Abstract
The mixed amide complexes [U(NEt 2) 2(N{SiMe 3} 2) 2] and [U(η-C 8H 8)(NEt 2)(N{SiMe 3} 2)] reacted in tetrahydrofuran (THF) with NEt 3HBPh 4 to give the cations [U(NEt 2)(N{SiMe 3} 2) 2(THF) x ] + and [U(η-C 8H 8)(N{SiMe 3} 2)(THF) x ] +. The bis(trimethylsilyl) amide complex [U(η-C 5Me 5) 2(N{SiMe 3} 2)] was inert towards NEt 3HBPh 4 but its treatment with NH 4BPh 4 afforded the cationic uranium(III) compound [U(η-C 5Me 5) 2(THF) 2][BPh 4], the crystal structure of which has been determined.
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