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Organoactinide complexes of the type Cp* 2 AcR 2 (Ac = Th, U) catalyze the intermolecular hydroamination of terminal alkynes with aliphatic amines. The regioselectivity of the products can be tuned by the alkyne and the metal. Mechanistic studies shows that the rate-limiting step is the formation of an actinide imido complex. For thorium, the imido intermediate has been characterized by standard techniques, including X-ray diffraction.
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Haskel et al. (1996) studied this question.
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