H5)(3)
Ln in THF gave [{-(Me3Si)(2)C5H3}(2)LnF](2) (Ln = La (1), Nd (2), Sm (
3), Gd (4)) or [(C5H5)(2)LnF(THF)](2) (Ln = Y (5), Yb (6)) in moderate
to good yield. All of them were fully characterized by elemental anal
yses, spectroscopy, and X-ray analyses. Compound 3 reacted with Na, Al
Cl3, (C6H5)(3)-SiOH, and 2,6-(Pr2C6H3OH)-C-i to form [(Me3Si)(2)C5H3](
2)Sm(THF), [{(Me3Si)(2)C5H3}(2)SmCl](2), [(C6H5)(3)SiO](3)Sm(THF)(3) (
7), and [2,6-(Pr2C6H3O)-C-i](3)Sm(THF)(3) (8), respectively. The molec
ular structures of [{(Me3Si)(2)C5H3}(2)SmCl](2), 7, and 8 were confirm
ed by X-ray diffraction study. The 3/NaH system can convert C6H5Br int
o C6H6 in 32% yield.