The reaction of 2,3,4,5‐tetramethylphospholylpotassium [C4Me4PK] with [LnCl3(THF)x] (Ln = Nd, Sm) in a 2:1 ratio gave unsolvated ate complexes of the formula [(C4Me4P)2LnCl2K]. Crystallisation of the samarium complex from ether afforded a polymeric ether solvate: {[(η5‐C4Me4P)Sm(μ3‐Cl)2(μ:η5,η1‐C4Me4P)K(Et2O)]∞}, which was characterised by X‐ray crystallography. Reaction of [(C4Me4P)2LnCl2K] with [LiCH(SiMe3)2] in toluene gave the alkyl complexes [(C4Me4P)2LnCH(SiMe3)2]; these complexes were most efficiently prepared from [LnCl3(THF)x], [KC4Me4P] and [LiCH(SiMe3)2] in a one‐pot procedure. Reaction of [(C4Me4P)2LnCH(SiMe3)2] with molecular hydrogen gave [(C4Me4P)2NdH], when Ln = Nd, whereas, when Ln = Sm, reduction occurred and the already known [(C4Me4P)2Sm] was isolated instead.
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